Scientific Program

Conference Series Ltd invites all the participants across the globe to attend 5th Global Nephrologists Annual Meeting Valencia, Spain.

Day 2 :

Keynote Forum

Bruce Hendry

The Renal Association, UK

Keynote: T-type calcium channel inhibition: A novel therapy in renal disease

Time : 10:00-10:40

Conference Series Nephrologists 2016 International Conference Keynote Speaker Bruce Hendry photo
Biography:

Bruce Hendry is President of the UK Renal Association and Emeritus Professor of Renal Medicine at Kings College London. He graduated in medicine from the University of Oxford and received his PhD in Biophysics from the University of Cambridge. His major research interests are in the cell and molecular biology of progressive renal fibrosis and in the design of novel therapeutic approaches. His current work is focused on the study of new approaches to the problem of aberrant renal cell proliferation leading to fibrosis; this work includes the use of antisense and small molecule strategies. Recent work has examined the role of antisense as therapy in renal fibrosis and ADPKD and the targeting of T-type calcium channels in glomerular disease. He has clinical research interests in diabetic nephropathy, HIV and the kidney and in polycystic kidney disease.

Abstract:

There is a lack of effective therapeutic options for patients with chronic kidney disease (CKD) related to IgA nephropathy and proteinuric nephropathies. Treatment with inhibitors of the renin angiotensin system (RAS) is standard but residual risk of progression of CKD remains high. In this context this lecture will explore an innovative strategy for therapy in CKD targeting T-type calcium channels. T-type calcium channels (TTCC) are closely related to the more familiar L-type calcium channels (LTCC). We have extended work on the role of TTCC in smooth muscle proliferation by demonstrating that TTCC have a role in mesangial cell function. TTCC are also expression in the efferent arteriole and TTCC inhibition reduces glomerular capillary pressure. In vitro human and rat mesangial cell proliferation is dependent on TTCC and not LTCC. Moreover, in models of glomerular cell proliferation, inhibition of TTCC reduces glomerular damage, reduces cell proliferation and inhibits monocyte infiltration, with improved renal function. In parallel with this work a series of studies in Japan has demonstrated that TTCC inhibition reduces glomerular proteinuria in animal studies and in small clinical studies of diabetic nephropathy. Taken together these studies provide the basis for optimism about TTCC inhibition as a new therapy in renal diseases where mesangial cell proliferation is coupled with significant proteinuria. Such diseases include IgA Nephropathy, Diabetic Nephropathy and lupus nephritis.

Break: Coffee Break 10:40-11:00 @ Foyer

Keynote Forum

Kveta Blahova

Charles University in Prague, Czech Republic

Keynote: D+ hemolytic-uremic syndrome: A systematic review

Time : 11:00-11:40

Conference Series Nephrologists 2016 International Conference Keynote Speaker Kveta Blahova photo
Biography:

KvÄ›ta Bláhová is an Associate Professor in the Department of Pediatrics at Charles University and University Hospital Motol in Prague. She received many awards. She has membership in prestigious European societies. She has published numerous papers in reputed journals.

Abstract:

Hemolytic-uremic syndrome (HUS) is the most common cause of acute renal failure in children below 3 years of age. It is defined by a triad of symptoms which associates hemolytic anemia with fragmented erythrocytes, thrombocytopenia and acute renal failure. Three types of HUS can be distinguished: typical HUS also called diarrhoea-associated (D+) HUS, atypical HUS (a-HUS/ D-HUS) and secondary HUS (drug induced, C+HUS, in patients receiving marrow transplantation, post partum etc.). The common event among these entities appears to be vascular endothelial cell injury, which induces mechanical destruction of erythrocytes, activation of platelet aggregation and local intravascular coagulation, especially in the renal microvasculature. D+ HUS represents nearly 90% of HUS in children. Evidence of exposure to Shiga toxin (STx 1, 2) producing Escherichia coli (STEC) - also called Enterohemorrhagic Escherichia coli (EHEC) - has been demonstrates in many countries in about 85% of cases. Recently serotypes O157:H7, O26 are the most frequent. Early and accurate supportive treatment and early start of dialysis is the major importance and allows a current mortality rate below 5%. Vital prognosis is compromised in cases with CNS or multi-visceral involvement. After 15 years or more of apparent recovery, 20% to 60% of patients have residual renal symptoms, with up to 20% having chronic renal insufficiency (CRI) or end-stage renal disease (ESRD). Atypical HUS represents less than 10% of HUS in children. Some of these cases (familial) are associated with low C3 levels, hereditary deficiency of factor H or with mutations in factor H gene. The deficiency of von Wille brand factor cleaving protease deficiency in D+HUS, as reported in adults with thrombotic thrombocytopenic purpura (TTP), is not present.

Keynote Forum

Hartmut H-J Schmidt

Universitätsklinikum Münster, Germany

Keynote: Challenges In Dialysis In Liver Associated Renal Failure

Time : 09:00-09:40

Conference Series Nephrologists 2016 International Conference Keynote Speaker Hartmut H-J Schmidt photo
Biography:

Prof. Dr. med. Hartmut Schmidt has completed his MD at the age of 25 years from Medical University of Hannover in Germany. He received postdoctoral training in gastroenterology at Medical University of Hannover, NIH (Bethesda), Charité (Berlin), and Universitätsklinikum Münster. Since 2010 he serves as director of Klinik für Transplantationsmedizin at Universitätsklinikum Münster. He has published more than 125 original articles. rn

Abstract:

Hepatorenal syndrome (HRS) is defined as a potentially reversible kidney failure in patients with liver cirrhosis, acute liver failure or steatohepatitis. Currently, classification is in discussion. Due to its very high short-term mortality, HRS is a life-threatening condition that has to be diagnosed and treated rapidly in order to improve the patient’s clinical outcome. The pathogenesis of HRS comprises portal hypertension with impaired kidney perfusion by vasoconstrictory endogenous mediators (including vasopressin, noradrenalin and renin / angiotensin), leading to oliguria, very low renal sodium excretion (<10 mmol/l) and water retention. Further diagnostic criteria include but are not restricted to creatinine serum concentrations rising above 1.5 mg/dL and clinical exclusion of other causes of acute kidney failure, structural kidney disease, shock, dehydration, and nephrotoxic medication. Systemic infections are potentially predisposing causes in some patients with HRS. Among the different therapies available, there is a discussion on different therapeutic approaches, the timing of dialysis, and the type of dialysis. Since there is little information in the literature in respect to superiority of different dialysis methods, the concepts of hemodialysis versus albumin dialysis will be compared. Furthermore, among different variables blood pressure and coagulation as important factors will be discussed.

  • Dialysis
    Kidney Transplantation
    Acute Kidney Injury
Location: Conference Hall

Session Introduction

Joachim Struck

Sphingo Tec GmbH, Germany

Title: Pro-enkephalin (Penkid): A novel plasma biomarker to assess renal impairment

Time : 11:40-12:10

Speaker
Biography:

Joachim Struck has received his PhD in Biochemistry at the Free University Berlin and worked as Post-doctoral fellow at UMASS Amherst. He has more than 20 years experience in industrial Basic and Clinical Research in vitro diagnostics (IVDs) and is currently CRO at Sphingo Tec GmbH, a company developing innovative IVDs for improved management of acutely diseased patients and for risk prediction in non-hospitalized subjects. He has co-authored more than 150 papers in peer-reviewed journals and is co-inventor of numerous patents.

Abstract:

Enkephalins are well known as small, unstable endogenous opioid peptides. Their peripheral functions are largely unknown, not least due to the fact that their reliable measurement has not been possible so far. To overcome this problem we devised a simple immunoassay method to detect as surrogate marker a stable peptide (“penKid”), which is stoichiometrically generated from the same precursor peptide as the Enkepahlins. Reported high expression levels of both Enkephalins and their receptors in the kidney prompted us to investigate plasma levels of penKid in various clinical settings, where kidney function is impaired. In patients undergoing coronay artery bypass graft surgery (CABG) plasma penKid increased quickly, when patients developed acute kidney injury (AKI). A study employing several thousand patients in various acute disease settings (sepsis, acute myocardial infarction, acute heart failure) consistently revealed a strong correlation of plasma penKid with eGFR and showed that eGFR is the major determinant for penKid. Elevated plasma penKid also predicted developing AKI, use of renal replacement therapy (RRT) and mortality risk. Serial measurements demonstrated penKid to be a dynamic marker, as concentration changes over time improved outcome risk prediction. It is especially noteworthy that penKid levels – as opposed to other kidney biomarkers currently discussed – were not raised over healthy normal concentrations by systemic inflammation only, when kidney function was not impaired. This aspect along with the fact that penKid is determined from plasma (not urine) makes it an especially attractive novel kidney biomarker for use in critically ill patients.

Kveta Blahova

Charles University in Prague, Czech Republic

Title: Chronic peritoneal dialysis (CPD) in children of the lowest age groups

Time : 12:10-12:40

Speaker
Biography:

KvÄ›ta Bláhová is an Associate Professor in the Department of Pediatrics at Charles University and University Hospital Motol in Prague. She received many awards. She has membership in prestigious European societies. She has published numerous papers in reputed journals.

Abstract:

Chronic peritoneal dialysis (CPD) is the most common dialysis treatment modality used to treat pediatric patients with end-stage renal disease (ESRD), particularly in children less than five years of age. Advantages of CPD include a less restricted diet, treatment at home, no need for vascular access. Contraindications to CPD include specific conditions that affect the integrity of the abdominal cavity and peritoneum. Total number of patients on CPD in our center is 43 in the last 6 years (11 of them are currently active - 5 patients under 1 years of age, 8 patients under 5 years of age). The causes of kidney failure in our center include con-genital kidney anomalies 41.9%, glomerulopathies 32.6%, ischemia 7.0%, pyelonephritis/ interstitial nephritis 2.3%, other 14.3%, unknown 2.3%. CPD modalities are divided into manual and automated options. Continuous ambulatory PD (CAPD) is the manual form of CPD that provides continuous solute and fluid removal throughout the day and night. CAPD is usually used especially in small infants before reaching of sufficient volume for the function of cycler (fill volume >120-130 ml). Automated PD (APD) uses a cycler that performs mul-tiple exchanges at night. APD is used in all child patients at home (20 % with dry day - NIPD, 80 % with wet day - CCPD). The regime of CPD should be individualized to the pa-tient needs for solute transfer and removal of fluid. Main parameters of prescription are osmo-lality of the dialysis solution, fill volume, and number of exchanges. Peritoneal equilibration test (PET) should be performed in all children undergoing CPD to determine the solute trans-fer characteristics of the peritoneal membrane. Fill volume in our center is 792±220 ml/m2 (920±434 ml/m2 in control group - data from 204 centers from International Pediatric Dialysis Network database), total dialysate turnover 8832±4384 ml/m2/day (9299±4703 ml/m2/day in control group), average PD fluid glucose concentration is 1.9±0.4% (1.8±0.5% in control group). Urine output is <100 ml/m2/day in 20 % and 100-500 ml/m2/day in 40% of patients. Infectious complications of CPD include peritonitis and catheter exit site/ tunnel infections. We use a two-cuffed Tenckhoff catheter to reduce the risk of peritonitis and we recommend daily care of the exit site. The incidence of peritonitis was 1 episode of peritonitis every 91.7 months of therapy in our group of patients (34.9 months in the control group). Noninfectious complications are divided into several categories - mechanical complications due to increased intra-peritoneal pressure (hernia, fluid leak, hydrothorax), ultrafiltration failure due to rapid solute transfer/ increased lymphatic flow/ aquaporin deficiency, catheter-related complications (dialysate leakage, catheter dislocation, catheter occlusion), and nutritional and metabolic problems - protein loss, hyponatremia due to sodium loss and subsequent hypovolemia, renal osteopathy. Body mass index (BMI) at CPD initiation was -0.42±1.25 SD and -0.20 ±1.67 SD at last visit. 20% of our patients have percutaneous endoscopic gastrostomy (PEG). CPD is safe and effective method for treatment of ESRD in children of the lowest age groups. Our results are fully comparable with the data from foreign centers for PD. The most severe risk factors for mortality are pulmonary and cardiovascular diseases, infections and severe oliguria/ anuria.

