First-Line Antiretroviral Regimen Failure and Determinants in an Urban HIV Clinic at Phramongkutklao Hospital, Bangkok, Thailand: 20 Years Experience.

PURPOSE: HIV treatment involves antiretroviral therapy (ART) endeavoring to suppress viral load to an undetectable level. Virologic failure occurs when ART fails to suppress and sustain an individual's viral load to less than 200 copies/mL after 6 months of therapy. In Thailand, the data among first-line antiretroviral regimen failure and determinants remains limited, especially in urban HIV clinics. We aimed to demonstrate factors of first-line antiretroviral regimen failures in an urban HIV/AIDS clinic at Phramongkutklao Hospital. PATIENTS AND METHODS: A nested case control 1:4 study was conducted. Data were collected from the electronic patient database among naïve people living with HIV/AIDS (PLWHA), aged ≥18 years and receiving ART continuously for at least 2 years at Phramongkutklao Hospital from 1 January 2000 to 31 December 2019. Multiple logistic regression was used to identify the determinants of virologic failure. Adjusted HRs (AHRs) with 95% CIs were used to declare statistical significance.
RESULTS: Of 200 PLWHA included in the study, 40 participants experienced HIV virologic failure. The median time after starting ART to virologic failure was 24 months (IQR 7-96.0). Univariate and multivariate analysis showed significant factors affecting first-line antiretroviral regimen failure included being female (37.5 vs 26.88%, adjusted odds ratio 5.08 [1.05-24.6, p-value 0.043], age ≤40 yr. (62.5 vs 49.6%, adjusted odds ratio 4.59 [1.47-14.37], p-value 0.009), CD4+count ≤200 cell/µL (77.5 vs 52.5%, adjusted odds ratio 4.83 [1.28-18.9], p value 0.02), tuberculosis (42.5 vs 7.5%, adjusted odds ratio 8.66 [2.37-31.56], p value <0.001) and initiation of ART at CD4+ count <350 cell/µL (72.5 vs 48.13%, adjusted odds ratio 31.36 [6.51-151.22], p value <0.001). Estimated prevalence of virologic failure in Phramongkutklao Hospital was 5.34%.
CONCLUSION: Our study revealed factors favoring virologic failure included being female, younger age, CD4+ count <200 cells/µL, tuberculosis and initiation of ART at CD4+ count <350 cell/µL. Multidisciplinary HIV comprehensive care teams should encourage patient adherence and support patients along HIV continuum of care to prevent virologic failure and drug resistance, especially among patients initiating ART at low CD4+ count and tuberculosis co-infection.

Introduction

HIV treatment involves antiretroviral therapy (ART), combining daily medications to inhibit the virus from replicating. The main goal of HIV treatment is to reduce a person’s viral load to an undetectable level. Durable viral suppression improves immune function and overall quality of life, lowers the risk of AIDS-defining and non-AIDS-defining complications, reduces the risk of HIV transmission, and allows people living with HIV/AIDS (PLWHA) to maximize their lifespan approaching that of individuals without HIV.1 The early marker for treatment failure is virologic failure. Suboptimal adherence and drug intolerance/toxicity are key contributors to virologic failure and regimen discontinuations.2,3 Furthermore, the presence of pre-existing (transmitted) HIV with drug resistance may also lead to virologic failure.4 Since 2014, Thailand’s national guidelines on HIV/AIDS treatment and prevention recommended initiating ART among all people living with HIV/AIDS (PLWHA) regardless of level of CD4+ count and all PLWHA in Thailand are able to access ART. The antiretroviral (ARV) regimens commonly used in Thailand include nonnucleoside reverse transcriptase inhibitor (NNRTI) based; nevirapine (NVP), efavirenz (EFV), rilpivirine (RPV) or protease inhibitor (PI) based; lopinavir/ritonavir (LPV/r) and atazanavir/ritonavir (ATA/r).5,6 Principal factors involving first-line antiretroviral regimen failure include poor adherence to medication, younger age, lower baseline CD4+ count and higher baseline viral load.7,8 Regarding the incidence of first-line antiretroviral regimen failure ranging from 4.1 to 24.6%,7,9,10 the diversity depended on different geographic areas and the study settings. One study from a university hospital in northern Thailand revealed the incidence of virologic failure was 9.6% that might have been affected by poor adherence, older age and low baseline CD4+ count.11 To date, the data among first-line antiretroviral regimen failure and determinants in Thailand remains limited especially in urban HIV clinics. We aimed to determine factors of first-line antiretroviral regimen failure in an urban HIV/AIDS clinic at Phramongkutklao Hospital to improve treatment strategies.

