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Verfasst von:Brückle, Maria-Sophie [VerfasserIn]   i
 Thomas, Elizabeth T. [VerfasserIn]   i
 Seide, Svenja [VerfasserIn]   i
 Pilz, Maximilian [VerfasserIn]   i
 Gonzalez-Gonzalez, Ana I. [VerfasserIn]   i
 Dinh, Truc Sophia [VerfasserIn]   i
 Gerlach, Ferdinand M. [VerfasserIn]   i
 Harder, Sebastian [VerfasserIn]   i
 Glasziou, Paul P. [VerfasserIn]   i
 Muth, Christiane [VerfasserIn]   i
Titel:Amitriptyline’s anticholinergic adverse drug reactions - a systematic multiple-indication review and meta-analysis
Verf.angabe:Maria-Sophie Brueckle, Elizabeth T. Thomas, Svenja Elisabeth Seide, Maximilian Pilz, Ana I. Gonzalez-Gonzalez, Truc Sophia Dinh, Ferdinand M. Gerlach, Sebastian Harder, Paul P. Glasziou, Christiane Muth
E-Jahr:2023
Jahr:April 5, 2023
Umfang:17 S.
Fussnoten:Gesehen am 21.06.2023
Titel Quelle:Enthalten in: PLOS ONE
Ort Quelle:San Francisco, California, US : PLOS, 2006
Jahr Quelle:2023
Band/Heft Quelle:18(2023), 4 vom: Apr., Artikel-ID e0284168, Seite 1-17
ISSN Quelle:1932-6203
Abstract:Background Half the US population uses drugs with anticholinergic properties. Their potential harms may outweigh their benefits. Amitriptyline is among the most frequently prescribed anticholinergic medicinal products, is used for multiple indications, and rated as strongly anticholinergic. Our objective was to explore and quantify (anticholinergic) adverse drug reactions (ADRs) in patients taking amitriptyline vs. placebo in randomized controlled trials (RCTs) involving adults and healthy individuals. Methods We searched electronic databases from their inception until 09/2022, and clinical trial registries from their inception until 09/2022. We also performed manual reference searches. Two independent reviewers selected RCTs with ≥100 participants of ≥18 years, that compared amitriptyline (taken orally) versus placebo for all indications. No language restrictions were applied. One reviewer extracted study data, ADRs, and assessed study quality, which two others verified. The primary outcome was frequency of anticholinergic ADRs as a binary outcome (absolute number of patients with/without anticholinergic ADRs) in amitriptyline vs. placebo groups. Results Twenty-three RCTs (mean dosage 5mg to 300mg amitriptyline/day) and 4217 patients (mean age 40.3 years) were included. The most frequently reported anticholinergic ADRs were dry mouth, drowsiness, somnolence, sedation, fatigue, constitutional, and unspecific anticholinergic ADRs. Random-effects meta-analyses showed anticholinergic ADRs had a higher odd’s ratio for amitriptyline versus placebo (OR = 7.41; [95% CI, 4.54 to 12.12]). Non-anticholinergic ADRs were as frequent for amitriptyline as placebo. Meta-regression analysis showed anticholinergic ADRs were not dose-dependent. Discussion The large OR in our analysis shows that ADRs indicative of anticholinergic activities can be attributed to amitriptyline. The low average age of participants in our study may limit the generalizability of the frequency of anticholinergic ADRs in older patients. A lack of dose-dependency may reflect limited reporting of the daily dosage when the ADRs occurred. The exclusion of small studies (<100 participants) decreased heterogeneity between studies, but may also have reduced our ability to detect rare events. Future studies should focus on older people, as they are more susceptible to anticholinergic ADRs. Registration PROSPERO: CRD42020111970.
DOI:doi:10.1371/journal.pone.0284168
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

kostenfrei: Volltext: https://doi.org/10.1371/journal.pone.0284168
 kostenfrei: Volltext: https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0284168
 DOI: https://doi.org/10.1371/journal.pone.0284168
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:Adverse reactions
 Depression
 Gastroenterology and hepatology
 Metaanalysis
 Ophthalmology
 Randomized controlled trials
 Receptor antagonist therapy
 Urology
K10plus-PPN:1850711828
Verknüpfungen:→ Zeitschrift

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