Break: Lunch Break 12:40-13:40 @ Restaurant
Speaker
Biography:

Bing He received his MD from Wuhan University School of Medicine, China and PhD from Karolinska Institute, Stockholm, Sweden. He is a senior researcher at Matrix Biology, Department of Medical Biochemistry and Biophysics, Karolinska Institute, Sweden. He has published more than 50 papers in the peer-reviewed scientific journals. His major research interests include molecular genetics of diabetic nephropathy, podocyte biology and molecular control of glomerular development.

Abstract:

Proteinuria usually indicates damage to the glomerular filtration barrier. Clinically, proteinuria is the hallmark of chronic kidney disease (CKD) leading to end-stage renal disease and is also an independent risk factor for cardiovascular disease. Glomerular podocytes play a central role in establishing and maintaining the complex cellular architecture of glomeruli. Dysfunction of podocytes contributes to development of CKD. To address the molecular basis of podocyte development and function, we first validated the phenotypic marker for zebra-fish pronephric podocyte injury by assessment of pericardial edema together with loss or decline of podocyte-specific GFP expression driven by the nphs2 promoter. Using this model, we further identified a podocyte-specific enhancer motif present in the nphs2 proximal promoter as well as its binding proteins. This finding allowed us to predict genome-wide a number of genes potentially co-expressed with Nphs2. Podocin encoded by Nphs2 is a key component of the slit diaphragm protein complex and is constitutively expressed in differentiated/mature podocytes. Accordingly, the predicted genes utilizing the same regulatory element as nphs2 are implicated in controlling podocyte differentiation and maintenance. Currently, four genes (Ccnc, Meis2, Ankrd6 and Slc16a9) have shown that their enhancer motifs predicted can drive reporter expression in zebrafish podocytes and their expression is detectable in mouse glomeruli. Ankrd6 is known to be involved in inhibition of Wnt/ß-catenin signaling, coincident with the absence of Wnt signaling in mature podocytes. Knockdown of zebra-fish homolog of Ankrd6 led to defect of glomerular development associated with up-regulation of active ß-catenin. The Wnt-dependent signaling inhibitor IWR suppressed increased Wnt signal activity in zebra-fish. These data suggest that Ankrd6 is required for podocyte terminal differentiation and maturation by silencing Wnt/ß-catenin signaling. Thus zebra-fish provides an excellent avenue towards revealing fundamental signal pathways controlling glomerular development and maintenance.

Speaker
Biography:

Pearl Pai qualified from University of Aberdeen, UK and received her MD from the University of Liverpool. She is the Chief of Service (Department of Medicine) and Chief of Nephrologist at University of Hong Kong – Shenzhen Hospital, Guangdong, China. She is also the Honorary Clinical Associate Professor at the Department of Medicine, the University of Hong Kong. She was a NHS Consultant Physician and Nephrologist in Sunderland Royal Hospital and then Royal Liverpool University Hospital before she returned to Hong Kong in 2012.

Abstract:

In China, the vision and direction of the Hospital; the patients’ behavior; the way the Doctors practice and finally the management of the institutions are very different from the UK National Health Service. The University of Hong Kong – Shenzhen Hospital (HKU-SZH) is a new affiliated hospital of the HKU set in China. It is hoped that the Hospital will act as a forerunner of reform Hospital and bring China healthcare closer to international standard. An account about China healthcare, its insurance cover, the preferential reimbursement of hospital hemodialysis compared to peritoneal dialysis will be given. Nephrologists training and competency are very variable. Patients are short of accurate medical information. It is not uncommon for uremia patients to seek medical attention late. Traditional Chinese Medicine is the preferred choice. The Chinese dialysis standard of operation of procedure (SOP) based itself on international guideline such as the KDOQI yet there is insufficient pressure on its reinforcement. The objectives of the HKU-SZH emphasize in prevention, health promotion, high quality and safe service. In spite of some shortcomings, there are also some excellent examples of ingenuity and adaptability in our dialysis setting. It is only through education, promotion of mutual trust and respect and when the facts, differences and difficulties are understood that we could move forward. So far, our approaches as cited are working and yielding results and will be presented here.

Speaker
Biography:

Dhanya Mohan currently works as Specialist Senior Registrar (Nephrology) at Dubai Hospital, Dubai Health Authority; UAE. She completed her Medical graduation from Christian Medical College, Vellore, India. She won many laurels including university medals and prizes and the ‘Best Outgoing Student’ award. She completed her Post-graduation in Internal Medicine from the same institute and won the B. Braun award instituted for outstanding performance. She went on to complete her MRCP (UK) and Specialty Certificate in Nephrology, her performance gaining her a special mention in the MRCP Annual Review 2010. Her areas of interest include chronic glomerulo-nephritis, peritoneal dialysis, kidney transplantation and medical education. With a keen interest in clinical research, she has publications in peer reviewed international journals. In addition, she is a tutor at the Dubai Medical College for Girls and enjoys teaching medical students.

Abstract:

Post transplant anemia is a common occurrence in kidney transplant recipients (KTRs). Common etiologies include ineffective erythropoietin, drug related erythroid suppression, iron deficiency and infections. Parvovirus B19 infection, though rare, needs to be always considered in the work up of chronic anemia in KTRs, especially in those patients with reticulocytopenia. A 36-year-old Arab male patient underwent living unrelated donor transplantation because of end-stage-renal disease resulting from diabetic nephropathy. He received induction therapy with anti-thymocyte globulin and maintenance with prednisolone, tacrolimus and mycophenolate mofetil (MMF). Allograft function was stable with serum creatinine around 1 mg/ dl. Eighteen months after transplantation, he was detected to have anemia and leucopenia (Hb: 7.3gm/ dl, WBC: 3500/ cc). Blood film revealed microcytosis. Bicytopenia was initially attributed to mycophenolate and the dosage was reduced. Over the next four months, he had recurrent admissions with severe anemia, requiring six units of packed red cell transfusion. Hemoglobin ranged from 4.6- 5.7 gm/ dl. Reticulocyte count varied from 0.41%- 2.22%. Folic acid and B12 levels were unrevealing. CMV DNA PCR was negative. The low reticulocyte count prompted us to consider pure red cell aplasia as a cause for the anemia. Further serologic evaluation was positive for anti parvovirus B19 Ig M, and PV B19 DNA PCR in blood was positive. He received five doses of intravenous immunoglobulin, 400mg/kg body weight daily. Dose of MMF was reduced and tacrolimus level maintained between 4-6 ng/ ml. Hemoglobin improved to 10.8 gm/ dl within a month, and has stabilized at 14 gm/ dl ever since. His clinical follow–up during the subsequent two years has not shown recurrence of anemia, though PV virus levels are just above detection threshold. Parvovirus B19 is a single stranded DNA virus, which has a pronounced tropism for erythroid precursor cells. PV B19 infection is a well-known cause of pure red cell aplasia and should be included in the workup of refractory anemia in KTRs, when more common causes have been excluded. Treatment includes reduction of immunosuppression and administration of intravenous immunoglobulin in severe cases.

Hisham Hussein Imam

Minia University, Egypt

Title: Pregnancy after renal transplantation

Time : 15:10-15:40

Speaker
Biography:

Hisham Hussein Imam, MD, obtained his primary medical qualification (MBBCH) from the Faculty of Medicine Ain Shams University, Egypt, with an Honor Degree in the year 1985. He obtained his Master and Doctorate Degrees from the Faculty of Medicine, Minia University, Egypt, in the years 1991 and 1995, respectively. He passed through the different grades of University teaching posts. He worked as Demonstrator, assistant Lecturer, Lecturer, assistant Professor and was appointed as Professor of Obstetrics & Gynecology at the Faculty of Medicine, Minia University, Egypt in the year 2005. He has very wide experience in all the aspects of women health both from academic and clinical perspectives. He has a lot of researches in the armamentarium of Obstetrics and Gynecology. He also supervised many candidates in their studies for Masters and Doctorates Degrees in the field of obstetrics and Gynecology. He has also special interest in Medical Education. He is an active member of many Scientific Societies and is a Referee and a peer reviewer for many nationally and internationally recognized scientific journals.

Abstract:

Recent advances in surgical techniques and immunosuppressive therapies allowed a marked increase in successful allogeneic organ transplantation in women. Kidney transplantation is the most frequently encountered transplanted organ. Since the first successful pregnancy in a renal transplantation recipient in 1958, thousands of patients have successful pregnancies after renal transplantation. In this article we will discuss the effect of pregnancy on the allograft function. We will address a discussion of the immunosuppressive agent and their use safety during pregnancy. We will also discuss the factors that affect the course of pregnancy and the co-morbid factors that influence the maternal and fetal outcome. Finally, we will go into a comprehensive discussion of the medical and obstetric management of pregnant women after renal transplantation and how to adequately monitor a woman who got pregnant after successful allogeneic renal transplantation.

Break: Coffee Break 15:40-16:00 @ Foyer
Speaker
Biography:

Khalid Bashar is a doctor at the department of Vascular Surgery in University Hospital Limerick, Ireland.

Abstract:

Introduction: With increasing number of patients diagnosed with ESRD, arterio-venous fistula (AVF) maturation has become a major factor in improving both dialysis related outcomes and quality of life of those patients. Compared to other types of access it has been established that a functional AVF access is least likely to be associated with thrombosis, infection, hospital admissions, secondary interventions to maintain patency and death. Aim: Study of demographic factors implicated in the functional maturation of arterio-venous fistulas and also to explore any possible association between pre-operative haematological investigations and functional maturation. Methods: We performed a retrospective chart review of all patients with ESRD who were referred to the vascular service in the University Hospital of Limerick for creation of vascular access for HD. We included patients with primary AVFs and excluded those who underwent secondary procedures. Results: The overall AVF functional maturation rate in our study was 53.7% (52/97). Female gender showed significant association with non-maturation (P=0.004) and was the only predictor for non-maturation in a logistic regression model (P=0.011). Patients who had history of renal transplant (P=0.036), had relatively lower haemoglobin levels (P=0.01) or were on calcium channel blockers (P=0.001) showed better functional maturation rates. Conclusion: Female gender was found to be associated with functional non-maturation, while a history of kidney transplant, calcium channel-blocker agents and low haemoglobin levels were all associated with successful functional maturation. In view of the conflicting evidence in the literature, large prospective multi-centre registry-based studies with well-defined outcomes are needed.

