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dc.contributor.authorHernandez, AV.
dc.contributor.authorThota, P.
dc.contributor.authorPellegrino, D.
dc.contributor.authorPasupuleti, V.
dc.contributor.authorBenites‐Zapata, VA.
dc.contributor.authorDeshpande, A.
dc.contributor.authorPenalva de Oliveira, AC.
dc.contributor.authorVidal, JE.
dc.date.accessioned2020-07-13T18:40:59Z
dc.date.available2020-07-13T18:40:59Z
dc.date.issued2017-01-10
dc.identifier.citationHernande AV., Thota P., Pellegrino D., Pasupuleti V., Benites VA., Deshpande A., et al. A systematic review and meta‐analysis of the relative efficacy and safety of treatment regimens for HIV ‐associated cerebral toxoplasmosis: is trimethoprim‐sulfamethoxazole a real option? HIV Medicine. 2017; 18(2): 115-124.es_PE
dc.identifier.issn1468-1293
dc.identifier.urihttps://hdl.handle.net/20.500.12727/6328
dc.description.abstractObjectives The objective of this study was to perform a systematic review and meta‐analysis of the literature to evaluate the efficacy and safety of therapies for cerebral toxoplasmosis in HIV ‐infected adults. The pyrimethamine plus sulfadiazine (P‐S) combination is considered the mainstay therapy for cerebral toxoplasmosis and pyrimethamine plus clindamycin (P‐C) is the most common alternative treatment. Although trimethoprim‐sulfamethoxazole (TMP ‐SMX ) has potential advantages, its use is infrequent. Methods We searched PubMed and four other databases to identify randomized controlled trials (RCT s) and cohort studies. Two independent reviewers searched the databases, identified studies and extracted data. Risk ratios (RR s) were pooled across studies using random‐effects models. Results Nine studies were included (five RCT s, three retrospective cohort studies and one prospective cohort study). In comparison to P‐S, treatment with P‐C or TMP ‐SMX was associated with similar rates of partial or complete clinical response [P‐C: RR 0.87; 95% confidence interval (CI ) 0.70–1.08; TMP ‐SMX : RR 0.97; 95% CI 0.78–1.21], radiological response (P‐C: RR 0.92; 95% CI 0.82–1.03), skin rash (P‐C: RR 0.81; 95% CI 0.56–1.17; TMP ‐SMX : RR 0.17; 95% CI 0.02–1.29), gastrointestinal impairment (P‐C: RR 5.16; 95% CI 0.66–40.11), and drug discontinuation because of adverse events (P‐C: RR 0.32; 95% CI 0.07–1.47). Liver impairment was more frequent with P‐S than P‐C (P‐C vs . P‐S: RR 0.48; 95% CI 0.24–0.97). Conclusions The current evidence fails to identify a superior regimen in terms of relative efficacy or safety for the treatment of HIV ‐associated cerebral toxoplasmosis. Use of TMP ‐SMX as preferred treatment may be consistent with the available evidence and other real‐world considerations. Larger comparative studies are needed.es_PE
dc.format.extentpp. 115-124es_PE
dc.language.isoenges_PE
dc.publisherBritish HIV Associationes_PE
dc.relation.ispartofseriesHIV Medicine;vol. 18; no. 2
dc.relation.urihttps://doi.org/10.1111/hiv.12402
dc.relation.urihttp://hdl.handle.net/10757/622311
dc.rightsinfo:eu-repo/semantics/openAccesses_PE
dc.sourceRepositorio Académico USMPes_PE
dc.sourceUniversidad San Martín de Porres - USMPes_PE
dc.subjectToxoplasmosis cerebrales_PE
dc.subjectEncefalitises_PE
dc.subjectVIHes_PE
dc.titleA systematic review and meta‐analysis of the relative efficacy and safety of treatment regimens for HIV ‐associated cerebral toxoplasmosis: is trimethoprim‐sulfamethoxazole a real option?es_PE
dc.typeinfo:eu-repo/semantics/articlees_PE
thesis.degree.nameMedicina Humana
thesis.degree.grantorUniversidad de San Martín de Porres. Facultad de Medicina Humana
thesis.degree.disciplineMedicina


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