Increased second-line antiretroviral therapy (ART) failure rate narrows future options for HIV/AIDS treatment. It has critical implications in resource-limited settings; including sub-Saharan Africa (SSA) where the burden of HIV-infection is immense. Hence, pooled estimate for second-line HIV treatment failure is relevant to suggest valid recommendations that optimize ART outcomes in SSA.
We retrieved literature systematically from PUBMED/MEDLINE, EMBASE, CINAHL, Google Scholar, and AJOL. The retrieved studies were screened and assessed for eligibility. We also assessed the eligible studies for their methodological quality using the Joanna Briggs Institute’s appraisal checklist. The pooled estimates for second-line HIV treatment failure and its associated factors were determined using STATA, version 15.0 and MEDCALC, version 18.11.3, respectively. We assessed publication bias using Comprehensive Meta-analysis software, version 3. Detailed study protocol for this review/meta-analysis is registered and found on PROSPERO (ID: CRD42018118959).
A total of 33 studies with the overall 18,550 participants and 19,988.45 person-years (PYs) of follow-up were included in the review. The pooled second-line HIV treatment failure rate was 15.0 per 100 PYs (95% CI: 13.0–18.0). It was slightly higher at 12–18 months of follow-up (19.0/100 PYs; 95% CI: 15.0–22.0), in children (19.0/100 PYs; 95% CI: 14.0–23.0) and in southern SSA (18.0/100 PYs; 95% CI: 14.0–23.0). Baseline values (high viral load (OR: 5.67; 95% CI: 13.40–9.45); advanced clinical stage (OR: 3.27; 95% CI: 2.07–5.19); and low CD4 counts (OR: 2.80; 95% CI: 1.83–4.29)) and suboptimal adherence to therapy (OR: 1.92; 95% CI: 1.28–2.86) were the factors associated with increased failure rates.
Second-line HIV treatment failure has become highly prevalent in SSA with alarming rates during the 12–18 month period of treatment start; in children; and southern SSA. Therefore, the second-line HIV treatment approach in SSA should critically consider excellent adherence to therapy, aggressive viral load suppression, and rapid immune recovery.
Citation: Edessa D, Sisay M, Asefa F (2019) Second-line HIV treatment failure in sub-Saharan Africa: A systematic review and meta-analysis. PLoS ONE 14(7): e0220159. https://doi.org/10.1371/journal.pone.0220159
Editor: Jason Blackard, University of Cincinnati College of Medicine, UNITED STATES
Published: July 29, 2019
Copyright: © 2019 Edessa et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are within the manuscript and its Supporting Information files.
Funding: We have received no funding for this work.
Competing interests: The authors have declared that no competing interests exist.
Abbreviations: AIDS, Acquired Immunodeficiency Syndrome; ART, Antiretroviral Therapy; CI, Confidence Interval; ES, Effect Size; HIV, Human Immunodeficiency Virus; JBI, Joanna Briggs Institute; OR, Odds Ratio; PRISMA, Preferred Reporting Items for Systematic review and Meta-analysis; RNA, Ribonucleic Acid; SSA, sub-Saharan Africa; VL, Viral Load; WHO, World Health Organization
In the past decade, rapid scale-up of antiretroviral therapy (ART) in sub-Saharan Africa (SSA) substantially reduced HIV/AIDS-related morbidity and mortality [1, 2]. It has also prolonged the average life expectancy of HIV-infected individuals . However, these benefits are being challenged by the increasing HIV treatment failure rates with first or second-line antiretroviral therapies [3–6]. HIV treatment failure can be defined in terms of clinical, immunological, or virological failures . Clinical failure is the occurrence of a new or recurrent stage III or stage IV clinical event (s). Immunological failure is the decline of CD4 counts either to less than the pre-treatment value or to <50% of a peak value on ART or persistently lower than 100 cells/ml . Virological failure could be a definite failure (i.e., when a single viral load (VL) is greater than 10,000 copies/ml at 12 months of follow-up) or a probable failure (i.e., when either a single VL is >1000 copies/ml at 12 months or a VL at 12 months is ≥ 400 copies/ml confirmed by a second measurement taken 30 days later) [8–10]. Clinical and immunological failure criteria are not sufficient for the definite diagnosis of treatment failure and each of them should be accompanied with VL tests as a confirmation . With this, VL testing is efficient to indicate direct plasma effects of ART on HIV ribonucleic acid (RNA) . It also helps preserve the limited HIV treatment options available by reducing the probability of incorrect switching to the next more expensive and toxic regimens .