Speaker
Biography:

Marwa Mounir Ismail graduated class 2008 from faculty of medicine, Alexandria University, Egypt. A master degree candidate. Working as a nephrologist in the Medical Research Institute, Alexandria University

Abstract:

Lupus nephritis develops in up to 75 % of SLE patients with 10 to 30 % progressing to ESRD. Urinary biomarkers to replace serial renal biopsies have been widely studied recently. Uromodulin, the most abundant urinary protein expressed exclusively by the TAL cells, showed its ability to elicit an inflammatory response and be a CKD biomarker. This study was conducted on 70 subjects divided as 23 SLE patients without LN, 27 SLE patients with LN and 20 control volunteers. Renal activity was assessed by SLICC Renal Activity score, positive anti-ds DNA and low complement levels. Urinary Uromodulin results showed lowest values among nephritis patients with mean 5.6 ± 3.4, followed by 9.9 ± 5.2 in SLE patients without nephritis and 12.9 ± 4.6 in the control group, with statistical significant difference (P <0.0001). Uromodulin also showed statistically significant positive correlation with eGFR (P = 0.03), while negative correlations were found with serum Creatinine, 24 hrs urinary proteins and SLICC renal activity score, with statistical significance (P = 0.001), (P = 0.000) and (P = 0.000) respectively. Thus, from the results of this study, we can conclude that decreasing urinary uromodulin levels can be a marker for renal activity in SLE patients, and a marker for CKD in absence of activity markers.

Hartmut H J Schmidt

Universitätsklinikum Münster, Germany

Title: Update on HCV therapy in renal disease and in renal transplant recipients

Time : 17:00-17:30

Speaker
Biography:

Hartmut H J Schmidt has completed his MD from Medical University of Hannover in Germany. He received Post-doctoral training in Gastroenterology at Medical University of Hannover, NIH (Bethesda), Charité (Berlin) and Universitätsklinikum Münster. Since 2010, he serves as Director of Klinik für Transplantations medizin at Universitätsklinikum Münster. He has published more than 125 original articles.

Abstract:

Hepatitis C virus (HCV) is a common infection especially in the cohort of patients with renal failure. Due to new antiviral approaches and the approval of direct-acting antiviral agents (DAA), HCV therapy has become more comfortable. Nevertheless, there are special patient groups, in whom treatment of HCV is still challenging. Due to only few data available, tolerability and efficacy of DAAs in special patient cohorts still remain unclear. Such special patient cohorts comprise HCV in patients with decompensated liver disease (Child-Pugh Class B or C), patients with chronic kidney disease and patients on waiting lists for renal/liver transplantation or those with HCV recurrence after transplantation. HCV infection in transplant recipients has been shown to be associated with increased morbidity and mortality and reduced graft survival. Successful eradication of HCV results in a better outcome concerning liver-related complications and in a better clinical outcome of these patients. In this update, the current therapeutic HCV strategies in patients with GFR < 30 ml/min and in renal transplant recipients will be discussed, but also the role of anti-HCV positive donors.

Speaker
Biography:

Ma. Eugenia Martínez is a doctoral candidate in Biochemical Engineering Sciences, focusing her thesis in Plant Biotechnology using Taraxacum as a scientific model for bioactives compounds recuperation and biomass valorization. She is currently working in the FP7 DISCO Project for bioactives production under "green chemistry" and further market commercialization

Abstract:

Currently, the most effective treatment for recurrent urinary tract infections in women is the use of antibiotics. However, limitation for this treatment is the duration and dosage of antibiotics and the resistance that bacteria develop after a long period of administration. Therefore, alternatives approaches need to be consider. The most common is the use traditional botanical remedies or preparations, in which the use of dandelion (Taraxacum sp.) has several references in treating bacterial infections. These properties have been attributed to the large number of bioactive compounds in their tissues, particularly triterpenes such as amyrin and lupeol, antioxidants and phenolics compounds. Antibacterial activity was evaluated in vitro by serial microdilution using a hexane extract from T. officinale leaves against Escherichia coli, Klebsiella pneumoniae and Proteus mirabilis as uropathogens, showing 100% inhibition at 400 mg/L for E. coli and 1600 mg/L for the other tested strains. Phytochemical analysis of plant tissue grown in vitro revealed the presence α-amyrin and lupeol both in leaves and in callus cultures, which extract would be further tested in rats. These results corroborate the folkloric use is given to the use of dandelion against bacterial infections and suggest the potential of these compounds for its potential use in the pharmaceutical industry, related to the formulation of natural products associated with improving urinary tract diseases. On the other hand, it can set the groundwork for a potential production system of these compounds for medicinal purposes, using biotechnology techniques that stimulate the synthesis and accumulation of these triterpenes into the plant cell.

Speaker
Biography:

Sevag Demirjian is the Director of Center for Critical Care Nephrology. He did his Residency in Internal Medicine and Nephrology at the Cleveland Clinic in 2004 and Internship, Cleveland Clinic in 2002. His current speciality interests are the Critical care nephrology, pre-operative risk assessment, continuous renal replacement therapy, acute kidney injury

Abstract:

Background: Hypophosphatemia is common in critically ill patients and has been associated with generalized muscle weakness, ventilatory failure and myocardial dysfunction. Continuous renal replacement therapy causes phosphate depletion, particularly with prolonged and intensive therapy. In a prospective observational cohort of critically ill patients with acute kidney injury (AKI), we examined the incidence of hypophosphatemia during dialysis, associated risk factors and its relationship with prolonged respiratory failure and 28-day mortality. Methods: This is a single-centre prospective observational study. Included in the study were 321 patients with AKI on continuous dialysis as initial treatment modality. Results: Four per cent of the patients had a phosphate level <2 mg/dL at initiation and 27% during dialysis. Low baseline phosphate was associated with older age, female gender, parenteral nutrition, vasopressor support, low calcium, and high urea, bilirubin and creatinine, whereas hypophosphatemia during dialysis correlated with the ischemic acute tubular necrosis etiology of renal failure, intensive dose and longer therapy. Serum phosphate decline during dialysis was associated with higher incidence of prolonged respiratory failure requiring tracheostomy [odds ratio (OR) =1.81; 95% confidence interval (CI) =1.07–3.08], but not 28-day mortality (OR =1.16; 95% CI =0.76–1.77) in multi-variable analysis. Conclusions: Hypophosphatemia occurs frequently during dialysis, particularly with long and intensive treatment. Decline in serum phosphate levels during dialysis is associated with higher incidence of prolonged respiratory failure requiring tracheostomy, but not 28-day mortality.

Speaker
Biography:

Dr Helena Genberg is a staff member at the Department of Transplantation Surgery, Karolinska University Hospital Huddinge, Stockholm, Sweden since 2002. In 2008 she defended her PhD thesis ABO-incompatible kidney transplantation using antigen-specific immunodasoption and rituximab at the Karolinska Institutet. As specialist in Surgery, her clinical as well as scientific work is focused on kidney transplantation. Dr Genberg is the author of several publications on ABO-incompatible kidney transplantation and rituximab. She has also had a number of assignments as reviewer of scientific manuscripts and was one of the organizers of The First International Workshop on ABO-incompatible kidney transplantation in 2007. Dr Genberg is the Secretary of The Swedish Transplantation Society.

Abstract:

ABO-incompatible (ABOi) living donor (LD) kidney transplantation has gained widespread popularity over the past 15 years. Worldwide over 3000 ABOi LD kidney transplantations have been reported. In Stockholm a protocol for ABOi transplantation was introduced in 2001 based on antigen-specific immunoadsorption for the anti-A/B antibody removal and rituximab to prevent antibody rebound. Since then some 100 ABOi transplantations have been performed there. The results of these transplantations have been evaluated in several studies and shown to be comparable with ABO-compatible LD kidney transplantation short-term. Similar results have also been reported from other centers. However, there are reports of inferior graft survival long-term following ABOi LD kidney transplantation when compared with ABO-compatible (ABOc) LD kidney transplantation. Yet, for the ABOi LD kidney recipients an ABOc living donor is rarely available. The alternative to dialysis or ABOi transplantation, is instead to enter the waiting list to possibly receive a deceased donor ABOc organ. In a recent study we compared the long-term results of ABOi LD kidney transplantation with wait listing. In this study the 10-year patient survival was 93% for the ABOi kidney recipients, 86% for the ABOc LD kidney recipients and 74% for patients entering the waiting list, p (overall) = 0.000. In conclusion, we argue that, for patients in the need of a kidney transplant, ABOi LD kidney transplantation is safe and a superior alternative to deceased donor wait listing.

Biography:

Erman Alci is a doctor at the department of surgery in Manisa State Hospital. His skills and expertise in Kidney Transplantation, Transplantation, Organ Transplantation and Transplant Surgery. His current speciality interests are surgery, clinical immunology and Nephrology.

Abstract:

DJ stents play an important role in modern urology to prevent undesirable side effects after surgery. With this study, we aimed to investigate the relationship of DJ stents with the demographic characteristics, surgical complications, UTI, hematuria of the patients who underwent renal tx. Data of 354 patients who underwent renal tx. between 2008 and 2011 in Ege University were evaluated retrospectively. 331 patients were included in this study. The term DJ (-) represents patients in whom DJ stent was not placed. Primary DJ term represents patients that the DJ stent was placed during the first tx. Secondary DJ term represents the patients who had DJ after tx. due to any complication. 254 (76.7%) patients were in DJ (-) group, 52 (15,7%) were in primary DJ group and 25 (7,6%) were in secondary DJ group. There was significant differences between the groups in terms of Anastomosis type (p =, 000), stay in hospital time (p =, 000), surgical complication (p =, 000), reoperation (p =, 000), percutaneous nephrostomy(p =, 000), UTÄ° (p =, 000), first UTÄ° time (p =, 000), recurrent UTÄ° (p =, 000), positive hemoculture (p =, 000), hematuria (p =, 000), duration of dialysis before tx (p =, 000), live/deceased donor (p =, 000), DGF (p =, 009). Our choice is to use the DJ stent in selected high-risk patients, and to keep the indications of DJ stent wider in deceased donor transplants by considering possible surgical complications. Using stent only in selected cases will decrease surgical complications due to stent placement.

Chandandeep Takkar

University of Texas, USA

Title: Calcific uremic arteriolopathy
Biography:

Takkar obtained her Bachelor of medicine and surgery (MBBS) from Government medical college, Amritsar, India and moved to the United States for further education. She completed her residency in Internal medicine at University of Texas Medical Branch (UTMB) at Galveston, Texas and served as a chief resident thereafter for a year. She completed her nephrology fellowship training at UTMB, Galveston as well and currently is an Assistant Professor in Nephrology, Internal medicine at University of Texas Health Science Center San Antonio, Texas.