Materials and Methods

Study Setting and Design

A nested case control study was conducted. Data were collected from the electronic patient database from January 2000 to December 2019 in Phramongkutklao Hospital, a 1200-bed teaching hospital of Phramongkutklao College of Medicine, Royal Thai Army, Bangkok, Thailand. The data included sex, age, mode of HIV transmission, antiretroviral regimens, opportunistic infections or tuberculosis (TB) before ART, hepatitis C virus infection, hepatitis B virus infection, underlying diseases, duration of virologic failure after ART initiation and viral load level at time of virologic failure. Inclusion criteria of participants in both case and control groups were naïve PLWHA, aged ≥18 years old and continuously on ART at Phramongkutklao Hospital ≥2 years. Participants in the virologic failure group were defined as having two consecutive plasma HIV-1 viral loads after 6 months of ART >1000 copies/mL, while those in the control group were defined as having plasma HIV-1 viral load after 6 months of ART <50 copies/mL. ()

In Thailand, the cumulative incidence of HIV virologic failure was 9.6%.11 The preliminary investigation showed 40 virologic failures from 1292 patient’s record files. To minimize statistical error, a study of all subjects should be conducted using a nested case control of 1:4. Hence, the sample size of the case group was 40, and that of the control group was 160. The study protocol followed the guidelines of the Declaration of Helsinki and ethics approval was obtained from the Institutional Review Board, Royal Thai Army Department (reference ID: R015h/62_Exp). Informed consent was waived because of unidentified patient data. All study-related information will be stored securely at the study site with confidentiality and anonymity.

Definitions

Virologic failure is defined as a plasma viral load above 1000 copies/mL based on 2 consecutive viral load measurements after 3 months with adherence support.12

Good adherence was defined as patients taking antiretroviral drug on time, regularly ≥95%, while <95% was categorized as poor adherence.2

The definition of good adherence in this study was assumed from medical records for patients that missed no appointments and continued ARV drugs as described for good adherence.

Statistical Analysis

Expected parameters affecting virologic failure were analyzed using the independent t-test for continuous data, Mann–Whitney U-test for continuous data without normal distribution and Chi-square or Fisher’s exact test for discrete data. Significant data from multivariate analysis (p < 0.05) was analyzed for covariates using multiple logistic regression. All statistical analyses were obtained using STATA/MP12 Software.

Results

From January 2000 to December 2019, 1292 HIV-positive patients were treated with ART and followed up at Phramongkutklao Hospital. Virologic failure occurred among 69 patients; however, 29 patients were excluded due to treatment experienced, referral from other hospitals and loss to follow up. From our nested case control study, 200 participants met eligible criteria (40 participants in the virologic failure group, 160 participants in the virologic suppressed group) (Figure 1). The characteristics of cases and controls are described in Table 1. The majority of participants in either virologic failure or virologic suppressed groups were male and heterosexual. The median CD4+count at presentation was significantly lower in the virologic failure group (98 cell/µL: [IQR 31–178.5] vs 186 cell/µL [IQR 52.3–329], p-value 0.014). The number of participants initiating ART at CD4+ count less than 350 cell/µL was significantly higher in the virologic failure group (77 vs 29%, p-value 0.006). According to ART regimens, the proportion of PI-based regimens in the virologic failure group were significantly higher (20 vs 4.38%, p-value 0.006). Only one half of participants (57.5%) in the virologic failure group had a currently undetectable HIV viral load. TB and pneumocystis pneumonia were the 2 most common opportunistic infections and in higher proportions in the virologic failure group (Figure 2). In the virologic failure group, the median time after ART initiation to virologic failure was 24 months (IQR 7–96). Annually median of CD4 + count, after 10 years longitudinal follow-up in the virologic suppressed group tended to be higher than that in the virologic failure group as shown in Figure 3.

Figure 1

Participants’ enrollment.