The HIV-infected patients on ART are recalling earlier fears of death from the infection because of treatment failures . Patients who experienced first-line HIV treatment failure may be switched to second-line regimens [15, 16]. Many countries in resource-limited settings switch a failed first-line ART to second-line regimen after an initial delay mainly related to inadequate VL tests . The inadequacy of VL informed differentiated care for the HIV-infected patients commenced with second-line ART  could increase the risks of death and opportunistic infections especially in patients with advanced HIV at the time of first-line HIV treatment failure .
The HIV treatment failure involving second-line regimens has very narrow options for further switching, and this is a serious concern in resource-limited settings . The World Health Organization (WHO) recommends few second-line regimens as preferred ART (i.e., ritonavir-boosted atazanavir- or lopinavir-based ART and dolutegravir-based ART) [20, 21]. Despite the limited second-line HIV treatment options, many countries in SSA have financial constraints to adopt third-line regimens [20, 21]. As a result, the optimal use of second-line therapies after the occurrence of first-line HIV treatment failure is alarmingly essential for SSA, the epicenter of HIV/AIDS. However, many countries in SSA have no national strategic guidelines for the optimal use of second-line therapy despite the occurrence of a number of treatment failures related to the therapies .
Suboptimal adherence (i.e., missing of any dose in the past 3 days  or 7 days ; or less than 95% adherence in the past 30 days  or less than 90% adherence in the past year ) was indicated as a key determinant of second-line HIV treatment failure [26, 27]. Suboptimal adherence could be a result of regimen toxicities . It may require a tailored adherence intervention based on the degree of suboptimal adherence [27, 29]. Baseline characteristics such as delayed initiation of second-line therapy  and high VL might result in unfavorable treatment outcomes . To maximize the durability of the second-line regimens, early identification of first-line treatment failure and switching to a second-line regimen at a relatively higher CD4 cell count is very important [31, 32]. Advanced clinical stage at baseline and lack of VL monitoring were also identified to have associations with second-line HIV treatment failures . In addition, the clinical status of patients such as baseline clinical stage IV and CD4 counts below 100 cells/mm3 were significantly linked with increased rates of treatment failure . As a result, pooling the proportion of second-line HIV treatment failures and factors associated with these failures are required to assist the optimization of HIV treatment outcomes in SSA. Therefore, the aim of this systematic review and meta-analysis was to estimate the proportion of second-line HIV treatment failure and its associated factors in SSA.
Materials and methods
The method of this systematic review and meta-analysis was reported as per the Preferred Reporting Items for Systematic Review and Meta-Analysis Protocols (PRISMA-P) 2015 statement recommendations . Identification of records, screening by titles and abstracts, and eligibility evaluation of full texts for final inclusion was conducted in accordance with the PRISMA flow diagram . During the execution of this systematic review and meta-analysis, the PRISMA checklist was strictly followed. The protocol is registered on the International Prospective Register of Systematic Reviews (PROSPERO) with a registration number of CRD42018118959 and it is available at https://www.crd.york.ac.uk/prospero/#recordDetails.php?ID=CRD42018118959 .
Data sources and searches
We performed a systematic literature search from PubMed, MEDLINE (Ovid), EMBASE (Ovid), CINAHL (EBSCOhost), Cochrane Library, Google Scholar, Health Technology Assessment, African Journals Online (AJOL) and ResearchGate. Websites of organizations and University repositories were also visited to retrieve any remaining relevant record including unpublished (gray) kinds of literature. In our search strategy, search terms we employed were “treatment failure”; “second-line”; “protease inhibitor”; “antiretroviral therapy”; and names of countries in the SSA. During the search, we accomplished a careful selection of keywords and indexing terms that did not limit the year of publication. In the search strategy, Boolean operators and truncations were also employed. The search was conducted from 15 December 2018 to 14 January 2019. Accordingly, all published and unpublished literature identified during the period of searching were retrieved.
We set predefined inclusion and exclusion criteria for initial screening by titles or abstracts and evaluation of full texts for their eligibility assessment. We considered articles with at least an outcome of failure to second-line ART for their potential to be included. Next, we assessed the original articles reporting second-line HIV treatment failure after at least 6 month period of follow-up; reported in English language; and conducted in countries of SSA for their eligibility. In addition, we assessed the eligible original articles for quality using the Joanna Briggs Institute’s (JBI) critical appraisal checklist and articles with moderate (50–75%) to high (>75%) quality were considered as per the appraisers’ evaluation results. However, we excluded articles with outcomes not related to second-line therapy failure; with no separate failure data for SSA patients in case of mixed multi-center study settings involving SSA and other countries; and with no separate data of second-line therapy failure in studies involving first and second-line therapies during the screening and eligibility assessments.
