Abstract
Purpose
Immunocompromised patients are postulated to be at elevated risk of unfavorable outcomes of COVID-19. The exact effect of HIV infection on the course of COVID-19 remains to be elucidated. The aim of the study was to describe the epidemiological and clinical aspects of SARS-CoV-2 infection in HIV-infected individuals.
Methods
The HIV-positive patients who were diagnosed with SARS-CoV-2 infection were identified through thirteen specialist HIV clinics routinely following them due to HIV treatment. The data were collected between November 2020 and May 2021 through an on-line electronical case report form (SurveyMonkey®). The collected information included demographics, lifestyle, comorbidities, HIV care history, COVID-19 clinical course and treatment. Logistic regression models were used to identify factors associated with the odds of death or hospitalization due to COVID-19.
Results
One hundred and seventy-three patients with HIV-SARS-CoV-2 coinfection were included in the analysis. One hundred and sixty-one (93.1%) subjects had a symptomatic course of the disease. Thirty-nine (23.1%) of them were hospitalized, 23 (13.3%) necessitated oxygen therapy. Three (1.8%) patients required admission to the intensive care unit and 6 (3.5%) patients died. The presence of comorbidities and an HIV viral load of more than 50 copies/mL were linked to the increased odds of hospitalization (OR 3.24 [95% CI 1.27–8.28]) and OR 5.12 [95% CI 1.35–19.6], respectively).
Conclusions
As depicted by our analyses, HIV-positive patients with comorbidities and/or uncontrolled HIV replication who are diagnosed with SARS-CoV-2 infection should be considered of high risk of poor COVID-19 outcome and followed up carefully.
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Introduction
Severe acute respiratory syndrome coronavirus 2 or SARS-CoV-2 emerged in Wuhan, China, in December 2019 and quickly disseminated causing a global pandemic [1].
The first cases were reported in Poland in March 2020 and by the end of July 2021, 2,883,120 people were infected and 75,261 of them died of COVID-19 [2]. As in many other countries, Polish health care system was overwhelmed, what resulted in serious limitations in access to health care.
People suffering from immunodeficiency, including those with HIV infection, are postulated to be at higher risk of acquiring infection and death from COVID-19 [3]. However, recent reports concerning HIV, yield contradictory results [4, 5]. One possible explanation is that people living with HIV (PLHIV) are not a homogeneous group and numerous factors contribute to the effect of HIV infection on SARS-CoV-2 response. The role of immune deficiency, effectiveness and components of antiretroviral therapy (ART), the history of opportunistic infections, including those affecting respiratory tract, remain to be elucidated. Moreover, local factors may contribute to the course of COVID-19, such as access to general healthcare, causal COVID-19 treatment and vaccine strategies [6,7,8].
On the other hand, COVID-19 pandemic may affect the linkage to and retention in HIV care. As reported by Euroguidelines in Central and Eastern Europe Network Group in the beginning of COVID-19 pandemic, 60% of HIV practitioners were also involved in COVID-19 care [9].
Therefore, it is necessary to review epidemiological and clinical characteristic of SARS-CoV-2–HIV coinfection in national healthcare systems.
Methods
In November 2020, the Polish AIDS Society initiated a project to identify HIV and SARS-CoV-2 coinfection cases in Poland. In Poland HIV-positive patients were tested for SARS-CoV-2 infection in the same settings and for the same purposes as the general population. The HIV-positive patients who were diagnosed with SARS-CoV-2 infection were identified through thirteen specialist HIV clinics routinely following them due to HIV infection. Patients with confirmed diagnosis were included in the study irrespective of the presence of symptoms. COVID-19 diagnosis, according to national standards, was based on the positive reverse transcriptase real-time polymerase chain reaction (RT-PCR) test or the presence of characteristic clinical and radiological symptoms in combination with epidemiological context.