Table 1

Baseline Characteristics in Virologic Failure and Virologic Suppressed Participants

	Virologic Failure (%)(n = 40)	Virologic Suppressed (%)(n = 160)	p-value
Sex			0.185
Male	25 (62.5)	117 (73.13)
Female	15 (37.5)	43 (26.88)
Age - yrs.
Mean ±SD (years)	38.62 ±11.04	41.19 ±11.79	0.214
≤ 40 yrs.	25 (62.5)	78 (49.6)	0.128
>40 yrs.	15 (37.5)	82 (50.4)
Underlying disease
Diabetes Mellitus	-	3 (1.88)	1.0
Chronic kidney disease	-	1 (0.63)	1.0
Marriage Status			0.887
Married	21 (52.5)	82(51.25)
Single	19 (47.5)	78 (48.7)
Occupation			0.106
Government officer	21 (52.5)	85 (53.13)
Employee	8(20)	41 (25.62)
Businessman	1 (2.5)	15 (9.38)
Other	10(25)	19 (11.8)
Start ART at CD4+ < 350 cell/µL	29 (72.5)	77 (48.13)	0.006
Mode of HIV transmission			0.319
Heterosexual	36 (90)	141 (88.3)
MSM	4(10)	19 (11.8)
ART regimens			0.006
NNRTI based	32 (80.0)	151 (94.38)
PI based	8 (20.0)	7 (4.38)
Integrase based	-	2 (1.25)
CD4+ count (cells/µL)
Median (IQR)	98 (31–178.5)	186 (52.5–329)	0.014
≤ 200 cells/µL	31 (77.5)	84 (52.5)	0.004
Single combination pill as initial regimen	7 (17.5)	33 (20.63)	0.659
Duration after initiation to virological failure [Median (IQR)]	-	24(7–96)	-
Good adherence	13 (22.5)	160 (100)	<0.001
Current undetectable HIV viral load	23 (57.5)	160 (100)	<0.001
Opportunistic disease	28 (70)	43 (26.9)	<0.001
PCP	9 (22.5)	17(10.63)	0.046
Cryptococcosis	2 (5.0)	6 (3.75)	0.662
Tuberculosis	16 (40)	12 (7.5)	0.001
Malignancy	1 (2.5)	1 (0.63)	0.36
Others	2 (5.0)	10 (8.3)	0.49
AIDS defining illness prior ART	17 (42.5)	33 (20.5)	0.005

Abbreviations: AIDS, acquired immunodeficiency syndrome; ART, antiretroviral therapy; HIV, The human immunodeficiency viruses; MSM, men who have sex with men; NNRTI, non-nucleoside reverse transcriptase inhibitor; PCP, pneumocystis pneumonia; PI, protease inhibitor.

Figure 2

Proportion of opportunistic infections stratified by virologic failure and virologic suppressed group.

Figure 3

Median CD4+ count in virologic failure and virologic suppressed groups during the 10-year follow-up.

Adherence

Most participants in the virologic failure group exhibited poor adherence. The rest (32.5%) showed good adherence in the virologic failure group, while 100% good adherence was observed in the control group.

Factors of First-Line Antiretroviral Regimen Failure

According to univariate and multivariate analysis, the significant factors of first-line antiretroviral regimen failures were: being female (37.5 vs 26.88%, adjusted odds ratio 5.08 [1.05–24.6], p-value 0.043), age ≤40 yr. (62.5 vs 49.6%, adjusted odds ratio 4.59 [1.47–14.37], p-value 0.009), CD4+ count ≤200 cell/µL (77.5 vs 52.5%, adjusted odds ratio 4.83 [1.28–18.9], p value 0.02), TB (42.5 vs 7.5%, adjusted odds ratio 8.66 [2.37–31.56], p value <0.001) and initiation of ART at CD4+ count ≤350 cell/µL (72.5 vs 48.13%, adjusted odds ratio 31.36 [6.51–151.22], p-value <0.001) (Table 2).

Table 2

Univariable and Multivariable Analysis of the Factors of the First-Line Antiretroviral Regimen Failures