Abstract:

Calcific Uremic Arteriolopathy (CUA) or Calciphylaxis is a rare and frequently fatal, necrotizing skin condition, encountered mostly in patients with ESRD on dialysis. The pathologic hallmark of calciphylaxis is medial calcification, intimal fibroplasia and luminal thrombosis of cutaneous arterioles, leading to ischemic ulceration. Clinical manifestations may include nodules or plaques that often progress to ulceration, frequently complicated by sepsis and death. The term CUA has recently been proposed over calciphylaxis to more accurately reflect the pathophysiology of the disorder, however one must realize that this entity has also been reported, albeit rarely, in non –uremic patients, including those with primary hyperparathyroidism, alcoholic liver disease, malignancy and certain connective tissue disorders. The estimated prevalence of CUA in patients with ESRD is about 4%, with an annual incidence of about 1/1000 cases. The six month mortality may reach upto 80% and a multifaceted approach to treatment is warranted, with emphasis to wound and pain management, optimization of mineral and bone parameters and possible use of sodium thiosulfate.

Speaker
Biography:

M Karavetian earned her PhD in “Health Promotion in Medical Sciences” from Maastricht University, Netherlands; and her dietetics degree from American University of Beirut, Lebanon. She has extensive experience in nutrition management of the chronically and critically ill; she shares her experience in conferences and workshops locally and regionally in the aim of improving health care. Her research is focused on finding effective strategies to change dietary behavior in chronically ill patients. Her publications focus on dietary management of hemodialysis patients and finding the optimal dietitian-to-patient ratio needed in the hemodialysis unit in the Arab world for optimal clinical outcomes.

Abstract:

The aim of this study was to assess the effect of intensive nutrition education by trained dedicated dietitians on osteodystrophy management among hemodialysis patients. This was done through a randomized controlled trial in 12 hospital-based hemodialysis units equally distributed over clusters 1 and 2. Cluster 1 patients were either assigned to usual care (n=96) or to individualized intensive staged-based nutrition education by a dedicated renal dietitian (n=88). Cluster 2 patients (n=210) received nutrition education from general hospital dietitians, educating their patients at their spare time from hospital duties. Main outcomes were: 1) dietary knowledge (%), 2) behavioral change, 3) serum phosphorus (mmol/L), each measured at T0 (baseline), T1 (post 6 month intervention) and T2 (post 6 month follow up). Analysis of results showed significant improvement only among patients receiving intensive education from a dedicated dietitian at T1; the change regressed at T2 without statistical significance: knowledge (T0: 40.3; T1: 64; T2: 63) and serum phosphorus (T0: 1.79; T1: 1.65; T2: 1.70); behavioral stages changed significantly throughout the study (T0: Preparation, T1: Action, T2: Preparation). In conclusion, the intensive protocol showed to be the most effective. Thus, integrating dedicated dietitians and stage-based education in hemodialysis units may improve the nutritional management of patients in Lebanon and countries with similar health care systems.

Biography:

Cristina Cacndido is a doctor at the department of Nephrology in Centro Hospitalar de Setúbal, Portugal.

Abstract:

Brachiocephalic arteriovenous fistula is the most commonly used and one of the favored hemodialysis access options. Often, these fistulas are associated with drainage disfunction in the Cephalic arch. This terminal portion of the cephalic vein is a frequent site for the development of stenosis. Various strategies have been applied to manage the stenosis, although, in some cases, it is not possible to intervene and access failure occurs. Cephalic vein transposition (CVT) to basilic vein is an alternative approach rarely described in literature for treatment of cephalic arch occlusive lesions. We report two haemodialysis patients, a 41 year-old woman and a 91 year-old man, with brachiocephalic fistula created 18 and 36 months ago respectively, that developed cephalic arch stenosis. In both cases the possibility of endovascular treatment was excluded, and surgical treatment was selected through CVT to basilica vein. In the first case, the access remains patent up to present day (6 months after CVT). In the second case, 9 months after surgical revision, a stenosis occurred close to the re-anastomosis and was treated by percutaneous balloon angioplasty, remaining patent also up to present day (12 months after CVT). The purpose of our study is to demonstrate an alternative approach for preserving brachiocephalic fistula with cephalic arch occlusive lesions. These results might encourage surgeons and nephrologists in Portugal to consider this strategy as a viable option.

Anupma Kaul

Sanjay Gandhi Postgraduate Institute of Medical Sciences, India

Title: Outcome of renal transplant recipients with cmv and bkv co-Infection nephropathy
Biography:

Anupma Kaul is a doctor at the department of Nephrology in Gandhi Postgraduate Institute of Medical Sciences, India. She has published 6 articles about kidney diseases.

Abstract:

Cytomegalovirus (CMV) and BK polyoma virus (BKV) are common infections in which the one acquires infection in childhood which becomes latent. Reactivation of both these viruses can occur in immunosuppressed states, such as renal transplantation, and can rarely result in virus-associated tubulointerstitial nephritis in renal allografts. The clinical picture can mimic, co-exist with or precipitate the rejection process. There is paucity of data comparing outcomes of renal transplant recipients with these viruses. We compared outcomes in patients with renal biopsy proven viral cytopathies. Method and Material: All patients are taken from in patients department of nephrology of a tertiary care teaching hospital in India. All those renal biopsy reports which are reported or suspicious as viral cytopathic changes in kidney were isolated. These biopsies were further examined by two independent renal histopathologist from our institute. They were classified on three groups: CMV viral cytopathic changes, BKV associated viral cytopathic changes and CMV-BKV co-infection associated viral cytopathic changes. Diagnoses were further confirmed with PCR technology in either serum or urine or both. All 20 patients were categorized in 3 groups: 10 in CMV only, 4 in BKV only and 6 were in CMV-BKV co-infection. Results: Out of 20 patients, 16 were male. Mean age is 37.95±11.09 years. Thirteen patients had chronic glomerulonephritis as basic disease, while chronic interstitial nephritis and diabetic nephropathy were basic disease in 2 each. One patient each had Henoch scholein purpura, hypertensive nephropathy and Ig A nephropathy as basic disease. In eight cases, donors 8 were parents (mother in 7 ), 5 were siblings (sister in 3) and 7 spousal ( wife in 5). One patient each had received ATG and Basiliximab as induction while 18 had no induction. All patients received triple drug immunosuppression, 9 received Tacrolimus, mycophenolate and prednisolone, another 9 received Cyclosporine, mycophenolate and prednisolone and 2 patients were started on cyclosporine, Azathioprine and prednisolone. Mean duration of graft survival was 62.70±30.78 months. In CMV subgroup mean graft survival was 65.40±25.25 months while in BKV subgroup was 61±46.46 months and in CMV and BKV co infection mean survival was 59.33±33.56 months. These are statistically not significant. At the end study period 10(50%) died. Conclusion: Cytomegalovirus and BK Virus infection are important infection in post renal transplant recipients. They can result in virus-associated tubulointerstitial nephritis and can mimic, co-exist or precipitate the rejection process. Although their co-infection is not common but they can co-exist. However their co-infection cannot change the graft survival and difference in not significant.

Biography:

Tanita Thaweethamcharoen obtained the Bachelor of Pharmacy and Bachelor of Public Administration Program in Public Administration, Master degree in the field of community pharmacy. She has completed her doctoral degree in the field of social and pharmacy administration program from Chulalongkorn University. She is the pharmacist and health economist of Siriraj Health Policy Unit, Faculty of Medicine, Siriraj Hospital, Mahidol University. She has published more than 10 papers in the international journals. She also has been serving as the reviewer board member of repute in research center of Mahidol University, Thailand and international journal. She is the first hospital pharmacist in Thailand who received the best poster presentation award from ISPOR in the ISPOR 4th Asia-Pacific Conference, 2010. She also received the Routine to Research (R2R) award and Lean R2R award of Thailand for two consecutive years (2013 and 2014). She is the lecturer and keynote speaker about the cost effective in health care, research methodology in routine to research project, quality of life in chronic kidney disease patient for the student and health personnel in many institutes such as Chulalongkorn University, Mahidol University, Siam University, Infectious Disease Association of Thailand, The Association of Hospital Pharmacy (Thailand), School of Pharmacy Institute Technology Bandung (ITB), Bandung, Indonesia.

Abstract:

Siriraj Hospital is the first university hospital in Thailand, with its vision to be the medical institute with international excellence in education, patient care, and research. Having about 2,100 inpatient beds, provides services to 80,000 admissions and over 3 million outpatients annually. Many health technology is offered to the hospital but the resource is limited thus Economic evaluation is an important tool involving examines consequences of the health care technology and evidence-based medicine in the hospital and societal perspective for policy decision. Economic evaluation research is one of the tools which impacts on decision making of treatments for individual patients because the result of the research concern both clinical outcome and ability to afford in the hospital or societal perspective. The results of the analysis can be a part of the process for the government decision, deciding whether drugs should be subsidized by the government, developing the intervention base on the cost effectiveness. The principles of economic evaluation and health technology assessment are the new challenge which can be applied to the processes as well as to improve patient care and will be useful in the overall movement towards the governance health care system. Role of the health care personnel cannot concern only the clinical outcome but healthcare expenditures also the important topic which are concerned so both of the effective and the expenditure should be considered. Our study start from the high expenditure of injectable drug; erythropoietin. Trend of Erythropoietin (EPO) expenditure was increasing between 2006 and 2009 and the highest expenditures for injectable drugs in 2009 of the large university hospital in Thailand. The major group of patient who use the erythropoietin is chronic kidney disease (CKD). CKD is the important chronic disease and the high expenditure in Thailand especially dialysis patient. Many tools of utility or the disease specific quality of life measurement were developed and applied in cost utility analysis to estimate the utility score and link to the QALYs which is one of the outcomes of the study. The results of the assessment since 2010 until the present are the evidence for many nephrologists and the Nephrology Society of Thailand to prioritize the health technology for health problem resolution and lead to an optimal care of people as well as good academic mission are challenge.

Biography:

Agnieszka Pozdzik has completed her medical study from University School of Medicine (Lublin, Poland) and has completed a PhD from Université Libre de Bruxelles (Brussels, Belgique). She is a nephrologist and Associate Professor at the Department of Nephrology. Since October 2012, she is the manager of the "Biobank of chronic kidney disease and urinary tract" (MARENVU) and, since June 2012, of the multidisciplinary center of nephrolithiasis. She has published more than 20 research papers in reputed journals and has been serving as a reviewer of repute journals

Abstract:

Tubulointerstitial nephritis (TIN) is a manifestation of IgG4-related diseases, which arecharacterized by infiltration of target organs by IgG4+ plasma cells and severe fibrosis. Cortico-sensitivity is one of the diagnostic criteria, but the treatment of steroid resistant and dependent forms is not well defined. We present a case of a 47-years-old patient with IgG4-related NTI followed for 72 months. He complained of fatigue and recurrent postprandial abdominal pain. With the exception of elevated levels of gamma-glutamyl transferase (GGT), transaminases and IgG4, kidney function remained normal (serum creatinine ≤ 0.9 mg/dL). After 2 cures of methylprednisolone (2010-11) azathioprine was associated in 2012. Due to the corticodependence and persistence of bilateral focal renal lesions detected by diffusion-weighted magnetic resonance imaging (DW-MRI), Rituximab (RTX) was given (2 × 376 mg/m²/15 days) in 2013. Before the first injection, positron emission tomography (PET) showed metabolic hyperactivity corresponding to axillary and abdominal aorta lymph nodes but not in the kidney. After 4 months of RTX, the patient became asymptomatic. All biological alterations disappeared. PET showed a decrease in metabolic activity at extrarenal lesions described above. A dramatic regression of bilateral renal lesions was noted by DW-MRI: the apparent diffusion coefficient had almost doubled (0.776 vs 1.111x10-3 mm²/sec) and the volume of renal lesions was reduced by 50%, which was never observed under other treatments. Our observations demonstrate: (1) the clinical, biological and radiological efficacy of rituximab in a steroid-dependent form of IgG4- related TIN and (2) the interest of DW-MRI as a non-nephrotoxic radiological and PET complementary approach not only in monitoring the effectiveness of immunosuppression but also in the early detection of renal involvement during IgG4 related disease.

