AIDS-related opportunistic illnesses and early initiation of HIV care remain critical in the contemporary HAART era: a retrospective cohort study in Taiwan
BMC Infectious Diseases volume 18, Article number: 352 (2018)
No study has reported the epidemiology of AIDS-related opportunistic illnesses (AOIs) in patients with newly diagnosed HIV infection in Taiwan in the past decade. Understanding the current trends in AOI-related morbidity/mortality is essential in improving patient care and optimizing current public health strategies to further reduce AOIs in Taiwan in the era of contemporary highly active antiretroviral therapy (HAART).
Eligible patients were evaluated at two referral centers between 2010 and 2015. The patients were stratified by date of diagnosis into three periods: 2010–2011, 2012–2013, and 2014–2015. The demographics, HIV stage at presentation according to the United States CDC 2014 case definition, laboratory variables, and the occurrence of AOIs and associated outcomes were compared among the patients. Logistic regression and Cox regression were respectively used to identify variables associated with the occurrence of AOIs within 90 days of HIV enrollment and all-cause mortality.
Over a mean observation period of 469 days, 1264 patients with newly diagnosed HIV with a mean age of 29 years and mean CD4 count of 275 cells/μL experienced 394 AOI episodes in 290 events. At presentation, 37.7% of the patients had AIDS; the frequency did not significantly differ across groups. The overall proportion of AOIs within the study period was 21.0%, and no decline across groups was observed. The majority of AOIs (91.7%) developed within 90 days of enrollment. All-cause and AOI-related mortality did not significantly differ across groups. Throughout the three study periods, AOIs remained the main cause of death (47/56, 83.9%), especially within 180 days of enrollment (40/42, 95.2%). A CD4 cell count of < 200 cells/μL at presentation was associated with increased adjusted odds of an AOI within 90 days [adjusted odds ratio, 40.84; 95% confidence intervals (CI), 12.59–132.49] and an elevated adjusted hazard of all-cause mortality (adjusted hazard ratio, 11.03; 95% CI, 1.51–80.64).
Despite efforts toward HIV prevention and management, early HIV care in Taiwan continues to be critically affected by AOI-related morbidity and mortality in the era of contemporary HAART. Additional targeted interventions are required for the earlier diagnosis of patients with HIV.
Prior to the era of highly active antiretroviral therapy (HAART) and effective antimicrobial therapy, AIDS-related opportunistic illnesses (AOIs) caused high morbidity and mortality rates in patients with HIV . In the late 1990s, AOI-related morbidity and mortality began to decline substantially in both resource-limited [2,3,4] and resource-rich regions [5,6,7] with the routine use of antimicrobial prophylaxis against Pneumocystis jiroveci pneumonia and Mycobacterium avium complex, widespread use of potent HAART, development of critical care , and enhanced retention across the HIV treatment cascade.
Although chronic non-AIDS-related diseases are emerging as a major cause of morbidity and mortality [9,10,11], AOIs remain common at presentation for HIV screening or at the first HIV-related medical visit in both developing (33.6–48.0%) [12, 13] and developed countries (15.3–53.8%) [14,15,16,17,18]. AOIs are also the leading cause of hospitalization [19, 20] and death [10, 21] in patients with HIV, and still present a considerable challenge for health care systems attempting to effectively manage HIV.
HIV infection has been a reportable disease in Taiwan since 1984, and was diagnosed in 33,423 patients by the end of 2016. Of these patients, 15,418 developed AIDS and 5569 died . Several strategies have been adopted to improve the HIV care continuum in Taiwan, including free access to HAART and management of AOIs since 1997; initiation of HAART at higher CD4 count thresholds (CD4 < 200 cells/μL in 2006, < 350 cells/μL in 2010, < 500 cells/μL in 2013, and in all patients, regardless of CD4 count in 2016); implementation of the HIV case management program since 2007; and development of LGBT community health centers since 2010. Although interventions have been implemented to combat the HIV epidemic in Taiwan , the number of HIV infections reported annually continue to increase , and only a few studies have investigated the epidemiology of AOI-related morbidity and mortality in patients with HIV about 10 years ago [24,25,26]. The epidemiology of AOI-related morbidity and mortality in patients with HIV has not been reported in Taiwan in the past decade. Moreover, both newly diagnosed patients and those with existing HIV diagnoses have been included in most reports [24, 25]. The combination of these two populations in a study design does not reflect the epidemiology of AOIs for newly diagnosed patients after seeking medical care for HIV. Understanding the current trends in AOI-related morbidity and mortality in patients newly diagnosed HIV is essential in improving patient care and optimizing current public health strategies.
This study was conducted at the two largest HIV-designated centers in southern Taiwan, and the current trends in AOI-related morbidity and mortality were analyzed in patients that were newly diagnosed as having HIV between January 1, 2010 and December 31, 2015.
