If you don't remember your password, you can reset it by entering your email address and clicking the Reset Password button. You will then receive an email that contains a secure link for resetting your password
If the address matches a valid account an email will be sent to __email__ with instructions for resetting your password
Comparison of antiviral effect for mild-to-moderate COVID-19 cases between lopinavir/ritonavir versus hydroxychloroquine: A nationwide propensity score-matched cohort study
Corresponding author at: Department of Preventive Medicine, Gil Medical Center, Gachon University College of Medicine, 34 Namdong-daero 774beon-gil, Namdong-gu, Incheon 21565, Republic of Korea.
Artificial Intelligence and Big-Data Convergence Center, Gil Medical Center, Gachon University College of Medicine, Incheon, Republic of KoreaDepartment of Preventive Medicine, Gachon University College of Medicine, Incheon, Republic of Korea
Corresponding author at: Division of Infectious Disease, Department of Internal Medicine, Korea University Guro Hospital, Korea University College of Medicine, 148, Gurodong-ro, Guro-gu, Seoul 08308, Republic of Korea.
We compared the antiviral effect of LPV/r and HCQ in patients with mild-to-moderate COVID-19 using a large sample size health insurance database.
•
SARS-CoV-2 viral shedding duration was similar between HCQ and LPV/r groups.
•
Neither HCQ nor LPV/r monotherapy showed any benefit in improving viral clearance compared with the control group.
Abstract
Objectives
We aimed to compare the antiviral effect of hydroxychloroquine (HCQ) and lopinavir/ritonavir (LPV/r) in patients with COVID-19.
Methods
Nationwide retrospective case-control study was conducted to compare the effect of HCQ and LPV/r on viral shedding duration among patients with mild-to-moderate COVID-19 using the reimbursement data of National Health Insurance Service. After propensity score matching (PSM), multivariate analysis was conducted to determine statistically significant risk factors associated with prolonged viral shedding.
Results
Overall, 4197 patients with mild-to-moderate COVID-19 were included. Patients were categorized into three groups: LPV/r (n = 1268), HCQ (n = 801), and standard care without HCQ or LPV/r (controls, n = 2128). The median viral shedding duration was 23 (IQR 17–32), 23 (IQR 16–32), and 18 (IQR 12–25) days in the LPV/r, HCQ, and control groups, respectively. Even after PSM, the viral shedding duration was not significantly different between LPV/r and HCQ groups: 23 (IQR, 17–32) days versus 23 (IQR, 16–32) days. On multivariate analysis, old age, malignancy, steroid use, and concomitant pneumonia were statistically significant risk factors for prolonged viral shedding.
Conclusion
The viral shedding duration was similar between HCQ and LPV/r treatment groups. There was no benefit in improving viral clearance compared to the control group.
Since the first emerging in December 2019, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has spread rapidly around the world, infecting over 38 million people globally and resulting in 1,089,047 deaths as of October 15, 2020 (
). To bring an end to this health crisis, vaccines are under development, but they are likely 1–2 years away. It is thus very important to minimize person-to-person transmission.
Antiviral agents are commonly used for improving clinical symptoms or ameliorating disease severity. Furthermore, they have an important clinical implication to suppress disease transmission by reducing the viral shedding duration, as shown from the effect of oseltamivir for influenza (
). Owing to the highly transmissible property of SARS-CoV-2, even asymptomatic and presymptomatic patients have transmitted the virus to their family members and colleagues (
). Moreover, as the pandemic has progressed, the number of deaths in high-risk groups has increased dramatically. Therefore, the treatment strategy for COVID-19 needs to be approached in two ways: reduction of mortality through combined antiviral therapy for severe patients and blockage of transmission through early antiviral treatment for patients with mild-to-moderate cases.
In the early pandemic periods, the most hopeful antiviral candidates were hydroxychloroquine (HCQ) and lopinavir/ritonavir (LPV/r), which had already been on the market for decades with other indications (
). Under urgent needs, many clinical trials using either candidate have been conducted, but there are still insufficient data to recommend HCQ or LPV/r use. Furthermore, most studies mainly focused on patients with moderate-to-severe COVID-19, and antiviral agents were administered at more than 7 days later from symptom onset (
Effect of high vs low doses of chloroquine diphosphate as adjunctive therapy for patients hospitalized with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection: a randomized clinical trial.
