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66 citation(s) found for "Ahmad, Ali".

Update on pharmacotherapies for cholestatic liver disease
Ali, Ahmad H. , Tabibian, James H. , Lindor, Keith D. , Tabibian, James H

Mayo Clinic

Hepatology Communications | December 21, 2016 | Volume: 1 | Issue: 1 | Pages: 7-17

10.1002/hep4.1013 | PMID 29404429 Get It

Cholestatic liver diseases are conditions with impaired bile formation and/or flow due to genetic, immunologic, environmental, or other causes. Unless successfully treated, this can lead to chronic liver injury and end‐stage liver disease. Primary biliary cholangitis (PBC) and primary sclerosing cholangitis (PSC) embody the most prominent adult cholestatic liver diseases with regard to incidence, morbidity, and mortality. A considerable proportion of patients with PBC and PSC experience progressive liver disease and ultimately liver‐related death due to a paucity of effective pharmacotherapy; however, novel pharmacologic developments offer substantial promise in this regard. Here, we provide a brief review and update on current and emerging pharmacotherapies for PBC and PSC. (Hepatology Communications 2017;1:7–17)
The Microbiome and Primary Sclerosing Cholangitis
Ali, Ahmad H. , Carey, Elizabeth J. , Lindor, Keith

Mayo Clinic

Seminars in Liver Disease | December 20, 2016 | Volume: 36 | Issue: 04 | Pages: 340-348

10.1055/s-0036-1594007 | PMID 27997974 Get It

Novel treatments in primary sclerosing cholangitis
Ali, Ahmad H. , Lindor, Keith D.

Mayo Clinic

Clinical Liver Disease | December 14, 2016 | Volume: 8 | Issue: 5 | Pages: 132-135

10.1002/cld.588 | PMID 31041081 Get It

Obeticholic acid for the treatment of primary biliary cholangitis
Ali, Ahmad H. , Lindor, Keith D.

Mayo Clinic

Expert Opinion on Pharmacotherapy | July 29, 2016 | Volume: 17 | Issue: 13 | Pages: 1809-1815

10.1080/14656566.2016.1218471 | PMID 27468093 Get It

A Randomized, Placebo-Controlled Clinical Trial of Efficacy and Safety: Modafinil in the Treatment of Fatigue in Patients With Primary Biliary Cirrhosis
Silveira, Marina G., Gossard, Andrea A., Stahler, Alisha C., Jorgensen, Roberta A., Petz, Janice L., Ali, Ahmad H. , Lindor, Keith D.

Mayo Clinic

American Journal of Therapeutics | May 12, 2016 | Volume: 24 | Issue: 2 | Pages: e167-e176

10.1097/mjt.0000000000000387 | PMID 27148676 Get It

Background and Aims: Fatigue is a common symptom of primary biliary cirrhosis (PBC), and is associated with an impaired quality of life. Study Question: No studies have assessed the use of modafinil in fatigue related to PBC in a controlled manner. Study Design, Measures, and Outcomes: A randomized, double-blind, placebo-controlled study was conducted to determine the safety and efficacy of modafinil for the treatment of fatigue in PBC. Forty patients were randomized to modafinil (n = 20) or placebo (n = 20) for 12 weeks. A verbal report of fatigue for at least 6 months was required for enrollment. Modafinil was administered at 100 mg by mouth once daily; a change by 50 mg every 2 weeks (maximum: 200 mg once daily) was allowed, depending on the subject's response to treatment. The primary outcome was defined as a ≥50% improvement in fatigue severity [quantified by the Fisk Fatigue Impact Scale (FFIS)] after 12 weeks of treatment, compared with baseline values. Results: Thirty-three PBC patients completed the study. After 12 weeks of therapy, only 5 patients had a ≥50% reduction in FFIS scores: 3 patients (17.6%) in the modafinil arm and 2 (12.5%) in the placebo arm (P = 1.00). Change in median FFIS score was not statistically different between patients in the 2 treatment groups (P = 0.36). Modafinil was associated with minimal adverse events (headaches, diarrhea, and rash). Conclusions: In patients with PBC who have fatigue, treatment with modafinil for 12 weeks was safe and fairly well tolerated; however, it did not result in beneficial effects on fatigue compared with patients treated with placebo (CONSORT Table 1). ClinicalTrials.gov identifier NCT00943176.
Current research on the treatment of primary sclerosing cholangitis
Ali, Ahmad H. , Carey, Elizabeth J. , Lindor, Keith D.

Mayo Clinic

Intractable & Rare Diseases Research | November 13, 2014 | Volume: 4 | Issue: 1 | Pages: 1-6

10.5582/irdr.2014.01018 | PMID 25674381 Get It