Unnikrishnan Gopalakrishnan
Amrita Institute of Medical Sciences and Research Centre
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Publication
Featured researches published by Unnikrishnan Gopalakrishnan.
Indian Journal of Gastroenterology | 2015
Vivek Saraf; Supriya Pande; Unnikrishnan Gopalakrishnan; Dinesh Balakrishnan; O. V. Sudheer; Puneet Dhar; S. Sudhindran
Zinc phosphide (ZnP) containing rodenticide poisoning is a recognized cause of acute liver failure (ALF) in India. When standard conservative measures fail, the sole option is liver transplantation. Records of 41 patients admitted to a single centre with ZnP-induced ALF were reviewed to identify prognostic indicators for requirement of liver transplantation. Patients were analyzed in two groups: group I (n = 22) consisted of patients who either underwent a liver transplant (n = 14) or died without a transplant (n = 8); group II (n = 19) comprised those who survived without liver transplantation. International normalized ratio (INR) in group I was 9 compared to 3 in group II (p < 0.001). Encephalopathy occurred only in group I. Model for End-Stage Liver Disease (MELD) score in group I was 41 compared to 24 in group II (p < 0.001). MELD score of 36 (sensitivity of 86.7 %, specificity of 90 %) or a combination of INR of 6 and encephalopathy (sensitivity of 100 %, specificity of 83 %) were the best indicators of mortality. Such patients should undergo urgent liver transplantation.
BMC Complementary and Alternative Medicine | 2017
Aswathy Sreedevi; Unnikrishnan Gopalakrishnan; Sundaram Karimassery Ramaiyer; Leelamoni Kamalamma
BackgroundType two diabetes is a complex and demanding chronic disease and its impact in a state (Kerala) which leads India in terms of the number of people with Diabetes is profound. Though the male to female ratio among the people with diabetes is roughly equal, women are uniquely and more severely affected. Management of type two Diabetes requires considerable dexterity on the part of the patient to manage drugs, diet and exercise. Therefore, in a low middle-income country like India it is necessary to look at low cost interventions that can empower the patient and build on available resources to help manage diabetes. Hence, we studied the feasibility and effect of two low cost interventions; yoga and peer support on glycaemic and other outcomes among women with type two diabetes.MethodsAn open label parallel three armed randomized control trial was conducted among 124 recruited women with Diabetes for three months. Block randomization with a block length of six was carried out with each group having at least 41 women. In the Yoga arm, sessions by an instructor, consisting of a group of postures coordinated with breathing were conducted for an hour, two days a week. In the peer support arm each peer mentor after training visited 13–14 women with diabetes every week followed by a phone call. The meeting was about applying disease management or prevention plans in daily life.ResultsThere was a trend in decline of fasting plasma glucose in the peer and yoga group and of glycosylated haemoglobin (HbA1c) in the yoga group only, though not significant. A significant decrease was observed in diastolic blood pressure and hip circumference in the yoga group. The process indicated that most (80%) of the women in the yoga group attended classes regularly and 90% of the women in the peer group reported that peer mentoring was useful.ConclusionThe effect of yoga and peer support on glycaemic outcomes was incremental. Longer term studies are necessary to ascertain the benefits shown by this feasibility study.Trial registrationCTRI/2011/12/002227 dated 14/12/2011.
Liver Transplantation | 2016
Viju Kumar Bharathan; Biju Chandran; Unnikrishnan Gopalakrishnan; Christi Titus Varghese; Dinesh Balakrishnan; O. V. Sudheer; Puneet Dhar; Sudhindran Surendran
The role of prostaglandin E1 (PGE1) infusion in improving early graft function has not been well defined, especially in the scenario of living donor liver transplantation (LDLT). We designed a randomized, double‐blind, placebo‐controlled trial to evaluate the role of perioperative PGE1 infusion in LDLT. Patients in the study arm received PGE1 (alprostadil) at the rate of 0.25 μg/kg/hour, starting at 1 hour after portal venous reperfusion, and continued for 96 hours. The primary endpoint was early allograft dysfunction (EAD). We analyzed multiple secondary endpoints including postoperative liver function and renal function parameters, acute kidney injury (AKI), hepatic artery thrombosis (HAT), postoperative bleeding, overall mortality, and posttransplant hospital stay. The incidence of EAD was lower in the PGE1 arm, although the difference did not reach statistical significance (22.4% versus 36%; P = 0.21). Among the secondary endpoints, the incidence of AKI was significantly lower in the PGE1 arm (8.2% versus 28%; P = 0.02), as were the peak and mean postoperative creatinine levels. The need for renal replacement therapy was similar between the 2 groups. Among the postoperative graft function parameters, postoperative alanine aminotransferase level was significantly lower in the PGE1 arm (P = 0.04), whereas the remaining parameters including serum bilirubin, aspartate aminotransferase, and international normalized ratio were similar between the 2 arms. There was no difference in the incidence of HAT and postoperative bleeding, in‐hospital mortality, and posttransplant hospital stay between the 2 arms. Perioperative PGE1 infusion reduces the incidence of posttransplant renal dysfunction in patients undergoing LDLT. Liver Transplantation 22 1067–1074 2016 AASLD
