Improving the outcomes of HIV/AIDS treatment programs in resource-limited settings requires successful linkage of patients testing positive for HIV to pre–antiretroviral therapy (ART) care and retention in pre-ART care until ART initiation. We conducted a systematic review of pre-ART retention in care in Africa.
Methods and Findings
We searched PubMed, ISI Web of Knowledge, conference abstracts, and reference lists for reports on the proportion of adult patients retained between any two points between testing positive for HIV and initiating ART in sub-Saharan African HIV/AIDS care programs. Results were categorized as Stage 1 (from HIV testing to receipt of CD4 count results or clinical staging), Stage 2 (from staging to ART eligibility), or Stage 3 (from ART eligibility to ART initiation). Medians (ranges) were reported for the proportions of patients retained in each stage. We identified 28 eligible studies. The median proportion retained in Stage 1 was 59% (35%–88%); Stage 2, 46% (31%–95%); and Stage 3, 68% (14%–84%). Most studies reported on only one stage; none followed a cohort of patients through all three stages. Enrollment criteria, terminology, end points, follow-up, and outcomes varied widely and were often poorly defined, making aggregation of results difficult. Synthesis of findings from multiple studies suggests that fewer than one-third of patients testing positive for HIV and not yet eligible for ART when diagnosed are retained continuously in care, though this estimate should be regarded with caution because of review limitations.
Studies of retention in pre-ART care report substantial loss of patients at every step, starting with patients who do not return for their initial CD4 count results and ending with those who do not initiate ART despite eligibility. Better health information systems that allow patients to be tracked between service delivery points are needed to properly evaluate pre-ART loss to care, and researchers should attempt to standardize the terminology, definitions, and time periods reported.
Please see later in the article for the Editors' Summary
Citation: Rosen S, Fox MP (2011) Retention in HIV Care between Testing and Treatment in Sub-Saharan Africa: A Systematic Review. PLoS Med 8(7): e1001056. doi:10.1371/journal.pmed.1001056
Academic Editor: John Bartlett, Duke University Medical Center, United States of America
Received: January 13, 2011; Accepted: May 31, 2011; Published: July 19, 2011
Copyright: © 2011 Rosen, Fox. 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.
Funding: Funding was provided by the United States Agency for International Development (USAID) (http://www.usaid.gov/) under Award Number 674-A-00-09-00018-00 with Boston University and by the National Institute of Allergy and Infectious Diseases (http://www.niaid.nih.gov/Pages/default.aspx) under Award Number K01AI083097. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. The content is solely the responsibility of the authors and does not necessarily represent the official views of USAID, the National Institute of Allergy and Infectious Diseases, the National Institutes of Health, or other parties.
Competing interests: The authors have declared that no competing interests exist.
Abbreviations: ART, antiretroviral therapy
Since 1981, AIDS has killed more than 25 million people, and about 33 million people (mostly living in low- and middle-income countries) are now infected with HIV, the virus that causes AIDS. HIV gradually destroys immune system cells (including CD4 cells, a type of lymphocyte), leaving infected individuals susceptible to other infections. Early in the AIDS epidemic, most HIV-infected people died within ten years of infection. Then, in 1996, highly active antiretroviral therapy (ART) became available, and, for people living in developed countries, HIV infection became a chronic condition. Unfortunately, ART was extremely expensive, and HIV/AIDS remained a fatal illness for people living in developing countries. In 2003, governments, international agencies, and funding bodies began to implement plans to increase ART coverage in resource-limited countries. By the end of 2009, about a third of the people in these countries who needed ART (HIV-positive people whose CD4 count had dropped so low that they could not fight other infections) were receiving treatment.
Why Was This Study Done?
Unfortunately, many HIV-positive people in resource-limited countries who receive ART still do not have a normal life expectancy, often because they start ART when they have a very low CD4 count. ART is more successful if it is started before the CD4 count falls far below 350 cells/mm3 of blood, the threshold recommended by the World Health Organization for ART initiation. Thus, if the outcomes of HIV/AIDS programs in resource-limited settings are to be improved, all individuals testing positive for HIV must receive continuous pre-ART care that includes regular CD4 counts to ensure that ART is initiated as soon as they become eligible for treatment. Before interventions can be developed to achieve this aim, it is necessary to understand where and when patients are lost to pre-ART care. In this systematic review (a study that uses predefined criteria to identify all the research on a given topic), the researchers investigate the retention of HIV-positive adults in pre-ART care in sub-Saharan Africa.
