Loss of HIV-infected patients on potent antiretroviral therapy programs in Togo: risk factors and the fate of these patients

Loss of HIV-infected patients on potent antiretroviral therapy programs in Togo: risk factors and the fate of these patients

 

Bayaki Saka¹, Dadja Essoya Landoh^2,&, Akouda Patassi³, Stephane d’Almeida⁴, Assetina Singo⁴, Bradford D Gessner⁵, Palokinam Vincent Pitché^1,4

 

¹Service de dermatologie et infections sexuellement transmissibles, Centre Hospitalier Universitaire Sylvanus Olympio, Lomé, Togo, ²Division de l’épidémiologie, Ministère de la Santé, Lomé, Togo, ³Service des maladies infectieuses, Centre Hospitalier Universitaire Sylvanus Olympio, Lomé, Togo, ⁴Programme national de lutte contre le SIDA et les IST (PNLS/IST), ministère de la Santé Togo, ⁵Agence de Médecine Préventive, Paris, France

 

 

^&Corresponding author
Dadja Essoya Landoh, Division de l’épidémiologie, Ministère de la Santé, Lomé, Togo

 

 

 

 

Human immunodeficiency virus (HIV) infection and acquired immunodeficiency syndrome (AIDS) are major public health problems in sub-Saharan Africa. Since the introduction of antiretroviral access programs in Togo, significant progress has been noted in the care of people living with HIV (PLWHA). From November 2008, antiretroviral therapy (ART) was provided free of charge to PLWHA while biological monitoring became free in 2010. Since then, the number of PLWHA support centers has increased from 70 in 2008 to 115 in late 2010, scaling-up treatment coverage of antiretroviral therapy from 2% in 2004 to 62.8% in late 2010 [1]. In the framework of scaling up the treatment at the sub-national levels, national programs are facing several challenges including the problem of loss to follow-up of PLWHA following the start of ART in treatment centers [2-6]. The current study aimed to highlight factors associated with early loss to follow-up of HIV-infected patients in treatment centers in Togo and the outcome of such patients.

 

 

This was a retrospective cross-sectional study carried out in 28 centers in Togo prescribing ART (two teaching hospitals, five regional hospitals, seven district hospitals/other public organizations, and 14 associations, NGOs, or accredited confessional structures). The choice of 28 treatment centers was done by convenience to cover the whole country, and targeted structures with large active patient populations. Indeed, over 80% of PLWHA in Togo are supported in these 28 centers. The study focused on medical records of PLWHA age older than 15 years on ART, who were lost to follow-up between January 2008 and October 2011. This period was selected because ART and biological screening became available for free during 2008 and 2011 was the last year of data available. According to the National AIDS control guidelines, a patient on ART was qualified as lost to follow-up when review of the medical records for the patient did not find evidence that he had died or moved four months after the last visit.

 

Once enrolled in a specific clinic, HIV-infected patients are requested to get all future treatment — provided at no charge — at that same clinic each month. Their contact numbers (if available) and information related to their clinic visits are recorded in their clinic record. To identify the outcome of patients lost to follow-up, study investigators called the patient's telephone number listed in the clinic record or his attendant's telephone number if this existed in the record. Patients were classified into two groups with respect to the time between the beginning of ART and lost of follow-up: early (less than or equal to 6 months) and late (more than 6 months).

 

Data were collected using a form validated by the Togolese National AIDS Program that had been tested in five clinics in Lomé. Six teams were deployed for data collection. Each team included two medical students who received two days of training on how to review patient's records in the HIV clinics; for each team, the two medical students reviewed the same patients' records and then the study team reconciled inconsistencies in the information collected by individual abstractors

 

Data were recorded using the software Epi Info version 3.5.1. For continuous variables, medians and interquartile ranges were calculated while for categorical variables we calculated proportions and respective 95% confidence intervals. Our main outcome variable was loss to follow-up at less than or equal to 6 months compared to loss to follow-up at greater than 6 months. The chi-square test or Fisher´s exact test were used when appropriate in bivariate analysis. Multivariate backwards stepwise logistic regression analysis was performed to identify independent risk factors for the dichotomous outcome lost to follow up or not lost to follow up. All variables significant during bivariate analysis at a p-value less than 0.05 and variables previously associated with lost to follow-up were included in the multivariate analysis. However, we excluded CD4 count as this is a component of the World Health Organization stage, and we used the latter as a measure of severity. We then removed variables in a stepwise fashion that were not significant at a p value > 0.1. We also assess for the level of significance of the likelihood ratio of the test. No interaction was identified for variables included in the model. Multivariate logistic regression analyses were performed using the method of MANOVA in Stata 11.

