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About:
Safety, tolerability, and clinical outcomes of hydroxychloroquine for hospitalized patients with coronavirus 2019 disease
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An Entity of Type :
schema:ScholarlyArticle
, within Data Space :
covidontheweb.inria.fr
associated with source
document(s)
Type:
Academic Article
research paper
schema:ScholarlyArticle
New Facet based on Instances of this Class
Attributes
Values
type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
Safety, tolerability, and clinical outcomes of hydroxychloroquine for hospitalized patients with coronavirus 2019 disease
Creator
Westblade, Lars
Choi, Justin
Goyal, Parag
Gulick, Roy
Kondoid, Maiko
Magleby, Reed
Maldarelli, Grace
Pham, Khanh
Rennert, Hanna
Safford, Monika
Satlin Id, Michael
Schenck, Edward
Source
Medline; PMC
abstract
BACKGROUND: Severe acute respiratory coronavirus 2 (SARS-CoV-2) has caused a devastating worldwide pandemic. Hydroxychloroquine (HCQ) has in vitro activity against SARS-CoV-2, but clinical data supporting HCQ for coronavirus disease 2019 (COVID-19) are limited. METHODS: This was a retrospective cohort study of hospitalized patients with COVID-19 who received ≥1 dose of HCQ at two New York City hospitals. We measured incident Grade 3 or 4 blood count and liver test abnormalities, ventricular arrhythmias, and vomiting and diarrhea within 10 days after HCQ initiation, and the proportion of patients who completed HCQ therapy. We also describe changes in Sequential Organ Failure Assessment hypoxia scores between baseline and day 10 after HCQ initiation and in-hospital mortality. RESULTS: None of the 153 hospitalized patients with COVID-19 who received HCQ developed a sustained ventricular tachyarrhythmia. Incident blood count and liver test abnormalities occurred in <15% of patients and incident vomiting or diarrhea was rare. Eighty-nine percent of patients completed their HCQ course and three patients discontinued therapy because of QT prolongation. Fifty-two percent of patients had improved hypoxia scores 10 days after starting HCQ. Thirty-one percent of patients who were receiving mechanical ventilation at the time of HCQ initiation died during their hospitalization, compared to 18% of patients who were receiving supplemental oxygen but not requiring mechanical ventilation, and 8% of patients who were not requiring supplemental oxygen. Co-administration of azithromycin was not associated with improved outcomes. CONCLUSIONS: HCQ appears to be reasonably safe and tolerable in most hospitalized patients with COVID-19. However, nearly one-half of patients did not improve with this treatment, highlighting the need to evaluate HCQ and alternate therapies in randomized trials.
has issue date
2020-07-23
(
xsd:dateTime
)
bibo:doi
10.1371/journal.pone.0236778
bibo:pmid
32701969
has license
cc-by
sha1sum (hex)
1a5f4148c39017226e4bad09933e6e5d2d276971
schema:url
https://doi.org/10.1371/journal.pone.0236778
resource representing a document's title
Safety, tolerability, and clinical outcomes of hydroxychloroquine for hospitalized patients with coronavirus 2019 disease
has PubMed Central identifier
PMC7377460
has PubMed identifier
32701969
schema:publication
PLoS One
resource representing a document's body
covid:1a5f4148c39017226e4bad09933e6e5d2d276971#body_text
is
schema:about
of
named entity 'pandemic'
named entity 'Hydroxychloroquine'
named entity 'hydroxychloroquine'
named entity 'SARS-CoV-2'
named entity 'hydroxychloroquine'
named entity 'intravenous infusion'
named entity '95% CI'
named entity 'HCQ'
named entity 'fever'
named entity 'HCQ'
named entity 'univariate analysis'
named entity 'Institutional Review Board'
named entity 'HCQ'
named entity 'afebrile'
named entity 'QTc interval'
named entity 'control group'
named entity 'HCQ'
named entity 'leukocytosis'
named entity 'partial pressure'
named entity 'adverse effects'
named entity 'HCQ'
named entity 'SARS-CoV-2'
named entity 'HCQ'
named entity 'vomiting'
named entity 'gastrointestinal'
named entity 'HCQ'
named entity 'New York City Department of Health'
named entity 'COVID-19'
named entity 'HCQ'
named entity 'anemia'
named entity 'azithromycin'
named entity 'HCQ'
named entity 'HCQ'
named entity 'HCQ'
named entity 'HCQ'
named entity 'diarrhea'
named entity 'Hydroxychloroquine'
named entity 'REDCap'
named entity 'HCQ'
named entity 'hypoxia'
named entity 'follow-up'
named entity 'WCMC'
named entity 'HCQ'
named entity 'remdesivir'
named entity 'tolerability'
named entity 'informed consent'
named entity 'EKG'
named entity 'mechanical ventilation'
named entity 'HCQ'
named entity 'HCQ'
named entity 'randomized trials'
named entity 'randomized trial'
named entity 'tachypnea'
named entity 'heart rate'
named entity 'HCQ'
named entity 'EKG'
named entity 'WCMC'
named entity 'arterial blood gas'
named entity 'follow-up'
named entity 'EKG'
named entity 'COVID'
named entity 'COVID'
named entity 'toxicity'
named entity 'hypotensive'
named entity 'HCQ'
named entity 'case series'
named entity 'white blood cell'
named entity 'HCQ'
named entity 'HCQ'
named entity 'virus'
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