Hydroxychloroquine/chloroquine for the treatment of hospitalized patients with COVID-19: An individual participant data meta-analysis

被引:6
作者
Di Stefano, Leon [1 ]
Ogburn, Elizabeth L. [1 ]
Ram, Malathi [2 ,3 ]
Scharfstein, Daniel O. [4 ]
Li, Tianjing [5 ]
Khanal, Preeti [3 ]
Baksh, Sheriza N. [6 ]
McBee, Nichol [3 ]
Gruber, Joshua [3 ]
Gildea, Marianne R. [3 ,26 ]
Clark, Megan R. [3 ]
Goldenberg, Neil A. [7 ,8 ,9 ]
Bennani, Yussef [10 ,11 ]
Brown, Samuel M. [12 ,13 ]
Buckel, Whitney R. [14 ]
Clement, Meredith E. [10 ,11 ]
Mulligan, Mark J. [15 ,16 ]
O'Halloran, Jane A. [17 ]
Rauseo, Adriana M. [17 ]
Self, Wesley H. [18 ]
Semler, Matthew W. [19 ]
Seto, Todd [20 ]
Stout, Jason E. [21 ]
Ulrich, Robert J. [15 ]
Victory, Jennifer [22 ]
Bierer, Barbara E. [23 ,24 ]
Hanley, Daniel F. [3 ]
Freilich, Daniel [25 ]
机构
[1] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Biostat, Baltimore, MD USA
[2] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Int Hlth, Baltimore, MD USA
[3] Johns Hopkins Sch Med, Div Brain Injury Outcomes, Baltimore, MD USA
[4] Univ Utah, Dept Populat Hlth Sci, Div Biostat, Sch Med, Salt Lake City, UT USA
[5] Univ Colorado, Anschutz Med Campus, Denver, CO 80202 USA
[6] Johns Hopkins Bloomberg Sch Publ Hlth, Baltimore, MD USA
[7] Johns Hopkins Sch Med, Dept Pediat, Baltimore, MD USA
[8] Johns Hopkins Sch Med, Dept Med, Baltimore, MD USA
[9] Johns Hopkins All Childrens Hosp, Johns Hopkins All Childrens Inst Clin & Translat, St Petersburg, FL USA
[10] Louisiana State Univ, Hlth Sci Ctr, New Orleans, LA USA
[11] Univ Med Ctr, New Orleans, LA USA
[12] Intermt Med Ctr, Div Pulm & Crit Care Med, Murray, UT USA
[13] Univ Utah, Salt Lake City, UT USA
[14] Intermt Healthcare, Pharm Serv, Murray, UT USA
[15] NYU, Dept Med, Div Infect Dis & Immunol, Grossman Sch Med, New York, NY USA
[16] NYU, Vaccine Ctr, Grossman Sch Med, New York, NY USA
[17] Washington Univ, Sch Med, Dept Med, St Louis, MO 63110 USA
[18] Vanderbilt Univ, Dept Emergency Med, Med Ctr, Nashville, TN USA
[19] Vanderbilt Univ, Med Ctr, Dept Med, Div Allergy Pulm & Crit Care Med, Nashville, TN USA
[20] Univ Hawaii, Dept Med, John Burns Sch Med, Honolulu, HI USA
[21] Duke Univ, Med Ctr, Div Infect Dis & Int Hlth, Durham, NC USA
[22] Bassett Med Ctr, Bassett Res Inst, Cooperstown, NY USA
[23] Brigham & Womens Hosp, Dept Med, Boston, MA 02115 USA
[24] Harvard Med Sch, Boston, MA 02115 USA
[25] Bassett Med Ctr, Dept Internal Med, Div Infect Dis, Cooperstown, NY 13326 USA
[26] FHI 360, Durham, NC USA
来源
PLOS ONE | 2022年 / 17卷 / 09期
基金
美国国家卫生研究院;
关键词
REMDESIVIR;
D O I
10.1371/journal.pone.0273526
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background Results from observational studies and randomized clinical trials (RCTs) have led to the consensus that hydroxychloroquine (HCQ) and chloroquine (CQ) are not effective for COVID-19 prevention or treatment. Pooling individual participant data, including unanalyzed data from trials terminated early, enables more detailed investigation of the efficacy and safety of HCQ/CQ among subgroups of hospitalized patients. Methods We searched ClinicalTrials.gov in May and June 2020 for US-based RCTs evaluating HCQ/ CQ in hospitalized COVID-19 patients in which the outcomes defined in this study were recorded or could be extrapolated. The primary outcome was a 7-point ordinal scale measured between day 28 and 35 post enrollment; comparisons used proportional odds ratios. Harmonized de-identified data were collected via a common template spreadsheet sent to each principal investigator. The data were analyzed by fitting a prespecified Bayesian ordinal regression model and standardizing the resulting predictions. Results Eight of 19 trials met eligibility criteria and agreed to participate. Patient-level data were available from 770 participants (412 HCQ/CQ vs 358 control). Baseline characteristics were similar between groups. We did not find evidence of a difference in COVID-19 ordinal scores between days 28 and 35 post-enrollment in the pooled patient population (odds ratio, 0.97; 95% credible interval, 0.76-1.24; higher favors HCQ/CQ), and found no convincing evidence of meaningful treatment effect heterogeneity among prespecified subgroups. Adverse event and serious adverse event rates were numerically higher with HCQ/CQ vs control (0.39 vs 0.29 and 0.13 vs 0.09 per patient, respectively). Conclusions The findings of this individual participant data meta-analysis reinforce those of individual RCTs that HCQ/CQ is not efficacious for treatment of COVID-19 in hospitalized patients.
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