Study design, setting, and data source
This study had a retrospective cohort design; it was conducted at Kaohsiung Medical University Chung-Ho Memorial Hospital (KMUH) and Kaohsiung Veterans General Hospital (VGHKS), the two largest referral centers for the treatment of patients with HIV in southern Taiwan. The health care staff at both KMUH and VGHKS have extensive experience in the treatment of patients with HIV and have been actively involved in voluntary counseling and testing (VCT) for HIV since 1997. The study was approved by the institutional review boards of both participating hospitals. The medical records of all eligible patients were reviewed by trained staff, who retrieved the patients’ age, sex, date of the first HIV-related medical visit, HIV diagnosis through active surveillance, presence of risk factors for HIV-1 acquisition, serum CD4+ T-cell counts, HIV viral load at presentation, HIV stage at presentation, and AOIs with associated outcomes.
We screened patients who presented at both hospitals for HIV-related care for the first time between January 1, 2010 and December 31, 2015. Those who had received follow-up care at both hospitals were counted once. Because both hospitals were designated to provide care for patients with HIV who were incarcerated, we included only patients who visited each hospital’s outpatient or inpatient department in person. We excluded patients without a new diagnosis, those younger than 15 years, and those seen only once as outpatients and were thus lost to follow-up during the observation period. We stratified the enrolled patients by the date of their initial HIV-related visit into three periods: period 1, from January 1, 2010 to December 31, 2011; period 2, from January 1, 2012 to December 31, 2013; and period 3, from January 1, 2014 to December 31, 2015. We compared demographic and clinical variables, comorbidities, baseline laboratory results, AOI events, and associated outcomes of the patients among the groups.
No consensus exists regarding the definition of a new diagnosis of HIV ; however, eligible patients received their initial HIV diagnosis at one of the study hospitals or had been diagnosed elsewhere but referred to one of the aforementioned hospitals within 1 month and had available medical records . The date of enrollment was defined as the date of the first visit at which the patient sought HIV care at either hospital. The date of an AOI event was defined as the date of the first visit at which the patient sought care for an AOI. The final patient observation was at 6 months after each study period, death, or the final outpatient visit or hospitalization for patients who were lost to follow-up, whichever occurred first. HIV diagnoses through active surveillance by VCT, military screening, screening at blood donation, prenatal screening, and screening at methadone clinics were included as initial diagnoses. Baseline CD4 cell count, HIV viral load, and laboratory test results were measured within 6 months of enrollment  or as close as possible to the date of HIV diagnosis. The stage of HIV infection at presentation was scaled in the range of 0–3 following the United States Centers for Disease Control and Prevention (CDC) 2014 case definition for HIV infection . Acute HIV infection was defined as acute retroviral syndrome with a negative or indeterminate Western blot in the presence of a positive p24-antigen or HIV-1 RNA test, either detectable or as a documented seroconversion, and with or without symptoms during the preceding 90 days . AOI-related mortality was defined as any death attributable to an AOI.
AOIs were defined according to the United States CDC 1993 AIDS case definition  with the addition of Penicillium marneffei infection, which is a common AOI in Southeast Asia, southern China, and Taiwan [19, 32]. If patients experienced more than one AOI episode during the same outpatient visit or hospitalization, the episodes were recorded as a single event. AOI episodes occurring during different outpatient visits or hospitalizations were recorded as separate events if no symptoms had been observed at previous outpatient visits or hospitalizations, and the associated laboratory results and outcomes were recorded sequentially.
Trends in AOI-related morbidity and mortality during the three study periods were the primary outcomes of interest. The AOI-related morbidity and mortality observed in each study period were then stratified by the interval from enrollment in HIV care. The identification of predictors of AOIs occurring within 90 days of enrollment for HIV care and of all-cause mortality was the secondary objective.
Categorical variables among the three subgroups were compared using the χ2 or Fisher’s exact test, and continuous variables were compared using analysis of variance. The probabilities of AOIs stratified by study period and all-cause mortality stratified by CD4 cell count at presentation were estimated using Kaplan–Meier survival curves and log-rank testing. In the univariable analysis, CD4 cell count at presentation was used instead of HIV stage at presentation due to the marked collinearity between these two variables. Variables associated with the occurrence of any AOIs within 90 days of enrollment for HIV care were identified using logistic regression analysis, and the factors associated with all-cause mortality were identified using Cox regression analysis. All variables in the univariable analysis were selected for subsequent multivariable analysis. The effects of each variable were estimated using odds ratios (ORs) or hazard ratios (HRs) with 95% confidence intervals (CIs). All tests were two-tailed, and p < 0.05 was considered significant. Statistical analyses were performed using SPSS version 22.0 (IBM Corp., Armonk, NY, USA).
Characteristics of study participants
Of the 2124 patients screened, 1950 met the inclusion criteria in terms of outpatient or inpatient department visits. A total of 686 patients were excluded because they were not newly diagnosed (n = 591), were not followed up for the second time (n = 94), or were younger than 15 years (n = 1). Of the remaining 1264 enrolled patients, 395 (31.2%) were included in period 1, 471 (37.3%) in period 2, and 398 (31.5%) in period 3.