The data were collected between November 2020 and May 2021 through an on-line electronical case report form (eCRF) build on SurveyMonkey® platform. The collected information included demographics, lifestyle, comorbidities, HIV care history and COVID-19 clinical course. The clinical course of COVID-19 infection was assessed on day 0, 7, 14 and 28 according to WHO Ordinal Scale [10] (Score 1—ambulatory, no limitation of activities, 2—ambulatory, limitation of activities or home oxygen therapy, 3—hospitalized with mild disease, no oxygen therapy, 4—hospitalized with mild disease, oxygen by mask or nasal cannula, 5—hospitalized with severe disease on non-invasive ventilation or high-flow oxygen, 6—hospitalized with severe disease on mechanical ventilation, 7—hospitalized with severe disease on mechanical ventilation or organ support, 8—death). Comorbidities groups included: respiratory, kidney, cardiovascular disease, diabetes and malignancy. In statistical analyses logistic regression models were used to identify factors associated with the odds of death or hospitalization due to COVID-19. Factors significant in univariate models (p < 0.1) were included in multivariate model. A confidence interval (CI) of 95% was accepted. All analyses were performed using SAS version 9.4 (SAS Institute, Cary, NC).
All patient information obtained was anonymized prior to data collection. The study received approval from Bioethical Committee of Medical University of Warsaw (Komisja Bietyczna Medycznego Uniwersytetu, Nr AKBE/155/2020) and a waiver for informed consent was granted.
A total of 193 patients with SARS-CoV-2 and HIV coinfection were reported and assessed for eligibility. Eleven of the patients were diagnosed with HIV during COVID-19 and they were excluded from the study as well as nine individuals who have not yet recovered by the end of the study and their clinical outcome was unknown. The study design is depicted in the flow chart (Fig. 1). The results are reported in concordance with STROBE statement. [11]
Results
Baseline characteristics
In total, 173 patients were included into analyses, of whom 32 were female (18.6%). Median age was 42 (IQR: 36–50), median BMI 24 (IQR: 22–27).
One hundred and forty-four patients (85.2%) were employed, among them 112 (80%) were working in close contact with other people. Ninety-nine (58.6%) patients stated to never have used drugs, 71 (42.3%) have never smoked. Sixty patients (34.9%) had preexisting comorbidities, 28 (15.4%) had HBV and/or HCV coinfection.
In terms of comorbidities, 85 patients (48.1%) had at least one underlying condition, the most common were: cardiovascular diseases—diagnosed in 39 patients (22.5%), respiratory—in 14 patients (8.1%) and malignancies—11 patients (6.4%). Psychiatric disorders were known in 9 patients (5.2%), diabetes in 7 patients (4%), inflammatory bowel diseases in 5 patients (3%), neurological diseases in 4 patients (2.3%), renal disease in one patient (0.6%). Twenty-six of the patients (15%) had more than one comorbid condition diagnosed before the onset of COVID-19.
HIV outcomes
Median time since HIV diagnosis was 8 years (IQR: 3–14). Route of transmission was identified as MSM contact in 111 (64.2%) subjects, heterosexual in 22 (12.7%), IDU in 32 (18.5%), in 8 (4.6%) patients it remained unknown. One hundred and sixty-nine (97.7%) patients have been receiving cART before COVID-19 and 149 of them (88,2%) had HIV viral load < 50 copies/mL. Median CD4 + cell count was 587 cells/µl (IQR: 375–790) before contracting SARS-CoV-2. In terms of antiretroviral therapy, 114 patients (67.5%) received an integrase inhibitor-based therapy, 32 patients (18.9%) were on a protease inhibitor based regimen and 30 patients (17.8%) were receiving a non-nucleoside reverse transcriptase inhibitors.
COVID-19 outcomes
COVID-19 diagnosis was based on the quantitative polymerase chain reaction (RT-PCR) in 137 (79.6%) patients. The remaining patients were diagnosed by serologic tests or the presence of characteristic signs and symptoms in combination with epidemiological context. This group includes mostly non-severe cases of the patients who were treated in outpatient clinics. One hundred and sixty-one (93.1%) patients had a symptomatic course of the disease. Thirty-nine (23.1%) of them were hospitalized, 27 (15.6%) received COVID-19 specific treatment and 23 (13.3%) necessitated oxygen therapy. Three (1.8%) patients required admission to the intensive care unit and 6 (3.5%) patients died. One hundred and forty-six (84.4%) subjects showed complete and 21 (12.1%) partial recovery.
In terms of COVID-19 therapy, 28 patients (16.2%) received heparin in prophylactic dose, five patients (2.9%) in therapeutic dose, 24 patients (13.9%) received dexamethasone, ten patients (5.8%) were treated with remdesivir, two patients (1.2%) were eligible for tocilizumab therapy and one of the patients (0.6%) received convalescent plasma.