Triple combination of interferon beta-1b, lopinavir-ritonavir, and ribavirin in the treatment of patients admitted to hospital with COVID-19: an open-label, randomised, phase 2 trial.
). It is necessary to comparatively evaluate the effect of viral suppression when the antiviral agent is administered in the early stage of symptom development. If effective for viral suppression, it has a very important meaning in terms of infection control and treatment (
An exploratory randomized controlled study on the efficacy and safety of lopinavir/ritonavir or arbidol treating adult patients hospitalized with mild/moderate COVID-19 (ELACOI).
This study aimed to compare the effect of HCQ and LPV/r on the viral shedding duration among patients with mild-to-moderate COVID-19 cases using South Korea’s National Health Insurance Service (NHIS) database.
Methods
Data source
This study used reimbursement data from the National Health Insurance Service (NHIS) of South Korea for the period from January 12, 2020 to May 15, 2020. The NHIS covers 97–98% of the population (51 million people). Data included age, sex, dates of admission and discharge, diagnoses coded according to the International Classification of Disease and Related Health Problems, 10th edition (ICD-10), and prescription of medications covered by NHIS.
Currently, the NHIS aggregates datasets for real-time reverse transcriptase polymerase chain reaction (rRT-PCR)-confirmed COVID-19 cases from information provided by the epidemiological investigation of
This nationwide retrospective study included patients with laboratory-confirmed COVID-19 diagnoses who were discharged during the study period from January 12, 2020 to May 15, 2020. Among these, only mild-to-moderate grade 1 patients were included in the analysis, and the effect of LPV/r or HCQ use on viral shedding duration was evaluated (Figure 1). We strictly included patients with mild or moderate grade 1 COVID-19, excluding severe patients for the following reasons: in severe cases, anti-viral agents might have been administered following late aggravation after initial supportive standard care and hospital stay may have been extended due to complications, although SARS-CoV-2 rRT-PCR test converted to be negative. Furthermore, the following two inclusion criteria should be met: (i) adults aged ≥19 years and (ii) hospitalization within 1 week after laboratory diagnosis for COVID-19. The criteria of ≤1 week from diagnosis to hospitalization is needed to assess the effect of early antiviral treatment. Exclusion criteria were as follows: (i) concomitant LPV/r and HCQ treatment; (ii) patients on LPV/r or HCQ medication prior to diagnosis; or (iii) those who received other antiviral agents thought to be effective against COVID-19 (ciclesonide, camostat, nafamostat, remdesivir, ribavirin, or interferon). For patients with multiple episodes of hospitalization, the first admission was only included for the analysis.
All included patients were categorized according to LPV/r or HCQ exposure: LPV/r-group, HCQ-group, and control group (supportive standard care only). LPV/r or HCQ use was defined as at least one prescription being recorded in the claim data. Data on the prescription of LPV/r, HCQ, or other drugs were extracted using drug codes based on the Anatomical Therapeutic Chemical Classification in the claim data of the study periods. Comorbidities were identified using ICD-10 codes entered within 1 year prior to COVID-19 diagnosis (Supplementary Table 2). Charlson Comorbidity Index (CCI) was also calculated to assess the general health status of study subjects (Supplementary Table 3). A subgroup analysis was conducted for mild cases only, moderate grade 1 cases only, and patients with pneumonia (defined as ICD-10 codes).
We defined patient’s length of hospitalization as viral shedding duration, which was assessed using rRT-PCR. This is reasonable, because all COVID-19 patients in South Korea required undetectable RNA from two consecutive nasopharyngeal swab specimens (24 h apart) to be discharged, according to the regulation of KCDC (
This study protocol was exempted for review by the Institutional Review Board of the Korea University Guro Hospital according to the exemption criteria (IRB No. 2020GR0260).
Statistical analysis
The data are presented using descriptive statistics for continuous and categorical variables. Differences between groups were analyzed with an analysis of variance (ANOVA) for continuous variables and chi-square tests for categorical variables.