The baseline demographic characteristics and comorbidities of the three groups are summarized in Table 1. The mean (±standard deviation, SD) duration of observation was 469 (±255) days, 98.3% of the patients were men, and the mean (±SD) age at presentation was 29 (±9) years. The mean (±SD) CD4 cell count at presentation was 275 (±205) cells/μL, and 38.8% of participants had a CD4 cell count of < 200 cells/μL. The frequency of diagnoses through active HIV surveillance was not significantly different among the three enrollment periods (P = 0.12), but those made during VCT significantly increased from 33.4% in period 1 to 43.0% in period 3 (P = 0.01). The three main routes of HIV transmission were homosexual or bisexual contact (87.2%), heterosexual contact (11.2%), and drug injection (1.1%). The distribution of HIV stages at presentation was not different among the three periods. The overall prevalence of AIDS at presentation according to the United States CDC 2014 case definition for HIV infection  (AOIs or CD4 cell count < 200 cells/μL) was 37.7% [38.5% in period 1, 38.4% in period 2, and 36.2% in period 3 (P = 0.74)]. The duration of observation, sex, mean age at presentation, comorbidities, mean CD4 cell count at presentation, and mean viral load at presentation did not differ significantly among the patients included in the three study periods.
Trends in AOI-related morbidity and risk of AOIs within 90 days of enrollment for HIV care
During 1622 person-years of observation, 394 AOI episodes occurred in 290 events, with 1.36 episodes per AOI event. The five most common AOIs during the study period were P. jirovecii pneumonia (43.4%), Cytomegalovirus disease (10.4%), M. tuberculosis (8.1%), wasting syndrome (8.1%), and Candidiasis (6.9%) (Additional file 1: Table S1). The prevalence of AOIs at presentation was 18.4%, and no decline was observed across groups (19.5% in period 1, 18.5% in period 2, and 17.3% in period 3; P = 0.74) (Table 1). Within the study period, the overall proportion of patients with an AOI was 21.0%, and no decline was observed across groups (22.5% in period 1, 21.0% in period 2, and 19.6% in period 3; P = 0.60). No significant difference was noted in the occurrence of the first AOI event among the three periods (log-rank test, P = 0.59; Fig. 1a).
By stratifying the AOI events (including repeated events) in each study period according to the interval since enrollment (≤90 days, 91–180 days, and ≥ 181 days; Fig. 1b), 91.7% of the events developed within 90 days, and among the three study periods, the proportion of events within each of the three intervals did not significantly differ (P = 0.11). Logistic regression results revealed that age [adjusted OR (AOR) per 10-year increase, 1.95; 95% CI, 1.58–2.41], heterosexual contact (vs. homosexual contact, AOR, 1.83; 95% CI, 1.05–3.19), and a CD4 cell count of < 200 cells/μL (vs. CD4 cell count ≥500 cells/μL at presentation, AOR, 40.84; 95% CI, 12.59–132.49) were associated with an AOI within 90 days of enrollment (Table 2).
Overall, the results indicated that the development of AOIs did not significantly differ among the study periods. Most AOIs developed shortly after enrollment, and age, heterosexual contact, and CD4 cell count < 200 cells/μL at presentation increased the risk of an AOI within 90 days.
Trends in AOI-related mortality and all-cause mortality
Of the 1264 enrolled patients, 1132 (89.6%) had survived, 56 (4.4%) had died, and 76 (6.0%) were lost to follow-up at the end of the study. The all-cause mortality within the study period was 4.4% [Total numbers: 56; AOI-related etiologies: 47 (83.9%), non-AOI-related infection: 4 (7.1%), liver disease: 3 (5.4%), cardiovascular disease: 2 (1.8%), and trauma: 1(1.8%)], and no decline was observed across groups (4.3% in period 1, 5.7% in period 2, and 3% in period 3, P = 0.15; Table 1). Within the entire study period, the overall proportion of AOI-related mortality was 3.7%; it did not significantly decreased from 3.3% in period 1 to 4.7% in period 2, and to 3.0% in period 3 (P = 0.38; Table 1). The overall mortality of each AOI event was 16.9%; it did not significantly improve across the three study periods (P = 0.82; Fig. 1b).
When all 56 all-cause deaths in each study period were stratified by interval since HIV enrollment (≤180 days and ≥ 181 days; Fig. 2a), it was revealed that 75% of the deaths occurred within 180 days of enrollment, and the proportions of deaths within each of the two intervals did not differ significantly among the three study periods (P = 0.47, Fig. 2a). AOIs accounted for 95.2 and 50.0% of overall all-cause deaths ≤180 days and ≥ 181 days after enrollment for HIV care, respectively. The proportion of AOI as the cause of death stratified by interval since enrollment for HIV care did not significantly differ among the three study periods (P = 0.62 and 0.26 for AOI(s) as the cause of mortality within 180 days and after 180 days of enrollment for HIV treatment, respectively; Fig. 2a).
Univariable analysis results revealed that the HR for all-cause mortality in patients with a CD4 count of < 200 cells/μL at presentation was 16.86 (95% CI, 2.33–122.04) compared with those with a CD4 count of ≥500 cells/μL at presentation (Fig. 2b, Table 3). In the multivariable analysis, a CD4 count of < 200 cells/μL at presentation (vs. a CD4 cell count of ≥500 cells/μL at presentation) remained significantly associated with an elevated risk of all-cause mortality [adjusted HR (AHR), 11.03; 95% CI, 1.51–80.64; Table 3]. Other factors associated with an elevated risk of all-cause mortality were age (AHR per 10-year increase, 1.47; 95% CI, 1.21–1.77), heterosexual contact (vs. homosexual contact, AHR, 2.61; 95% CI, 1.32–5.16), unknown contact (vs. homosexual contact, AHR, 5.87; 95% CI, 1.27–27.08), and HBsAg seropositivity (AHR, 2.65; 95% CI, 1.42–4.94).