 

This study was approved by the Ministry of Health of Togo's board committee. Reference No 01/2011/MS/DGS/DSSP/PNLS-IST. We obtained verbal consent from study subjects that participated in the phone call.

 

 

From January 2008 to October 2011, 16,617 patients were placed on ART in the 28 included medical care structures. Among the total of 16,617 PLWHA, 1216 (7.3%) were lost to follow after the initiation of ART. Of these 1216, 290 had early loss to follow-up while 926 had late loss to follow-up. Baseline characteristics of the 1216 patients are summarized in Table 1.

 

During bivariate analysis, of the 1216 people lost to follow-up, those with early compared to late loss to follow-up were more likely to be under age 35 years (RR 1.6; 95% CI: 1.3 - 2.0; p<0.001), to be female (RR = 1.8; 95% CI: 1.4 - 2.2; p<0.001), to have WHO stage III or IV compared to stage I or II (RR = 1.5; 95%CI: 1.2 - 1.8; p = 0.0003), to have a CD4 count below 50 cells/mm3 (RR = 1.6; 95%CI: 1.4 - 2.1; p < 0.001), to have had an opportunistic infection at the beginning of ART (RR = 1.7; 95% CI: 1.4 - 2.1), to live in a rural area (RR = 1.6; 95%CI: 1.2 - 2.1; p < 0.001), and to have received treatment in a public structure (RR = 1.3; 95%CI: 1.1 - 1.9; p = 0.05) (Table 2).

 

During multivariate analysis, we included variables significant at p<0.05 on bivariate analysis. Of the 1216 patients, 1119 (93%) had data for all relevant variables and were included in the model. In the model, hemoglobinemia was removed (p=0.3). The following factors remained significantly associated with early lost to follow up of PLWHA on ART: age below 35 years (OR = 1.6; 95% CI: 1.2-2.2), female sex (OR = 1.8; 95% CI: 1.3-2.5), WHO stage III or IV (OR = 1.7; 95% CI: 1.3-2.2), existence of an opportunistic infection (OR = 2.3; 95% CI: 1.5-3.1), and follow-up in a public structure (OR 1.9; 95% CI: 1.2-3.3) (Table 3).

 

Among the 1216 patients, no telephone number was mentioned in the medical records of 212 patients and for 802 patients, the listed telephone number did not work. Of the remaining 202 patients, 114 patients (56%) were alive and 88 (44%) had died.

 

 

This study shows that the factors in Togo associated with early loss to follow of PLWHA on ART are age, gender, WHO stage of disease, existence of an opportunistic infection and type of clinic delivering HIV/AIDS care. Among the subset of patients for whom this information was available, we have demonstrated that a major reason for lost to follow-up is death; it is possible that a major reason we could not contact many people by telephone is because of death, and if this occurred, our mortality estimates will be conservative. In summary, lost to follow-up frequently follows severe disease, including death, and particularly among women and younger adults.

 

The proportion of patients lost to follow reported in Togo was significantly lower than the 13-40% reported by other studies in sub-Saharan Africa [4,7]. This may have resulted from different time intervals used to define loss to follow: in our study this was 4 months, while other studies used values of 60 days [8], 6 months [2, 9] or 14 months [7]. A multicenter study in Africa, Asia, and Latin America recently recommended using 6 months as the standard definition to improve comparability [10].

 

The severity of disease also likely played a role in determining our results. The CD4 count in our study was less than 200 / mm3 for 76% of patients at the beginning of ART with a median count of 119/mm3. Thus, in Togo most patients begin ART once they meet the clinical criteria for AIDS. While this is consistent with other studies from sub-Saharan Africa [2, 11] it will not be true in other more affluent areas or possibly in Africa over time.

