Prevention and management of diarrhea associated with naldemedine among patients receiving opioids: a retrospective cohort study
Autor: | Gakuji Osawa, Yoriko Kato, Yusuke Takagi, Etsuko Aruga, Chika Kobayashi, Eri Ikezawa |
---|---|
Jazyk: | angličtina |
Rok vydání: | 2020 |
Předmět: |
Adult
Male Diarrhea medicine.medical_specialty Constipation Palliative care Narcotic Antagonists Naldemedine Receptors Opioid mu 03 medical and health sciences 0302 clinical medicine Internal medicine Neoplasms medicine Humans 030212 general & internal medicine Peripherally-acting mu-opioid receptor antagonist lcsh:RC799-869 Adverse effect Aged Retrospective Studies Aged 80 and over Performance status business.industry Palliative Care Gastroenterology Retrospective cohort study General Medicine Middle Aged Opioid-induced constipation Naltrexone Analgesics Opioid 030220 oncology & carcinogenesis Adverse events Defecation Female lcsh:Diseases of the digestive system. Gastroenterology medicine.symptom business Research Article |
Zdroj: | BMC Gastroenterology, Vol 20, Iss 1, Pp 1-8 (2020) BMC Gastroenterology |
Popis: | Background Naldemedine, a novel peripherally-acting mu-opioid receptor antagonist, has improved opioid-induced constipation in randomized controlled trials. The most frequent adverse event of naldemedine is diarrhea, which can cause abdominal pain and often leads to treatment discontinuation. We aimed to identify risk factors and appropriate management strategies for key adverse events including diarrhea associated with naldemedine, since those have not been extensively studied. Methods We conducted a multi-center retrospective cohort study. Eligible patients had cancer, had undergone palliative care at participating centers, had been prescribed regular opioids, and had taken at least one dose of naldemedine between June 2017 and March 2018. The primary endpoint was the incidence of diarrhea according to baseline characteristics. Secondary endpoints included the duration of naldemedine administration, daily defecation counts before and after starting naldemedine, duration and severity of diarrhea as an adverse event of naldemedine, other adverse events, and the incidence of constipation within 7 days after recovery from diarrhea. We defined patients who started naldemedine within three days of starting a regularly prescribed opioid as the early group, and the remainder as the late group. Results Among 103 patients who received naldemedine, 98 fulfilled the eligibility criteria. The median age was 68 years and 48% of the patients were female. Median performance status was 3, and the median oral intake was 50%. The median duration of naldemedine administration and overall survival were 25 and 64 days, respectively. The incidence of diarrhea in the early group (n = 26) was significantly lower than in the late group (n = 72) (3.9% vs. 22.2%, p = 0.02). Daily defecation counts increased after late (median 0.43 to 0.88, p p = 0.34). Constipation after the diarrhea was resolved was common (53%), especially among patients who stopped naldemedine (78%). The diarrhea was improved within three days in 92% of patients who stopped other laxatives. Conclusions The early administration of naldemedine is beneficial because it reduces adverse events including diarrhea. Diarrhea caused by naldemedine can be effectively managed by stopping other laxatives while continuing naldemedine. |
Databáze: | OpenAIRE |
Externí odkaz: | |
Nepřihlášeným uživatelům se plný text nezobrazuje | K zobrazení výsledku je třeba se přihlásit. |