No significant differences in all-cause mortality and AOI-related mortality were observed among the study periods. Throughout all study periods and especially within 180 days of enrollment, AOIs remained the main cause of death. Age, a CD4 count of < 200 cells/μL at presentation, heterosexual and unknown contact, and HBsAg seropositivity were independent risk factors for all-cause mortality.
Throughout the three study periods, no significant differences were observed in the prevalence of AOI-related morbidity and mortality in patients with newly diagnosed HIV. AOI events were generally diagnosed at or shortly after presentation and enrollment (Figs. 1a, b). Throughout the study periods, particularly within 180 days of enrollment (95.2%; Fig. 2a), AOIs remained the main cause of death. The findings reveal that in Taiwan, in this era of contemporary HAART, AOI-related morbidity and mortality continue to pose a major challenge to patients with HIV at presentation or shortly after receiving a diagnosis of HIV.
Consistent with the Collaboration of Observational HIV Epidemiological Research (COHERE) study , the present study revealed that late presentation of HIV (CD4 count < 200 cells/μL at presentation) was associated with increased AOI-related morbidity and mortality (Tables 2 and 3). Late presentation has negative consequences not only for the patient but also for the general population. These include increased transmission of HIV to sexual partners [33, 34] and an increased demand for medical resources [15, 35]. Although several strategies for improving HIV care, including antimicrobial prophylaxis against Pneumocystis jiroveci pneumonia and Mycobacterium avium complex, have been adopted in Taiwan , further interventions to identify patients with HIV and initiate care earlier is urgently required to reduce AOI-related morbidity and mortality.
The substantial proportion of patients with late presentation HIV infection (CD4 count < 200 cells/μL at presentation) in this study (Table 1) is consistent with findings in studies conducted in both developing [12, 13] and developed [14,15,16,17,18] countries. In Taiwan, several active HIV surveillance programs have been adopted among specific populations, including blood and organ donors in 1988, military draftees in 1989, prison inmates in 1990, pregnant women in 2005, and people with sexually transmitted diseases and intravenous drug users (IDUs) in 2008. In 1997, a nationwide program of free anonymous VCT for HIV among high-risk populations was initiated at several hospitals, clinics, and nongovernmental organizations. It is unclear why the proportion of late-presenting patients did not change over the three study periods despite the implementation of active surveillance. Moreover, the proportion of patients with AIDS at presentation (37.7%) in this study was even higher than that reported (15%) during 1984–2005 in a previous nationwide cohort study . In that study, the proportion of patients that received an AIDS diagnosis within 1 month of an HIV diagnosis was 21.1% in the pre-HAART (January 1, 1984 to March 31, 1997), 26.% in the early HAART (April 1, 1997 to December 31, 2001), and 10.9% in the late HAART eras (January 1, 2002 to December 31, 2005) . The low proportion of such diagnoses during the late HAART era may have resulted from a rapid increase in IDUs with HIV infections (from 1.7% in 2002 to 68.6% in 2006) [36, 37], most of whom were diagnosed through active surveillance in the penal system [26, 38]. However, HIV infection in IDUs has consistently decreased since the Taiwan CDC launched harm reduction programs in August 2005 . Starting in 2008, the epidemic changed, with infections mainly occurring through sexual transmission, especially among men who have sex with men (MSM), as reported in other Asian countries [40, 41]. The higher rate of AIDS at presentation observed in the present study compared with that in previous studies  may have resulted from a growing population of MSM who are unable to access HIV testing and subsequent care due to the dual stigma and discrimination of both homosexuality and HIV . Therefore, to alleviate the recent surge of late HIV presentation among MSM, investigating the risks associated with late presentation and adopting consequent interventions in this high-risk population should be a priority.
The early diagnosis of patients with HIV infection is challenging; however, Taiwan presents various opportunities for the implementation of interventions. The first opportunity is provided by surveys of trends in late presentation in known risk groups to identify those at increased risk of late presentation [12, 13, 18, 43, 44]. The second opportunity involves identifying barriers to HIV testing and subsequent care in groups at increased risk of late presentation. The present guidelines recommend that sexually active homosexual and bisexual men get tested for HIV at least annually . In many Asian countries, the estimated frequency of testing in those high-risk populations is below the recommended level of 60–80%, which is crucial for reducing the incidence of HIV in a population [41, 46]. Although the proportion of HIV infections diagnosed through VCT programs increased from 33.4% in period 1 to 43.0% in period 3 (Table 1), almost half of the new diagnoses were not made through active surveillance for HIV infection. Efforts to identify social [47,48,49], psychological , geographical , and economic barriers  that prevent high-risk groups from receiving regular HIV testing or timely medical care  should be increased. The third opportunity involves adopting novel approaches to HIV testing. In addition to facility-based testing, which is widely used in Taiwan, flexible approaches such as peer-led , indicator condition-guided , and home-based  testing should be targeted by incorporating the current knowledge of HIV prevalence and the causes of late presentation. For example, in Taiwan, rapid oral HIV testing by IDUs after release from the criminal justice system has been accepted . The fourth opportunity for intervention is educating primary physicians on the early presentation of HIV infection and acute retroviral syndrome. Primary physicians may not be sufficiently sensitive to the indicators of such HIV-associated conditions or the symptoms of acute retroviral syndrome that cause patients with HIV to seek medical care . In this study, no significant decline in the proportion of HIV diagnoses at an acute HIV status was observed over the three study periods (Table 1). This might be reversed by increasing the awareness of primary-care physicians.