Liver Transplantation | 2018
Christi Titus Varghese; Viju Kumar Bharathan; Unnikrishnan Gopalakrishnan; Dinesh Balakrishnan; O. V. Sudheer; Puneet Dhar; S. Sudhindran
Despite advances in the practice of living donor liver transplantation (LDLT), the optimum surgical approach with respect to the middle hepatic vein (MHV) in right lobe LDLT remains undefined. We designed a randomized trial to compare the early postoperative outcomes in recipients and donors between extended right lobe grafts (ERGs; transection plane was maintained to the left of MHV and division of MHV performed beyond the segment VIII vein) and modified right lobe grafts (MRGs; transection plane was maintained to the right of MHV; the segment V and VIII drainage was reconstructed using a conduit of recipient portal vein). Eligible patients (n = 86) were prospectively randomized into the ERG arm (n = 43) and the MRG arm (n = 43) at the beginning of donor hepatectomy. The primary endpoint considered in this equivalence trial was patency of the MHV or the reconstructed “neo‐MHV” in the recipient. The secondary endpoints included biochemical parameters, postoperative complications, mortality in recipients as well as donors and volume regeneration of remnant liver in donors, measured at 2 months. The patency of the MHV was comparable in the ERG and MRG arms (90.7% versus 81.4%; difference, 9.3%; 95% confidence interval [CI], –5.8 to 24.4; z score, 1.245; P = 0.21). Volume regeneration of the remnant liver in donors was significantly better in the MRG arm (111.3% versus 87.3%; mean difference, 24%; 95% CI, 14.6‐33.3; P < 0.001). The remaining secondary endpoints in donors and recipients were similar between the 2 arms. To conclude, MRG with reconstructed neo‐MHV has comparable patency to native MHV in ERG and confers equivalent graft outflow in the recipient. Furthermore, it allows better remnant liver regeneration in the donor at 2 months. Liver Transplantation 24 888–896 2018 AASLD.
Annals of Transplantation | 2017
Raghavendra Babu; Pulkit Sethi; Sudhindran Surendran; Puneet Dhar; Unnikrishnan Gopalakrishnan; Dinesh Balakrishnan; Binoj Sivasankarapillai Thankamonyamma; Sudheer Othiyil Vayoth; Manoj Thillai
BACKGROUND Recipient outcomes in adult living donor liver transplantation depend on various characteristics in both recipient and donor. We aimed to derive a score based upon preoperative characteristics in donor and recipient that could predict the recipient mortality in adult living donor liver transplantation. MATERIAL AND METHODS Retrospective data of 100 living donor liver transplantation recipients and their respective donors were analyzed for preoperative factors that correlated with recipient mortality. Statistically significant factors were weighted appropriately to derive a regression equation to obtain a donor-to-recipient match (DORMAT) score. This score was applied to 71 patients prospectively and their outcome was analyzed. RESULTS Donor-recipient match (DORMAT) score, derived using regression analysis of the significant variables was [0.002 (Recipient age) + 0.013 (Recipient BMI) + 0.055 (SBP) + 0.344 (HRS) + 0.022 (Pre-op culture positivity) + 0.01 (Donor age) - 0.639]×100. DORMAT score, when validated to a prospective cohort of 71 adult-to-adult LDLT patients, had a C-statistic (area under ROC curve) of 0.712. The mortality rate was seen to increase with increasing DORMAT score. CONCLUSIONS DORMAT score is a useful clinical decision-making tool to predict recipient mortality in adult living donor liver transplantation.
Journal of The American College of Surgeons | 2017
K.Y. Santosh Kumar; Johns Shaji Mathew; Dinesh Balakrishnan; Viju Kumar Bharathan; Binoj Sivasankara Pillai Thankamony Amma; Unnikrishnan Gopalakrishnan; Puneet Dhar; Sudheer Othiyil Vayoth; S. Sudhindran
Journal of clinical and experimental hepatology | 2017
Amol Vijay Kanetkar; Dinesh Balakrishnan; Sudhindran Sudhindran; Puneet Dhar; Unnikrishnan Gopalakrishnan; O. V. Sudheer
Indian Journal of Thoracic and Cardiovascular Surgery | 2018
Lokesh Sreedharan; Neethu Krishna; Unnikrishnan Gopalakrishnan; Praveen Kerala Varma
Hpb | 2018
M. Kathirvel; S. Mallick; M.S. Durairaj; K. Nair; J. Shaji Mathew; S.T. Binoj; R.N. Menon; Dinesh Balakrishnan; Unnikrishnan Gopalakrishnan; S. Sudhindran
Hpb | 2018
S. Mallick; M. Kathirvel; M. Thillai; P. Sethi; M.S. Durairaj; K. Nair; R.N. Menon; Dinesh Balakrishnan; Unnikrishnan Gopalakrishnan; S. Sudhindran
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Amrita Institute of Medical Sciences and Research Centre
View shared research outputsAmrita Institute of Medical Sciences and Research Centre
View shared research outputsAmrita Institute of Medical Sciences and Research Centre
View shared research outputsAmrita Institute of Medical Sciences and Research Centre
View shared research outputsBinoj Sivasankarapillai Thankamonyamma
Amrita Institute of Medical Sciences and Research Centre
View shared research outputsAmrita Institute of Medical Sciences and Research Centre
View shared research outputsAmrita Institute of Medical Sciences and Research Centre
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