Screening and eligibility
We identified and selected records retrieved through a search of the electronic databases and indexing services. Following this, we exported them to ENDNOTE reference software version 8.2 (Thomson Reuters, Stamford, CT, USA). Next, we identified, registered, and removed duplicates by the use of ENDNOTE. Accordingly, two authors, Dumessa Edessa (DE) and Mekonnen Sisay (MS), independently screened titles and abstracts of the retained records based on the predefined inclusion criteria. A third author, Fekede Asefa (FA), was consulted in case of disagreement between the two authors. With this, DE and FA individually collected and evaluated full texts of the retained articles for their quality and final eligibility assessment. In the end, we included articles that fulfilled the quality evaluation criteria.
Quality assessment and data extraction
We accomplished quality assessment for the articles by employing the JBI’s critical appraisal checklist for cohort and analytical cross-sectional studies [38, 39]. Two authors (DE and MS) critically appraised the articles. For the final decision of inclusion, we considered scores of the two authors in consultation with the third author’s score (in case of disagreement between the two authors’ appraisal results). Lastly, we ranked the articles by their methodological qualities based on the total number of appraisers’ score marked as ‘yes’ to questions of the JBI’s critical appraisal checklist. Accordingly, we included all studies with their overall positive responses in ranges of 50% to 75% (moderate quality studies) or higher than 75% (high quality studies) for the review and meta-analysis.
To extract relevant data, we employed a customized data abstraction format that has been prepared in a Microsoft Excel sheet. Two of the authors independently abstracted data pertaining to first author; year of publication; study design (analytical cross-sectional, follow-up); study region/country; study participants (children, adults, mixed-age groups); types of second-line ART (ritonavir-boosted protease inhibitor (PI)-based ART, PI-based ART with no ritonavir-boosting); sample size; median months of follow-up; person/patient-years (PYs) of follow-up; and event of interest (number of second-line therapy failure and factors associated with the failure).
Proportion of second-line HIV treatment failure that includes clinical, immunological or virological failure, as defined by the WHO [7, 9] was the primary outcome variable we estimated in this systematic review and meta-analysis. The secondary outcome measure we estimated was factors associated with the second-line HIV treatment failures.
Data synthesis and analysis
Proportion of second-line HIV treatment failure we pooled together was accomplished with the help of STATA software, version 15.0. Again, we performed sensitivity and subgroup analyses to minimize the risks of bias. With this, we used forest plots to graphically report the various meta-analysis results. We also applied the Mantel-Haenszel random-effects model to conduct meta-analyses at a 95% confidence level. Likewise, we assessed the heterogeneity status of the included studies and presented it with the use of Cochran’s Q test (chi-squared (I2) statistic). We also accomplished tests for factors associated with second-line therapy failure by using MEDCALC statistical software (MedCalc Software bvba, Ostend, Belgium), version 18.11.3. Besides, we employed Comprehensive Meta-analysis software (Biostat, Englewood, New Jersey, USA), version 3, for publication bias assessment. Similarly, we evaluated the presence of publication bias with the use of Egger's regression and Begg’s correlation tests. Lastly, we considered all statistical tests with p-values less than 0.05 (two-tailed) as significant.
We identified a total of 1,608 records from the search of legitimate databases and indexing services. After the removal of 368 duplicates, we retained 1240 records for screening by titles and abstracts. Again, we excluded a total of 1,142 literature by screening titles (n = 294) and abstracts (n = 848). Of this 1,142 literature, 947 of them had unrelated outcomes of interest; 73 of them were discussion papers; 72 of them had outcomes of first-line therapy failure; 46 of them had mixed and/or other country studies, and 4 of them reported their outcomes with non-English languages. Accordingly, we conducted an eligibility evaluation of 98 full texts as per the predefined eligibility criteria for inclusion. Again, we excluded 65 studies with justifiable reasons (i.e., 56 of them with irrelevant/insufficient outcomes of interest; 9 of them with mixed first and second-line HIV treatment failures and no separate data for second-line therapy failure). PRISMA flow chart depicting the selection, screening, and eligibility assessment process is shown in Fig 1 and S1 Table. We also assessed these records for their methodological quality by employing the JBI’s critical appraisal checklists (Table 1). Finally, we included 33 articles with the primary outcome of interest and with a high or moderate percentage in its score of methodological quality assessment for the systematic reviews and meta-analysis.