Biography:

Abstract:

Background: Although conventional chest radiograph remains the first routine radiologic examination in mechanically ventilated patients, chest ultrasound provides more accurate information, with less ionizing radiation and less time delay. Objective: To compare between sensitivity of chest ultrasound and routine daily chest X- ray in diagnosis and follow up of diseases in mechanically ventilated patients admitted at Respiratory ICU of Ain Shams University Hospital. Design: The study was carried out as a prospective analytical study. Patients and methods: The study was conducted upon twenty five mechanically ventilated patients( 16 male patients and 9 female patients ) , with mean of age 58.8 years (SD ± 15.64 ) who were admitted at the Respiratory Intensive Care Unit of Ain Shams University Hospital during the period from October 2012 till May 2013. Chest ultrasound examination was done for patients on mechanical ventilation on first day of enrollment prior to seeing their chest X-ray, then follow up daily chest ultrasound examination was done all over the period of mechanical ventilation with comparison of examination results with that of chest X- ray. Results: Initial chest ultrasound was more sensitive in detection of pleural effusion (40% of cases) than chest X-ray (8% of cases). This superiority of chest ultrasound over chest X-ray persisted in follow up studies (44%, 8% respectively).As regards consolidation, there was no statistically significant difference between chest ultrasound (consolidation was detected in 16 out of 25 cases ) and chest X-ray ( consolidation was detected in 15 out of 25 cases) at the initial studies , and also along the follow up period ,chest ultrasound detected consolidation in17/25 patients, while CXR detected consolidation in 18/25 patients. In the follow up of five mechanically ventilated patients with no obvious radiologic abnormalities on chest X-ray, initial and follow-up ultrasound was also free and detected no localized abnormality. There was statistically significant relationship between chest ultrasound findings in cases with pleural effusion and in cases with consolidation and clinical progress. Conclusion: Chest ultrasound is a reliable tool for evaluation of mechanically ventilated patients.

Biography:

Veena Joshi (M.Sc; Ph.D) has completed her education in India. She has over 25 years of experience in Epidemiology and social research at Ministry of Health in Singapore and various hospitals in India. She has published several papers in reputed journals and has been serving as reviewer board member of repute.

Abstract:

Aim of the study was to conduct a systematic review to summarize the outcome of renal transplantation in adult patients with history of DM [DMRTx] in 1.DMRTx , 2. type 2 DMRTx 3.DM and type 2 DM in comparisons with Non-DMRTx, 4. Type2DMRTx vs dialysis and 5. Preemptive Kidney Transplant (prekTx) vs non prekTx. MEDLINE, EMBASE, Renal transplant registries were searched for observational / cohort/ case-control studies from 1980 to 2014. Type2DM compared to DM studies recruited fewer (<100) and older(>50 years) patients. We identified 22 studies reporting survival after RTx [in DM (1),DM vs Non-DM (10), Type DM (2), Type2DM vs Non-DM (6), Type2DMRTx vs Dialysis (1), PreKTx vs Non PreKTx (2)]. 16, 7, 12, and 3 single center studies showed 1,3, 5 and 10 year patient survival respectively. Seven studies in DM group have reported 5 yr graft and patient survival where one study showed graft survival was significantly (p<.05)better in Non-DM group compared to DM group. Patient survival did not differ. Among five type2DM studies, one and three studies showed graft and patient survival in non-DM to be significantly (p<.05) better than type2DM group. 5 yr survival after RTx was significantly (p=.001) better in RTx patients compared to patients on dialysis. At 10 year, patient survival of non-DM was significantly better than DM or type2DM and survival of preemptive was similar to non-preemptive (p<.05). There is an urgent need for multi-center studies with prediabetes, especially type2DM patients to look at long term survival after renal transplant.

Speaker
Biography:

Phuong-Thu Pham is Professor of Medicine and Director of Outpatient Services of the Kidney Transplant Program at UCLA Medical Center. Her major areas of interest and research include recurrence of glomerular diseases following primary kidney transplantation, new onset diabetes after transplantation, BK virus screening and management after kidney transplantation, the link between hypomagnesemia and renal function decline in patients with diabetes mellitus type 2 as well as in recipients of kidney transplant, and acute and chronic kidney injury following liver transplantation. Her interests in these topics have resulted in publications in well-known Nephrology textbooks and journals as well as invitations to speak at both national and international meetings. She has written over thirty book chapters for major Nephrology and solid organ transplantation textbooks including Comprehensive Clinical Nephrology, Textbook of Organ Transplantation, Transplantation of the Liver, Pancreas, islet, and stem cell transplantation for diabetes, Chronic Kidney Disease: Dialysis and Transplantation, and Handbook of Kidney Transplantation. She has also served as moderator for transplant-related conferences at the American Society of Nephrology and World Congress of Nephrology, editorial board member for the Case Reports in Nephrology and Transplantation Technologies and Research journals, and member of the organizing committee for the International Conference on Nephrology and Therapeutics.

Abstract:

Over the past two decades, while the proportion of failed kidney transplant patients returning to dialysis has remained stable and comprises of 4- 5% of all incident dialysis patients in the United States, the absolute number of patients reinitiating dialysis after a failed transplant has more than doubled. More importantly, the United States Renal Data System (USRDS) database revealed a greater than 3-fold increase in the annual adjusted mortality rates for patients returning to dialysis after graft loss compared with those with a functioning graft (9.4% vs. 2.8%, respectively). The Canadian Organ Replacement Registry database similarly demonstrated a greater than 3-fold increase in the risk of death among patients with a failed allograft compared with those with a functioning graft. Continuation of low-dose immunosuppression to maintain residual allograft function has been suggested as a contributing factor, presumably via treatment-related infectious and cardiovascular complications, among others. In contrast, a survival advantage in maintaining patients on long-term immunosuppression has been suggested among those returning to peritoneal dialysis. Whether early versus late reinitiation of dialysis or whether allograft nephrectomy has an impact on patient survival remains poorly defined. Despite the significant number of patients requiring reinitiation of some form of renal replacement therapy after a failed transplant and the increasing evidence suggesting their high mortality and morbidity rates, management of the failed allograft in these patients has received little attention. An overview of the literature on the management of immunosuppression after allograft failure, the ideal timing of dialysis reinitiation, a review on the pros and cons of allograft nephrectomy, and the author' perspectives on the management of this special patient population are presented.

  • Kidney
    Chronic Kidney Diseases
    Clinical Nephrology
Location: Conference Hall

Session Introduction

Dawn S. Milliner

Mayo Clinic, USA

Title: Hyperoxaluria: An underappreciated cause of kidney stones and kidney disease

Time : 11:40-12:10

Speaker
Biography:

Dr. Milliner is a member of the Divisions of Nephrology and Pediatric Nephrology, Departments of Internal Medicine and Pediatrics at the Mayo Clinic College of Medicine. She conducts research in pediatric stone disease, oxalate, and inherited forms of nephrolithiasis. She chaired the Seventh International Workshop on Primary Hyperoxaluria, served as chair of the Scientific Advisory Board of the Oxalosis and Hyperoxaluria Foundation and is past president of the Research on Calculus Kinetics Society. Dr. Milliner is medical director for the Mayo Clinic Hyperoxaluria Center and is principal investigator for the Rare Kidney Stone Consortium, funded by the NIH.

Abstract:

The prevalence of kidney stones is high and stone formation is associated with CKD and end stage kidney disease. High concentrations of oxalate in the urine pose risk not only for calcium oxalate urolithiasis, but also for kidney disease caused by deposition of calcium oxalate crystals in kidney tubules and interstitium. Crystal induced inflammation and subsequent fibrosis can cause chronic progressive, or acute, loss of kidney function. Gut flora play a role in bioavailability of oxalate in the intestinal lumen and a number of disease states increase oxalate absorption from the gut. Any intestinal disease that impairs fat absorption, such as Crohn’s disase, pancreatic insufficiency, or short bowel syndrome can lead to enteric hyperoxaluria. Management of the epidemic of obesity is increasing the frequency of enteric hyperoxaluria through use of medications such as orlistat and increasing numbers of gastric bypass procedures performed in many parts of the world. Malabsorbtive procedures, more effective for weight loss, are associated with hyperoxaluria and stones. Inherited forms of primary hyperoxaluria result in the highest urine oxalate observed in human disease. The hyperoxaluria is lifelong and kidney failure is frequent. Three types of primary hyperoxaluria have been recognized. They differ in the severity of hyperoxaluria and stone disease, and in the frequency of end stage kidney disease. Kidney stones and kidney failure related to hyperoxaluria are increasingly recognized. Mechanisms of kidney injury, treatments available and under investigation, and clinical management of patients with advanced oxalate related kidney disease will be discussed.

Ahmed Zeidan

Hull York Medical School, UK

Title: Effects of intravenous iron in chronic kidney disease and heart failure

Time : 12:10-12:40

Speaker
Biography:

Dr. Ahmed Zeidan, BSc.(Hons), MB ChB, is currently pursuing a Doctorate in Medical Science under the supervision of Professor Sunil Bhandari. He received his first degree in Medical Microbiology & Immunology from Newcastle University and obtained his Medical degree from the University of Sheffield in 2010. Following his undergraduate studies he worked as a junior doctor in Manchester and completed his training in General/Internal Medicine at Hull and East Yorkshire Hospitals Trust. As a research fellow in Cardiology and Nephrology he was offered a scholarship for his current PhD at York University. Beside his clinical and research work, he is also actively involved in hospital-based teaching, tutoring medical students and lecturing at Hull-York Medical School. He is also a final year undergraduate examiner at Manchester Medical School.

