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3045 citation(s) found for "Ha, Patrick K".

Comparison of Therapies for Primary Prevention of Esophageal Variceal Bleeding: A Systematic Review and Network Meta‐analysis
Sharma, Mayank , Singh, Siddharth , Desai, Vivek, Shah, Vijay H. , Kamath, Patrick S. , Murad, M. Hassan , Simonetto, Douglas A. , Murad, Mohammad Hassan, Murad, M Hassan , Simonetto, Douglas A

Hepatology | August 20, 2018 | Volume: 69 | Issue: 4 | Pages: 1657-1675

10.1002/hep.30220 | PMID 30125369 Get It

We performed a systematic review with network meta‐analysis (NMA) to compare the efficacy of different approaches in primary prevention of esophageal variceal bleeding and overall survival in patients with cirrhosis with large varices. Thirty‐two randomized clinical trials (RCTs) with 3,362 adults with cirrhosis with large esophageal varices and no prior history of bleeding, with a minimum of 12 months of follow‐up, were included. Nonselective beta‐blockers (NSBB), isosorbide‐mononitrate (ISMN), carvedilol, and variceal band ligation (VBL), alone or in combination, were compared with each other or placebo. Primary outcomes were reduction of all‐cause mortality and prevention of esophageal variceal bleeding. Random‐effects NMA was performed and summary estimates were expressed as odds ratio and 95% confidence intervals (OR; CI). Quality of evidence was critically appraised using the Grading of Recommendations, Assessment, Development and Evaluation approach. Moderate quality evidence supports NSBB monotherapy (0.70; 0.49‐1.00) or in combination with VBL (0.49; 0.23‐1.02) or ISMN (0.44; 0.21‐0.93) for decreasing mortality in patients with cirrhosis with large esophageal varices and no prior history of bleeding. Moderate‐quality evidence supports carvedilol (0.21; 0.08‐0.56) and VBL monotherapy (0.33; 0.19‐0.55) or in combination with NSBB (0.34; 0.14‐0.86), and low‐quality evidence supports NSBB monotherapy (0.64; 0.38‐1.07) for primary prevention of variceal bleeding. VBL carries a higher risk of serious adverse events compared with NSBB.Conclusion:NSBB monotherapy may decrease all‐cause mortality and the risk of first variceal bleeding in patients with cirrhosis with large esophageal varices. Additionally, NSBB carries a lower risk of serious complications compared with VBL. Therefore, NSBB may be the preferred initial approach for primary prophylaxis of esophageal variceal bleeding.
Proposed response assessment and endpoints for meningioma clinical trials: report from the Response Assessment in Neuro-Oncology Working Group
Huang, Raymond Y. , Weller, Michael , Dunn, Ian F. , Preusser, Matthias , Rogers, Leland , Raizer, Jeffrey J. , Schiff, David , Soffietti, Riccardo , Tonn, Jörg-Christian, Vogelbaum, Michael A. , Reardon, David A. , Wen, Patrick Y. , Galanis, Evanthia , Weller, Michael , Soffietti, Riccardo , Preusser, Matthias , Huang, Raymond , Bi, Wenya Linda , Kaley, Thomas , Blakeley, Jaishri O. , McDermott, Michael , Weber, Damien Charles , Wen, Patrick Yung

Neuro-Oncology | August 17, 2018 | Volume: 21 | Issue: 1 | Pages: 26-36

10.1093/neuonc/noy137 | PMID 30137421 Get It

Multi-ingredient pre-workout supplements, safety implications, and performance outcomes: a brief review
Harty, Patrick S. , Zabriskie, Hannah A. , Erickson, Jacob L. , Molling, Paul , Jagim, Andrew R. , Molling, Paul E, Jagim, Andrew R , Harty, Patrick S , Zabriskie, Hannah A , Kerksick, Chad M.

Journal of the International Society of Sports Nutrition | August 8, 2018 | Volume: 15 | Issue: 1 | Pages: No page available

10.1186/s12970-018-0247-6 | PMID 30089501 Get It

Posttraumatic Stress Disorder in Patients with Heavy Alcohol Consumption and Alcoholic Hepatitis
Samala, Niharika , Lourens, Spencer, Shah, Vijay H. , Kamath, Patrick S. , Crabb, David W. , Tang, Qing , Radaeva, Svetlana , Liangpunsakul, Suthat , Chalasani, Naga , Crabb, David W , Liangpunsakul, Suthat , Sanyal, Arun J.