Considering the significant differences in baseline characteristics among study groups, propensity score matching (PSM) was taken between two groups to be compared. To compare the viral shedding duration, we created propensity scores for the LPV/r-group, HCQ-group, and control group. All sets of propensity scores were estimated via multinomial logistic regression using baseline covariates including age, sex, comorbidities, disease severity, and concomitant pneumonia. To compare the viral shedding duration, three data sets were made (LPV/r-group vs. HCQ-group; LPV/r-group vs. control group; HCQ-group vs. control group), and each of the sets were propensity score matched in 1:1 proportion. Age and sex were perfectly matched, and Greedy nearest neighbor matching was used for other covariates on the logit of the propensity score.
After PSM, multiple linear regression was used to determine statistically significant factors associated with viral shedding duration. Variables included in the models were age, sex, comorbidities, disease severity, concomitant pneumonia, concomitant use of steroid, azithromycin or oseltamivir, and elapsed days from laboratory diagnosis to hospitalization.
All tests were two tailed, and results were considered statistically significant at p-value <0.05. SAS version 9.4 (SAS Institute Inc, Cary, NC) was used for the analyses.
Results
During study periods, a total of 5720 COVID-19 patients were discharged (or death occurred) in South Korea. Most cases (>95%) were hospitalized within a day from laboratory diagnosis, and more than 98% were hospitalized within 7 days. Regarding disease severity, children and adolescents were milder in severity: 99.1% (214/216) were mild, 1.4% (2/216) were moderate grade 1, and none were moderate grade 2 or severe (Supplementary Table 4). Similarly, mild cases accounted for the large portion in adults aged 19–64 year (91.7%, 4037/4402). However, in the elderly, less than two-thirds of cases (59.5%, 656/1102) were mild, while the rest required oxygen therapy; one-third of cases on oxygen therapy required high flow oxygen supply or mechanical ventilation. Since the first emergence of COVID-19 in South Korea, the prescription trend of LPV/r and HCQ is shown in Supplementary Figure 1. Overall, LPV/r and HCQ prescription tended to decrease, and preference appeared to change significantly depending on the literature published at that time. Sequentially, LPV/r was replaced by HCQ and supportive standard care.
Baseline characteristics of patients with mild-to-moderate grade 1 COVID-19
A total of 4197 patients with mild-to-moderate grade 1 COVID-19 were included in this study. Patients were categorized into three different groups: those treated with LPV/r (LPV/r-group, n = 1268), those treated with HCQ (HCQ-group, n = 801), and those with supportive standard care without HCQ or LPV/r (control group, n = 2128) (Supplementary Table 5). There were some significant differences among the three groups in the baseline characteristics. Compared to LPV/r or HCQ-groups, the control group was significantly younger, had fewer comorbidities, and included more males. The oseltamivir combination rate was less than 0.5% in all groups.
The median time of viral RNA shedding was 23 (IQR 17–32) days in the LPV/r-group, 23 (IQR 16–32) days in the HCQ-group, and 18 (IQR 12–25) days in the control group. There was no significant difference between the LPV/r-group and the HCQ-group, but the viral shedding duration was estimated to be significantly longer in both treatment groups compared to the control group.
Propensity score matched comparison of the antiviral effect on viral shedding duration — LPV/r versus HCQ treatment
As the baseline characteristics showed significant difference across the three groups, we computed propensity scores for LPV/r use and HCQ use based on age and sex. After PSM, most of the baseline characteristics were similar, including comorbidities. However, the disease severity and proportion of accompanying pneumonia were still significantly higher in the LPV/r and HCQ-group, especially in the LPV/r-group (Table 1).
Table 1Baseline characteristics after propensity score matching between the two groups.
