Coronavirus (Covid-19)
A collection of articles and other resources on the Coronavirus (Covid-19) outbreak, including clinical reports, management guidelines, and commentary.
CORONAVIRUS (COVID-19) VACCINE RESOURCES VACCINE FAQ
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Original Article
Sotrovimab for Early Covid-19
A. Gupta and Others
In this ongoing, randomized, phase 3 trial, sotrovimab (a SARS-CoV-2–targeted monoclonal antibody) or placebo was administered to outpatients within 5 days after the onset of Covid-19 symptoms. The incidence of hospitalization for any cause was lower among patients who received sotrovimab (1% vs. 7%).
Oct 27
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Original Article
Casirivimab and Imdevimab in Outpatients
D.M. Weinreich and Others
This phase 3, placebo-controlled platform trial evaluated a single infusion of casirivimab and imdevimab (REGEN-COV) at 2400-mg and 1200-mg doses in outpatients with acute SARS-CoV-2 infection. The incidence of Covid-19–related hospitalization was lower and recovery was faster among patients who received the antibody combination than among those who received placebo.
Sep 29 -
Correspondence
Toxic Effects from Ivermectin Use
C. Temple, R. Hoang, and R.G. Hendrickson
The Oregon Poison Center received calls at a rate of 0.25 per month in all of 2020, as compared with 21 calls in August 2021 alone, regarding toxic effects from ivermectin in persons who used the drug for the prevention or treatment of Covid-19. Symptoms included gastrointestinal distress, confusion, ataxia, and seizures, and 6 of the 21 persons were hospitalized.
Oct 20
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Original Article
Casirivimab and Imdevimab in Outpatients
D.M. Weinreich and Others
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Original Article
Subcutaneous Antibody Combination and Covid-19
M.P. O’Brien and Others
Household contacts of persons infected with SARS-CoV-2 are at risk for infection. A single subcutaneous injection of two anti–SARS-CoV-2 monoclonal antibodies in such persons within 4 days after the detection of infection in a household contact reduced this risk by two thirds in the first 28 days after exposure.
Sep 23
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Original Article
Subcutaneous Antibody Combination and Covid-19
M.P. O’Brien and Others
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Original Article
Convalescent Plasma for High-Risk Covid-19
F.K. Korley and Others
Patients who were seen in emergency departments within 7 days after the onset of Covid-19 symptoms and were considered appropriate for discharge were randomly assigned to receive either convalescent plasma or placebo. Convalescent plasma did not prevent disease progression.
Aug 18
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Original Article
Convalescent Plasma for High-Risk Covid-19
F.K. Korley and Others
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Original Article
Anticoagulation in Critically Ill Patients with Covid-19
The REMAP-CAP, ACTIV-4a, and ATTACC Investigators
In a randomized trial, patients with severe Covid-19 were assigned to receive either therapeutic-dose anticoagulation or usual-care pharmacologic thromboprophylaxis. At 21 days, therapeutic-dose anticoagulation did not improve hospital survival or the number of days free of cardiovascular or respiratory organ support.
Aug 26Editorial Surviving Covid-19 with Heparin?
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Original Article
Anticoagulation in Critically Ill Patients with Covid-19
The REMAP-CAP, ACTIV-4a, and ATTACC Investigators
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Original Article
Anticoagulation in Moderate Covid-19
The ATTACC, ACTIV-4a, and REMAP-CAP Investigators
In a randomized trial, patients with moderately severe Covid-19 were assigned to receive either therapeutic-dose anticoagulation or usual-care thromboprophylaxis. At 21 days, therapeutic-dose anticoagulation resulted in a higher probability of survival until hospital discharge without organ support.
Aug 26
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Original Article
Anticoagulation in Moderate Covid-19
The ATTACC, ACTIV-4a, and REMAP-CAP Investigators
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Original Article
Waning Immunity among Covid-19–Vaccinated Israelis
Y. Goldberg and Others
A resurgence of Covid-19 in mid-June prompted an examination of Covid-19 immunity as a function of month of vaccination in Israel. Data on confirmed infection and severe disease among fully vaccinated persons were collected from July 11 to 31, 2021. Relative and absolute rates of infection and severe disease increased with time since the second vaccine dose in all age groups.
Oct 27
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Original Article
Waning Covid-19 Immunity in Israel
E.G. Levin and Others
In a longitudinal study involving nearly 4000 health care workers in Israel who had received two doses of BNT162b2 vaccine, levels of spike-binding IgG and neutralizing antibody decreased and did so to a greater extent in men, persons 65 years of age or older, and persons with immunosuppression. Obese persons had higher levels of antibody than nonobese persons.
Oct 06 -
Original Article
Waning Vaccine Protection against SARS-CoV-2 in Qatar
H. Chemaitelly and Others
In a test-negative, case–control study involving more than 900,000 participants in Qatar, vaccine effectiveness peaked at 77.5% in the first month after the second dose. The effectiveness fell thereafter to as low as 20% in months 5 through 7 after vaccination, but protection against serious Covid-19 remained greater than 90% for at least 6 months.
Oct 06
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Original Article
Waning Covid-19 Immunity in Israel
E.G. Levin and Others
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Correspondence
Immune Response to a Third Dose of BNT162b2
A.R. Falsey and Others
A third dose of the BNT162b2 vaccine was administered to 23 volunteers 8 to 9 months after the second dose, and the immune response was assessed. Local reactions were similar to those seen after the second dose. One month after the third dose, neutralization titers were 5 to 7 times as high as those before the third dose, and neutralization extended to the delta variant.
Oct 21 -
Correspondence
A Third Vaccine Dose in Organ-Transplant Recipients
V.G. Hall and Others
It is known that people receiving immune suppressive therapy, such as recipients of solid-organ transplants, have a suboptimal response to SARS-CoV-2 vaccination. In a randomized, double-blind trial, a third dose of the mRNA-1273 vaccine was compared with placebo. The third dose of vaccine produced a significant boost in neutralizing antibodies.
