Cosmas Rinaldi Adithya Lesmana

Dr. Cosmas Rinaldi Adithya Lesmana


Research Focus & Metrics

Academic Career Length

18Years (2009-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
12 December 2015 in BMC Gastroenterology
Verified
Journal Article
Open access
PDF file
CLCosmas Rinaldi Adithya Lesmana
Cosmas Rinaldi Adithya Lesmana
LPLevina S. Pakasi
Levina S. Pakasi
SISri Inggriani
Sri Inggriani
MAMaria L. Aidawati
Maria L. Aidawati
LLLaurentius A. Lesmana
Laurentius A. Lesmana
The clinical significance of non-alcoholic fatty pancreatic disease (NAFPD) or fatty pancreas is largely unknown. It is often an incidental finding on abdominal ultrasound, which is not explored further, especially its association with metabolic condition and the risk of pancreatic malignancy. The aim of this study is to evaluate the presence of NAFPD and its associated risk factors among adult medical check-up patients. A large cross-sectional study was done among adult medical check-up patients underwent abdominal ultrasound between January and December 2013 in Medistra Hospital, Jakarta. Data was obtained from the patients’ medical record and include demographic data, blood pressures, fasting blood glucose level, and lipid profile. The presence of fatty pancreas was diagnosed by ultrasound. Bivariate and multivariate analyses were done to find associated risk factors for NAFPD. Statistical analysis was done using SPSS version 17. A total of 1054 cases were included in this study; pancreas cannot be visualized in 153 cases and were excluded from the analysis. Fatty pancreas was present in 315 (35.0 %) patients. Bivariate analyses found associations among fatty pancreas and several risk factors such as gender, age, systolic and diastolic blood pressures, body mass index (BMI), fasting plasma glucose (FPG), triglycerides (TG) and cholesterol levels. Fatty pancreas is a common finding during medical check-up with a prevalence of 35 %. Fatty pancreas has significant association with metabolic factors and it might have an important role in risk of malignancy.

1 October 2020 in Clinical and Molecular Hepatology
Verified
Journal Article
Open access
PDF file
CLCosmas Rinaldi Adithya Lesmana
Cosmas Rinaldi Adithya Lesmana
MRMonica Raharjo
Monica Raharjo
RGRino A. Gani
Rino A. Gani
Managing liver cirrhosis in clinical practice is still a challenging problem as its progression is associated with serious complications, such as variceal bleeding that may increase mortality. Portal hypertension (PH) is the main key for the development of liver cirrhosis complications. Portal pressure above 10 mmHg, termed as clinically significant portal hypertension, is associated with formation of varices; meanwhile, portal pressure above 12 mmHg is associated with variceal bleeding. Hepatic vein pressure gradient measurement and esophagogastroduodenoscopy remain the gold standard for assessing portal pressure and detecting varices. Recently, non-invasive methods have been studied for evaluation of portal pressure and varices detection in liver cirrhotic patients. Various guidelines have been published for clinicians’ guidance in the management of esophagogastric varices which aims to prevent development of varices, acute variceal bleeding, and variceal rebleeding. This writing provides a comprehensive review on development of PH and varices in liver cirrhosis patients and its management based on current international guidelines and real experience in Indonesia.

23 July 2009 in Journal of Digestive Diseases
Verified
Journal Article
Closed access
PDF file
CLCosmas Rinaldi Adithya Lesmana
Cosmas Rinaldi Adithya Lesmana
IHIrsan Hasan
Irsan Hasan
UBUnggul Budihusodo
Unggul Budihusodo
RGRino A. Gani
Rino A. Gani
EKEning Krisnuhoni
Ening Krisnuhoni
LLLaurentius A. Lesmana
Laurentius A. Lesmana