Abstract:

The heart is subject to a number of adaptive and subsequently maladaptive changes in patients with chronic kidney disease (CKD). There are structural changes with both concentric and eccentric hypertrophy in part linked to FGF-23; changes in energetics, with a switch from fatty acids to glucose metabolism; ischaemic vulnerability from both iron and erythropoietin deficiency; oxidative stress and changes in calcium cycling within the mitochondria. However, the key components in the process are the adjustments in mitochondrial function which serve as the powerhouse for all tissues.Iron plays a pivotal role in oxygen uptake, transport, storage and metabolism in both skeletal and cardiac muscle. In models of stressed hearts with CKD, there is an increase in stage 4 respiration in addition to an increase in uncoupling proteins leading to mitochondrial dysfunction and an increase in transition pore formation leading to impaired contractile function of cardiomyocytes. Therefore a deficiency of iron may lead to impaired mitochondrial function via effects on transition pore opening and subsequent inhibition of the pro-survival pathway and activation of apoptotic pathways. Also chronic iron deficiency may cause structural abnormalities in cardiac myocytes leading to reduced exercise capacity and performance. However, both in vitro and in vivo data suggest that there may be an increase in oxidative stress with intravenous iron administration whilst clinical data suggest improved functional capacity. Few studies have examined the effects of intravenous iron in patients with heart failure, anaemia, iron deficiency, and renal dysfunction and none have examined whether a single large dose of iron may lead to improvements in functional capacity without adverse effects. Therefore we have been examining the effect of iron and whether it leads to improvement in mitochondrial function and hence symptom improvement and cardiac function independent of haemoglobin in patients with CKD. In addition we are assessing if intravenous iron therapy affect markers of kidney injury and oxidative stress via generation of labile or catalytic iron. The results of these studies will provide an insight into the mechanisms underlying the conundrum with the benefits of iron related to incorporation into the iron sulphur clusters as part of the electron transport chain and TCA cycle, the changes in mitochondrial function and the potential iron related increase in oxidative stress and subsequent adverse effects.

Break: Lunch Break 12:40-13:40 @ Restaurant

Barbara Schraml

Klinikum der Universität München, Germany

Title: Defining Dendritic Cells by Ontogeny

Time : 13:40-14:10

Speaker
Biography:

Barbara Schraml has completed her PhD at Washington University in St. Louis and her postdoctoral studies in the laboratory of Caetano Reis e Sousa at the London Research Institute. She has been and independent Emmy-Noether Research group leader since 2014. Her group at the Walter-Brendel-Centre for Experimental Medicine of the Ludwig Maximilians University Munich focuses on understanding tissue specific immune responses.

Abstract:

Mononuclear phagocytes sample the environment for signs of damage or infection. The classification of these cells as macrophages or dendritic cells (DC) has traditionally been done on the basis of differences in cell morphology, expression of specific markers or of select functional attributes. However, these attributes are not absolute and often overlap, leading to difficulties in cell type identification. To circumvent these issues, we have generated a model to define DC based on their ontogenetic descendence from a committed precursor. We show that in mice precursors of conventional DC but not other leukocytes are marked by expression of DNGR-1/CLEC9A. We generated a mouse model to genetically label Clec9a-expressing conventional DC precursors and their progeny with yellow fluorescent protein (YFP). Genetic labeling of these cells and their progeny specifically traces cells traditionally ascribed to the DC lineage and the restriction is maintained after infection. Notably, in some tissues cells previously thought monocytes/macrophages are in fact descendants from DC precursors. These studies provide the first in vivo model for lineage tracing of DC and allow the definition of DC based on ontogenetic rather than phenotypic, morphological or functional criteria. These studies establish DC as an independent immune lineage and distinguish them from other leukocytes, thus paving the way to unraveling the functional complexity of the mononuclear phagocyte system.

Levent Yucetin

Medicalpark Antalya Transplant center, Turkey

Title: An investigation of post-traumatic growth experiences among living kidney donors

Time : 14:10-14:40

Speaker
Biography:

Levent Yucetin is the director of Antalya Medicalpark Transplant Center Coordination. He studied and trained in Oxford, Cambridge, Harefield transplant centers, Barcelona University and TPM organisation between 1999-2001. He was the president of Turkish Transplant Coordinator's Society between 2005-2009, National Key Member of ETCO between 2002-2012. Turkey's leader at European Union projects ETPOD,ELIPSY,LIDOPS and ODEQUS. Member of Turkish Health Ministery's Transplant Coordinators and Organ Donation board. Trainer of Transplant coordinators at Helath Ministery Certification organisation. He has published more than 29 papers in reputed journals and 10 chapters at 4 repute books.

Abstract:

More than 1 million patients are estimated to have undergone transplantation in the past years. In recent years, living-donor kidney transplantation accounted for more than 50% of all transplantations. Kidney transplantation from living donors is regarded as a contradictory case to the “do no harm” principle as a major surgical intervention is performed on a normal and healthy person at the expense of recovery of the organ recipient. The purpose of this study was to investigate positive psychological experiences, specifically posttraumatic growth (PTG), among living kidney donors. The sample consisted of a total of 184 kidney donors. The age of donors ranged between 21-76 (mean, 50.76; SD, 10.93). In this study 67.9% of donors were female. The recipients on dialysis group had higher scores than the recipients who did not have dialysis; the mean difference was significant on the subscales of change in life philosophy, change in relationships, change in self-perception, and in the PTGI score. The donors with higher education levels received higher scores on the subscale of change in relationships in comparison with donors with low education. The donors who were married and older than 51 years had higher scores than donors who were not married or younger on the subscale of change in self-perception. This is a singlecenter study; this center performs more than 500 kidney transplantations per year. There is a good system and experience at each step before and after transplantation for donor and recipient and relatives. It is a really big potential trauma to donate a kidney to your relative; you can change this negative effect to a positive effect with a good system. The present study also showed that when compared with the scale’s absolute midpoint, kidney donors in the study sample experienced moderate-to-high levels of PTG.

Speaker
Biography:

Donald Silverberg Graduated from Medical School University of Manitoba in 1962. He did his Residency in Internal Medicine and Nephrology at the Mayo Clinic Rochester Minnesota in 1962-1966 and Residency in Nephrology, University of Lund, Sweden in 1966-1967. He worked as Nephrologist University Hospital, Edmonton Canada during l968-1976. Has been living in Israel and practicing nephrology since 1976 in Tel Hashomer and Beilinson and Tel Aviv Medical Center. National Director of Hypertension Control Division, Kupat Holim Sick Fund 1978-1986 (Organizing the detection and treatment of hypertension for the Israeli population).

Abstract:

Anemia (Hb <13g% in men and <12g% in women) is present in about 40% of Heart Failure (HF) patients. Iron deficiency (ID), if defined as either a serum ferritin of <100ug/l or a serum ferritin of 100-300 ug/l along with % Transferrin Saturation of <20%, is present in about 60% of the patients with anemia (about 24% of all HF patients) and in about 40% of patients without anemia (about 24% of all HF patients). Thus ID is present in about half the patients with HF. The ID in HF is associated with reduced iron stores in the bone marrow and the heart. ID is an independent risk factor for severity and worsening of the HF. Correction of ID with intravenous (IV) iron usually corrects both the anemia and the ID. Currently used IV iron preparations are very safe and effective in treating the ID in HF whereas little information is available on the effectiveness of oral iron. In metanalysis IV iron correction of ID in HF is associated with improvement in NYHA functional status, exercise capacity, C Reactive Protein, quality of life, rate of hospitalization for HF, cardiac dilation and hypertrophy, cardiac function, and renal function. Correction of the ID is also highly cost effective. The improvement seem to be related more to the correction of the iron deficiency than to correction of the anemia. The large placebo- controlled studies have only been done with Ferric sucrose and Ferric carboxymaltose. The incidence of adverse effects of these agents is similar to placebo. However large long-term adequately-controlled mortality-driven intervention studies are still needed to clarify the effect of IV iron in HF. Several Heart Associations, including the European, Australian and New Zealand Heart Associations, suggest that ID should now be routinely sought for in all HF patients and corrected if present.

Speaker
Biography:

LAIDOUDI Aicha has completed her PhD at the age of 25 years from Ferhat Abbas University and she is in the postdoctoral studies, Mohamed Maherzi University School of Medicine. She is a doctor in the department of internal medicine, Mohamed Lamine Debaghine Hospital. She is in 5th and latest year of post-doctoral studies.

Abstract:

Introduction:The NITU syndrome is a rare combination characterized by the occurrence of tubulointerstitial nephritis (TIN) and uveitis (U), it is a rare disease of the adolescent and the young woman, its pathogenesis is unknown, autoimmune origin has recently been proposed including humoral and cellular immunity. In general, renal and eye damage tended to resolve with corticosteroid therapy. We report two cases of TINU syndrome occurring in adults in which the recovery of renal function was incomplete despite corticotherapy in the first observation, and immunological disorders which can create differential diagnostic difficulties. Case reports: Observation 1: A 25 year old woman, nurse, admitted to explore asthenia and weight loss of 6 Kg, associated with severe hypertension and acute unilateral anterior uveitis. She was taking no medications. Clinical examination revealed: a blood pressure (BP) of 170/130 mmHg, class II dyspnea (NYHA), a holosystolic heart murmur in the mitral area without heart failure signs, a mucocutaneous pallor but no signs of vasculitis, urine dipstick test finds traces of protein and hematuria; ocular fundus exam found grade I hypertensive retinopathy, the rest of the examination was normal. Biological studies showed kidney failure with GFR of 18.71 ml/mn/1.73m2 , proteinuria was 540 mg / 24h. Erythrocyte sedimentation rate between 37 and 76 mm (3-12) mm/hour. Kidney biopsy with histological examination showed a non caseating granuloma in the interstitial tissue with presence of rare hyaline casts in the kidney tubules, and tubulointerstitial nephritis with granulomatous lesions in the medullary parenchyma. Further exploration was done mainly oriented to sarcoidosis and tuberculosis and the other differential diagnosis was all negative but Quantiferon was 10 times normal with negativity of all other examinations to KB (koch’s bacillus). No other sites of granulomas. The patient responded to corticoid treatment (pulse IV followed by high-dose daily glucocorticoids then gradually tapered off but without normalization. The patient untimely stopped corticosteroids after 4 months of treatment that caused a decreased renal function that required a 2nd pulse then high-dose daily glucocorticoids. Glucocorticoid-sparing was provided by mycophenolate mofetil (MMF). The patient remained well without recurrence of uveitis 2 years later but without complete recovery of renal function which improved gradually with immunosuppressive treatment. Observation 2: A 46 year old patient, without specific personal history, but a mother who died of chronic kidney failure, presented a recurrent anterior uveitis, associated with an increase in serum creatinine; The clinical examination is unremarkable, the urine dipstick showed proteinuria (+), glycosuria: traces; Biological studies showed kidney failure with a GFR of 14 mL / min/1.73m2, inflammatory syndrome, proteinuria of 650 mg /day, research of infectious agents or auto-immunity origin was negative. Renal biopsy showed tubulointerstitial nephritis lesions in subacute stage; biopsy of the salivary glands showed stage III chronic lymphocytic sialadenitis (the Chisholm and Mason classification) without xerostomia, AntiSSA, antiSSB negative. Gallium scintigraphy did not find any signs suggesting a type of sarcoidosis inflammatory. The diagnosis of TINU syndrome was retained after exclusion of other differential diagnosis. The patient received corticosteroid treatment. Serum creatinine improved quickly with normalization 2 months later. The patient remained well without recurrence of the disease 6 years later. Discussion: TINU syndrome diagnosis is based on a combination of the bipolar impairment: renal and eye; and excluding other causes (infectious, drug and autoimmune). The treatment protocol is not yet codified, but corticosteroids at high-dose are first-line treatment of renal disease. In our patients, the presence of TIN in the renal biopsy, recurrent anterior uveitis, no notion of drug intake, the response to corticosteroids and exclusion of other diagnoses, so the diagnostic of TINU syndrome was retained. In the first observation, positivity of Quantiferon is explained by the fact that the TINU syndrome is associated with elevation of serological markers in the absence of their corresponding diseases, in the 2nd observation, the presence of stage III chronic lymphocytic sialadenitis can be explained by these immunological disorders in the absence of Sjogren syndrome. Conclusion: TINU syndrome is a rare entity, the pathogenesis is unknown, and its association with autoimmune diseases suggests its autoimmune origin. TINU syndrome is secondary to immunological disorders as evidenced interstitial infiltrate of the renal parenchyma, the inflammatory disease of the uvea and good response to corticosteroid therapy.