Sep 23Editorial Third Time’s a Charm — Covid-19 Vaccine Hope for Solid-Organ Transplant Recipients
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Correspondence
Immune Response to a Third Dose of BNT162b2
A.R. Falsey and Others
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Correspondence
Kinetics of Immune Response to Covid-19 Vaccines
A.-r.Y. Collier and Others
B-cell and T-cell responses were measured to assess the stability and duration of vaccine-induced immunity. Responses to BNT162b2 and mRNA-1273 peaked early and declined over 6 to 8 months. The response to Ad26.CoV2.S reached a lower peak but continued without evidence of notable decline for 8 months. Response levels correlating with protection have not yet been defined.
Oct 15 -
Correspondence
Three Covid-19 Vaccine Doses in Transplant Recipients
N. Kamar and Others
Solid-organ transplant recipients receiving immunosuppressive therapy appear to have a poor response to Covid-19 vaccination. A group of 101 consecutive transplant recipients received two doses of the BNT162b2 vaccine 1 month apart and a third dose 2 months after the second dose; 40% had antibodies after the second dose and 68% had antibodies after the third dose.
Aug 12
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Correspondence
Kinetics of Immune Response to Covid-19 Vaccines
A.-r.Y. Collier and Others
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Correspondence
Detailed Tabulation of Adverse Events in Clalit Study
N. Dagan, N. Barda, and R.D. Balicer
Questions arose after the publication of a study from Clalit Health Services in Israel, in which adverse events from BNT162b2 vaccination and from SARS-CoV-2 infection were examined. To address the many questions raised, the authors have generated a comprehensive table that provides the raw data on the consequences of vaccination and of infection.
Oct 27 -
Correspondence
Local Hypersensitivity Reactions to mRNA Vaccines
P.W. Askenase
The rare florid local reactions to Covid-19 vaccines bear gross and microscopic similarity to previously reported cutaneous basophil hypersensitivity reactions to injection of rabbit serum proteins and keyhole limpet hemocyanin in humans.
Oct 28
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Correspondence
Detailed Tabulation of Adverse Events in Clalit Study
N. Dagan, N. Barda, and R.D. Balicer
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Original Article
Phase 3 Trial of the ChAdOx1 nCoV-19 Vaccine
A.R. Falsey and Others
In a randomized, double-blind, placebo-controlled phase 3 trial of the ChAdOx1 nCoV-19 vaccine in over 32,000 participants from the United States, Chile, and Peru, the incidence of serious adverse effects was low (including no cases of vaccine-induced immune thrombotic thrombocytopenia) and the vaccine efficacy was 74%. Efficacy was documented in a range of demographic subgroups.
Sep 29
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Correspondence
Delta SARS-CoV-2 Outbreak in a California Prison
E.T. Chin and Others
In a 1-month period, 15% of a prison population became infected with Covid-19. There were 122 infections among 468 vaccinated and 359 unvaccinated residents; 27 cases were symptomatic. The efficacy of the mRNA-1273 vaccine was 57% against infection and 84% against symptomatic infection.
Oct 20
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Correspondence
Delta SARS-CoV-2 Outbreak in a California Prison
E.T. Chin and Others
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Correspondence
Vaccine Efficacy against the Delta Variant in Scotland
A. Sheikh, C. Robertson, and B. Taylor
An analysis of mortality among more than 114,000 SARS-CoV-2–infected people in Scotland revealed that vaccine effectiveness against death caused by the delta variant 14 days or more after the second dose was 90% for the BNT162b2 vaccine and 91% for the ChAdOx1 nCoV-19 vaccine.
Oct 20
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Correspondence
Vaccine Efficacy against the Delta Variant in Scotland
A. Sheikh, C. Robertson, and B. Taylor
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Correspondence
BNT162b2 Effectiveness against Delta Variant in Adolescents
B.Y. Reis and Others
A study involving more than 94,000 vaccinated and unvaccinated adolescents between the ages of 12 and 18 years in Israel showed increasing levels of protection against Covid-19 during the first month after receipt of two vaccine doses. The estimated vaccine efficacy at 7 to 21 days after receipt of two doses was 90% against infection and 93% against symptomatic disease.
Oct 20 -
Original Article
BNT162b2 Vaccination against Covid-19 in 12-to-15-Year-Old Adolescents
R.W. Frenck, Jr., and Others
This randomized trial of the BNT162b2 vaccine involved 2260 adolescents 12 to 15 years of age. Similar levels of antibody to SARS-CoV-2 were elicited in the 12-to-15-year-old participants and in 16-to-25-year-old participants in a parallel trial. Among participants with no evidence of previous infection, no cases of Covid-19 were diagnosed in vaccine recipients, as compared with 16 cases in placebo recipients.
Jul 15Correspondence BNT162b2 Covid-19 Vaccine in Adolescents
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Correspondence
BNT162b2 Effectiveness against Delta Variant in Adolescents
B.Y. Reis and Others
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Original Article
The mRNA-1273 Vaccine in Adolescents
K. Ali and Others
In a trial of mRNA-1273 or placebo involving 3700 adolescents 12 to 17 years of age, two doses of vaccine stimulated high levels of neutralizing antibodies, with a side-effect profile similar to that seen in other age groups. The incidence of Covid-19 in the unvaccinated group was too low to gauge protection, but Covid-19 did not develop in any vaccinated participants.
Aug 11
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Correspondence
Covid-19 Vaccination in Early Pregnancy and Miscarriage
M.C. Magnus and Others
In this case–control study performed with the use of registry data in Norway, there was no evidence of an increased risk of first-trimester pregnancy loss associated with Covid-19 vaccination during early pregnancy.
Oct 20 -
Correspondence
On Preliminary Findings of mRNA Covid-19 Vaccine Safety in Pregnant Persons
H. Sun
Shimabukuro et al. (June 17 issue) reported preliminary data on the safety of mRNA Covid-19 vaccines in pregnancy from the v-safe surveillance system and pregnancy registry. In these letters, Hong Sun raises questions about the proportion of women reporting spontaneous abortion in the article, and Shimabukuro et al. respond.