Alcoholism: Clinical and Experimental Research | August 7, 2018 | Volume: 42 | Issue: 10 | Pages: 1933-1938

10.1111/acer.13862 | PMID 30080255 Get It

BackgroundLifetime prevalence of posttraumatic stress disorder (PTSD) in the general population is reported to be 6.8%. Individuals with alcohol dependence and substance abuse have high prevalence of PTSD. However, the prevalence of PTSD in heavy drinkers with alcoholic hepatitis (AH) is not known.The study's aim was to determine the prevalence of PTSD in heavy drinkers with and without AH.MethodsWe screened for PTSD using the Primary Care‐PTSD questionnaire among heavy drinkers with (n = 115) and without (n = 64) AH participating in a multicenter observational study in which participants were followed up to 12 months following their enrollment.ResultsThe prevalence of PTSD in heavy drinkers with AH was 34% and was not different from heavy drinking controls without liver disease (34%). In the entire group screened for PTSD, the presence of PTSD was associated with higher alcohol consumption as reported by average drinks per last 30 days and average grams of alcohol consumed per day (p = 0.047 for both tests), but not associated with relapse of heavy drinking or mortality. Similarly, patients with AH and PTSD did not have higher relapse rate or higher mortality compared to patients with AH but no PTSD.ConclusionsCompared to previously reported prevalence in general population, heavy drinking individuals with or without AH have significantly higher prevalence of PTSD. However, PTSD was not associated with higher relapse rate or higher mortality in this population.
Medicare Beneficiary Out-of-Pocket Costs for Generic Cardiovascular Medications Available Through $4 Generic Drug Discount Programs
Liu, Patrick , Dhruva, Sanket S. , Shah, Nilay D. , Ross, Joseph S. , Ross, Joseph S

Annals of Internal Medicine | July 24, 2018 | Volume: 169 | Issue: 11 | Pages: 817-819

10.7326/m18-0965 | PMID 30039170 Get It

Laboratory Utilization and Analytical Validation of Fecal Electrolyte Tests
Parakh, Rugvedita , Greene, Dina N. , Block, Darci R , Ranjitkar, Pratistha , Greene, Dina , Mathias, Patrick C

The Journal of Applied Laboratory Medicine | July 23, 2018 | Volume: 1 | Issue: 6 | Pages: 668-677

10.1373/jalm.2016.022590 | PMID 33379818 Get It

Abstract Background Chronic diarrhea can be categorized as fatty, watery, or inflammatory. Watery diarrhea is further divided into secretory or osmotic types and can be differentiated by measuring fecal electrolytes and osmotic gap. However, with widespread use of endoscopy, it is unclear if these measurements are being used clinically. Furthermore, because stool is not a validated specimen type for Food and Drug Administration–approved electrolyte assays, utilization is a practical concern for laboratories before analytical validation. Here, we determined the clinical utility and validated the performance characteristics of stool electrolytes on the Beckman Coulter AU680. Methods Historical results and literature review were used to determine the clinically relevant ranges for stool electrolytes (Na+, Cl−, K+, phosphate, and Mg2+). Additionally, medical chart review was performed (n = 44 patients) on results to evaluate their clinical utility in chronic diarrhea work-up. Linearity, precision, and stability studies were performed on the AU680. Accuracy was evaluated by comparing results to the Roche Cobas 6000 c501. Results For all cases, stool electrolytes and osmotic gap proved valuable in chronic diarrhea work-up. The imprecision of the assays ranged from 0% to 5.9%. All assays were found to be linear within the instrument's analytical measurement range with appropriate slopes and intercepts. The bias between the AU680 and the Roche c501 ranged from −0.48 to 2.39 (mmol/L or mg/dL). Na+, Cl−, and K+ were stable refrigerated for 5 days and up to 1 freeze-thaw cycle. Phosphate and Mg2+ were stable refrigerated for 48 h, but unstable to freeze-thaw cycles. Conclusions Stool osmotic gap is valuable for evaluating chronic diarrhea and can be calculated using electrolyte concentrations measured on the AU680.
Proenkephalin (PENK) as a Novel Biomarker for Kidney Function
Struck, Joachim , Wu, Alan H.B. , Zarbock, Alexander , Somma, Salvatore Di , Mehta, Ravindra L. , Nadim, Mitra K. , Maisel, Alan S. , Neath, Sean‐Xavier , Jaffe, Allan S. , Pickkers, Peter , Jaffe, Allan, Mehta, Ravindra L , Beunders, Remi , Koyner, Jay L. , Murray, Patrick T. , Jaffe, Allan S.

