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¿Ayuda la amitriptilina para el manejo del dolor del síndrome del intestino irritable?: Una revisión sistemática y
Raghad Alhajaji1,2, Manal Alfahmi3, Eatedal Mohammed Alshareef4
1Makkah Branch of Ministry of Health, Saudi Ministry of Health, Makkah, Saudi Arabia.
La amitriptilina mejora eficazmente el dolor en el síndrome del intestino irritable (SII). Esta revisión sistemática encontró un alivio significativo del dolor a corto plazo para los pacientes con SII tratados con amitriptilina en comparación con placebo.
Área de la Ciencia:
- Gastroenterology; Pharmacology; Clinical Medicine
Sus antecedentes:
- Irritable bowel syndrome (IBS) is a prevalent functional gastrointestinal disorder globally.
- Amitriptyline is a frequently used second-line pharmacological agent for managing IBS symptoms.
- Evidence regarding the pain-therapeutic efficacy of amitriptyline in IBS requires consolidation.
Objetivo del estudio:
- To systematically review and meta-analyze the existing evidence on the pain therapeutic efficacy of amitriptyline in adult patients diagnosed with IBS.
- To consolidate current research findings on amitriptyline's effectiveness in alleviating IBS-related pain.
Principales métodos:
- An updated systematic review and meta-analysis adhering to PRISMA guidelines.
- Searched four major databases (PubMed, Scopus, Web of Science, Cochrane) from inception to March 15, 2024.
- Included observational studies and randomized controlled trials.
Principales resultados:
- Analyzed 15 studies with 1497 IBS patients; 12 studies were included in the meta-analysis.
- Pooled improvement rate for amitriptyline was 66.61% (fixed model, p=0.31, I²=55%).
- Amitriptyline showed a statistically significant pooled odds ratio of 2.07 over placebo (fixed model, p=0.40, I²=1%) for pain management.
Conclusiones:
- Amitriptyline demonstrates significant short-term efficacy in improving abdominal pain and global IBS symptoms.
- The certainty of evidence is limited by short follow-up periods, variable study quality, and incomplete safety reporting.
- Further well-designed, longer-term trials with standardized outcomes and adverse event monitoring are necessary.
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