Oct 14Original Article Preliminary Findings of mRNA Covid-19 Vaccine Safety in Pregnant PersonsCorrection Preliminary Findings of mRNA Covid-19 Vaccine Safety in Pregnant Persons Correction mRNA Covid-19 Vaccines in Pregnant Women
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Correspondence
Covid-19 Vaccination in Early Pregnancy and Miscarriage
M.C. Magnus and Others
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Correspondence
mRNA Covid-19 Vaccines and Risk of Spontaneous Abortion
L.H. Zauche and Others
In this updated analysis from the CDC v-safe pregnancy registry, the cumulative risk of pregnancy loss at 6 to less than 20 weeks of gestation after receipt of Covid-19 vaccination soon after conception or in early pregnancy was consistent with rates of pregnancy loss over the same gestational age range reported in historical cohorts.
Oct 14
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Original Article
Efficacy of mRNA-1273 Vaccine at End of Blinded Phase
H.M. El Sahly and Others
The mRNA-1273 vaccine was approved for emergency use in December 2020; trial participants who received placebo were informed of the results and offered vaccination. At the close of the blinded phase of the trial, the vaccine efficacy in preventing Covid-19 illness was 93.2%, and the efficacy against severe disease was 98.2%. No new safety issues were identified.
Sep 22
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Original Article
BNT162b2 Vaccine at 6 Months of Follow-up
S.J. Thomas and Others
In a multinational, observer-blinded, randomized trial involving 44,165 participants 16 years of age or older and 2264 participants 12 to 15 years of age, the efficacy of the BNT162b2 vaccine was 91% against Covid-19 and 97% against severe disease through 6 months of follow-up. In South Africa, where the beta variant was widespread, vaccine efficacy was 100%. Late toxic effects from the vaccine were not observed.
Sep 15 -
Original Article
Vaccine Effectiveness among U.S. Health Care Personnel
T. Pilishvili and Others
In a test-negative case–control study involving 1482 vaccinated health care workers and 3449 controls, the BNT162b2 and mRNA-1273 SARS-CoV-2 vaccines were 88.8% and 96.3% effective, respectively, at preventing symptomatic Covid-19. Efficacy was similar in subgroups according to age (<50 or ≥50 years), racial and ethnic groups, underlying conditions, and various levels of patient contact.
Sep 22
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Original Article
BNT162b2 Vaccine at 6 Months of Follow-up
S.J. Thomas and Others
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Original Article
Covid-19 Vaccine Effectiveness in Medical Settings
M.G. Thompson and Others
A study with a test-negative design analyzed 41,552 admissions to 187 hospitals and 21,522 visits to 221 EDs or urgent care clinics. The mRNA-based vaccines (≥14 days after the second dose) were highly effective against SARS-CoV-2 infection leading to hospitalization (89%), ICU admission (90%), or an urgent care visit (91%).
Sep 08Editorial Covid-19 Vaccine Effectiveness and the Test-Negative DesignLetters responding to this article are now published: Prevention of Covid-19 with the BNT162b2 and mRNA-1273 Vaccines
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Original Article
Covid-19 Vaccine Effectiveness in Medical Settings
M.G. Thompson and Others
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Original Article
Third Dose of Covid-19 Vaccine in Israel
Y.M. Bar-On and Others
Since July 30, 2021, more than a million fully vaccinated Israeli residents who were 60 years of age or older have received a third dose of the BNT162b2 mRNA vaccine. As of August 31, the rate of confirmed Covid-19 infection was lower in the booster group than in the nonbooster group by a factor of 11.3, and the rate of severe illness was lower by a factor of 19.5.
Oct 07
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Original Article
Third Dose of Covid-19 Vaccine in Israel
Y.M. Bar-On and Others
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Case Records of the Massachusetts General Hospital
A Man with Sore Throat, Epistaxis, and Oropharyngeal Petechiae
H. Hock and Others
A 21-year-old man with sickle cell trait presented with sore throat, epistaxis, and petechiae of the oropharynx. The hemoglobin level was 9.8 g per deciliter, the platelet count 1000 per microliter, and the white-cell count 670 per microliter. A test for SARS-CoV-2 RNA was positive. What is the diagnosis?
Oct 14
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Case Records of the Massachusetts General Hospital
A Man with Headache and Covid-19
H.M. Heller and Others
A 24-year-old man was admitted to the hospital with a 3-week history of headache and a positive test for SARS-CoV-2 RNA. MRI showed multiple small hyperintense foci in the caudate nuclei and putamina. On lumbar puncture, the opening pressure was higher than 55 cm of water; the CSF white-cell count was 108 per microliter. What is the diagnosis?
Dec 24 -
Correspondence
SARS-CoV-2 in an Immunocompromised Host
B. Choi and Others
This letter describes an immunocompromised patient who had persistent infection with SARS-CoV-2 over a period of months, despite several courses of remdesivir. Phylogenetic analysis showed accelerated viral evolution.
Dec 03
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Case Records of the Massachusetts General Hospital
A Man with Headache and Covid-19
H.M. Heller and Others
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Case Records of the Massachusetts General Hospital
A Woman with Chest Pain, Dyspnea, and Shock
C. Newton-Cheh and Others
A 44-year-old woman presented with cough, dyspnea, and chest pain. On examination, she had tachycardia and hypotension. Evaluation revealed SARS-CoV-2 RNA in a nasopharyngeal swab, as well as elevated levels of troponin and lactic acid and a decline in urine output. Urgent management decisions were made.
Jul 30
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Case Records of the Massachusetts General Hospital
A Woman with Chest Pain, Dyspnea, and Shock
C. Newton-Cheh and Others
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Correspondence
Type I Interferonopathy in Muscle in a Man with Covid-19
G.S. Manzano, J.K. Woods, and A.A. Amato
Generalized, predominantly proximal weakness and a greatly elevated creatine kinase level developed in a man with Covid-19. Immunohistochemical analysis of a muscle-biopsy specimen revealed abnormal expression of MHC-1 and myxovirus resistance protein A on muscle fibers, suggesting type I interferonopathy.