The Journal of Applied Laboratory Medicine | July 23, 2018 | Volume: 2 | Issue: 3 | Pages: 400-412

10.1373/jalm.2017.023598 | PMID 33636859 Get It

Abstract Background The assessment of kidney function and detection of acute kidney injury (AKI) remain cumbersome. On the one hand, because of limited accuracy of established tests: The most widely used methods are creatinine based, which lack in sensitivity, as creatinine is not purely filtrated by the kidney and rises relatively late after onset of AKI. On the other hand, because of labor-intensiveness: Gold standard inulin clearance and comparable methods involve intravenous compound infusion, blood sampling at several time points, and have error-sensitive determination methods. In recent years, several biomarkers have been put forward (e.g., NGAL, KIM-1, TIMP-2*IGFBP-7), but clinical implementation is limited up to now. Content Proenkephalin (PENK) represents a new candidate to determine kidney function. This peptide is cleaved from the precursor peptide preproenkephalin A alongside enkephalins (endogenous opioids) and is filtrated in the glomerulus. PENK plasma concentration appears to accurately represent glomerular filtration rate in patients diagnosed with sepsis or cardiac diseases. Moreover, increased PENK concentration is found to be associated with longer-term outcome concerning AKI and cardiac diseases. Lastly, the predominant receptor of enkephalins, the δ-opioid receptor, is expressed with the highest density in the kidney, suggesting that enkephalins could also exert a direct effect on kidney function. Summary In this review, we present an overview of enkephalins and the assessment of kidney function using this possible new functional biomarker PENK and compare it with established and novel biomarkers.
The Utility of MR Elastography to Differentiate Nodular Regenerative Hyperplasia from Cirrhosis
Navin, Patrick J. , Hilscher, Moira , Welle, Christopher L. , Mounajjed, Taofic, Kamath, Patrick S. , Venkatesh, Sudhakar K. , Hilscher, Moira B, Venkatesh, Sudhakar K , Navin, Patrick , Torbenson, Michael

Hepatology | July 17, 2018 | Volume: 69 | Issue: 1 | Pages: 452-454

10.1002/hep.30175 | PMID 30014488 Get It

Vitamin C for Vasoplegia After Cardiopulmonary Bypass: A Case Series
Wieruszewski, Patrick M. , Nei, Scott D. , Maltais, Simon, Schaff, Hartzell V. , Wittwer, Erica D. , Schaff, Hartzell , Wieruszewski, Patrick M

A&A Practice | July 11, 2018 | Volume: 11 | Issue: 4 | Pages: 96-99

10.1213/xaa.0000000000000752 | PMID 29634537 Get It

Cardiac vasoplegia remains a significant contributor of morbidity and mortality in cardiac surgery patients after cardiopulmonary bypass. Effective therapeutic options for vasopressor-refractory vasoplegia are limited. We report 3 patients in whom we administered high-dose intravenous ascorbic acid (vitamin C), a cofactor for endogenous catecholamine synthesis, to treat vasoplegia refractory to epinephrine, vasopressin, and norepinephrine after surgery requiring cardiopulmonary bypass. Reductions in vasopressor requirements were observed in all 3 patients, and, in 2 patients, norepinephrine was completely discontinued within 24 hours. Ascorbic acid is a novel potential therapeutic option for cardiac vasoplegia that warrants rigorous prospective studies.
Harmonization of technology across an integrated delivery network
Anderson, Jared , Cooley, T., Torre, Charlie De la, Rocco, James Anthony Della, Dorn, Mitchell, Ferer, Darren S., Friudenberg, Patrick, Ganio, Michael C, Lim, Dennison, McGregory, Michael E., Nickman, Nancy A. , Schenkat, Daniel H, Shah, Shailly, Tjhio, David, Urbanski, Chris, Volpe, Gwen

American Journal of Health-System Pharmacy | July 9, 2018 | Volume: 75 | Issue: 14 | Pages: 1073-1078

10.2146/ajhp170301 | PMID 29987061 Get It