The key strength of this study is that it is the first in this era of contemporary HAART to analyze the current trends in AOI-related morbidity and mortality in newly diagnosed patients with HIV infection in Taiwan after the implementation of harm reduction programs in August 2005. The findings are critical for public health policies in terms of regulating HIV control and may be generalizable to other Asia-Pacific [40, 41] and North American countries  with similar HIV epidemics among the MSM population who may be unable to access HIV testing due to stigma and discrimination of both homosexuality and HIV . However, our research had several limitations. First, the results may not be generalizable to the entire population of Taiwan. During the study period, 12,786 patients with newly diagnosed HIV were registered with the Taiwan CDC. Of these, 9.9% (1264/12,786) were enrolled in this study. Most of the participants (97%) were men, and the three main transmission routes were MSM (78.5%), heterosexual contact (13.4%), and intravenous drug use (3.7%) [56,57,58,59,60,61]. Although the sex distribution and HIV transmission routes are similar to those in the present study, our findings must be confirmed through nationwide surveillance. Second, there is no single definition of late presentation with HIV infection ; previously used definitions considered different CD4 cell counts (in the range of < 50 to < 350 cells/μL) [14, 15, 63]. In this study, late presentation was defined as a CD4 cell count of < 200 cells/μL at presentation. Therefore, the prevalence of late presentation in this study may not be comparable to that in other studies. Finally, 94 patients were excluded from the present study because they visited the outpatient clinic only once and were lost to follow-up during the observation period. Because the etiologies of patients lost to follow-up could not be determined, the effect on the prevalence of late presentation and AOI-related morbidity and mortality remains unknown. However, a comparison of the 1264 enrolled patients and 94 patients excluded due to being lost to follow-up revealed no significant differences between these two groups with respect to sex, age, and risk of HIV transmission.
Although considerable progress in reducing the burden of HIV and AOI-related morbidity and mortality has been made in Taiwan since the early 1980s, further improvements are warranted. The prevalence and timing of AOIs remain a critical challenge in delivering early HIV care. Nationwide surveillance to investigate the trends in late presentation among different risk groups and analyze the associated risks is urgently required. Improved surveillance is warranted for implementing effective, targeted interventions to improve early diagnosis of HIV infection and further reduce AOI-related morbidity and mortality.
Acquired immune deficiency syndrome
AIDS-related opportunistic illnesses
Highly active antiretroviral therapy
Hepatitis B surface antigen
Hepatitis C virus
Human immunodeficiency virus
Intravenous drug users drug users
Voluntary counseling and testing
Mocroft A, Lundgren J, Monforte AA, Ledergerber B, Barton S, Vella S, et al. Survival of AIDS patients according to type of AIDS-defining event. The AIDS in Europe study group. Int J Epidemiol. 1997;26(2):400–7.
Marie-Renée B, Drouin O, Bartlett G, Nguyen Q, Low A, Gavriilidis G, et al. Incidence and prevalence of opportunistic and other infections and the impact of antiretroviral therapy among HIV-infected children in low-and middle-income countries: a systematic review and meta-analysis. Clin Infect Dis. 2016;62(12):1586–94.
Tanuma J, Lee KH, Haneuse S, Matsumoto S, Nguyen DT, Nguyen DTH, et al. Incidence of AIDS-defining opportunistic infections and mortality during antiretroviral therapy in a cohort of adult HIV-infected individuals in Hanoi, 2007-2014. PLoS One. 2016;11(3):e0150781.
Rubaihayo J, Tumwesigye NM, Konde-Lule J. Trends in prevalence of selected opportunistic infections associated with HIV/AIDS in Uganda. BMC Infect Dis. 2015;15(1):1.
Buchacz K, Baker RK, Palella FJ Jr, Chmiel JS, Lichtenstein KA, Novak RM, et al. AIDS-defining opportunistic illnesses in US patients, 1994–2007: a cohort study. AIDS. 2010;24(10):1549–59.
Schwarcz L, Chen M-J, Vittinghoff E, Hsu L, Schwarcz S. Declining incidence of AIDS-defining opportunistic illnesses: results from 16 years of population-based AIDS surveillance. AIDS. 2013;27(4):597–605.
Djawe K, Buchacz K, Hsu L, Chen M-J, Selik RM, Rose C, et al. Mortality risk after AIDS-defining opportunistic illness among HIV-infected persons—San Francisco, 1981–2012. J Infect Dis. 2015;212(9):1366–75.