Dec 10
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Correspondence
Type I Interferonopathy in Muscle in a Man with Covid-19
G.S. Manzano, J.K. Woods, and A.A. Amato
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Original Article
Myocarditis after BNT162b2 Vaccine in Israel
D. Mevorach and Others
In an Israeli Ministry of Health database, 136 definite or probable cases of myocarditis were detected among 5 million vaccinated persons. The rate ratio after two doses as compared with unvaccinated persons was 2.35, with the highest risk among male recipients between the ages of 16 and 19 years.
Oct 06
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Original Article
Myocarditis after Covid-19 mRNA Vaccine
G. Witberg and Others
Among 2.5 million patients who received the BNT162b2 mRNA vaccine in a large Israeli health care system, the incidence of myocarditis at 42 days was 2.13 cases per 100,000 persons, with the highest incidence (10.69 per 100,000 persons) among male patients between the ages of 16 and 29 years. Most cases of myocarditis were mild or moderate.
Oct 06 -
Correspondence
Myocarditis after Covid-19 Vaccination
A.K. Verma, K.J. Lavine, and C.-Y. Lin
Two patients who had received Covid-19 mRNA vaccination are described. One received the BNT162b2 vaccine; the other received the mRNA-1273 vaccine. Myocarditis, confirmed on histologic examination, developed in both patients within 2 weeks after vaccination. One patient died and the other recovered.
Sep 30
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Original Article
Myocarditis after Covid-19 mRNA Vaccine
G. Witberg and Others
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Original Article
Safety of the BNT162b2 mRNA Covid-19 Vaccine
N. Barda and Others
Among more than 1.7 million persons, BNT162b2 vaccination was associated with increased risks of myocarditis (risk ratio, 3.24), lymphadenopathy, appendicitis, and herpes zoster infection; in comparison, Covid-19 increased the risks of myocarditis (risk ratio, 18.28), pericarditis, arrhythmia, deep-vein thrombosis, pulmonary embolism, myocardial infarction, intracranial hemorrhage, and thrombocytopenia.
Aug 25Editorial The Importance of Context in Covid-19 Vaccine Safety
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Correspondence
A High-Risk VITT Prodrome
F. Salih and Others
A group of 11 patients had elements of VITT (thrombocytopenia, high d-dimer levels, and positivity for anti-PF4 antibodies) associated with severe headache but no other evidence of thrombosis during the period after ChAdOx1 nCoV-19 vaccination. Four of the patients went on to have thromboses and intracerebral hemorrhage, which suggests that the findings are a VITT prodrome.
Sep 15 -
Correspondence
Decline in Pathogenic Antibodies in VITT
L. Schönborn and Others
Platelet-activating antibodies can develop after adenoviral vector vaccination against Covid-19, leading to a potentially fatal procoagulant state. In an analysis involving 35 patients with these antibodies, platelet activation declined in nearly every patient within 12 weeks, despite the persistence of positivity on ELISA, and 5 patients received additional vaccination without sequelae.
Sep 08
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Correspondence
A High-Risk VITT Prodrome
F. Salih and Others
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Original Article
Vaccine-Induced Thrombocytopenia and Thrombosis
S. Pavord and Others
The phenotypes of VITT were defined in 220 patients in the United Kingdom who presented a median of 14 days after the first ChAdOx1 nCoV-19 vaccination. Half had cerebral venous sinus thrombosis, a third of whom also had intracranial hemorrhage. Mortality was 22%. Intravenous immune globulin may reverse VITT.
Aug 11
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Original Article
Vaccine-Induced Thrombocytopenia and Thrombosis
S. Pavord and Others
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Correspondence
Pathogenic Antibodies in Patients with VITT
G. Uzun, K. Althaus, and T. Bakchoul
Vaccine-induced immune thrombotic thrombocytopenia is caused by the induction of anti-PF4 polyanion antibodies in response to the vaccine. A survey of patients with anti-PF4 antibodies showed no cross-recognition of the SARS-CoV-2 spike protein, and the antiviral antibody levels in response to the vaccine were not correlated with the development of VITT.
Aug 25
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Correspondence
Pathogenic Antibodies in Patients with VITT
G. Uzun, K. Althaus, and T. Bakchoul
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Correspondence
Therapeutic Plasma Exchange in Refractory VITT
C.J. Patriquin and Others
Three patients with severe manifestations of VITT after Covid-19 vaccination had a poor response to initial therapy with anticoagulants and intravenous immune globulin. Their conditions improved after therapeutic plasma exchange was initiated, and they were able to leave the hospital.
Aug 26
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Correspondence
Therapeutic Plasma Exchange in Refractory VITT
C.J. Patriquin and Others
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Original Article
Brief Report
VITT — Diagnosis and Treatment
A. Bourguignon and Others
A rare side effect of ChAdOx1 nCoV-19 vaccination against Covid-19 — venous or arterial thrombosis, which has been termed vaccine-induced immune thrombotic thrombocytopenia — has been reported in recent months. In this Brief Report, investigators describe the use of intravenous immune globulin in the treatment of three such vaccine recipients in Canada.
Aug 19
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Original Article
Brief Report
VITT — Diagnosis and Treatment
A. Bourguignon and Others
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Original Article
Brief Report
Broadly Neutralizing Antibodies against All Coronaviruses
C.-W. Tan and Others
People who recovered from SARS-CoV-1 infection in 2002–2003 have neutralizing antibodies documented for up to 17 years. Vaccinating such people with the BNT162b2 SARS-CoV-2 vaccine elicited high titers of antibodies capable of neutralizing not only all SARS-CoV-2 variants of concern but also coronavirus types found in bats and pangolins. Immunity against all beta-coronaviruses may be achievable.
Aug 18
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Correspondence
Cross-Reactive Antibody Responses Elicited by the 501Y.V2 Variant
T. Moyo-Gwete and Others
Convalescent serum from persons who had recovered from infection with 501Y.V2 (B.1.351), a SARS-CoV-2 variant first identified in South Africa, showed potent neutralization of the original variant (D614G), the 501Y.V2 variant, and the P.1 variant first identified in Brazil. These results suggest that vaccines based on the 501Y.V2 spike protein may be broadly effective against two common variants of SARS-CoV-2.