Number of the patients assigned to each WHO category in on days 0, 7, 14 and 28 is depicted in Fig. 2.
The characteristics of the patients stratified by the adverse outcomes are shown in Tables 1 and 2.
In general, patients admitted to the hospital, as compared to those who were not hospitalized, were less likely to be employed (66.7% vs. 90.5%; p = 0.0007), but more likely to acquire HIV through injecting drug use (30.3 vs. 17.2%; p = 0.0003) or heterosexual mode (21.2% vs. 10.9%; p = 0.0003), to be virologically unsuppressed (34.3% vs. 5.4%; p < 0.0001), to have at least one comorbidity (53.8% vs. 30.2%; p = 0.0124) and to have lower CD4 count (488 cells/µl vs. 604 cells/µl; p = 0.0402) (Table 1).
Patients who died, as compared to those who survived, were less likely to be employed (50.0% vs. 86.5%; p = 0.0426) and more likely to be virologically unsuppressed (66.7% vs. 9.82%; p = 0.0019) and to have at least one comorbidity (83.3% vs. 33.1%; p = 0.0201) (Table 2).
The odds of hospitalization
In univariate regression models, being employed, having comorbidity or coinfections, unknown route of HIV transmission, VL > 50 copies/ml and the CD4 + count before COVID-19 were associated with the odds of hospitalization.
After adjustment, two factors were independently associated with the increased odds of hospitalization, namely the presence of comorbidities (OR 3.24 [95% CI 1.27–8.28]) and VL > 50 copies/mL (OR 5.12 [95% CI 1.35–19.6]). Being employed was identified as a factor lowering the odds of hospitalization (OR 0.31 [95% CI 0.10–0.95]) (Table 3).
The odds of death
In univariate regression models, BMI, being employed, having comorbidity and a VL > 50 copies/ml were associated with the odds of death. After adjusting for all the significant factors in the multivariate model, none of them continued to be independently associated with death in the course of COVID-19, most likely in relation to low statistical power (Table 4).
Discussion
More than ninety percent of our patients presented symptoms of SARS-CoV-2 infection. Similar percentage was reported in the systematic review of 252 patients with SARS-CoV-2–HIV coinfection [12]. Estimates of the prevalence of asymptomatic COVID-19 in general population are varying, but seem to oscillate around 17%. [13]. As asymptomatic individuals are less likely to be tested and do not seek medical consultations it is possible that our study is overestimating the proportion of symptomatic COVID-19 among HIV-positive persons. It is important to note that the most patients included in our analysis were relatively young, with normal BMI and on antiretroviral therapy with well-controlled infection. This reflects well the general population of HIV-infected individuals in Poland [14,15,16].
At the time, when our study was conducted, the new SARS-CoV-2 variant, B.1.1.7, emerged in the United Kingdom and began to dominate in Poland, accounting for more than 90% of all infections by March 2021 [17]. COVID-19 vaccines have been available in Poland, as in the rest of Europe, since late December 2020. Initially, vaccines were distributed among healthcare professionals, followed by selected populations (PLHIV not being one of them). Universal access to the vaccines was granted in May 2021. [18] We did not include the vaccination status of the patients in our analyses, but based on the time of the data collection (November 2020–May 2021), it is safe to assume that a great majority of our patients were not vaccinated.
Thirty-nine of our patients (22.5%) required hospitalization (WHO Ordinal Scale 3 and more). According to the literature, hospitalization rates vary widely, depending on multiple factors. One of them is the period of the pandemic. Marchant et al. reported a drop in case hospitalization rate from 65% in the first pandemic wave to 15% in November 2020. [19] Mahajan et al. pointed to the fact, that the case hospitalization rate (referring to the number of hospitalizations divided by the number of confirmed COVID-19 cases) is much larger than the infection hospitalization rate (related to the assessed number of actual cases based on the SARS-CoV-2 antibodies seroprevalence in the population) 6,9% vs. 14% at the same time [20].
Overall mortality reported in our analysis (6 out of 173 patients, 3.47%) is consistent with the results of the large meta-analysis, where 1416 out of 41,113 (3.44%) HIV–SARS-CoV-2-coinfected individuals died [21] and slightly lower than the overall case-fatality ratio of 5.43% estimated by a large Polish study conducted in the first months of pandemic, before the first variants of concern were identified [22].
