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Tratamiento antirretroviral de la infección por el VIH - libdoc.who.int

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111<br />

Autores: George Rutherford, Alicen Spaulding<br />

Fecha: 8 Oct 2009<br />

Pregunta: ¿Debe utilizarse AZT o d4T en <strong>el</strong> TARV inicial? (Estudios observacionales)<br />

Entornos: Multiples entornos<br />

Bibliografía: 1. George C, Yesoda A, Jayakumar B, Lal L. A prospective study evaluating clinical outcomes and costs of three<br />

NNRTI-based HAART regimens in Kera<strong>la</strong>, India. J Clin Pharm Ther 2009;34:33-40. 2. Laurent C, Bourgeois A, Mpoudi-<br />

Ngolé E, Ciaffi L, Kouanfack C, Mougnutou R, Nkoué N, Calmy A, Koul<strong>la</strong>-Shiro S, De<strong>la</strong><strong>por</strong>te E. Tolerability and<br />

effectiveness of first-line regimens combining nevirapine and <strong>la</strong>mivudine plus zidovudine or stavudine in Cameroon.<br />

AIDS Res Hum Retroviruses 2008;24:393-9. 3. Mocroft A, Phillips AN, Le<strong>de</strong>rgerber B, Kat<strong>la</strong>ma C, Chiesi A, Goeb<strong>el</strong> FD,<br />

Knysz B, Antunes F, Reiss P, Lundgren JD. Re<strong>la</strong>tionship between antiretrovirals used as part of a cART régimen and<br />

CD4 c<strong>el</strong>l count increases in patients with suppressed viremia. AIDS 2006;20:1141-50. 4. Njoroge J, Reidy W, John-<br />

Stewart G, Attwa M, Kiguru J, Ngumo R, Wambua N, Chung MH. Inci<strong>de</strong>nce of peripheral neuropathy among patients<br />

receiving HAART regimens containing stavudine vs. zidovudine in Kenya [Abstract TUPEB179]. 5th Conference on HIV<br />

Pathogenesis and Treatment and Prevention, Cape Town, South Africa, 19−22 July 2009. 5. Pazare AR, Khirsagar N,<br />

Gogatay N, Bajpai S. Comparative study of inci<strong>de</strong>nce of hyper<strong>la</strong>ctetemia/ <strong>la</strong>ctic acidosis in stavudine vs. AZT based<br />

regime [Abstract THPE0159]. XVII International AIDS Conference, Mexico City, Mexico, 3−8 August 2008.<br />

Evaluación <strong>de</strong> calidad<br />

N° <strong>de</strong><br />

estudios<br />

Diseño<br />

Limitaciones<br />

Mortalidad (observacional)<br />

1 Estudio<br />

observacional<br />

Sin<br />

limitaciones<br />

im<strong>por</strong>tantes<br />

Inconsistencia<br />

Sin<br />

inconsistencias<br />

im<strong>por</strong>tantes<br />

Incertidumbre<br />

<strong>por</strong><br />

evi<strong>de</strong>ncia<br />

indirecta<br />

Imprecisiones<br />

No grave im<strong>por</strong>tantes<br />

4<br />

Otros<br />

factores a<br />

consi<strong>de</strong>rar<br />

Ninguno<br />

Resumen <strong>de</strong> hal<strong>la</strong>zgos<br />

N° <strong>de</strong> pacientes Efecto<br />

AZT d4T<br />

8/85 (9.4%)<br />

11/84<br />

(13.1%)<br />

Re<strong>la</strong>tivo<br />

(IC <strong>de</strong>l<br />

95%)<br />

RR 0.72<br />

(0.3 a 1.7)<br />

Absoluto<br />

37 menos<br />

<strong>por</strong> 1000<br />

(<strong>de</strong> 92<br />

menos a 92<br />

más)<br />

Calidad<br />

⊕⊕OO<br />

BAJA<br />

Im<strong>por</strong>tancia<br />

CRÍTICA

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