 

In multivariate analysis, five factors (age, sex, WHO stage III or IV, presence of opportunistic infections and type of HIV care center) were associated with early loss to follow up of PLWHA on ART. Our study could not determine further why these factors contributed to loss to follow-up. Three of the factors — WHO stage [12,13], opportunistic infections [11,14,15], and among a subset death — are all consistent and illustrate that in our setting the most ill patients become lost to the medical care system. The other factors require more investigation to explain. Unlike our study, Ekouevi et al. [2] reported that in West Africa males were more likely than females to have low retention on ART. Early lost to follow up in young patients may be related to psychological denial of HIV infection or by the use of other types of treatment [16]. Use of a public clinic may reflect socioeconomic status with poorer patients more likely to be lost to follow-up.

 

In our study, 80% of patients whose phone numbers existed in their medical record could not be reached on these numbers. Previous studies have reported values of 35% [17] and 27% [18]. The explanation for this discrepancy, but may relate to socio-cultural issues, such as patients providing incorrect telephone numbers because of fear of stigmatization, denial of infection or a preference for traditional treatment. Alternatively, it could be that most patients whom we could not track had died, since this outcome had occurred for almost half of the patients whom we could track. Other studies support this theory: Yu et al [18] reported that 73% of all patients could be tracked, 50% had died and 23% were alive while a meta-analysis from sub-Saharan Africa reported that 40% of patients lost to follow-up had died [19].

 

The national STI/HIV/AIDS control program should take these results into account to strengthen the medical support of PLWHA in Togo, targeting young patients, those seeking care in public centers, and those with the most severe disease. For example, community health workers could actively track persons with HIV. Less expensively, health care providers could send SMS text messaging reminders, targeting high risk groups, a method that has worked in other settings [20-21]. Most generally, to the extent that severe disease and mortality are key factors in loss to follow-up, improvements in clinical care — such as better laboratory monitoring, sustained access to ART, and increased patient education on the utility of modern medical interventions — may provide the best long-term solution.

 

Limitations

 

As with many retrospective studies, data were missing from many patients, particularly for information collected during the phone follow-up component. Consequently, we likely did not fully evaluate some important risk factors. Additionally, data may have been incompletely recorded in medical records. This could have affected risk factor data (e.g., incorrect or missing CD4 counts) or outcome data (e.g., lack of accurate recording of death or change of residence for patients on ART). This is a necessary limitation for our study, where we aimed to determine risk factors for lost to follow-up in actual practice. While we could have performed a prospective study with periodic patient tracking (e.g., weekly) this design would have altered usual care seeking behaviors.

 

 

Factors associated with the early loss to follow-up of PLWHA on ART in Togo were age, sex, clinical WHO stage III or IV, presence of opportunistic infection, and type of HIV care center; moreover, many patients lost to follow-up died. These results suggest specific groups that could be targeted with active case follow-up or SMS messaging.

 

 

BDG works for AMP, which receives grant-specific funding for vaccine related work from GSK, Pfizer, Crucell, Merck, and Sanofi Aventis, as well as unrestricted funding from Sanofi Aventis; neither he nor AMP has received funding for work on HIV infection. The other authors declare no competing interests.

 

 

BS participated to the study design, undertook the field study, conducted the data collection, analysis and interpretation, and wrote the manuscript. DEL was involved in the field study, in data collection, analysis and interpretation and wrote the manuscript. AP; SD; and AS participated in data analysis and interpretation of results, and reviewed the manuscript. BG was involved in the scientific management, data analysis and interpretation, and guided the manuscript writing and its finalization. PVP was responsible for the conception of the study and its overall scientific management, for analysis and interpretation, and the preparation of the final manuscript. All the authors have read and approved the final manuscript to be submitted for publication.

 

 

The authors wish to thank the Ministry of Health of Togo for permitting this study to be conducted. Many thank to Makawa-Sy Makawa, Badawassou Leloua and Tetouyaba Blatome for their help during data collection in the field.

 

 

Table 1: Base line characteristics of 1216 patients with human immunodeficiency virus infection on anti-retroviral therapy who were lost to follow-up; Togo, 2008-2011

Table 2: Factors associated with lost to follow-up (LFU) at ≤ 6 months compared to greater than 6 months among patients with human immunodeficiency virus (HIV) infection taking antiretroviral therapy (ART); Togo, 2008- 2011. (n=1216)

Table 3: Multivariate analysis of factors associated with lost to follow-up at ≤ 6 months compared to greater than 6 months among patients with human immunodeficiency virus (HIV) infection on antiretroviral therapy; Togo, 2008-2011

 

 

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