The 33 studies included for the systematic reviews and meta-analysis had a total of 18,550 participants, and 2,473 of them experienced treatment failures to their second-line HIV treatment. The study participants had a total of 19,988.45 PYs of follow-up. All the included studies were published during the year 2009 to 2018. Sample sizes for the included studies range from 40 patients enrolled by a study conducted in Uganda  to 6,714 patients enrolled by a study accomplished in Nigeria . The study participants of 26 studies were adults [19, 23–25, 27, 34, 40, 42–60], while that of 2 studies [22, 61] and 5 studies [6, 41, 62–64] were children and mixed age groups, respectively. Sixteen studies (n = 16) were from southern Africa [23, 27, 43, 45–52, 57, 58, 60, 62, 64]; 7 studies were from eastern Africa [22, 34, 40, 53, 55, 61, 63]; 5 studies were from western Africa [25, 41, 42, 44, 54]; and 5 studies were from mixed regions in SSA [6, 19, 24, 55, 59]. The second-line HIV treatment regimens received by the study participants were PI-based, 18 of them with ritonavir-boosted PI-based ART [24, 25, 27, 40, 42, 44, 45, 48, 49, 52–56, 58, 60, 61, 63] and 15 of them with no ritonavir in their PI-based ART regimens [6, 19, 22, 23, 34, 41, 43, 46, 47, 50, 51, 57, 59, 62, 64]. Thirteen studies (n = 13) defined the second-line HIV treatment failure by using the WHO definition of RNA VL more than 400 copies/ml [6, 19, 24, 25, 27, 42, 47, 49, 53, 54, 56–58] while 16 of the studies employed the WHO criteria of HIV RNA VL above 1000 copies/ml [22, 23, 40, 43–46, 48, 50–52, 55, 59–61, 63]. However, 4 of the studies employed mixed definitions of the WHO criteria for ART failure that included clinical, immunological and virological failures and/or death/lost to follow-up [34, 41, 62, 64] (Table 2 and S2 Table).
Proportion of patients with second-line ART failure
The pooled estimate for rate of second-line HIV treatment failure was 15.0 per 100 PYs of follow-up (95% CI: 13.0–18.0 per 100 PYs; I2 = 97.69%; P<0.001). The second-line treatment failures among the included studies range from 1.0/100 PYs (95% CI: 0.0–3.0 per 100 PYs) to 40.0/100 PYs (95% CI: 30.0–50.0) (Fig 2).
Sensitivity and subgroup analyses
We performed sensitivity analyses by excluding outliers [44, 58] and one or more studies. They did not have significant changes in the extent of pooled outcome measures. As a result, we included all the studies for the meta-analysis. We performed subgroup analyses on the basis of month period of follow-up after second-line ART initiation (less than 12 months, 12–18 months, above 18 months); patient groups (children, adults, mixed age-groups); regions in SSA (southern Africa, eastern Africa, western Africa, mixed regions of SSA); and type of second-line ART (PI-based ART, ritonavir-boosted PI-based ART). Accordingly, the pooled estimates of second-line ART failure were 19.0/100 PYs (95% CI: 15.0–22.0/100 PYs; I2 = 97.58%; P<0.001) at 12–18 month period of follow-up after second-line therapy initiation; 19.0/100PYs (95% CI: 14.0–23.0/100PYs; I2 = 0.0%) among children; and 18.0/100 PYs (95% CI: 14.0–23.0/100 PYs; I2 = 97.60%; P < 0.001) among patients in the southern SSA (Fig 3A–3D and S3 Table).
(a) Forest pilot describing failure by months of follow-up. (b) Forest pilot describing failure by regions of SSA. (c) Forest pilot describing failure by age group of participants. (d) Forest pilot describing failure by ritonavir boosting status of PI-based ART.
Factors associated with second-line ART failure
The pooled estimate for factors associated with second-line HIV treatment failure revealed that certain factors were influencing the failure rates. High baseline viral load (OR: 5.67; 95% CI: 13.40–9.45); advanced clinical stage of HIV at baseline (OR: 3.27; 95% CI: 2.07–5.19); low peak CD4 cell counts at baseline (<100 cells/mm3) (OR: 2.80; 95% CI: 1.83–4.29); and suboptimal adherence to second-line therapy (OR: 1.92; 95% CI: 1.28–2.86) were patient factors associated with the significantly increased occurrence of second-line ART failures (Table 3).