What Did the Researchers Do and Find?
The researchers identified 28 studies that included data on the proportion of adult patients retained between any two time points between testing positive for HIV and starting ART in HIV/AIDS care programs in sub-Saharan Africa. They defined three stages of pre-ART care: Stage 1, the interval between testing positive for HIV and receiving CD4 count results or being clinically assessed; Stage 2, the interval between enrollment in pre-ART care and the determination of eligibility for ART; and Stage 3, the interval between being deemed eligible for ART and treatment initiation. A median of 59% of patients were retained in Stage 1 of pre-ART care, 46% were retained in Stage 2, and 68% were retained in Stage 3. Retention rates in each stage differed greatly between studies—between 14% and 84% for Stage 3 pre-ART care, for example. Because the enrollment criteria and other characteristics of the identified studies varied widely and were often poorly defined, it was hard to combine study results. Nevertheless, the researchers estimate that, taking all the studies together, less than one-third of patients testing positive for HIV but not eligible for ART when diagnosed were retained in pre-ART care continuously.
What Do These Findings Mean?
These findings suggest that there is a substantial loss of HIV-positive patients at every stage of pre-ART care in sub-Saharan Africa. Thus, some patients receiving a positive HIV test never return for the results of their initial CD4 count, some disappear between having an initial CD4 count and becoming eligible for ART, and others fail to initiate ART after having been found eligible for treatment. Because only a few studies were identified (half of which were undertaken in South Africa) and because the quality and design of some of these studies were suboptimal, the findings of this systematic review must be treated with caution. In particular, the estimate of the overall loss of patients during pre-ART care is likely to be imprecise. The researchers call, therefore, for the implementation of better health information systems that would allow patients to be tracked between service delivery points as a way to improve the evaluation and understanding of the loss of HIV-positive patients to pre-ART care in resource-limited countries.
Please access these Web sites via the online version of this summary at http://dx.doi.org/10.1371/journal.pmed.1001056.
- Information is available from the US National Institute of Allergy and Infectious Diseases on HIV infection and AIDS
- HIV InSite has comprehensive information on all aspects of HIV/AIDS
- Information is available from Avert, an international AIDS charity on many aspects of HIV/AIDS, including information on HIV/AIDS treatment and care, on HIV and AIDS in Africa and on universal access to AIDS treatment (in English and Spanish)
- The World Health Organization provides information about universal access to AIDS treatment, including the 2010 progress report (in English, French and Spanish); its 2010 ART guidelines can be downloaded (in several languages)
- The International AIDS Economics Network posts information about economic, social, and behavioral aspects of HIV care and treatment
- Up-to-date research findings about HIV care and treatment are summarized by NAM/aidsmap
The remarkable expansion of access to antiretroviral therapy (ART) for HIV/AIDS in resource-constrained countries has given nearly four million HIV-positive adults in sub-Saharan Africa the opportunity to achieve what for many may be nearly normal life expectancies . Others, however, do not make it past their first year on treatment. The rate of early mortality and loss to follow-up, which itself portends mortality for many, averages 23% across the region . For patients initiating ART late, with very low CD4 counts, the odds of success are even lower: in a pooled analysis of data from multiple resource-limited countries, patients with starting CD4 counts below 25 cells/mm3 faced a more than 3-fold increased risk of death compared to those with starting CD4 counts above 50 cells/mm3 . Those who survive suffer more morbidity and utilize more medical care resources than would otherwise have been necessary .
Earlier initiation of ART requires earlier diagnosis and regular monitoring until treatment eligibility. Despite large-scale HIV testing campaigns to hasten diagnosis  and the raising of CD4 count thresholds to allow earlier ART eligibility , late presentation for AIDS treatment remains the norm. Median baseline CD4 counts have increased only modestly in the years since treatment became available ,, and most programs still report medians well below even the very low threshold of 200 cells/mm3 previously allowed by most treatment guidelines .
The persistence of low starting CD4 counts points to a problem that has just begun to be recognized in the research literature: poor pre-ART retention in care, or the failure to link patients from HIV testing to HIV care and retain them in care until they are eligible for ART. Without effective retention in pre-ART care, beginning with HIV testing and continuing until the first antiretrovirals are dispensed, even patients who have long been aware of their HIV status will access care only when seriously ill, which is often well after treatment eligibility.
A prerequisite to developing interventions to retain patients in care between testing and treatment is an understanding of where and when they are being lost. Research on retention in pre-ART care is challenging, as it requires long periods of follow-up and consistent information systems that allow individuals to be tracked as they move in and out of care at multiple facilities. As a result, only a handful of quantitative studies reporting on rates of pre-ART linkage and loss have been published. In this paper, we review those studies and summarize what is known about this issue in sub-Saharan Africa. Our objective is to determine whether existing data allow us to estimate what proportion of adult patients who test positive for HIV are staged, enroll, and remain in pre-ART care until ART-eligible, and initiate ART as soon as eligible.
An ethics statement was not required for this work.
We conducted a systematic literature review of patient retention between HIV testing and ART initiation in sub-Saharan Africa. Following a detailed search protocol and standard systematic review procedures (Texts S1 and S2), we searched the published literature and major conference abstract archives for reports containing primary, patient- or facility-level data from routine health-care delivery settings on the proportion of patients retained in care between HIV testing and ART initiation and/or rates of linkage between any two intermediate points between testing and ART. We excluded patients who were in care solely for the purpose of preventing mother-to-child transmission of HIV, patients who were in pediatric care, modeled estimates without primary data, qualitative studies, and clinical trials that did not take place under routine care conditions. We included reports of trials of procedural changes within facilities. Where multiple reports described the same data, the one reporting the most complete follow-up or with the clearest definitions of outcomes was used. We did not place a language restriction on the papers included in our search but did limit the search to English-language indices.
We searched PubMed and the ISI Web of Knowledge through January 5, 2011, with the combined terms “Africa” and “HIV” plus “retention,” “linkage,” or “pre-ART.” We searched the African Indicus Medicus through April 1, 2011, using the same terms. We also searched abstracts from the conferences of the International AIDS Society from 2008 to 2010 and from the Conference on Retroviruses and Opportunistic Infections from 1997 to 2011, and scanned the titles of abstracts presented at the HIV Implementers Meetings in 2008 and 2009 and the 5th International Conference on HIV Treatment Adherence (2010). Finally, we reviewed the reference lists of all papers found through the PubMed and ISI Web of Knowledge searches.
S. R. assessed the eligibility of all abstracts and journal articles that met our initial criteria, and M. P. F. confirmed eligibility. Using a standard data extraction form, both authors extracted and reviewed the relevant data, including study site, sample size and inclusion criteria, dates of data collection, study design and outcomes, and quantitative results.
We anticipated that wide variation in definitions, outcomes, and specific components of pre-ART care evaluated in the studies would prevent aggregate statistical analysis of findings beyond a basic descriptive level. We therefore began by describing each study, identifying the start and end points of the data presented, and specifying the proportions of patients retained or linked. We defined “loss to care” as failing to reach the next step in the care sequence for any reason (death or discontinuation), but we also accepted each study's own criteria for determining which patients died or discontinued care. Transfers were rarely distinguished from losses in the published studies. Where possible, we used the reported data to calculate a 95% confidence interval for the proportion of patients retained or linked. Next, we grouped the findings into stages within the testing-to-ART-initiation sequence, as described below, and illustrated the results using forest plots. Finally, for each stage we estimated the median proportion of patients completing the stage and reported the median and range.
Classification of Results
Preliminary review of the literature suggested that the sequence of events that starts with testing positive for HIV and ends with initiating ART can usefully be grouped into three stages, as illustrated in Figure 1. For analysis, we categorized each study by stage, allowing some studies to be included in more than one stage as appropriate.
Figure 1. Stages of pre-ART care.doi:10.1371/journal.pmed.1001056.g001
Stage 1, in which the patient is staged for referral to either pre-ART care or ART, starts immediately after a patient tests positive for HIV infection. Depending on the technology available and the testing setting, Stage 1 typically requires the patient to make one or two additional visits to a clinic. A blood sample for a CD4 count can be given during the same visit as the HIV test if the test is conducted at a clinic; if the test is done at a stand-alone testing site, the patient is typically referred elsewhere to provide a blood sample. Once the sample has been taken, patients are asked to return 2 d to 2 wk later to receive their results, with the time interval dependent on laboratory processing capacity and location. Completion of Stage 1 requires that patients receive their CD4 count results (or clinical staging outcome) and be referred onward for pre-ART care or ART.
Stage 2 lasts from enrollment in pre-ART care until eligibility for ART. Stage 2 pertains only to patients who complete Stage 1 prior to ART eligibility, as those already eligible for ART at staging will be referred directly to Stage 3. The steps included in Stage 2 are generally poorly defined in the literature and vary widely from program to program. In some programs “enrollment in care” happens automatically when a patient presents at a site, regardless of patient intention, while in others it requires active patient participation. Patients may be considered enrolled in care prior to staging or only after having been found not-yet-eligible for ART. At a minimum, retention in pre-ART care requires regular clinic visits for monitoring of patient condition. The frequency and content of these visits varies widely: patients with very high CD4 counts may be asked to return as infrequently as once a year, while those approaching treatment eligibility may be monitored on a monthly or quarterly basis. Similarly, some programs routinely dispense cotrimoxazole, isoniazid, vitamins, and/or food supplements to pre-ART patients, while others simply assess condition. For practical purposes, completion of Stage 2 requires that ART eligibility be determined prior to the patient's CD4 count falling substantially below the eligibility threshold or the patient becoming severely ill.
Finally, Stage 3 encompasses the steps between determination of ART eligibility and ART initiation. Programs in sub-Saharan Africa typically require two or more “treatment readiness” visits during this stage, and the full course of treatment education and adherence training can last for up to 8 wk. Completion of Stage 3 requires that the patient be dispensed a first dose of antiretrovirals.
We identified 668 full-length journal articles and 1,145 abstracts potentially relevant to our review. As shown in the search flowchart in Figure 2, after excluding duplicates and studies that did not meet the geographic, population, content, or design criteria of our review, 20 full-length articles and eight abstracts were eligible for the review. Most (23/28) were published or presented in 2009 or later. Seven countries are represented, but half the studies (14/28) were conducted in just one, South Africa. Most (18/28) were designed as retrospective cohorts using routinely collected patient-level data; the remaining were program evaluations, trials of procedural changes, and a prospective cohort. The studies are described in Table 1, which also contains the study codes we will use to refer to individual studies throughout this paper. Of the 28 studies included, 20 reported information relevant to only one stage in the testing-to-treatment sequence, six addressed two stages, and two addressed to all three stages. We thus had a total of 38 stage-specific observations.
Figure 2. Flow chart of literature search on pre-ART retention in care.
Adherence conference, 5th International Conference on HIV Treatment Adherence; CROI, Conference on Retroviruses and Opportunistic Infections; IAS, International AIDS Society; Implementers conference, HIV Implementers Meetings.doi:10.1371/journal.pmed.1001056.g002
Table 1. Studies included in this review of retention in pre-ART HIV care in sub-Saharan Africa.doi:10.1371/journal.pmed.1001056.t001
Stage 1: Testing to Staging
Ten studies reported rates of staging after a positive HIV test (Table 2 and Figure 3). Time intervals for evaluating results varied widely, from 1 wk to 6 mo. In general, between one-third and two-thirds of patients testing positive for HIV provided samples for CD4 counts and/or returned for results within 2–3 mo of the HIV test. For all the studies in Table 2, the median proportion of patients completing one or both of the steps in Stage 1 was 59% (range 35%–88%).
Figure 3. Forest plot of the ten studies reporting on the proportion of patients completing Stage 1 or steps within Stage 1.
Bars indicate 95% confidence intervals. Studies shown in the plot report to differing end points; refer to Table 2 for details.doi:10.1371/journal.pmed.1001056.g003
Table 2. Reported rates of retention or linkage in Stage 1 (HIV testing to staging).doi:10.1371/journal.pmed.1001056.t002
Stage 2: Staging to ART Eligibility
Fourteen studies reporting on retention in pre-ART care between staging and ART eligibility (Stage 2) are shown in Table 3 and Figure 4. The upper rows of Table 3, which report on enrollment in pre-ART care after a positive HIV test, clearly overlap with some of the studies classified as Stage 1 and presented in Table 2, but we placed them in Stage 2 because they focus on pre-ART care rather than staging. Similarly, many of the studies in the lower rows of Table 3, which report on retention in pre-ART care after enrollment, use ART initiation as an end point, overlapping with Stage 3.
Figure 4. Forest plot of the 14 studies reporting on the proportion of patients completing Stage 2 or steps within Stage 2.
Bars indicate 95% confidence intervals. Studies shown in the plot report to differing end points; refer to Table 3 for details.doi:10.1371/journal.pmed.1001056.g004
Table 3. Reported rates of retention or linkage in Stage 2 (staging to ART eligibility).doi:10.1371/journal.pmed.1001056.t003
The first eight studies in Table 3 reported the proportion of patients who enrolled in an HIV care program after testing. Time intervals allowed for completing this step varied from “immediately” after the HIV test to a year after staging, and “enrollment in care” was itself not consistently defined. Across the studies, the median proportion of patients enrolling in care after a positive HIV test was 44% (range 31%–68%).
The last six studies in Table 3 reported on retention in ART care after enrollment. Four provided results up to the date of data censoring, rather than up to a clinically meaningful end point within the stage or to a consistent duration of follow-up of all patients in the cohort. In most of these cases, the outcome assessed was the proportion of patients who either initiated ART or remained in pre-ART care at the censoring date. In these studies, a median of 55% (range 42%–95%) of patients reached the study end point (repeat CD4 count, ART initiation, 12 months of follow-up, or data censoring), while the rest died or were lost to follow-up before the end point.
Stage 3: ART Eligibility to ART Initiation
The 14 studies reporting on Stage 3 are summarized in Table 4 and illustrated in Figure 5. Stage 3 has the most consistent and precise start and end points: from a clearly defined threshold, treatment eligibility, to a definite event, ART initiation. Across all the studies in Table 4, a median of 68% (range 14%–84%) of patients eligible for ART actually initiated treatment within the study periods of observation. As with Stage 1 and Stage 2, the time intervals allowed for the completion of Stage 3 varied widely and were in some cases unclear.
Figure 5. Forest plot of the 14 studies reporting on the proportion of patients completing Stage 3 or steps within Stage 3.
Bars indicate 95% confidence intervals. Studies shown in the plot report to differing end points; refer to Table 4 for details.doi:10.1371/journal.pmed.1001056.g005
Table 4. Reported rates of retention or linkage in Stage 3 (ART eligibility to ART initiation).doi:10.1371/journal.pmed.1001056.t004
Eight studies contained data pertaining to more than one stage between testing and treatment initiation. These studies are listed multiple times in Tables 2–4 above, but the patient samples assessed at each stage did not remain consistent between stages in all of the studies. In Table 5, we provide multi-stage results for the relevant studies. Even the most comprehensive studies, such as Malawi 2 and SA 6, did not report outcomes to the end of a stage for all patients enrolled. Four of the seven studies that started with Stage 1 followed through to Stage 3 only those patients who were already eligible for ART in Stage 1—no further follow-up was reported of patients who were not yet eligible for ART and should have progressed to Stage 2.
During the early years of HIV/AIDS treatment scale up in sub-Saharan Africa, attention was focused on initiating eligible patients on ART and, more recently, on long-term retention in care of those patients on treatment. Growing awareness of the negative consequences of late presentation for treatment, combined with new enthusiasm for test-and-treat strategies, is now leading to renewed interest in the pre-ART period, which is after HIV diagnosis but before treatment.
Our analysis of 24 studies documenting rates of retention of patients from testing positive for HIV infection to initiating ART suggests that patient management during this period poses serious challenges. Most studies reported a substantial reduction in patient numbers at every step of the process. This reduction in patient numbers is clearly illustrated in Figure 6, which summarizes findings from all the reports. Studies are few, however, and offering a definitive answer to our core question—what proportion of patients who test positive for HIV are staged, enroll and remain in pre-ART care until ART eligibility, and initiate ART—is not possible with the data available. Only a handful of countries are represented, and most by no more than one or two studies. No study provides all the information needed to answer this question, even for a single setting, and combining results from multiple studies appears ill-advised. To examine the implications of doing this, we multiplied the median proportions of patients achieving the study end point in each stage (Stage 1, 59%; Stage 2, 46%; Stage 3, 68%), and found that the information available suggests that only about 18% of patients who are not yet eligible for ART when they are diagnosed with HIV remain continuously in care until ART eligibility. When we instead multiplied all combinations of estimates from each of the three stages, we estimated a median completion of all three stages of 17%, with an interval from the 10th to the 90th percentile of 7%–32%.
Figure 6. Summary of proportions of patients completing steps within each stage of pre-ART care in the studies reviewed.doi:10.1371/journal.pmed.1001056.g006
If we make one optimistic assumption, we can use the data in the most complete study in our review—SA 6, which tracked patients from provision of a sample for a CD4 count to either ART initiation or a repeat CD4 count—to answer the question for one setting. In SA 6, 988 patients were enrolled after testing positive for HIV. By the end of the study, 141 had initiated ART, and 189 had returned for at least one repeat CD4 count. If we optimistically assume all 189 in the latter group remained in pre-ART care until ART initiation, then the overall retention rate for this population was 33%, better than what we estimated by multiplying the medians but still very low. While it is difficult to believe that only a sixth to a third of patients remain continuously in care, the evidence does not allow us to make a more definitive estimate.
There appear to be several main reasons for the poor performance of pre-ART care in retaining patients. Most patients during this stage are asymptomatic and may not perceive themselves as requiring medical care. Since very little therapeutic care is offered during the pre-ART period, patients must take it on faith that making the effort to come to the clinic for monitoring is worth the costs of doing so. Current approaches to providing care often require multiple clinic visits, for example, to first provide a blood sample for a CD4 count and then return a week later to receive the results. Choosing to “wait and see what happens” may well be a preferred strategy for patients who lack resources for transport, risk losing employment by taking time off work, or fear being recognized as a client of an HIV clinic. Other patients, those who already have very low CD4 counts at their first presentation for HIV care, do not complete Stage 3 because they die before doing so. A number of the papers we reviewed stratified results by CD4 count range and/or identified other factors associated with pre-ART attrition, and a review of these findings would be valuable.
In interpreting the results summarized above, it should also be kept in mind that there is far more mobility among HIV patients than had been anticipated . Loss to follow-up at any one site may or may not indicate that a patient has dropped out of care permanently. Some patients may have returned to the same site after the data for the study were censored or the study's definition of loss to care reached. Many patients may have simply transferred, usually informally, from one site to another. Difficult as this problem is for managing ART patients, it is even worse during the pre-ART period, because patients are expected to visit the clinic less frequently, and more clinics are able to provide pre-ART services than are accredited to offer ART. For individual patients, dropping out of pre-ART care is less likely to represent a death sentence than is loss to follow-up after initiating treatment. Patients lost to pre-ART care mainly risk becoming late presenters to treatment, not dying. It is reasonable to assume that many, if not most, patients who drop out of pre-ART care will return to the health-care system at some later date, most likely once they become seriously ill. Without an effective health information system that allows patients to be tracked from site to site and over time, as they come and go from care, it is nearly impossible to assess the extent to which patient mobility mitigates the observed loss to care rates.
While pre-ART loss to care may not pose as immediate a mortality threat as loss of patients who already have clinical AIDS, it is still a major impediment to improving the outcomes of HIV care and treatment overall, is itself a contributor to the high mortality observed during the first year on ART, and wastes scarce health system resources. What can be done to begin to address this problem? We have heard of several operational solutions currently being evaluated, involving adjustments in referral procedures, improvements in the information provided to patients, reminders conveyed by text message or phone, or an increase in the number of steps that can be completed in a single visit. We have seen few rigorous evaluations of interventions, however. One exception, which is currently being evaluated in several settings, is the use of point-of-care CD4 count technology to reduce the number of visits to the clinic in Stage 1 –. Another promising strategy is to dispense prophylaxis for opportunistic infections, such as cotrimoxazole and isoniazid, more actively to pre-ART patients; a study in Kenya reported that retention of pre-ART patients 12 mo after enrollment improved from 63% to 84% after provision of cotrimoxazole was introduced .
A discussion of interventions is beyond the scope of this paper but would warrant further investigation. What we do wish to discuss are two issues that arise directly from this review. First, the review made painfully clear the need for standardization of terminology, definitions, time intervals, and end points that should be reported for the pre-ART period. The three-stage structure presented here may provide a framework for classifying results, but it is no more than a starting point. We have three recommendations for how researchers might begin to address this issue. First, proposals for clearly defined outcomes within each stage, and standard terminology to describe those outcomes and to label the phenomenon of pre-ART loss to care overall, would be helpful. Suggestions from researchers involved in work in this area, and thus familiar with data availability and limitations, would be welcome. Second, more effort should be made to report quantitative data comprehensively. We were forced to exclude from our review one paper and several conference abstracts that indicated that the authors likely had the data required to make quantitative estimates of retention in pre-ART care but did not report them or reported them incompletely. Having a standard set of indicators and outcomes, as suggested above, would also help to solve this second problem. And third, using data censoring as an end point should be avoided when possible, in favor of a clinically meaningful end point or a fixed duration of follow-up.
