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Comparative profiles of lubiprostone, linaclotide, and elobixibat for chronic constipation: a systematic literature review with meta-analysis and number needed to treat/harm.
Rao, Satish S; Manabe, Noriaki; Karasawa, Yusuke; Hasebe, Yuko; Nozawa, Kazutaka; Nakajima, Atsushi; Fukudo, Shin.
Afiliación
  • Rao SS; Division of Gastroenterology and Hepatology, Medical College of Georgia, Augusta University, Augusta, GA, USA.
  • Manabe N; Division of Endoscopy and Ultrasonography, Department of Clinical Pathology and Laboratory Medicine, Kawasaki Medical School General Medical Center, Okayama, Japan.
  • Karasawa Y; Medical Affairs, Viatris Pharmaceuticals Japan Inc, Tokyo, Japan. Yusuke.Karasawa@viatris.com.
  • Hasebe Y; Medical Affairs, Viatris Pharmaceuticals Japan Inc, Tokyo, Japan.
  • Nozawa K; Medical Affairs, Viatris Pharmaceuticals Japan Inc, Tokyo, Japan.
  • Nakajima A; Department of Gastroenterology and Hepatology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Fukudo S; Department of Behavioral Medicine, Tohoku University Graduate School of Medicine, Sendai, Japan.
BMC Gastroenterol ; 24(1): 12, 2024 Jan 02.
Article en En | MEDLINE | ID: mdl-38166671
ABSTRACT

OBJECTIVE:

To comprehensively evaluate the efficacy, safety, patient symptoms, and quality-of-life (QoL) of lubiprostone, linaclotide, and elobixibat as treatment for chronic constipation (CC).

DESIGN:

Systematic literature review (SLR) and meta-analysis (MA). Literature searches were conducted on PubMed and Embase using the Ovid platform.

METHODS:

SLR including randomized controlled trials (RCTs) and observational studies was conducted to identify the overall efficacy and safety of lubiprostone, linaclotide, and elobixibat. Thereafter, MA was performed using only RCTs. The number needed to treat (NNT) and number needed to harm (NNH) analyses were additionally conducted. PRIMARY AND SECONDARY OUTCOME

MEASURES:

The primary outcome was efficacy regarding change in spontaneous bowel movements. Secondary outcomes included safety, constipation-related symptoms, and QoL.

RESULTS:

Twenty-four studies met the inclusion criteria for the SLR 17 RCTs, 4 observational studies, and 3 single-arm trials. Feasibility assessment for the MA resulted in 14 studies available for safety data analysis, and 8 available for efficacy analysis, respectively. Three drugs showed similar efficacy in the MA and NNT analysis. However, the NNH analysis revealed distinct safety profiles lubiprostone, linaclotide, and elobixibat were linked to the highest risk of nausea, diarrhea, and abdominal pain, respectively.

CONCLUSION:

The current study provides an updated overview of the efficacy, safety, patient symptoms, and QoL of the three drugs with different mechanisms of action for CC treatment.The findings could help physicians adopt an individualized approach for treating patients with CC in clinical practice.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Péptidos / Estreñimiento Tipo de estudio: Clinical_trials / Observational_studies / Prognostic_studies / Systematic_reviews Límite: Humans Idioma: En Revista: BMC Gastroenterol Asunto de la revista: GASTROENTEROLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Péptidos / Estreñimiento Tipo de estudio: Clinical_trials / Observational_studies / Prognostic_studies / Systematic_reviews Límite: Humans Idioma: En Revista: BMC Gastroenterol Asunto de la revista: GASTROENTEROLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos