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Dive into the research topics where Puneet Dhar is active.

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Featured researches published by Puneet Dhar.


Indian Journal of Surgical Oncology | 2015

Pancreatic Cancer in Chronic Pancreatitis

Puneet Dhar; S. Kalghatgi; Vivek Saraf

Data exists to indicate a definite association between chronic pancreatitis and pancreatic cancer. The strength of this association varies between various causes of pancreatitis, with hereditary and tropical pancreatitis more likely to result in malignancy. Pathogenesis may involve genetic factors, diabetes, smoking and alcohol consumption. Clinically a significant overlap exists between the two conditions, with histology difficult to obtain and interpret in this setting. Biomarkers like CA19-9 and others may be useful, as is a variety of newer imaging modalities. Treatment needs to be individualised as surgery offers the only chance of cure, albeit in but a few.


World Journal of Surgical Oncology | 2005

Spontaneous rupture of giant gastric stromal tumor into gastric lumen

Rajiv Mehta; Vayoth O Sudheer; Anil John; Raghavan R Nandakumar; Puneet Dhar; S. Sudhindran; Vallath Balakrishnan

BackgroundGastrointestinal stromal tumors (GIST) constitute a large majority of mesenchymal tumors of the gastrointestinal (GI) tract, which express the c-kit proto-oncogene protein, a cell membrane receptor with tyrosine kinase activity. GI stromal tumors of the stomach are usually associated with bleeding, abdominal pain or a palpable mass.Case presentationA 75-year-old male presented with upper abdominal pain and palpable mass. Computed tomographic (CT) scan of the abdomen showed a large mass arising in the posterior aspect of fundus, body, and greater curvature of the stomach. Second day after the admission, there was significant reduction in the size of the tumor, clinically as well as radiologically. Endoscopic biopsy showed large bulge in fundus and corpus of the stomach posteriorly with an opening in the posterior part of the corpus, and biopsy from the edge of the opening reveled GIST. Patient underwent curative resection.ConclusionSpontaneous ruptured of giant gastric stromal tumor is very rare presentation of stomach GIST. Thorough clinical examination and timely investigation can diagnose rare complication.


Anz Journal of Surgery | 2008

LAPAROSCOPY IN SUSPECTED ABDOMINAL TUBERCULOSIS IS USEFUL AS AN EARLY DIAGNOSTIC METHOD

Prasad Krishnan; Sudheer Othiyil Vayoth; Puneet Dhar; Sudhindran Surendran; Shaji Ponnambathayil

Background:  Establishing a histological diagnosis in abdominal tuberculosis can be difficult, frequently delaying treatment. The aim of the study was to evaluate the role of laparoscopy for ascertaining the diagnosis in suspected abdominal tuberculosis.


Indian Journal of Gastroenterology | 2015

Acute liver failure due to zinc phosphide containing rodenticide poisoning: Clinical features and prognostic indicators of need for liver transplantation

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.


Liver Transplantation | 2016

Perioperative prostaglandin e1 infusion in living donor liver transplantation: A double‐blind, placebo‐controlled randomized trial

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

Randomized trial on extended versus modified right lobe grafts in living donor liver transplantation

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

A New Score to Predict Recipient Mortality from Preoperative Donor and Recipient Characteristics in Living Donor Liver Transplantation (DORMAT Score).

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.


Indian Journal of Gastroenterology | 2014

Gastrointestinal intramural hematoma-Analysis of clinical and radiological features for early differentiation from mesenteric ischemia

R. Subhash; G. Unnikrishnan; Dinesh Balakrishnan; O. V. Sudheer; Puneet Dhar; S. Sudhindran

IntroductionLong-term anticoagulation is associated with hemorrhage at various sites. Gastrointestinal intramural bleeds and hematomas (IMH) often mimic mesenteric ischemia (MI) due to similar clinical settings and imaging features, making early differentiation difficult.AimTo compare the demography, clinical features and imaging characteristics of patients presenting with IMH with those of MI, so as to help in evolving clinical and imaging guidelines to differentiate both early in the course of the disease.MethodsAll radiologically (contrast-enhanced computed tomogram [CT]) diagnosed cases of gastrointestinal IMH from the hospital database during the period between 2006 and 2012 were retrospectively analyzed. This data was compared with the clinical and imaging features of a group of surgically confirmed MI during the same period. Patients not on anticoagulation therapy at the time of presentation and those with incomplete clinical or radiological data were excluded from the study.ResultsThere were 16 patients in IMH group and 54 patients in MI group. Clinical features like overt rectal bleeding or melena, and prolonged prothrombin time-international normalized ratio (PT-INR) more than three, and CT features like proximal location in the bowel, increased bowel wall thickness, hyperdensity on plain scan (>40 Hounsfield units (HU)), and short segment bowel involvement were significantly associated with IMH. Visualization of embolus and absent mesenteric vasculature to a segment of intestine in CT was significantly associated with MI.ConclusionAttention to clinical features and early CT scan can aid in early differentiation of IMH from MI, facilitating appropriate intervention early in the course of disease.


Journal of clinical and experimental hepatology | 2011

44 hepatic steatosis-quantification by non-enhanced ct scan.

U Dattaram; St Binoj; Puneet Dhar; O. V. Sudheer; G Unnikrishnan; R Menon; Dinesh Balakrishnan; S. Sudhindran

152


Journal of clinical and experimental hepatology | 2011

19 cost of immunosuppression using generic products after liver transplantation.

St Binoj; S Abubacker; R Menon; B Dinesh; G Unnikrishnan; O. V. Sudheer; Puneet Dhar; S. Sudhindran

142

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O. V. Sudheer

Amrita Institute of Medical Sciences and Research Centre

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S. Sudhindran

Amrita Institute of Medical Sciences and Research Centre

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Dinesh Balakrishnan

Amrita Institute of Medical Sciences and Research Centre

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G. Unnikrishnan

Amrita Institute of Medical Sciences and Research Centre

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Unnikrishnan Gopalakrishnan

Amrita Institute of Medical Sciences and Research Centre

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Akshay P. Bavikatte

Amrita Institute of Medical Sciences and Research Centre

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Sudheer Othiyil Vayoth

Amrita Institute of Medical Sciences and Research Centre

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Sudhindran Surendran

Amrita Institute of Medical Sciences and Research Centre

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K.Y. Santosh Kumar

Amrita Institute of Medical Sciences and Research Centre

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Viju Kumar Bharathan

Amrita Institute of Medical Sciences and Research Centre

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