The second issue highlighted by this review is the absence of health information systems that allow patients to be tracked between service delivery points. We did not find a single study that was able to follow a cohort of HIV-positive adults all the way from testing to treatment initiation if they were not already eligible for ART when diagnosed. While in retrospect this points to a failure of the research community to establish prospective cohorts several years ago, it also reflects the sheer difficulty posed by such research. In most settings we are familiar with, it is virtually impossible to determine retrospectively what happens to patients after testing positive for HIV, as there is no tracking system in place to indicate whether they have sought further care or not. In our experience, even where sophisticated electronic record systems are in use for managing ART patients, they are rarely kept up to date or complete for those who have not initiated ART.
A starting point for understanding the nature and scope of the problem of pre-ART loss to care might thus be to implement effective patient tracking systems in selected geographic catchment areas that will generate accurate information on attrition between and within stages and help researchers assess the role of patient mobility in offsetting observed attrition, identify characteristics of patients most likely to be lost, and explore the extent to which attrition from pre-ART care is temporary—i.e., delay in action by patients who will later return to care, albeit sicker—or represents permanent loss from the health-care system, which will likely ultimately lead to death. Even doing this on a relatively small scale will be challenging, as it has been for ART patients , but it is a vital intervention for improving pre-ART care.
Limitations and a Call for Data
The heterogeneity of the literature identified, and the sheer scarcity of studies found for most sub-Saharan countries, led to a number of review limitations that are important to bear in mind in interpreting our findings. Most of these limitations have been alluded to already but warrant reiteration here. First, the quality and heterogeneity of the studies prevented meaningful synthesis of the results, which should therefore be regarded as suggestive rather than conclusive. The lack of standard definitions among reports, or even clear definitions of outcome measures within some (but not all) of the reports, combined with inconsistent or unreported durations of follow-up, stymied aggregate analysis. This limitation should be kept in mind in interpreting the forest plots and the summary figure (Figure 6) in particular. Second, double-counting likely affects some of the studies. Patients who are lost from one stage of care can return to care later and either successfully complete the stage or be lost again. Single-stage studies can tell us whether patients remain continuously in care until the end of the stage but should not be combined with studies of other stages, as demonstrated by our multiplying of median estimates above. Third, there is likely important heterogeneity among study populations that could not be discerned from most reports. For example, patients who enroll in pre-ART care (Stage 2) with low CD4 counts, close to the ART eligibility threshold, have less time at risk of being lost from care than those who enroll earlier, with higher CD4 counts, but few studies reported this information. Fourth, half of the studies eligible for inclusion in our review came from just one country, South Africa, and only six other countries are represented by the rest of the studies. This may diminish the generalizability of the findings to the sub-Saharan region as a whole. Fifth, eight of the 28 studies included were in abstract form only and were thus not subjected to peer review. Finally, publication bias may have affected our summary estimates. Only a few HIV clinics in sub-Saharan Africa have published information about pre-ART loss to care, and most of these sites collaborate with nongovernmental organizations, universities, or other external partners. If sites that have the ability and resources to report on such data have either lower or higher than average retention rates, our summary estimates will be biased.
Needless to say, new health information systems or studies launched now—the best solution to the problems described above—will require several years to accumulate the duration of follow-up needed. We therefore conclude with a call to HIV/AIDS service delivery organizations in the field. We think it likely that some programs have captured the data needed to analyze pre-ART loss to care through all three stages. We speculate that in some geographic areas, a single organization is the sole provider of every step of HIV care and treatment delivery. If that organization has also assigned a unique patient identification number to all those served, beginning with HIV testing, then an adequate data set may exist. We hope that this paper will inspire those who may have such data to try to answer the questions raised here, and that we will soon begin to see the results of this effort in the literature.
We thank Bruce Larson for input on the conceptual framework, Megan Coffman for assistance with the literature search, and in particular Melinda Wilson, who originally encouraged us to investigate the issue of pre-ART loss to care.
Conceived and designed the experiments: SR MPF. Performed the experiments: SR MPF. Analyzed the data: SR MPF. Contributed reagents/materials/analysis tools: SR MPF. Wrote the paper: SR MPF. ICMJE criteria for authorship read and met: SR MPF. Agree with the manuscript's results and conclusions: SR MPF. Wrote the first draft of the paper: SR.
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