LPV/r-group (n = 1047)
Control (n = 1047)
p-Value
HCQ-group (n = 701)
Control (n = 701)
p-Value
LPV/r-group (n = 735)
HCQ-group (n = 735)
p-Value
Age, years, mean (SD)
45.95 (15.64)
45.95 (15.64)
1
48.73 (16.33)
48.73 (16.33)
1
50.72 (16.78)
50.72 (16.78)
1
Age, groups
1
1
1
19–49 years
565 (53.96%)
565 (53.96%)
–
315 (44.94%)
315 (44.94%)
–
301 (40.95%)
301 (40.95%)
–
50–64 years
367 (35.05%)
367 (35.05%)
–
290 (41.37%)
290 (41.37%)
–
298 (40.54%)
298 (40.54%)
–
≥65 years
115 (10.98%)
115 (10.98%)
–
96 (13.69%)
96 (13.69%)
–
136 (18.50%)
136 (18.50%)
–
Male, no (%)
404 (38.59%)
404 (38.59%)
–
246 (35.09%)
246 (35.09%)
1
246 (33.47%)
246 (33.47%)
1
From diagnosis to admission, days
0.09 (0.63)
0.07 (0.57)
0.4895
0.03 (0.27)
0.02 (0.29)
0.8497
0.14 (0.84)
0.20 (0.26)
0.0003
CCI (SD)
1.15 (1.47)
1.07 (1.34)
0.1925
1.35 (1.62)
1.2 (1.49)
0.0594
1.38 (1.63)
1.39 (1.61)
0.8341
Comorbidities
578 (49.15%)
598 (50.85%)
0.3784
412 (58.77%)
406 (57.92%)
0.7451
458 (62.31%)
449 (61.09%)
0.6292
Diabetes
159 (15.19%)
139 (13.28%)
0.2109
127 (18.12%)
132 (18.83%)
0.7308
126 (17.14%)
139 (18.91%)
0.3778
Thyroid disease
69 (6.59%)
68 (6.49%)
0.9296
75 (10.70%)
76 (10.84%)
0.9313
47 (6.39%)
79 (10.75%)
0.0029
Cardiac disease
62 (5.92%)
75 (7.16%)
0.2506
65 (9.27%)
59 (8.42%)
0.5725
61 (8.30%)
68 (9.25%)
0.5187
Chronic respiratory disease
305 (29.13%)
331 (31.61%)
0.2166
185 (26.39%)
176 (25.11%)
0.5825
253 (34.42%)
199 (27.07%)
0.0023
Renal disease
20 (1.91%)
22 (2.10%)
0.7552
16 (2.28%)
15 (2.14%)
0.8559
28 (3.81%)
16 (2.18%)
0.0662
Chronic liver disease
134 (12.8%)
107 (10.22%)
0.0645
109 (15.55%)
94 (13.41%)
0.2549
96 (13.06%)
118 (16.05%)
0.1037
Chronic neurologic disease
97 (9.26%)
81 (7.74%)
0.2099
108 (15.41%)
106 (15.12%)
0.8819
88 (11.97%)
130 (17.69%)
0.0021
Malignancy
45 (4.30%)
53 (5.06%)
0.4078
40 (5.71%)
38 (5.42%)
0.8157
36 (4.90%)
39 (5.31%)
0.7221
Rheumatologic disease
29 (2.77%)
28 (2.67%)
0.8932
22 (3.14%)
14 (2.00%)
0.1768
2 (2.99%)
22 (2.99%)
1
Anemia
78 (7.45%)
95 (9.07%)
0.1772
69 (9.84%)
60 (8.56%)
0.4056
73 (9.93%)
70 (9.52%)
0.7917
Hematologic disease
18 (1.72%)
12 (1.15%)
0.2699
4 (0.57%)
1 (0.14%)
0.3741
19 (2.59%)
7 (0.95%)
0.0176
Mental and behavioral disorder
184 (17.57%)
173 (16.52%)
0.5227
147 (20.97%)
163 (23.25%)
0.3032
129 (17.55%)
167 (22.72%)
0.0135
HIV
1 (0.10%)
1 (0.10%)
1
1 (0.14%)
1 (0.14%)
1
1 (0.07%)
1 (0.07%)
1
Disease severity
<0.0001
0.0025
<0.0001
Mild
911 (87.01%)
1012 (96.66%)
–
645 (92.01%)
672 (95.86%)
–
600 (81.63%)
680 (92.52%)
–
Moderate, grade 1
136 (12.99%)
35 (3.34%)
–
56 (7.99%)
29 (4.14%)
–
135 (18.37%)
55 (7.48%)
–
Pneumonia, no (%)
602 (57.50%)
129 (12.32%)
<0.0001
305 (43.51%)
108 (15.41%)
<0.0001
501 (68.16%)
313 (42.59%)
<0.0001
Steroid use, no (%)
33 (3.15%)
13 (1.24%)
0.0029
20 (2.85%)
10 (1.43%)
0.065
24 (3.27%)
18 (2.45%)
0.3476
Azithromycin use, no (%)
211 (20.15%)
12 (1.15%)
<0.0001
222 (31.67%)
10 (1.43%)
<0.0001
82 (11.16%)
212 (28.84%)
<0.0001
Oseltamivir use, no (%)
5 (0.48%)
1 (0.1%)
0.2181
2 (0.29%)
1 (0.14%)
1
5 (0.68%)
2 (0.27%)
0.452
LPV/r = lopinavir/ritonavir; HCQ = hydroxychloroquine; SD = standard deviation; CCI = Charlson Comorbidity Index.