Jun 03 -
Original Article
Antibodies and SARS-CoV-2 Infection in Health Workers
S.F. Lumley and Others
In a longitudinal study of seropositive and seronegative health care workers undergoing asymptomatic and symptomatic SARS-CoV-2 testing, the presence of anti-spike or anti-nucleocapsid IgG antibodies was associated with a substantially reduced risk of SARS-CoV-2 reinfection in the ensuing 6 months.
Feb 11
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Correspondence
Cross-Reactive Antibody Responses Elicited by the 501Y.V2 Variant
T. Moyo-Gwete and Others
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Original Article
Bamlanivimab plus Etesevimab for Covid-19
M. Dougan and Others
In a phase 3 trial involving 1035 outpatients who were at increased risk for severe Covid-19, those who received two monoclonal antibodies targeting SARS-CoV-2 had a significant reduction in the viral load and a significantly lower incidence of progression to severe illness than those who received placebo.
Jul 14 -
Original Article
Tofacitinib for Covid-19 Pneumonia
P.O. Guimarães and Others
Patients who were hospitalized with Covid-19 pneumonia were randomly assigned, at a median of 10 days after symptom onset, to receive tofacitinib or placebo. At 28 days, the risk of death or respiratory failure was lower in the tofacitinib group.
Jul 29Editorial JAK Inhibitors — More Than Just Glucocorticoids
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Original Article
Bamlanivimab plus Etesevimab for Covid-19
M. Dougan and Others
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Original Article
Convalescent Plasma in Early Covid-19 Infection
R. Libster and Others
High-titer convalescent plasma was compared with placebo in older adult patients within the first 3 days after the onset of symptoms of Covid-19 and documented SARS-CoV-2 infection. Disease progression was approximately half as common in patients who received convalescent plasma (16%) as in those who received placebo (31%).
Feb 18Letters responding to this article are now published: Plasma Therapy to Prevent Severe Covid-19 in Older Adults
Editorial (A Little) Clarity on Convalescent Plasma for Covid-19
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Original Article
Dexamethasone Treatment in Covid-19
The RECOVERY Collaborative Group
Among hospitalized patients with Covid-19, treatment with dexamethasone resulted in lower 28-day mortality than usual care, according to the level of respiratory support the patients were receiving, indicating a possible correlation between efficacy and the stage of infection.
Feb 25Editorial Research in the Context of a Pandemic
Editorial The RECOVERY Platform
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Original Article
Dexamethasone Treatment in Covid-19
The RECOVERY Collaborative Group
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Original Article
Neutralizing-Antibody Therapy in Covid-19
P. Chen and Others
In a phase 2 trial, outpatients with Covid-19 who received a single infusion of a 2800-mg dose of the neutralizing antibody LY-CoV555 had a greater reduction from baseline in viral load than those who received placebo. Hospitalization was less frequent among antibody-treated patients (1.6% vs. 6.3%).
Jan 21Editorial Monoclonal Antibodies to Disrupt Progression of Early Covid-19 Infection
Original Article REGN-COV2, a Neutralizing Antibody Cocktail, in Outpatients with Covid-19
Correspondence Neutralizing Antibody LY-CoV555 for Outpatient Covid-19
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Original Article
Neutralizing-Antibody Therapy in Covid-19
P. Chen and Others
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Original Article
Breakthrough Covid-19 in Health Care Workers
M. Bergwerk and Others
Among 1497 health care workers who were fully vaccinated against Covid-19 and had full testing results, 39 breakthrough infections were detected between January 20 and April 28, 2021. The infected workers had mild symptoms or were asymptomatic and had lower titers of peri-infection neutralizing antibody than coworkers who were not infected.
Jul 28
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Correspondence
Resurgence of Covid-19 in Vaccinated Health Workers
J. Keehner and Others
From March through July 2021, a total of 227 health care workers at UCSD, 57% of whom were fully vaccinated, tested positive for SARS-CoV-2; the delta variant was the dominant isolate. No deaths were recorded. Vaccine effectiveness fell from over 90% in March to 65.5% in July. A trend was observed for greater risk as a function of time since full vaccination.
Sep 01 -
Perspective
Public Health Law after Covid-19
M.M. Mello and W.E. Parmet
To combat the pandemic, officials imposed extensive mitigation measures using their emergency powers. In response, more than 1000 suits challenged orders shuttering businesses, banning indoor worship services, restricting travel, and mandating mask wearing.
Sep 01
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Correspondence
Resurgence of Covid-19 in Vaccinated Health Workers
J. Keehner and Others
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Correspondence
Breakthrough SARS-CoV-2 Infections in Health Care Workers
B. Lange, M. Gerigk, and T. Tenenbaum
In a German study, 4 health care workers out of 1137 (0.35%) who had received one of the mRNA SARS-CoV-2 vaccines had mildly symptomatic Covid-19 a median of 62 days after the second vaccine dose. All four infections were with the B.1.1.7 strain. The infected persons had high viral loads and viral shedding up to 32 days after diagnosis.
Aug 18
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Correspondence
Breakthrough SARS-CoV-2 Infections in Health Care Workers
B. Lange, M. Gerigk, and T. Tenenbaum
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Original Article
Covid-19 Prevention and Attenuation with mRNA Vaccines
M.G. Thompson and Others
In a study involving 3975 health care personnel, first responders, and other essential workers, the effectiveness of mRNA vaccines against SARS-CoV-2 infection was 91% with full vaccination. The vaccines attenuated the viral RNA load, febrile symptoms, and illness duration among those who became infected despite vaccination.
Jul 22
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Original Article
Covid-19 Prevention and Attenuation with mRNA Vaccines
M.G. Thompson and Others
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Original Article
Brief Report
Variant SARS-CoV-2 Infection after Vaccination
E. Hacisuleyman and Others
Mild Covid-19 symptoms developed in two fully vaccinated persons. Serum tests showed high titers of antibodies capable of neutralizing the wild-type strain of SARS-CoV-2 first identified in Wuhan, China, but sequencing of the virus isolates revealed novel variants. Some mutations in the receptor-binding domain of the spike protein were shared by the two variant strains.