	Virologic Failure (%) (n = 40)	Virologic Suppressed (%) (n = 160)	ORcrude (95% CI)	p-value	ORadjusted (95% CI)	p-value
Female	15 (37.50)	43 (26.88)	1.63 (0.79–3.39)	0.188	5.08 (1.05–24.6)	0.043
Age ≤40 yrs.	25 (62.50)	78 (49.6)	1.73 (0.85–3.53)	0.131	4.59 (1.47–14.37)	0.009
CD4+ count ≤ 200 cells/µL	31 (77.50)	84 (52.50)	3.12 (1.39–6.97)	0.006	4.83 (1.28–18.9)	0.020
PCP	9 (22.50)	17 (10.63)	2.44 (1.00–5.99)	0.051	3.58 (0.58–22.17)	0.170
Tuberculosis	17 (42.5)	12 (7.50)	9.12 (3.86–21.54)	<0.001	8.66 (2.37–31.56)	<0.001
PIs vs NNRTI base ART	8 (20.00)	9 (5.62)	3.56 (1.24–10.24)	0.019	1.75 (0.34–9.13)	0.505
Initiation ART at CD4+ count < 350 cell/µL	29 (72.5)	77 (48.13)	2.84 (1.33–6.08)	0.007	31.36 (6.51–151.22)	<0.001
AIDS defining illness prior ART	17 (42.5)	33 (20.75)	2.82 (1.35–5.88)	0.006	0.99 (0.21–4.71)	0.985

Abbreviations: AIDS, acquired immunodeficiency syndrome; ART, antiretroviral therapy; NNRTI, non-nucleoside reverse transcriptase inhibitor; PCP, pneumocystis pneumonia; PI, protease inhibitor.

Prevalence of HIV Virologic Failure in Phramongkutklao Hospital

From January 2000 to December 2019, 1292 HIV-positive patients were treated with ART and followed-up at Phramongkutklao Hospital. Sixty-nine patients presented virologic failure, and the estimated prevalence of virologic failure in Phramongkutklao Hospital was 5.34%.

Genotypic Resistance Profiles

Among subjects in the virologic failure group showing good adherence, 4 participants presented virologic failure within 6 months of ART initiation despite good adherence, indicating pretreatment HIV drug resistance (PDR) (). The majority of HIV genotypic resistance in PDR comprised NRTI and NNRTI resistance.

Nine participants in this group developed acquired HIV drug resistance irrespective of good adherence, and 2 cases were suspected to have received the drug resistant virus from their partners. However, the determination of acquired HIV drug resistance was not described in the other 7 cases.

In our cohort, the most common NRTI-associated mutations were M184V followed by K65R, while K103N was the most common NRTI-associated mutation.

Discussion

Globally, UNAIDS endeavored to have 90% of people on ART and virally suppressed by 2030, and as a result, HIV treatment failure would be prevented13 by implementing recommended strategies worldwide. These include improving ART adherence, taking medication based on the most appropriate prescription, preventing drug-to-drug interaction and increasing knowledge to improve attitudes of patients towards ART.

In our study, factors affecting virologic failure in first-line antiretroviral regimen were being female, younger age (≤40 yrs.), CD4 + count ≤200 cells/µL, TB and initiating ART at CD4+ count ≤350 cell/µL. Similarly, one related study in Thailand demonstrated that poor adherence, a low CD4+ count at baseline (<100 cells/µL), and old age were the predictors for treatment failure.11 As well as some reports from Africa, virologic failure was associated with nonadherence to medications, age >40 years, a CD4 + count <250 cell/µ, tuberculosis and being male.14,15 Age and sex were found to be the predictors of virologic failure in several reports. However, the results were diverse in that being either male or female, and older or younger age correlated with virologic failure revealed different outcomes in each report. These might be explained by different geographic areas and socioeconomic statuses among studies.10,11,14,15

In 2015, one study described initiating antiretroviral therapy among HIV-positive adults with a CD4 + count of >500 cells/µL provided net benefits over starting such therapy among patients after the CD4+ count had declined to 350 cells/µL.16 In our study, subjects presenting a CD4+ count ≤200 cells/µL were found to be 3.55 times higher at risk of virologic failure. Further, subjects initiating ART at CD4+ count <350 cell/µL were found to be 31.36 times higher at risk of virologic failure. Due to the decline of HIV-1-specific CD4 T helper cells, qualitative impairments of CD4 T cell function and functional impairment of CD4 T cells indirectly led to functional impairment of HIV-1 specific CD8 T cells or B cell responses to control viral replication.17 Subsequently, the number of viruses in the body increased, possibly leading to virologic resistance.18 Early initiation of ART after diagnosis of HIV/AIDS regardless of CD4 + count level not only showed better outcome in reducing HIV/AIDS-related illness, but might reduce the risk of virologic failure.