Total dosage of LPV/r was 3884/971 mg on average, which was considered to have been administered for about 5 days when calculated based on 800/200 mg/day as recommended by the guidelines (
). HCQ was used on average of 2376 mg, which was equivalent to dosage for 5–6 days, calculated based on 400 mg/day recommended by the guideline.
The median time of viral RNA shedding was not significantly different between the LPV/r and HCQ-group: 23 (IQR, 17–32) days versus 23 (IQR, 16–32) days (Table 2). Neither agent shortened the viral shedding duration compared to the control group.
Table 2Comparison of viral shedding duration based on antiviral treatment groups among patients with mild-to-moderate grade 1 COVID-19.
Subgroup and multivariate analyses for the viral shedding duration
On multivariate analysis using propensity score-matched data sets comparing each antiviral group versus control group, LPV/r or HCQ still showed a significantly longer viral shedding duration compared to the control group. However, the significance due to the use of antiviral agents disappeared in the subgroup analysis which includes only moderate cases or pneumonia cases (Supplementary Tables 6 and 7).
On multivariate analysis using dataset comparing LPV/r and HCQ groups, neither of the agents showed a significant difference in terms of the viral shedding duration. The factors that significantly influence the viral shedding duration were age, malignancy, steroid use, and concomitant pneumonia (Table 3). As the elapsed time from diagnosis to hospitalization is longer, in-hospital shedding duration was much shorter. In the subgroup analysis for patients with moderate grade 1 severity or concomitant pneumonia, cardiac disease was identified as a factor that significantly increased the viral shedding duration.
Table 3Multivariate analysis for the viral shedding duration among antiviral users (LPV/r or HCQ) for COVID-19.
Currently, no specific antiviral agent is available for the prevention or treatment of COVID-19, so drug repurposing has been considered as a promising approach to rapidly identify an effective therapy. HCQ and LPV/r are the candidates at the forefront of drug repurposing. This nationwide retrospective study was conducted to evaluate the antiviral effect of HCQ and LPV/r in the treatment of patients with mild COVID-19 using the NHIS reimbursement dataset. In this study, the viral shedding duration of SARS-CoV-2 was similar between HCQ and LPV/r treatment groups. When analyzing the effect of antiviral agents, the timing of antiviral therapy is an important issue to be considered. Early (within 7 days from symptom onset) initiation of antiviral therapy may be critical in reducing SARS-CoV-2 viral load, as previously noted (
Factors associated with prolonged viral shedding and impact of lopinavir/ritonavir treatment in hospitalised non-critically ill patients with SARS-CoV-2 infection.
). Due to the limitation of our database, it was difficult to know the initiation timing of antiviral treatment in each individual patient; however, the government of South Korea had launched a series of aggressive measures to perform tight contact tracing and mass screening tests, which enabled early diagnosis within 3–5 days from symptom onset (
). As shown in this study, >95% were hospitalized within a day from laboratory diagnosis. It took more than 1 week to be hospitalized in only a small number of patients, and those were excluded in this study considering the timing issue.