Different independent study reports also described depressive symptoms ; tuberculosis co-treatment with HIV/AIDS ; traditional medicine use ; delayed second-line HIV treatment initiation ; and younger age  as factors that favored second-line therapy failure. On the other hand, a study report indicated obesity  and elevated total bilirubin  as factors that protected second-line ART failure.
Egger’s regression test did not show any evidence for publication bias among the included studies (P = 0.0992, one-tailed). In addition, Begg’s correlation test did not also show any evidence of publication bias (P = 0.154, one-tailed) (Fig 4).
In this meta-analysis, the pooled estimate of proportion for second-line HIV treatment failure was 15.0 per 100 PYs of follow-up. This evidence is in line with reports from several studies that revealed a proportion of second-line HIV treatment failure as high as 25% [32, 65–69]. With this, the rate of second-line therapy failure among HIV-infected children was estimated to be 19.0 per 100 PYs. Aligned with this finding, 19% of children treated with PI-based second-line therapy in Thailand encountered treatment failures . Another study conducted in Thailand also reported up to 49% virological failure rates in children treated with second-line therapies . Additionally, an ART audit for pediatric patients in London indicated that 37% of the patients achieved HIV-RNA VL less than 400 copies/ml . Lack of VL monitoring, insufficient early diagnosis of failure, and unstructured and inadequate adherence counseling were the few reasons implicated for the increased treatment failure rates in children .
The pooled treatment failure rates before 12 months and 12–18 months of follow-up after second-line therapy initiation were 17.0/100 PYs and 19.0/100 PYs, respectively. The failure rate was 9.0/100 PYs after 18 months of follow-up. This indicated that a relatively sustained virological response is expected after the 18 months of follow-up. Similarly, a multi-centered study in Asia and Africa found that the most frequent experience of second-line therapy failure (i.e., 250.0/1000 PYs) occurred during 6 to 11 months of follow-up compared to the 18 months and more duration of follow-up (i.e., 212.0/1000 PYs) .
Subgroup analyses by regions revealed lower second-line HIV treatment failure rates in western (11.0/100 PYs) and eastern (13.0/100 PYs) regions of SSA compared to the rate in southern (18.0/100 PYs) region. These estimates are in line with the 19.6 million people living with HIV in southern and eastern regions compared to the 6.1 million people living with the infection in western and central Africa regions in 2017 . Since a minimal failure rate can naturally occur toward antimicrobial agents, an increased probability of failure might be expected in the southern/eastern regions of Africa with a higher HIV burden. Indeed, in the presence of infection and antimicrobial agent use, there is always a natural phenomenon of drug resistance and failure . This phenomenon can also be accelerated with improper infection control practices and suboptimal adherence to the ART . In addition, two studies indicated consistent findings with the second-line HIV treatment failure rates in southern (19%)  and western/eastern regions (11.1%) .
High VL (≥ 5000 copies/ml) at second-line HIV treatment initiation increased the odds of treatment failure (odds ratio (OR) 5.67; 95% CI: 3.40–9.45; P<0.0001). Patients who experienced virologic failure with first-line therapy and switched to second-line therapy after 12 months were more likely to experience a further increase in VL as a potential indicator for second-line therapy failure . Several studies indicated that second-line therapy failure was associated with higher baseline VL measurements [26, 78–84]. Patients who had an experience of suboptimal adherence to second-line therapy were more likely to develop treatment failure compared to patients with optimal adherence (OR 1.92; 95% CI: 1.28, 2.86; P = 0.0013). Several published reports explained a relationship between suboptimal adherence to second-line therapy and the increase in failure rates [6, 22, 26, 71, 79, 81, 85–88]. In addition, patients with histories of suboptimal adherence to first-line therapy were also more likely to have suboptimal adherence to second-line therapy [50, 89]. It could increase the odds of second-line HIV treatment failure rate. This increased failure rate may also be linked to poor treatment adherence resulting from the more frequent toxicities associated with second-line ART regimens .