Break: Coffee Break 15:50-16:10 @ Foyer

Francesco Fontana

University of Modena and Reggio Emilia, Italy

Title: Wearable artificial kidney - back to the future: A review

Time : 16:10-16:40

Speaker
Biography:

Francesco Fontana, MD, is currently terminating his training in Nephrology at University of Modena and Reggio Emilia, Modena, Italy. In 2014 he attended an internship at the Instituto de Fisiologia Molecular, Instituto de Nutricion, Mexico City, Mexico. In 2015 he entered as a PhD student the Doctorate School of Clinical and Experimental Medicine at University of Modena and Reggio Emilia. His research interests focused on hemorheology in kidney transplantation and dialysis, acute kidney injury (AKI) models in rats and AKI – chronic kidney disease transition, biocompatibility and clinical aspects of miniaturized devices for chronic dialysis.

Abstract:

Although the burden of end stage renal disease is worldwide expanding, current dialytic options are unsatisfactory, mainly due to their intermittent character. Benefits of continuous treatments on rates of complications and mortality are clearly demonstrated, and a miniaturization of dialysis devices would allow delivery of continuous treatment without limiting patient’s freedom. Miniaturization poses several technical challenges, in terms of dialysis membranes, dialysate regeneration, vascular access, patient monitoring, power sources and pumping systems. First attempts in the creation of a portable/wearable artificial kidney (WAK) for hemodialysis (HD) date back to the seventies, but technology later needed to be refined with development of dialysate regeneration modules based on sorbents and enzymes. These advances paved the way to first, short-term validations in humans obtaining promising results in terms of safety and effectiveness but needing further confirmations. WAK have also been proposed to enhance the efficacy of peritoneal dialysis (PD), circumventing the problems of a direct access to blood system and continuous anticoagulation, main bottlenecks for a widespread use in HD. Dialysis market is presently offering some options for portable/home devices, but no WAK is marketed. Hot topics in recent researches on under development WAKs have been the selectivity and regenereability of sorbents and a reappraisal of electro-oxidation for urea elimination. Furthermore, promising, although preliminary, advances have been made in the development of implantable devices, most promising consisting in a combination of sorbents and a scaffold with renal epithelial cells.

Speaker
Biography:

Alsayed Alnahal is currently working as Assistant Professor at Zagzaig University Hospital and is a previous Director of the dialysis unit. He is graduated in 1996 and obtained his Post-graduate in Zagazig University. He has published more than 12 publications in reputed journals

Abstract:

Introduction: Serum creatinine is unreliable early biomarker for diagnosis of acute kidney injury (AKI) after cardiac surgery requiring cardiopulmonary bypass, we need to search for rapid and dependable marker for detection of AKI. Aim of work: This study was designed to test urinary netrin-1as marker of early kidney injury post-cardiac surgery. Our study included 39 subjects with preoperative normal creatinine. All patients underwent full history and routine laboratory investigation. Both serum creatinine and urinary netrin-1 were measured at 0, 6 and 24 hours after cardiac surgery. Results: 14 patient developed AKI after cardiac surgery. A statistically significant elevation in urinary netrin-1 is found at 6 and 24 hours after CPB surgery in the AKI group; while serum creatinine failed to show any statistically significant elevation at 6 hours after CPB in the same group. No statistically significant change in level of creatinine or urinary netrin-1 at 6 and 24 hours after CPB surgery in the non AKI group. The sensitivity and specificity of urinary netrin-1 to detect AKI at 6 h after CPB surgery was 86.7% and 91.7% respectively at a cutoff value of 107.3 pg/ml. Combined urinary netrin-1 and serum creatinine have the same sensitivity and specificity. Conclusion: Urinary netrin-1 may be considered as early sensitive biomarker of acute kidney injury at 6 hours after cadio-pulmonary bypass surgery instead of serum creatinine that rise only 24 hours after CPB surgery in cardiac surgery associated- acute kidney injury patients.

Speaker
Biography:

Francois Cachat has completed his MD from Lausanne Medical School in Switzerland in 1991. After training in pediatrics in Switzerland, he completed a fellowship in pediatric nephrology in Charlottesville, VA, USA, where he conducted research on experimental obstructive uropathy. His current research interests are the measurement of renal function in children, and the application of Evidence-Based Medicine in the field of pediatric Nephrology. He is currently chief of pediatric nephrology at the Inselspital Bern, Switzerland. He has authored more than 70 peer-reviewed papers, and serves in more than 20 Journals as reviewer or member of the Editorial board.

Abstract:

Background Microalbuminuria (MA) has been shown to be an early biomarker of renal damage. It is postulated that MA is the early result of hyperfiltration, which could evolve into glomerular sclerosis and renal failure if hyperfiltration is left untreated. We hypothesized that MA is a good indicator of hyperfiltration in children with kidney disorders, obviating the need to calculate the filtration fraction (FF). Methods 155 children or young adults were prospectively included [42 single kidney (SK), 61 vesicoureteral reflux, 23 obstructive uropathies, 29 other kidney diseases]. We measured inulin, para-aminohippuric acid clearances, FF and MA. Prediction of hyperfiltration was explored by studying the association between FF and other variables such as urinary albumin (Alb), urinary albumin–creatinine ratio (ACR), creatinine clearance. Results A significant but weak association between urinary Alb or ACR and FF was found in subjects with SK (Spearman correlation coefficients 0.32 and 0.19, respectively). Multivariate analysis also showed that urinary Alb and ACR significantly predict FF only in subjects with a SK (r2 = 0.17, P = 0.01 and r2 = 0.13, P = 0.02, respectively). This holds true only in subjects with a SK and inulin clearance >90 mL/min/1.73 m2 (r2 = 0.41, P < 0.001). There was no association between creatinine clearance and FF. Conclusions MA is not associated with FF in subjects with nephro-urological disorders, except in those with a SK, where the association is weak, indicating that MA is due to other mechanisms than high FF and cannot predict hyperfiltration in such groups.

Biography:

Jose Luis Gorriz is a doctor at the department of Nephrology in Doctor Peset university Hospital and department of Medicine in University of Valencia, Spain

Abstract:

Abstract: Renal insufficiency increases the risk of stroke and bleeding in atrial fibrillation patients. Although vitamin K antagonists reduce the risk of stroke in patients with moderate renal dysfunction, this observation is less clear in patients with renal impairment. Moreover, the risk of bleeding with vitamin K antagonists increases as renal function worsens. Maintaining international normalized ratio values within therapeutic targets is more difficult in patients with renal dysfunction, and those agents may cause warfarin-related nephropathy and vascular calcification. Rivaroxaban is the only nonvitamin K oral anticoagulant with a dose specifically tested in patients with moderate renal insufficiency. Rivaroxaban is effective for the prevention of stroke in atrial fibrillation patients with moderate renal dysfunction, with a lower risk of intracranial and fatal bleeding. Key words: Atrial fibrillation , chronic kidney disease , new oral anticoagulant, nonvitamin K oral anticoagulant , renal function , renal insufficiency , rivaroxaban, vitamin K antagonist.

Speaker
Biography:

Juan Pablo Preciado is a medical student currently enrolled in the 6th semester of medicine school from Universidad de Guadalajara, in the campus of Puerto Vallarta, Jalisco. Mexico. He has participated actively in numerous national conferences and actualization courses, nowadays want to attend to an international event, this, in order to gain experience on the international arena, that will be useful to practice in medical sciences and broaden his personal experience in medical investigation area. Currently my strongest engagement is with my career. Volunteering and getting involved in various scholar activities allow me to develop skills and attitude to effectively participate in multiple areas of medical sciences. The Knowledge and love to my career have given me the motivation to give the best of me every day and act responsibly

Abstract:

Background: End-Stage Kidney Disease is directly related to hypertension, diabetes and dyslipidemia, which is today diseases that have reached epidemic proportions in our country. Methods: We conducted an analytical, observational, cross-sectional, retrospective study based on individuals, involving 18 patients assigned to the ISSSTE Hospital located in Puerto Vallarta, Jalisco. México, diagnosed with End-Stage Kidney Disease, in which we seek to establish an approximate time frame for the diagnosis of End-Stage Kidney Disease in patients with a previous diagnosis of Systemic Hypertension, Diabetes Mellitus Type 2 and both associated. Statistical analysis was performed using the Excel Analysis ToolPak for Microsoft Office Excel 2013. Results: Data were collected from 18 patients diagnosed with End Stage Kidney Disease, of which only 15 patient's (83.33%) were analyzed, otherwise 3 patient's (16.66%) were excluded, 2 of them by presenting a diagnosis of ESKD simultaneously to Type 2 Diabetes or Systemic Hypertension, and the remaining patient did not present any comorbidity when establishing the diagnosis of ESKD. Of the selected patients it was found that the category who took a shorter time to have as diagnosed ESKD were patients with Hypertension as unique comorbidity, with an average of 5.6 years, while the category of type 2 diabetes mellitus and associated hypertension, had an average of 9 years, and finally patients with type 2 diabetes mellitus only, showed an average of 20 years of evolution before they make a diagnosis of ESRD. Conclusions/Discussion: The results show a direct causal link between type 2 diabetes mellitus and hypertension, with the onset of chronic kidney failure, this time depending on the evolution of the disease. Being patients with hypertension as the only comorbidity those with the shortest period to develop terminal chronic renal impairment compared to patients with diabetes mellitus as one comorbidity, who show a slow and progressive deterioration, perhaps associated with various factors, a major by inhibiting the renin-angiotensin system, which slows the progression of kidney disease.

Biography:

Agnieszka Pozdzik has completed her medical study from University School of Medicine (Lublin, Poland) and has completed a PhD from Université Libre de Bruxelles (Brussels, Belgique). She is a nephrologist and Associate Professor at the Department of Nephrology. Since October 2012, she is the manager of the "Biobank of chronic kidney disease and urinary tract" (MARENVU) and, since June 2012, of the multidisciplinary center of nephrolithiasis. She has published more than 20 research papers in reputed journals and has been serving as a reviewer of repute journals.