HCQ or LPV/r monotherapy showed no benefit for improving viral clearance compared to the control group. The viral shedding duration seemed to be rather prolonged in the treatment groups (median viral shedding duration, 22–23 days in the antiviral treatment groups vs. 18 days in the control group). However, it would be possible that the viral shedding duration in the control group was estimated to be shorter than it really is because of the following reasons. First, community treatment centers (CTC), which were introduced in Korea as a measure to efficiently distribute limited medical resources during the declared epidemic starting in early March 2020, could make a bias in the claim database. Some patients with mild symptoms were transferred from the hospital to CTCs if they were medically stable but needed to maintain isolation (
). Although supportive care is maintained in CTCs, some CTCs might not claim reimbursement due to neglectable medical costs and complex process, potentially contributing to the shortened length of hospitalization in the control group. Second, during the earlier period of the COVID-19 pandemic in South Korea, many mild COVID-19 patients diagnosed at the airport quarantine received supportive care without antiviral treatment at the CTC. Actually, a majority of them had symptoms for more than a week before traveling, so the viral shedding duration might have been estimated shorter. In the previous studies including mild COVID-19 patients in CTCs, the mean viral shedding duration from symptom onset was 21–24.5 days, which is longer than the results of our control group (
). When we compared the viral shedding duration between the HCQ or LPV/r-groups and the control group in subgroup analyses including only moderate cases or those with concomitant pneumonia, there was no significant difference, which reflected the selection bias of mild cases who were mainly included in the control groups.
One of the most effective treatment strategies would be to stop the viral replication at the beginning, thereby minimizing the peak viral load and shedding duration (
). It is unclear why HCQ or LPV/r did not show favorable antiviral effect in this study. One possible reason is that a higher dose is required to successfully suppress SARS-CoV-2 in patients as shown in vitro cytotoxicity test (
In vitro activity of lopinavir/ritonavir and hydroxychloroquine against severe acute respiratory syndrome coronavirus 2 at concentrations achievable by usual doses.
). Insufficient data are available regarding the optimal dose to ensure the safety and efficacy of both drugs for COVID-19. Another possible reason is the inadequate target tissue concentration of those antiviral agents. LPV/r is an anti-HIV drug, innovated to get high plasma and lymphatic tissue concentration, not lung tissue (
). There are no pharmacokinetic data on respiratory tract concentration of LPV/r. Although pharmacokinetic data indicate HCQ exhibits extensive tissue distribution, the tissue concentration of the respiratory tract might be variable depending on intestinal resorption and hepatic first-pass metabolism (
Use of hydroxychloroquine in hospitalized COVID-19 patients is associated with reduced mortality: Findings from the observational multicentre Italian CORIST study.
). The inverse association of HCQ with mortality was more evident in elderly, in patients who experienced more severe manifestation or especially having elevated C-reactive protein. Furthermore, the beneficial impact was observed even in the late treatment groups, suggesting that the anti-inflammatory and anti-thrombotic potential of HCQ may have had more important role rather than its antiviral properties.
On multivariate analysis, old age, malignancy, steroid use, and concomitant pneumonia were identified as risk factors for prolonged viral shedding in this study, consistent with previous studies (
Factors associated with prolonged viral shedding and impact of lopinavir/ritonavir treatment in hospitalised non-critically ill patients with SARS-CoV-2 infection.
Prolonged SARS-CoV-2 viral shedding in patients with COVID-19 was associated with delayed initiation of arbidol treatment: a retrospective cohort study.