Poor adherence was the major cause of virologic failure, similar to other reports.11,14,15 The remaining patients (32.5%) presented good adherence regarding virologic failure, while all patients in the control group showed good adherence. In this study, adherence was measured by patient self-reporting and pill counts between visits without using a standardized questionnaire. The type of adherence measurement was debated concerning its reliability resulting in a discordance effect in some studies.19,20 Despite the reported good adherence in our cohort, virologic failure and acquired HIV drug resistance also occurred. Consequently, care plans should be developed to include reliable adherence measurements, for instance, a standardized questionnaire21,22 and electronically shared medical records.23

Females also faced increased risk of virologic failure in this cohort that might be explained by dependency status. From one related study featuring numerous female subjects, specific determinants of HIV virologic failure included lack of income, unemployment, dependent living situation and financial dependency.24 Similarly, younger age group (<40 yr.) also exhibited increased risk of virologic failure and was possibly related to maturity of life and disease-specific education which influenced long-term adherence and subsequently developed virologic failure.25,26

Interestingly, TB incidence was found to be 8.66 times higher among subjects at risk of virologic failure. TB was also described as the factor of either HIV virologic or immunologic failure.9,27,28 Several reasons can explain these phenomena, eg, M.tuberculosis induced apoptosis of CD4+ cells, subsequently leading to depletion of CD4+ cells, impairs cellular immune responses and results in immunologic failure.29 Furthermore, in treatment aspects of TB and HIV co-infection, antiretroviral and anti-TB constituted major obstacles for patients. Pill burden, adverse drug-to-drug interaction and unfavorable reactions of these drugs might have posed challenges leading to intolerance, poor adherence and subsequent virologic failure.

Surprisingly, the estimated prevalence of virologic failure in Phramongkutklao Hospital (5.34%) was relatively low compared with related studies indicating it ranged from 4.1 to 14.7%.7,9 The observed variation may have been a result of different geographic areas, study settings, the endpoint of virologic failure and patient adherence. Nevertheless, the low prevalence of virologic failure in our cohort could be explained in that almost one half of participants were government officers having obtained high education level and stable life activities resulting in good adherence to their ART.9,30

In our urban HIV clinic, the strongest risk factors of virologic failure including delayed initiation of ART, opportunistic infections and low CD4 + count resembled those found in rural HIV clinics.31 Multisector strategies should be implemented to solve this problem. Improving public health policy focused on active HIV-positive case findings as well as early initiation of ART and linkage to care should be encouraged.32 Innovative HIV care models should be developed and assessed, eg, telemedicine and smartphone applications to enhance adherence which have been reported as acceptable by young PLWHA.33,34 Developing multidisciplinary comprehensive HIV care teams, to support patients as they experience the HIV continuum of care from diagnosis to viral suppression and retention in the system, should be warranted and initially target PLWHA presenting a high risk of HIV virologic failure.35

This study constituted a large urban HIV cohort assembled from 20 years’ treatment experiences of PLWHA in a Thai university hospital and demonstrated the determinants of first-line antiretroviral failure in an urban HIV clinic setting exhibiting a low prevalence of HIV virologic failure and high education level of patients. Nevertheless, our study encountered several limitations. First, pretreatment HIV-viral loads were not performed among all patients, so we could not evaluate HIV-viral load level as a predictor of virologic failure. Second, adherence measurement and documentation were unstandardized. However, this represented usual clinical practices and adherence was and remained the strongest predictor for virologic failure. Third, we collected retrospective data; therefore, the accuracy of analysis depended on the completeness of data entry in the hospital database. Fourth, according to the low prevalence of HIV virologic failure in our cohort, the case control study was designed. Selection bias constituted a major concern, so we used a nested case control study to minimize this bias. Finally, this involved a limited single center experience. Thus, the less generalizable findings should be appraised and compared with other cohorts. A prospective multicenter study using standardized adherence measurement should be further investigated.

Despite these limitations, this study provided important information which would be useful for ART treatment programs in clinical practice especially in the urban HIV clinic setting.

Conclusion

Our study revealed that factors favoring virologic failure included CD4+ count <200 cells/µL, TB and starting ARV at CD4+ count <350 cell/µL. Integrative multisector strategies should be implemented including improving public health policy focused on active HIV-positive case findings, early initiation of ART and linkage to care, developing innovative HIV care models as well as setting up multidisciplinary comprehensive HIV care teams to support patients along the HIV continuum of care to prevent virologic failure and drug resistance, especially among patients initiating ART at low CD4+ counts and TB co-infection.