23 December 2017 in JGH Open
Verified
Journal Article
Open access
PDF file
CLCosmas Rinaldi Adithya Lesmana
Cosmas Rinaldi Adithya Lesmana
RGRino A Gani
Rino A Gani
LLLaurentius A Lesmana
Laurentius A Lesmana
Background and Aim: Non‐alcoholic fatty pancreas disease (NAFPD) is a disease that ranges from simple steatosis and can further lead to chronic pancreatitis and possible pancreatic cancer development. Its exact pathogenesis and impact on clinical practice are still largely unknown. Pancreatic cancer is still the most lethal malignancy in the world. Studies about the relationship between NAFPD and pancreatic cancer are still lacking. This study aims to find the possible role of endoscopic ultrasound (EUS) examination as a screening tool in NAFPD patients based on EUS examination among pancreatic cancer patients.Methods: EUS hospital data were collected within a 2‐year period, and all patients who underwent EUS procedures were analyzed. Pancreatic malignancy was diagnosed based on imaging and tumor markers and cytopathology using the endoscopic ultrasound fine needle aspiration (EUS‐FNA) procedure. Patients with pre‐existing pancreatic diseases, significant alcohol consumption, or other primary cancer with metastasis to the pancreas were excluded. Statistical analysis was performed using SPSS version 23.0.Results: In total, 162 patients (75 females and 87 males) were recruited for database analysis.^ Pancreatic malignancy was found in 43 (26.5%) patients, whereas fatty pancreas was found in 53 (32.7%) patients, and this was commonly found among pancreatic cancer patients.^ Based on logistic regression analysis, factors such as age, gender, diabetes, and chronic pancreatitis were not found to be significant risk factors for pancreatic malignancy where fatty pancreas is the only significant risk factor for pancreatic cancer (odds ratio: 18.027 [95% CI: 7.288–44.588]).Conclusion: Prevalence of NAFPD among pancreatic cancer patients is high. Future studies can be conducted to show whether EUS can be considered a screening tool for the early detection of pancreatic malignancy in NAFPD patients; a cohort prospective study might also be needed to show clear causality between fatty pancreas and pancreatic cancer.

19 July 2022 in Journal of Clinical and Translational Hepatology
Verified
Journal Article
Open access
PDF file
SNSaut Horas H. Nababan
Saut Horas H. Nababan
CLCosmas Rinaldi Adithya Lesmana
Cosmas Rinaldi Adithya Lesmana
Portal hypertension in nonalcoholic fatty liver disease (NAFLD) mostly occur in cirrhotic stage. However, several experimental and clinical studies showed evidence of portal hypertension in NAFLD without significant or advance fibrosis. This early development of portal hypertension in NAFLD is associated with liver sinusoidal contraction by hepatocellular lipid accumulation and ballooning, which is also accompanied by capillarization and dysfunction of liver sinusoidal endothelial cells. Both of these impaired mechanical and molecular components can cause an increase in intrahepatic vascular resistance which lead to the increase of portal pressure in the absence of significant liver fibrosis. Extrahepatic factors such as insulin resistance and gut dysbiosis may also contribute to liver sinusoidal endothelial dysfunction and early portal hypertension in NAFLD. The clinical impact of early portal hypertension in NAFLD is still unclear. However, clinical tools for diagnosis and monitoring of portal hypertension in NAFLD are being investigated to predict high-risk patients and to guide therapy.

13 June 2011 in Journal of Clinical Pathology
Verified
Journal Article
Closed access
PDF file
CLCosmas Rinaldi Adithya Lesmana
Cosmas Rinaldi Adithya Lesmana
SSSimon Salim
Simon Salim
IHIrsan Hasan
Irsan Hasan
ASAndri S Sulaiman
Andri S Sulaiman
RGRino A Gani
Rino A Gani
UBUnggul Budihusodo
Unggul Budihusodo
Background: A non-invasive method to assess liver fibrosis by measuring liver stiffness with transient elastography (TE) has been recently introduced. The role of TE among chronic hepatitis B (CHB) patients in starting antiviral therapy in the primary care setting is still controversial because of its high cost. The AST to platelet ratio index (APRI) could be a much cheaper alternative. Objectives: This study compares the diagnostic accuracy of TE and APRI in assessing liver fibrosis in CHB patients. Patients and Methods: A cross-sectional study in CHB patients intending to start antiviral treatment. Liver fibrosis was staged according to the METAVIR scoring system. Liver stiffness was measured by TE performed on the same day with liver biopsy, while APRI was calculated as follows: APRI=(AST/upper limit of normal)×100/platelet count (109/l). Cutoff levels of liver stiffness and APRI were calculated by using the receiver operating characteristic curve to detect significant liver fibrosis, defined as fibrosis stage F2 or more. Results: 117 patients were enrolled in the study; their mean age was 40.6±10.97 years. The median liver stiffness was 5.9 kPa (2.5–48 kPa) and the median APRI was 0.239 (0.09–2.73). The cutoff level of liver stiffness was 5.85 kPa for ≥F2 with an AUC of 0.614, 60.3% sensitivity, 63.6% specificity, 73.3% PPV, 49.1% NPV and a LR+ of 1.66. The APRI cutoff level was 0.235 for F≥2 with an AUC of 0.693, 64.4% sensitivity, 70.5% specificity, 78.3% PPV, 54.4% NPV and a LR+ of 2.18. Both methods gave comparable diagnostic accuracy. Conclusion: APRI is a useful marker to screen liver fibrosis in the primary care setting when TE is not available.