Jun 10Correspondence Vaccine Breakthrough Infections with SARS-CoV-2 Variants
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Original Article
Brief Report
Variant SARS-CoV-2 Infection after Vaccination
E. Hacisuleyman and Others
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Correspondence
Vaccination and Household Transmission of SARS-CoV-2
R.J. Harris and Others
In this study involving household contacts of persons with laboratory-confirmed Covid-19, the risk of household transmission was 40 to 50% lower among household contacts of index patients who had received one dose of vaccine 21 days or more before testing positive than among contacts of unvaccinated index patients.
Jun 23
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Correspondence
Vaccination and Household Transmission of SARS-CoV-2
R.J. Harris and Others
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Original Article
Treatment of MIS-C
A.J. McArdle and Others
An observational cohort study evaluated immunomodulatory therapy of multisystem inflammatory syndrome in children by comparing IVIG, IVIG plus glucocorticoids, or glucocorticoids alone. The investigators found no evidence of the superiority of any of the three therapies, although significant differences may emerge as more data accrue.
Jun 16Editorial Immunotherapy for MIS-C — IVIG, Glucocorticoids, and Biologics
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Correspondence
Household Transmission of SARS-CoV-2 from Children
V.T. Chu and Others
In an outbreak of Covid-19 at a summer camp, 224 confirmed cases in children and adolescents 7 to 19 years of age were identified. After the campers returned home, transmission of SARS-CoV-2 occurred in 35 of 194 (18%) households, with a secondary attack rate of 45% among household members.
Jul 21 -
Original Article
MIS-C — Initial Therapy and Outcomes
M.B.F. Son and Others
An analysis of surveillance data on inpatients younger than 21 years of age who had multisystem inflammatory syndrome in children and were hospitalized between March 15 and October 31, 2020, showed that initial treatment with IVIG plus glucocorticoids was associated with a lower risk of cardiovascular dysfunction and a lower incidence of adjunctive therapy use than IVIG alone.
Jul 01Editorial Immunotherapy for MIS-C — IVIG, Glucocorticoids, and Biologics
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Correspondence
Household Transmission of SARS-CoV-2 from Children
V.T. Chu and Others
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Original Article
Vaccine Effectiveness against Delta Covid-19 Variant
J. Lopez Bernal and Others
The B.1.617.2 (delta) Covid-19 variant has surged in India and spread worldwide. In a test-negative case–control study, the effectiveness of two doses of BNT162b2 was 94% against the B.1.1.7 (alpha) variant and 88% against delta; with the ChAdOx1 nCoV-19 vaccine, effectiveness was 74% and 67%, respectively. Protection after a single vaccine injection was low; two doses are needed.
Jul 21Editorial Vaccine Effectiveness Studies in the Field
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Original Article
Efficacy of the ChAdOx1 Vaccine against the B.1.351 Variant
S.A. Madhi and Others
A double-blind randomized trial in South Africa documented poor efficacy of two doses of the ChAdOx1 nCoV-19 vaccine against the B.1.351 variant of SARS-CoV-2 that emerged in South Africa. Infections occurred in 3.2% of placebo recipients and in 2.5% of vaccine recipients. Thirty-nine of the 42 virus isolates were the B.1.351 variant. None of the cases led to hospitalization or death.
May 20Editorial Interplay between Emerging SARS-CoV-2 Variants and Pandemic Control
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Correspondence
Heterologous Vaccination with ChAdOx1 nCoV-19 and mRNA-1273
J. Normark and Others
Health care workers who had received a dose of ChAdOx1 nCoV-19 were offered a choice of receiving either ChAdOx1 nCoV-19 or mRNA-1273 9 to 12 weeks after the initial dose. Levels of S-specific and RBD-specific IgG increased by a factor of 5 after a ChAdOx1 nCoV-19 boost and by a factor of 115 to 125 after an mRNA-1273 boost.
Jul 14
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Original Article
Efficacy of the ChAdOx1 Vaccine against the B.1.351 Variant
S.A. Madhi and Others
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Correspondence
Durability of Response after Ad26.COV2.S Vaccination
D.H. Barouch and Others
In this study, investigators measured immune responses in 20 participants who had received either one or two doses of the Ad26.COV2.S vaccine and in 5 who had received placebo. A high level of neutralizing antibodies against SARS-CoV-2 was maintained for at least 8 months after single-dose injection, with a median decrease by a factor of 1.8 in the titer.
Jul 14
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Correspondence
Durability of Response after Ad26.COV2.S Vaccination
D.H. Barouch and Others
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Original Article
Ad26.COV2.S Vaccine Efficacy against Covid-19
J. Sadoff and Others
Ad26.COV2.S vaccine is a replication-incompetent human adenovirus type 26 vector containing the gene sequence that produces SARS-CoV-2 spike protein in a prefusion-stabilized conformation. In a randomized trial involving nearly 40,000 persons, vaccine efficacy was 66% against moderate to severe–critical Covid-19 and 85% against severe–critical Covid-19. Efficacy against the variant first identified in South Africa was 64% against moderate disease and 82% against severe–critical disease.
Jun 10
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Original Article
Ad26.COV2.S Vaccine Efficacy against Covid-19
J. Sadoff and Others
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Special Report
SARS-CoV-2 Variants and Vaccines
P.R. Krause and Others
The emergence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) viral variants of concern arouses concern regarding possible escape from vaccine-elicited immunity. Global strategies involving integration of clinical rollout with systematic investigation are presented.
Jun 23 -
Correspondence
Neutralization of SARS-CoV-2 Variants by Convalescent and Vaccinee Serum
G.-L. Wang and Others
Serum samples from patients convalescing after SARS-CoV-2 infection and after vaccination with BBIBP-CorV or CoronaVac in China neutralized pseudoviruses expressing spike proteins from the B.1.1.7 variant at levels that were similar to those from the wild-type (Wuhan) isolate but lower than those from the B.1.351 variant.