Non-HIV-related comorbidities are among main mortality risk factors in COVID-19 [23, 24]. Since the advent of antiretroviral therapy, life expectancy of PLHIV has risen and they are more likely to develop chronic conditions characteristic to older population. Furthermore, it has been reported that PLHIV develop comorbidities more often and earlier than general population [25], what combined with impaired immune system makes HIV-positive people a particularly vulnerable population [26]. According to WHO report, HIV infection and multimorbidity independently elevate the risk of death from COVID-19 [27].
In our study, comorbidities were fairly common and were also the main driving factor for the severe course of SARS-CoV-2 infection requiring hospitalization. Our analysis did not directly link multimorbidity to the risk of death from COVID-19 in PLHIV what may be caused by a relatively small sample size and few reported deaths.
Above results point out to the importance of timely diagnosis of comorbid conditions in HIV-positive patients. Healthcare professionals should be aware of the early signs and symptoms of cardiovascular, metabolic and renal diseases, malignancy, as well as known side effects of antiretroviral therapy and address them properly according to local or European guidelines [28]. Taking into account the possibility of underdiagnosed comorbidities, as well as lack of certainty for the course of COVID-19 and possible drug–drug interactions, it seems rational to propose different indications for hospitalization in this group of patients [29].
The other factor that influenced the course of COVID-19 in our patients was a detectable viral load of more than 50 copies/mL. The exact impact of HIV viral load on COVID-19 severity remains unclear and many reports lack the appropriate subgroup analysis.
In a case series of 33 patients described by Härter et al., only two patients were not virally suppressed and both of them required intensive care, one of them died [30]. Analogous results were reported by the Euroguidelines in Central and Eastern Europe (ECEE) Network Group in a cohort of 34 patients. Two of the three patients necessitating admission to intensive care unit had a detectable HIV RNA, one of these patients died [31]. The opposite pattern was observed by Patel et al. in a larger cohort [32]. In a meta-analysis by Lee et al., no correlation was found between HIV viral load and severity of COVID-19 [5]. Tesoriero et al. found that the hospitalization rate was higher in those patients who were not virally suppressed and was also increasing with the stage of HIV infection (defined by CD4 + count) [33].
Several studies have investigated the occupational risk for SARS-CoV-2 infection. In a large study based in UK, the authors postulated that healthcare workers were at higher risk of severe COVID-19 [34], whereas the analysis of excess mortality associated with COVID-19 revealed that other groups of essential workers may be even more affected [35]. We observed that being employed reduced the risk of hospitalization, however, had no effect on COVID-19 mortality. The possible explanation of this effect is the reluctance of the employed patients, who are in good condition, to stay in hospital in order to continue working from home and avoid sick leave.
Limitations to our study include the lack of the control group of HIV-negative individuals and a limited number of endpoints included in the analysis. Unfortunately, a low number of study outcomes prevent in depth analyses of related risk factors, both in our study and in already existing reports. On the other hand, this is, to our knowledge, the first Polish study investigating COVID-19 course and epidemiology in the population of people living with HIV/AIDS.
Conclusions
As depicted by our analyses, HIV-positive patients with comorbidities and/or uncontrolled HIV replication who are diagnosed with SARS-CoV-2 infection should be considered of high risk of poor COVID-19 outcome and followed up carefully.
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JDK: study design, data collection, data analysis, writing. ML: data collection, writing. MH: Data collection. EM: data collection. EJ: data collection. ES: data collection. AW: data collection. MW-J: data collection. AO: data collection. MB-J: data collection. MS: data collection. JS-R: data collection. PW: data collection. MP: data collection. All authors read and approved the final manuscript.
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The study received approval from Bioethical Committee of Medical University of Warsaw (Komisja Bietyczna Medycznego Uniwersytetu, Nr AKBE/155/2020) and a waiver for informed consent was granted.
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Kowalska, J.D., Lara, M., Hlebowicz, M. et al. Non-HIV-related comorbidities and uncontrolled HIV replication are independent factors increasing the odds of hospitalization due to COVID-19 among HIV-positive patients in Poland. Infection 51, 379–387 (2023). https://doi.org/10.1007/s15010-022-01887-8
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DOI: https://doi.org/10.1007/s15010-022-01887-8