Akgün KM, Tate JP, Pisani M, Fried T, Butt AA, Gibert CL, et al. Medical ICU admission diagnoses and outcomes in human immunodeficiency virus–infected and virus–uninfected veterans in the combination antiretroviral era. Crit Care Med. 2013;41(6):1458.
Uhlenkott MC, Buskin SE, Kahle EM, Barash E, Aboulafia DM. Causes of death in the era of highly active antiretroviral therapy: a retrospective analysis of a hybrid hematology-oncology and HIV practice and the Seattle/king county adult/adolescent spectrum of HIV-related diseases project. Am J Med Sci. 2008;336(3):217–23.
Palella FJ Jr, Baker RK, Moorman AC, Chmiel JS, Wood KC, Brooks JT, et al. Mortality in the highly active antiretroviral therapy era: changing causes of death and disease in the HIV outpatient study. J Acquir Immune Defic Syndr. 2006;43(1):27–34.
Kim JH, Psevdos G Jr, Gonzalez E, Singh S, Kilayko MC, Sharp V. All-cause mortality in hospitalized HIV-infected patients at an acute tertiary care hospital with a comprehensive outpatient HIV care program in new York City in the era of highly active antiretroviral therapy (HAART). Infection. 2013;41(2):545–51.
Honge BL, Jespersen S, Aunsborg J, Mendes DV, Medina C, da Silva Te D, et al. High prevalence and excess mortality of late presenters among HIV-1, HIV-2 and HIV-1/2 dually infected patients in Guinea-Bissau - a cohort study from West Africa. Pan Afr Med J. 2016;25:40.
Drain PK, Losina E, Parker G, Giddy J, Ross D, Katz JN, et al. Risk factors for late-stage HIV disease presentation at initial HIV diagnosis in Durban, South Africa. PLoS One. 2013;8(1):e55305.
Mocroft A, Lundgren JD, Sabin ML, Monforte A, Brockmeyer N, Casabona J, et al. Risk factors and outcomes for late presentation for HIV-positive persons in Europe: results from the collaboration of observational HIV epidemiological research Europe study (COHERE). PLoS Med. 2013;10(9):e1001510.
Sabin CA, Smith CJ, Gumley H, Murphy G, Lampe FC, Phillips AN, et al. Late presenters in the era of highly active antiretroviral therapy: uptake of and responses to antiretroviral therapy. AIDS. 2004;18(16):2145–51.
Brannstrom J, Svedhem Johansson V, Marrone G, Wendahl S, Yilmaz A, Blaxhult A, et al. Deficiencies in the health care system contribute to a high rate of late HIV diagnosis in Sweden. HIV Med. 2016;17(6):425–35.
Perbost I, Malafronte B, Pradier C, Santo L, Dunais B, Counillon E, et al. In the era of highly active antiretroviral therapy, why are HIV-infected patients still admitted to hospital for an inaugural opportunistic infection? HIV Med. 2005;6(4):232–9.
O'Connell S, Enkelmann J, Sadlier C, Bergin C. Late HIV presentation - missed opportunities and factors associated with a changing pattern over time. Int J STD AIDS. 2017;28(8):814–21.
Xiao J, Gao G, Li Y, Zhang W, Tian Y, Huang Y, et al. Spectrums of opportunistic infections and malignancies in HIV-infected patients in tertiary care hospital, China. PLoS One. 2013;8(10):e75915.
Gebo KA, Fleishman JA, Moore RD. Hospitalizations for metabolic conditions, opportunistic infections, and injection drug use among HIV patients: trends between 1996 and 2000 in 12 states. J Acquir Immune Defic Syndr. 2005;40(5):609–16.
Mirani G, Williams PL, Chernoff M, Abzug MJ, Levin MJ, Seage GR, et al. Changing trends in complications and mortality rates among US youth and young adults with HIV infection in the era of combination antiretroviral therapy. Clin Infect Dis. 2015;61(12):1850–61.
Centers for Disease Control DoH, R.O.C. (Taiwan). HIV/AIDS http://www.cdc.gov.tw/english/info.aspx?treeid=e79c7a9e1e9b1cdf&nowtreeid=e02c24f0dacdd729&tid=7D01A79F5FD3B63D. Accessed 10 Dec 2017.
Centers for Disease Control DoH, R.O.C. (Taiwan). AIDS Control Program http://www.cdc.gov.tw/english/info.aspx?treeid=9d909a43ebf2819d&nowtreeid=0a4848283dfe9c40&tid=3DD1C7FFFF550913. Accessed 10 Dec 2017.
Hung C-C, Chen M-Y, Hsieh S-M, Sheng W-H, Chang S-C. Clinical spectrum, morbidity, and mortality of acquired immunodeficiency syndrome in Taiwan: a 5-year prospective study. J Acquir Immune Defic Syndr. 2000;24(4):378–85.
Sun H, Chen M, Hsieh S, Sheng W, Chang S, Hsiao C, et al. Changes in the clinical spectrum of opportunistic illnesses in persons with HIV infection in Taiwan in the era of highly active antiretroviral therapy. Jpn J Infect Dis. 2006;59(5):311.