Jun 17
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Special Report
SARS-CoV-2 Variants and Vaccines
P.R. Krause and Others
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Correspondence
BNT162b2 Vaccine and Emerging SARS-CoV-2 Variants
Y. Liu and Others
A total of 20 serum samples from 15 persons who received the BNT162b2 vaccine showed strong neutralization activity against recombinant viruses engineered to express the spike protein from the Wuhan-Hu-1 strain and B.1.429, B.1.526, and B.1.1.7 variants. These in vitro neutralization assays are not clearly predictive of activity in vivo.
Jul 29 -
Clinical Implications of Basic Research
SARS-CoV-2 Vaccine Design
P.-A. Koenig and F.I. Schmidt
A recent study of the D614G variant spike protein of SARS-CoV-2 sheds light on a mechanism underlying the relatively increased infectivity of virions expressing it and has implications for vaccine design.
Jun 17
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Correspondence
BNT162b2 Vaccine and Emerging SARS-CoV-2 Variants
Y. Liu and Others
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Original Article
Inactivated SARS-CoV-2 Vaccine in Chile
A. Jara and Others
In a national prospective cohort study involving 10.2 million participants in Chile, the effectiveness of an inactivated SARS-CoV-2 vaccine, which had been developed in China and administered in two doses 28 days apart, was estimated. Effectiveness among fully immunized persons was estimated at 65.9% for Covid-19 and at 87.5% for hospitalization, 90.3% for ICU admission, and 86.3% for death.
Jul 07
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Original Article
Safety and Efficacy of NVX-CoV2373 Vaccine
P.T. Heath and Others
In a phase 3 trial involving more than 15,000 participants, two doses of NVX-CoV2373, a recombinant SARS-CoV-2 nanoparticle vaccine, administered 21 days apart had a vaccine efficacy of 89.7%. Reactogenicity was generally mild and transient, and adverse events were infrequent and of low grade.
Jun 30 -
Original Article
NVX-CoV2373 Vaccine Efficacy against B.1.351 in South Africa
V. Shinde and Others
A randomized, phase 2 trial compared the NVX-CoV2373 nanoparticle vaccine with placebo in participants in South Africa, including 30% who were seropositive at baseline. Overall vaccine efficacy was 49.4%, with the B.1.351 variant identified in more than 90% of isolates.
May 20Editorial Interplay between Emerging SARS-CoV-2 Variants and Pandemic Control
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Original Article
Safety and Efficacy of NVX-CoV2373 Vaccine
P.T. Heath and Others
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Correspondence
Local Covid-19 Vaccine Reactions in Non-White Persons
U. Samarakoon, S. Alvarez-Arango, and K.G. Blumenthal
Previous reports document a small risk of delayed large local reactions to Covid-19 vaccines; however, clinical photos most often show White persons. Reactions have also been noted in vaccine recipients who are Black, Indigenous, or People of Color (BIPOC). Photos of eight such delayed reactions are shown.
Aug 12
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Correspondence
Local Covid-19 Vaccine Reactions in Non-White Persons
U. Samarakoon, S. Alvarez-Arango, and K.G. Blumenthal
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Original Article
Effectiveness of the BNT162b2 mRNA Vaccine in Israel
N. Dagan and Others
Nearly 600,000 people in a large health care organization were followed after vaccination for infection, hospitalization, and severe Covid-19. Estimated vaccine effectiveness in preventing death was 72% during the period from day 14 through day 20 after the first dose, and for the period 7 or more days after the second dose, hospitalization was reduced by 87%. These results were similar to those reported in a randomized trial.
Apr 15
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Original Article
Effectiveness of the BNT162b2 mRNA Vaccine in Israel
N. Dagan and Others
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Clinical Practice
Mild or Moderate Covid-19
R.T. Gandhi, J.B. Lynch, and C. del Rio
The diagnosis of Covid-19 is usually based on SARS-CoV-2 PCR testing of a nasopharyngeal swab or other specimen. Remdesivir and dexamethasone have benefits in hospitalized patients with severe Covid-19, but in patients with moderate disease, dexamethasone is not efficacious and data are insufficient to recommend for or against routine use of remdesivir.
Oct 29
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Perspective
Protecting Olympic Participants from Covid-19
A.K. Sparrow and Others
Plans to protect participants and the public from Covid-19 during the Olympics aren’t built on rigorous risk assessment. They fail to consider the ways in which exposure occurs, the factors that contribute to exposure, and which participants may be at highest risk.
May 25 -
Clinical Practice
Severe Covid-19
D.A. Berlin, R.M. Gulick, and F.J. Martinez
Patients with severe Covid-19 should be closely monitored regarding the need for endotracheal intubation; intubated patients should receive lung-protective ventilation. Data from randomized, controlled trials are awaited to inform the use of antiviral and immunomodulatory therapies; preliminary data support benefits of remdesivir in this population.
May 15See Also Chinese Translation in NEJM 医学前沿
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Perspective
Protecting Olympic Participants from Covid-19
A.K. Sparrow and Others
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Videos in Clinical Medicine
Emergency Intubation in Covid-19
G.S. Shrestha and Others
This video demonstrates the procedure for emergency endotracheal intubation in patients with suspected or proven Covid-19. Endotracheal intubation in such patients poses a risk of infection for the health care personnel involved. Meticulous planning and preparation and the use of practice drills can minimize this risk.
Feb 18Letters responding to this article are now published: Emergency Intubation in Covid-19
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Videos in Clinical Medicine
Percutaneous Tracheostomy
D.A. Hashimoto, A.L. Axtell, and H.G. Auchincloss
A tracheostomy is a surgically created airway that is kept open with a breathing tube, or tracheostomy tube. This video demonstrates percutaneous tracheostomy, a procedure that may be performed at the patient’s bedside, including patients with Covid-19, who may require a tracheostomy in the course of severe respiratory distress.
Oct 28Correspondence Percutaneous Tracheostomy
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Videos in Clinical Medicine
Family Meetings on Behalf of Patients with Serious Illness
E. Widera and Others
Effective family meetings build rapport and offer support, provide updates about a patient’s medical status and prognosis, and ensure treatment that is consistent with the patient’s goals. Such meetings can result in better use of health care resources. This video demonstrates how to have an effective family meeting.