Abstract:

Tubulointerstitial nephritis (TIN) is a manifestation of IgG4-related diseases, which arecharacterized by infiltration of target organs by IgG4+ plasma cells and severe fibrosis. Cortico-sensitivity is one of the diagnostic criteria, but the treatment of steroid resistant and dependent forms is not well defined. We present a case of a 47-years-old patient with IgG4-related NTI followed for 72 months. He complained of fatigue and recurrent postprandial abdominal pain. With the exception of elevated levels of gamma-glutamyl transferase (GGT), transaminases and IgG4, kidney function remained normal (serum creatinine ≤ 0.9 mg/dL). After 2 cures of methylprednisolone (2010-11) azathioprine was associated in 2012. Due to the corticodependence and persistence of bilateral focal renal lesions detected by diffusion-weighted magnetic resonance imaging (DW-MRI), Rituximab (RTX) was given (2 × 376 mg/m²/15 days) in 2013. Before the first injection, positron emission tomography (PET) showed metabolic hyperactivity corresponding to axillary and abdominal aorta lymph nodes but not in the kidney. After 4 months of RTX, the patient became asymptomatic. All biological alterations disappeared. PET showed a decrease in metabolic activity at extrarenal lesions described above. A dramatic regression of bilateral renal lesions was noted by DW-MRI: the apparent diffusion coefficient had almost doubled (0.776 vs 1.111x10-3 mm²/sec) and the volume of renal lesions was reduced by 50%, which was never observed under other treatments. Our observations demonstrate: (1) the clinical, biological and radiological efficacy of rituximab in a steroid-dependent form of IgG4- related TIN and (2) the interest of DW-MRI as a non-nephrotoxic radiological and PET complementary approach not only in monitoring the effectiveness of immunosuppression but also in the early detection of renal involvement during IgG4 related disease. key words : chronic kidney diseases, renal fibrosis, membranous nephropathy, renal pathology, peritoneal dialysis, nephrolithiasis

Speaker
Biography:

Aamir Jalal Al Mosawi, advisor doctor, Iraqi ministry of Health is currently the Head of Iraq Headquarter of Copernicus Scientists International Panel. He published more than 25 scientific papers in international journals and published many books and book chapters with international publishers. He joined the International Association of Pediatric Nephrology (IPNA) during the year 2000. He is the founding editor of an international peer-reviewed medical journal “The New Iraqi Journal of Medicine (2005-2013)”, and member of the World Association of Medical Editors (WAME). He also served as a member of the advisory council the International Association of Medical Colleges (IAMC).

Abstract:

The use of new dietary therapies to lower urea levels simulating dialysis procedures has been recently described and has been sometimes called intestinal or dietary dialysis. In the commonest form of this new dietary approach, the patient consumes relatively a large amount of soluble fiber. The most commonly used soluble fiber acacia gum is digested by colonic flora, thereby increasing the amount of nitrogen that is eliminated as fecal waste. When acacia fibers gum are added to a low protein diet in patients with advanced chronic kidney disease (CKD) who do not have access to dialysis, their serum BUN levels can be lowered and they experienced a decrease in uremic symptoms. In a series of 80 patients with chronic renal failure (CRF), 14 (16.5%) patients were treated with a new therapeutic dietary regimen. This new dietary regimen consists of using acacia gum as dietary supplement in addition to the traditional conservative measures used in the management of CRF. The use of this novel technology resulted in amelioration of the uremic symptoms and lowering of blood urea levels and delaying the need for dialysis. In this sample of 80 patients the longest survival of 5 years was achieved in 2 patients, both treated initially with IPD. One of them was transplanted and the other was treated with new dietary technology.

Biography:

Mustapha Bouatia is professor at department of medicine and pharmacy in Mohammed V University, Morocco

Abstract:

Biography:

Khalfaoui Mohamed Amine is a doctor at the department of Nephrology at University Hospital Ibn Rushd Casablanca, Morocco. His current speciality interests are the Nephrology-Hemodialysis and renal transplantation.

Abstract:

Introduction: The immunodeficiency, moderate in patients with chronic renal failure (IRC), explains a susceptibility greater to viral infections including viral hepatitis B, unfortunately these patients respond badly to vaccination against hepatitis B. In addition, their rate of Ac protectors decreases more rapidly than in the general population. We have studied the decay of the rate of Ac Hbs in renal failure chronic non-dialysis and vaccinated against hepatitis B. Patients and methods: We have measured the rate of Ac Hbs every 3 to 6 months in renal failure not on dialysis followed in consultation and having been vaccinated with success against hepatitis B (Ac Hbs>10 IU/ml). Result : Forty patients aged 48±11years, with creatinine clearance to 28±13ml/min which 57.5 per cent of men and 42.5 per cent of women have been followed on average 12 months (min 6 months/max 18 months). The initial nephropathy was a diabetic nephropathy in 18 patients (45 % ), the nephroangiosclerose 11 patients (27.5 % ), and finally of chronic glomerulonephrites in 7 patients (17.5 %) and 4 patients with an indeterminate nephropathy. The rate of Ac at the beginning of the follow-up was on average to 260 IU/ml . This rate declined by an average of 30 IU/ml per month. The threshold of 10 IU/ml below which patients are no longer protected was reached in 10 months on average. Among the factors studied (creatinine clearance, sex, weight, diabetes, baseline albumin, protidemie, type of nephropathy) none was predictive of the rate of reduction of the Ac. Discussion: The decrease in the rate of Ac HBS is fast among the IRC which makes necessary a serological monitoring regular all the more that nothing allows you to predict the speed of decay for a given patient. Our study allows giving an estimate of the rate of the monitoring and of the delay before a new vaccination in function of the initial rate of Ac. Conclusion: The renal disease loses their protection against hepatitis B in 12 months on average which makes the serological surveillance necessary.

Biography:

Mohamed Alqadhi is a doctor at the department of Nephrology and Urology in National Institute of Urology & Nephrology, Egypt

Abstract:

Objective: To review our 5 years’ experience with ureteroscopy treatment of distal ureteric calculi. Patients and methods: We reviewed the medical records of 136 patients who underwent ureteroscopic procedures for the treatment of distal ureteric calculi from February 2007 to October 2012. Patient and stone characteristics, treatment modality and outcome were assessed. Procedure’s duration, status “stone free” and hospital stay were also evaluated. The mean clinical and radiological follow-up period was 31.8 months for 74.2% of eligible patients. Results: The stone free rate following an initial ureteroscopy was 79.4. The ultimate success rate for stone removal after “second look” improved to 95.9%. The mean operative duration was 51 minutes. The intraoperative complication rate was 8.6%, the postoperative complication rate was 7.5%, and the mean hospital stay was 1.1 days. We could detect one ureteric stricture and one vesico-ureteric reflux (0.9% for each). A significant ureteric perforation was detected in 4.1% and ureteric perforation in 0.7% of the study group. We could find that the longer the operative duration, the greater the complications. Stone impaction and size were also found associated with higher morbidity. Conclusion: Growing skills and experience of ureteroscopy will lead to a significant increase in the success rate and also reducing serious complications.

Speaker
Biography:

Bruce Hendry is President of the UK Renal Association and Emeritus Professor of Renal Medicine at King's College London. He graduated in medicine from the University of Oxford and received his PhD in Biophysics from the University of Cambridge. His major research interests are in the cell and molecular biology of progressive renalfibrosis and in the design of novel therapeutic approaches. His current work is focused on the study of new approaches to the problem of aberrant renal cell proliferation leading to fibrosis; this work includes the use of antisense and small molecule strategies. Recent work has examined the role of antisense as therapy in renal fibrosis and ADPKD and the targeting of T-type calcium channels in glomerular disease. He has clinical research interests in diabetic nephropathy, HIV and the kidney and in polycystickidney disease.

Abstract:

There is a lack of effective therapeutic options for patients with Chronic Kidney Disease (CKD) related to IgA nephropathy and proteinuric nephropathies. Treatment with inhibitors of the Renin Angiotensin System (RAS) is standard but residual risk of progression of CKD remains high. In this context this lecture will explore an innovative strategy for therapy in CKD targeting T-type calcium channels. T-Type Calcium Channels (TTCC) are closely related to the more familiar L-Type Calcium Channels (LTCC). We have extended work on the role of TTCC in smooth muscle proliferation by demonstrating that TTCC have a role in mesangial cell function. TTCC are also expression in the efferent arteriole and TTCC inhibition reduces glomerular capillary pressure. In vitro human and rat mesangial cell proliferation is dependent on TTCC and not LTCC. Moreover, in models of glomerular cell proliferation, inhibition of TTCC reduces glomerular damage, reduces cell proliferation and inhibits monocyte infiltration, with improved renal function. In parallel with this work a series of studies in Japan has demonstrated that TTCC inhibition reduces glomerular proteinuria in animal studies and in small clinical studies of diabetic nephropathy. Taken together these studies provide the basis for optimism about TTCC inhibition as a new therapy in renal diseases where mesangial cell proliferation is coupled with significant proteinuria. Such diseases include IgA Nephropathy, Diabetic Nephropathy and lupus nephritis

Kveta Blahova

Charles University in Prague, Czech Republic

Title: D+ hemolytic-uremic syndrome: A systematic review
Speaker
Biography:

Květa Bláhová is an Associate Professor in the Department of Pediatrics at Charles University and University Hospital Motol in Prague. She received many awards. She has membership in prestigious European societies. She has published numerous papers in reputed journals

Abstract:

Hemolytic-Uremic Syndrome (HUS) is the most common cause of acute renal failure in children below 3 years of age. It is defined by a triad of symptoms which associates hemolytic anemia with fragmented erythrocytes, thrombocytopenia and acute renal failure. Three types of HUS can be distinguished: typical HUS also called diarrhoea-associated (D+) HUS, atypical HUS (a-HUS/ D-HUS) and secondary HUS (drug induced, C+HUS, in patients receiving marrow transplantation, post partum etc.). The common event among these entities appears to be vascular endothelial cell injury, which induces mechanical destruction of erythrocytes, activation of platelet aggregation and local intravascular coagulation, especially in the renal microvasculature. D+ HUS represents nearly 90% of HUS in children. Evidence of exposure to Shiga toxin (STx 1, 2) producing Escherichia Coli (STEC) - also called Enterohemorrhagic Escherichia Coli (EHEC) - has been demonstrates in many countries in about 85% of cases. Recently serotypes O157:H7, O26 are the most frequent. Early and accurate supportive treatment and early start of dialysis is the major importance and allows a current mortality rate below 5%. Vital prognosis is compromised in cases with CNS or multi-visceral involvement. After 15 years or more of apparent recovery, 20% to 60% of patients have residual renal symptoms, with up to 20% having Chronic Renal Insufficiency (CRI) or End-Stage Renal Disease (ESRD). Atypical HUS represents less than 10% of HUS in children. Some of these cases (familial) are associated with low C3 levels, hereditary deficiency of factor H or with mutations in factor H gene. The deficiency of von Wille brand factor cleaving protease deficiency in D+HUS, as reported in adults with Thrombotic Thrombocytopenic Purpura (TTP), is not present.