An advanced clinical stage (stage III or IV) of HIV at the commencement of second-line therapy increased the odds of treatment failure (OR 3.27; 95% CI: 2.07–5.19; P<0.0001). With this, baseline CD4 cell counts of < 100 cells/ml were linked to increased odds of treatment failure (OR 2.80; 95% CI: 1.83–4.29; P<0.0001). Growing evidence relate the advanced HIV and lower peak CD4 cell counts at baseline to the increased rates of failure with second-line therapy [6, 69, 77, 87, 90].
Some of the included studies also reported that patients with lengthy delays in initiating second-line therapy ; who were underweight ; who were on tuberculosis co-treatment ; who had depressive symptoms ; who were with practice of herbal or traditional medicine use ; and who were at younger age  had increased rates of treatment failure [63, 71, 77, 80, 90]. Although the relationship among depression, adherence and treatment failure is yet to be fully investigated, more than one-third of HIV-infected patients with depressive symptoms were found to have an elevated HIV-RNA VL in South Africa . Patients with higher depression rating scales, with higher HIV-RNA VL and at a younger age were indicated to have increased patterns of ART missed doses . A high probability of suboptimal adherence to ART among alcohol users was also reported  which can contribute to the ART failure. Despite widespread concern about concurrent traditional medicine use and ART, yet there is no sufficient evidence of whether traditional medicine use results in adverse effects or interactions that could limit the effectiveness of the ART or not . With regard to HIV-tuberculosis co-treatment, suboptimal adherence to treatments was explained by a study report  and this interpretation could be related to the outcome of ART.
Contrary to other studies, one of the included studies reports that obese or overweight patients had a reduced proportion of failure to second-line ART . Obese HIV patients were found to have higher CD4 counts compared to normal-weight patients . A higher plasma concentration of second-line regimen containing darunavir-boosted with ritonavir was revealed in obese patients . The WHO recommended second-line therapies for HIV-infection involve mainly ritonavir-boosted PI-based regimen. The ritonavir inhibits cytochrome P450 enzymes to which many of the medications are substrate . The ritonavir-enzyme interaction can increase the plasma concentration of second-line therapy thereby protects treatment failure experience . Although the relationship between elevated total bilirubin and second-line therapy failure is not fully clear, up to one-third of patients treated with atazanavir had elevated bilirubin as a marker of hepatotoxicity [100, 101]. Aligned with this, a higher discontinuation rate of ritonavir-boosted atazanavir  and super-boosting of lopinavir-ritonavir were linked with co-administration of a medication that inhibits hepatic cytochrome P450 enzymes .
Although the overall sample size was large enough, there are some limitations to note. First, the majority of data were derived from observational studies which resulted in a high degree of heterogeneity and a range of potential biases. As a result, we have used a random-effects model which is more appropriate in such anticipated heterogeneity. A series of subgroup analyses were also considered to reduce the degree of heterogeneity and presented them in percentages to indicate the extent of differences. Second, other additional potential explanations for second-line therapy failures including medication toxicities and drug-drug interactions might not have been adequately addressed. Third, we have included articles published only in the English language and this could under-or over-estimate the pooled proportion of second-line therapy failure in the SSA. Finally, the reporting of some variables pertaining to clinical and programmatic follow-ups were inconsistent, limiting the conclusiveness of the pooled factors associated with the second-line HIV treatment failure.
The pooled proportion of second-line HIV treatment failure experienced by HIV-infected patients in SSA was found to be high. More common failure rates occurred at a 12–18 month period of follow-up after second-line therapy start, in children, and in the southern region of the SSA. Suboptimal adherence to second-line ART, higher HIV-RNA VL at baseline, lower peak values for CD4 cells, and advanced WHO clinical stages were among the key factors that have accelerated second-line HIV treatment failure in the setting. With this, prolonged delays in switching prior therapy, tuberculosis co-treatment, and other patient factors including younger age, depressive symptoms, underweight, and traditional medicine use were linked with the occurrence of second-line treatment failure. Therefore, optimal second-line HIV treatment approaches should critically consider immediate and aggressive VL suppression, rapid immune recovery, and excellent adherence to the therapy. Together with these approaches, more frequent clinical follow-ups and VL monitoring are recommended for the HIV-infected patients in SSA that help in rapid identification and intervention of failure cases. Finally, countries in the SSA should develop strategies and guidelines related to containment of second-line HIV treatment including intensive adherence support and intervention as routine clinical practice especially for patients with slow response to the therapies.
S2 Table. Definition and month of treatment failure report for the included studies.
We would like to thank Haramaya University, College of Health and Medical Sciences’ staff without them this systematic review and meta-analysis would not have been realized.
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