). Old age, comorbidities, and steroid use might blunt the host immune response, thereby promoting viral replication. In the subgroup analyses, chronic neurologic diseases were also associated with increased risk of prolonged viral shedding in the cases with mild COVID-19, while cardiovascular disease was identified as a risk factor in the moderate cases or cases with concomitant pneumonia. Since ACE2, the SARS-CoV-2 binding receptors, is widely expressed in the various organ including the lungs, heart, and vessels, it is possible that greater number of ACE2 receptors—along with blunted host response encountered in many comorbid conditions—might promote viral replication, resulting in prolonged viral shedding. Recent studies suggested that the negative outcomes in patients with underlying cerebrovascular disease might be due to elevated expression of ACE2 (
). Although unclear, COVID-19 might trigger acute coronary syndrome, arrhythmia, or acute exacerbation of heart failure, similar to influenza viral infection (
). SARS-CoV-2 itself might induce new cardiac pathology or exacerbation of underlying cardiovascular diseases under the systemic and/or localized inflammatory host response, resulting in cytokine storm in some severe cases (
). In this study, cardiovascular disease was a significant risk factor for longer hospitalization only in the analyses including the HCQ-group. Although generally safe when used for approved indications, including autoimmune inflammatory rheumatic diseases or malaria, the safety and benefit of HCQ treatment are poorly evaluated in COVID-19, and potential safety hazards have been announced recently, especially among severe patients and/or high-dose users (
Effect of high vs low doses of chloroquine diphosphate as adjunctive therapy for patients hospitalized with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection: a randomized clinical trial.
This study has some limitations. First, this was a retrospective cohort study. Although large number of cases were included, with propensity score matched for relevant variables, we could not rule out residual confounders. Second, we did not compare the viability of SARS-CoV-2 with the duration of infectivity. This study focused on the comparison of rRT-PCR-based viral clearance between LPV/r and HCQ. Third, this study did not include cases with severe COVID-19, having a limitation in evaluating the potential anti-inflammatory impact of HCQ or LPV/r in the prevention of complications and fatality. Fourth, environmental factors were not considered in this study. Environmental factors such as temperature, humidity and food might influence transmission, severity and mortality of COVID-19 (
). As the severity of COVID-19 and the effect of antiviral treatment may vary by region with different environments, further studies from various countries or regions would be required. Fifth, there was significant differences in baseline characteristics between HCQ and LPV/r groups. To overcome the differences, this study used PSM and subgroup/multivariate analyses. Finally, because of the limitation of study design using claim database, data on drug concentration and related metabolic factors were not available.
In conclusion, we compared the antiviral effect of LPV/r and HCQ in patients with mild-to-moderate COVID-19 using a large sample size health insurance database. The viral shedding duration was similar between HCQ and LPV/r groups. Neither HCQ nor LPV/r monotherapy showed benefits in improving viral clearance compared to the control group. Given such a limited effectiveness of HCQ or LPV/r monotherapy, a combination strategy needs to be considered. In fact, studies have shown beneficial effects when combining ribavirin and interferon rather than LPV/r alone (34), and several combination therapies have been tried.
Funding source
This work was supported by the National Research Foundation of Korea (NRF) grant [2020M3A9I2081699] to JYS and grants from the Gachon University Gil Medical Center [2018−17 and 2019−11] to JJ.
Ethical approval
This study protocol was exempted for review by the Institutional Review Board of the Korea University Guro Hospital according to the exemption criteria (IRB No. 2020GR0260).
Conflict of interest
We declare no conflict of interest.
Appendix A. Supplementary data
The following is Supplementary data to this article:
Effect of high vs low doses of chloroquine diphosphate as adjunctive therapy for patients hospitalized with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection: a randomized clinical trial.
Use of hydroxychloroquine in hospitalized COVID-19 patients is associated with reduced mortality: Findings from the observational multicentre Italian CORIST study.
Triple combination of interferon beta-1b, lopinavir-ritonavir, and ribavirin in the treatment of patients admitted to hospital with COVID-19: an open-label, randomised, phase 2 trial.
In vitro activity of lopinavir/ritonavir and hydroxychloroquine against severe acute respiratory syndrome coronavirus 2 at concentrations achievable by usual doses.
An exploratory randomized controlled study on the efficacy and safety of lopinavir/ritonavir or arbidol treating adult patients hospitalized with mild/moderate COVID-19 (ELACOI).
Factors associated with prolonged viral shedding and impact of lopinavir/ritonavir treatment in hospitalised non-critically ill patients with SARS-CoV-2 infection.
Prolonged SARS-CoV-2 viral shedding in patients with COVID-19 was associated with delayed initiation of arbidol treatment: a retrospective cohort study.
32266-9&id=gr1.jpg){kind=link}