Yang CH, Huang YF, Hsiao CF, Yeh YL, Liou HR, Hung CC, et al. Trends of mortality and causes of death among HIV-infected patients in Taiwan, 1984-2005. HIV Med. 2008;9(7):535–43.
Lesko CR, Cole SR, Zinski A, Poole C, Mugavero MJ. A systematic review and meta-regression of temporal trends in adult CD4+ cell count at presentation to HIV care, 1992–2011. Clin Infect Dis. 2013;57(7):1027–37.
Barry SM, Lloyd-Owen SJ, Madge SJ, Cozzi-Lepri A, Evans AJ, Phillips AN, et al. The changing demographics of new HIV diagnoses at a London Centre from 1994 to 2000. HIV Med. 2002;3(2):129–34.
Selik RM, Mokotoff ED, Branson B, Owen SM, Whitmore S, Hall HI. Centers for Disease Control and Prevention (CDC). Revised surveillance case definition for HIV infection—United States, 2014. MMWR Recomm Rep. 2014;63:1–0.
Braun DL, Kouyos RD, Balmer B, Grube C, Weber R, Günthard HF. Frequency and spectrum of unexpected clinical manifestations of primary HIV-1 infection. Clin Infect Dis. 2015;61(6):1013–21. civ398
Centers for Disease Control. Revised classification system for HIV infection and expanded surveillance case definition for AIDS among adolescents and adults. MMWR Recomm Rep. 1992;41(RR-17):1–19.
Sun HY, Chen MY, Hsiao CF, Hsieh SM, Hung CC, Chang SC. Endemic fungal infections caused by Cryptococcus neoformans and Penicillium marneffei in patients infected with human immunodeficiency virus and treated with highly active anti-retroviral therapy. Clin Microbiol Infect. 2006;12(4):381–8.
Skarbinski J, Rosenberg E, Paz-Bailey G, Hall HI, Rose CE, Viall AH, et al. Human immunodeficiency virus transmission at each step of the care continuum in the United States. JAMA Intern Med. 2015;175(4):588–96.
Marks G, Crepaz N, Janssen RS. Estimating sexual transmission of HIV from persons aware and unaware that they are infected with the virus in the USA. AIDS. 2006;20(10):1447–50.
Guillon M, Celse M, Geoffard PY. Economic and public health consequences of delayed access to medical care for migrants living with HIV in France. Eur J Health Econ. 2018;19(3):327–40.
Chen YJ, Lee CM, Chen M, Chuang SY, Liu HF, Wong WW, et al. Molecular epidemiology of HIV-1 infection in Taiwan from 2005 to 2008: further spread of CRF07_BC and emergence of CRF07_BC/subtype B dual infection. J Acquir Immune Defic Syndr. 2012;59(5):438–46.
Chen YM, Kuo SH. HIV-1 in Taiwan. Lancet. 2007;369(9562):623–5.
Yang CH, Yang SY, Shen MH, Kuo HS. The changing epidemiology of prevalent diagnosed HIV infections in Taiwan, 1984-2005. Int J Drug Policy. 2008;19(4):317–23.
Lin T, Chen CH, Chou P. Effects of combination approach on harm reduction programs: the Taiwan experience. Harm Reduct J. 2016;13(1):23.
Dokubo EK, Kim AA, Le LV, Nadol PJ, Prybylski D, Wolfe MI. HIV incidence in Asia: a review of available data and assessment of the epidemic. AIDS Rev. 2013;15(2):67–76.
van Griensven F, JWdL VW. A review of the epidemiology of HIV infection and prevention responses among MSM in Asia. AIDS. 2010;24:S30–40.
Beyrer C, Sullivan PS, Sanchez J, Dowdy D, Altman D, Trapence G, et al. A call to action for comprehensive HIV services for men who have sex with men. Lancet. 2012;380(9839):424–38.
Kigozi IM, Dobkin LM, Martin JN, Geng EH, Muyindike W, Emenyonu NI, et al. Late-disease stage at presentation to an HIV clinic in the era of free antiretroviral therapy in sub-Saharan Africa. J Acquir Immune Defic Syndr. 2009;52(2):280–9.
Desta WG, Sinishaw MA. Factors Affecting Utilization of Voluntary HIV Counseling and Testing Services among Teachers in Awi Zone, Northwest Ethiopia. AIDS Res Treat. 2017;2017:9034282.
Patel RR, Patel S, Clarke E, Khan AW, Doshi B, Radcliffe KW. Guidance and practice on frequency of HIV and sexually transmitted infection testing in men who have sex with men - what is the European situation? Int J STD AIDS. 2014;25(3):213–8.
Zablotska I, Holt M, de Wit J, McKechnie M, Mao L, Prestage G. Gay men who are not getting tested for HIV. AIDS Behav. 2012;16(7):1887–94.
Ransome Y, Batson A, Galea S, Kawachi I, Nash D, Mayer KH. The relationship between higher social trust and lower late HIV diagnosis and mortality differs by race/ethnicity: results from a state-level analysis. J Int AIDS Soc. 2017;20(1):1–9.
Bertrand T, Chan PA, Howe K, Comella J, Marak T, Bandy U. Health Equity, Social justice, and HIV in Rhode Island: a contemporary challenge. R I Med J. 2016;99(11):21–4.
