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Table 1 Characteristics of included studies

From: Efficacy and safety of abacavir-containing combination antiretroviral therapy as first-line treatment of HIV infected children and adolescents: a systematic review and meta-analysis

Studies

Brennan 2014 [29]

Musiime 2014 [28]

PENTA 2002 [31, 32]

Technau 2014 [14, 15]

Type of study

Prospective cohort study

Randomised controlled trial

Randomised controlled trial

Retrospective cohort study

Age range

5 to 14 years

1 month to 13 years

3 months to 16 years

4 to 129 months

Countries included

South Africa

Uganda Zambia

Belgium, Brazil, France, Germany, Ireland, Italy, Portugal, Spain and UK

South Africa

Period of enrollment

April 2009 to March 2011

May 2010 to September 2013

January 1998 to July 2000

August 1998 to April 2013

Sample size (n)

557

365

130

9543

Intervention

Abacavir, Lamivudine and Efavirenz

Abacavir, Lamivudine and NNRTI

Abacavir and Lamivudine ± Nelfinavir

Abacavir, Lamivudine and Lopinavir/ritonavir or Efavirenz

Comparators

Stavudine, Lamivudine and Efavirenz

Zidovudine, Lamivudine and NNRTI

Abacavir and Zidovudine ± Nelfinavir

Stavudine, Lamivudine and Lopinavir/ritonavir or Efavirenz

Stavudine, Lamivudine and NNRTI

Lamivudine and Stavudine ± Nelfinavir

Length of follow up

Up to 24 months

Up to 96 weeks

Up to 5 years

Up to 48 weeks

Funding sources

United States Agency for International Development (USAID)

Medical Research Council UK

European Commission, Medical Research Council, the Istituto Superiore di Sanità, Comunidad Autonoma de, Glaxo-Wellcome and Agouron

National Institutes of Health