Gesesew HA, Tesfay Gebremedhin A, Demissie TD, Kerie MW, Sudhakar M, Mwanri L. Significant association between perceived HIV related stigma and late presentation for HIV/AIDS care in low and middle-income countries: a systematic review and meta-analysis. PLoS One. 2017;12(3):e0173928.
Shangani S, Escudero D, Kirwa K, Harrison A, Marshall B, Operario D. Effectiveness of peer-led interventions to increase HIV testing among men who have sex with men: a systematic review and meta-analysis. AIDS Care. 2017;29(8):1003–13.
Sullivan AK, Raben D, Reekie J, Rayment M, Mocroft A, Esser S, et al. Feasibility and effectiveness of indicator condition-guided testing for HIV: results from HIDES I (HIV indicator diseases across Europe study). PLoS One. 2013;8(1):e52845.
Wolff B, Nyanzi B, Katongole G, Ssesanga D, Ruberantwari A, Whitworth J. Evaluation of a home-based voluntary counselling and testing intervention in rural Uganda. Health Policy Plan. 2005;20(2):109–16.
Lyu SY, Morisky DE, Yeh CY, Twu SJ, Peng EY, Malow RM. Acceptability of rapid oral fluid HIV testing among male injection drug users in Taiwan, 1997 and 2007. AIDS Care. 2011;23(4):508–14.
Lazarus JV, Hoekstra M, Raben D, Delpech V, Coenen T, Lundgren JD. The case for indicator condition-guided HIV screening. HIV Med. 2013;14(7):445–8.
Althoff KN, Gange SJ, Klein MB, Brooks JT, Hogg RS, Bosch RJ, et al. Late presentation for human immunodeficiency virus care in the United States and Canada. Clin Infect Dis. 2010;50(11):1512–20.
Centers for Disease Control DoH, R.O.C. (Taiwan). Statistics of Communicable Diseases and Surveillance Report 2010 http://www.cdc.gov.tw/professional/infectionreportinfo.aspx?treeid=56ca56252a0fa705&nowtreeid=2AA8435E1709FBFB&tid=A64090AD33AEA54B. Accessed 10 Dec 2017.
Centers for Disease Control DoH, R.O.C. (Taiwan). Statistics of Communicable Diseases and Surveillance Report 2011 http://www.cdc.gov.tw/professional/infectionreportinfo.aspx?treeid=56ca56252a0fa705&nowtreeid=2AA8435E1709FBFB&tid=E6F157600F310E3D. Accessed 10 Dec 2017.
Centers for Disease Control DoH, R.O.C. (Taiwan). Statistics of Communicable Diseases and Surveillance Report 2012 http://www.cdc.gov.tw/professional/infectionreportinfo.aspx?treeid=56ca56252a0fa705&nowtreeid=2AA8435E1709FBFB&tid=464F496EE012F03C. Accessed 10 Dece 2017.
Centers for Disease Control DoH, R.O.C. (Taiwan). Statistics of Communicable Diseases and Surveillance Report 2013 http://www.cdc.gov.tw/professional/infectionreportinfo.aspx?treeid=56ca56252a0fa705&nowtreeid=2AA8435E1709FBFB&tid=F811D601B49E2955. Accessed 10 Dec 2017.
Centers for Disease Control DoH, R.O.C. (Taiwan). Statistics of Communicable Diseases and Surveillance Report 2014 http://www.cdc.gov.tw/professional/infectionreportinfo.aspx?treeid=56ca56252a0fa705&nowtreeid=2AA8435E1709FBFB&tid=15B0DEB6406CAF71. Accessed 10 Dec 2017.
Centers for Disease Control DoH, R.O.C. (Taiwan). Statistics of Communicable Diseases and Surveillance Report 2015 [http://www.cdc.gov.tw/professional/infectionreportinfo.aspx?treeid=56ca56252a0fa705&nowtreeid=2AA8435E1709FBFB&tid=2535D9B0B8D8C633]. Accessed 10 Dec 2017.
Waters L, Sabin CA. Late HIV presentation: epidemiology, clinical implications and management. Expert Rev Anti-Infect Ther. 2011;9(10):877–89.
Girardi E, Sabin CA, Monforte AD. Late diagnosis of HIV infection: epidemiological features, consequences and strategies to encourage earlier testing. J Acquir Immune Defic Syndr. 2007;46(Suppl 1):S3–8.
This manuscript was edited by Wallace Academic Editing.
No funding was received for this study.
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The data set used during the present study is available from the corresponding author on reasonable request.
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This study was approved by the VGHKS and KMUH ethics committees [VGHKS17-CT4–20, KMUHIRB-SV(II)-20,170,003] and adhered to the ethical principles of the Declaration of Helsinki. The requirement for informed consent was waived by the institutional review boards of both participating hospitals.
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Lee, CY., Tseng, YT., Lin, WR. et al. AIDS-related opportunistic illnesses and early initiation of HIV care remain critical in the contemporary HAART era: a retrospective cohort study in Taiwan. BMC Infect Dis 18, 352 (2018). https://doi.org/10.1186/s12879-018-3251-1
- Late presentation
- Opportunistic illness