Sep 10
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Videos in Clinical Medicine
Percutaneous Tracheostomy
D.A. Hashimoto, A.L. Axtell, and H.G. Auchincloss
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Perspective
SARS-CoV-2 Testing and School Reopening
Y. Rafiei and M.M. Mello
Most U.S. school reopening plans focus on screening for Covid-19 symptoms. But because an estimated 40% of Covid-19 cases are asymptomatic and 50% of transmissions occur from asymptomatic persons, screening testing is critical.
Dec 03 -
Correspondence
Detection of SARS-CoV-2 with a CRISPR-Based Test
J. Joung and Others
A new method for the detection of SARS-CoV-2 combines simplified extraction of RNA with isothermal amplification and CRISPR (clustered regularly interspaced short palindromic repeats)–mediated detection. Testing of 402 samples indicated a sensitivity of 93.1% and a specificity of 98.5%.
Oct 08
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Perspective
SARS-CoV-2 Testing and School Reopening
Y. Rafiei and M.M. Mello
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Videos in Clinical Medicine
How to Obtain a Nasopharyngeal Swab Specimen
F.M. Marty, K. Chen, and K.A. Verrill
Collecting specimens from the surface of the respiratory mucosa with nasopharyngeal swabs is a procedure used to diagnose Covid-19 as well as other respiratory viral infections and certain bacterial infections in adults and children. This video describes the collection of specimens for detection of Covid-19.
May 28Correspondence How to Obtain a Nasopharyngeal Swab SpecimenSee Also Chinese Translation in NEJM 医学前沿
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Correspondence
Patient-Collected Swabs for SARS-CoV-2 Testing
Y.-P. Tu and Others
Tongue, nasal, and mid-turbinate swabs to detect SARS-CoV-2 were collected by 530 outpatients before a health care worker collected nasopharyngeal swabs from these patients. Both the mid-turbinate and the nasal samples collected by the patients themselves may be clinically acceptable, with estimated sensitivities above 90%.
Jul 30
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Correspondence
Patient-Collected Swabs for SARS-CoV-2 Testing
Y.-P. Tu and Others
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Correspondence
Saliva Specimens to Detect SARS-CoV-2 Infection
A.L. Wyllie and Others
In this letter, the investigators report that saliva specimens and nasopharyngeal swab specimens had similar sensitivity in the detection of SARS-CoV-2 RNA in both symptomatic and asymptomatic persons.
Sep 24Correspondence Saliva for Detection of SARS-CoV-2
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Correspondence
Saliva Specimens to Detect SARS-CoV-2 Infection
A.L. Wyllie and Others
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Correspondence
Microvascular Changes in the Brain in Covid-19
M.-H. Lee and Others
High-resolution MRI and histopathological study of the brains of patients who had died from Covid-19 showed punctate hyperintensities and punctate or linear hypointensities, which represented various forms of pauci-inflammatory microvasculopathy. No evidence of active viral infection was found.
Dec 30 -
Original Article
Nimble GWAS on Covid-19
The Severe Covid-19 GWAS Group
During the peak of hospitalizations of patients with severe Covid-19 in Italy and Spain in March, a group of researchers in these and other countries obtained and analyzed samples, resulting in the identification of two chromosomal loci associated with the disorder.
Oct 15Editorial Genetic Risk of Severe Covid-19
Correspondence Mining a GWAS of Severe Covid-19See Also Chinese Translation in NEJM 医学前沿
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Correspondence
Microvascular Changes in the Brain in Covid-19
M.-H. Lee and Others
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Review Article
Cytokine Storm
D.C. Fajgenbaum and C.H. June
Cytokine storm, a life-threatening disorder involving cytokine elevations and immune-cell hyperactivation, has various causes and is characterized by constitutional symptoms, systemic inflammation, and multiorgan dysfunction. Selective interventions can ameliorate the illness.
Dec 03See Also Chinese Translation in NEJM 医学前沿
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Original Article
Baricitinib plus Remdesivir for Adults with Covid-19
A.C. Kalil and Others
In a trial involving 1033 patients hospitalized with Covid-19, the addition of baricitinib to remdesivir was associated with shorter recovery time, particularly among patients receiving high-flow oxygen, and with a 30% higher odds of improvement at day 15 than remdesivir alone. Adverse events were less frequent with the combination therapy.
Dec 11
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Original Article
Repurposed Antiviral Drugs for Covid-19
WHO Solidarity Trial Consortium
The authors report interim results of the WHO Solidarity trial of four repurposed antiviral drugs — remdesivir, hydroxychloroquine, lopinavir, and interferon beta-1a — in patients hospitalized with Covid-19. Effects on overall mortality, initiation of ventilation, and duration of hospital stay are compared.
Dec 02Editorial A Large, Simple Trial Leading to Complex Questions
Perspective FDA Approval of Remdesivir — A Step in the Right Direction -
Original Article
Remdesivir for Covid-19 — Final Report
J.H. Beigel and Others
In this randomized, double-blind trial in 1062 adults hospitalized with Covid-19, remdesivir was superior to placebo in shortening the time to recovery (10 days, vs. 15 days with placebo). The estimates of mortality by day 29 were 11.4% with remdesivir and 15.2% with placebo. The benefit of remdesivir was most apparent in patients who were receiving low-flow oxygen at baseline.
Nov 05Correspondence Remdesivir for the Treatment of Covid-19 — Preliminary Report
See Also Chinese Translation in NEJM 医学前沿
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Original Article
Repurposed Antiviral Drugs for Covid-19
WHO Solidarity Trial Consortium
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Original Article
Remdesivir for 5 Days or 10 Days in Covid-19
J.D. Goldman and Others
A randomized trial comparing a 5-day course of intravenous remdesivir with a 10-day course in patients with Covid-19 pneumonia and hypoxemia who were not yet receiving mechanical ventilation showed no significant differences in outcome related to the duration of treatment.
Nov 05Editorial Remdesivir — An Important First Step
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Original Article
Remdesivir for 5 Days or 10 Days in Covid-19
J.D. Goldman and Others
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Original Article
Compassionate-Use Remdesivir for Severe Covid-19
J. Grein and Others
A cohort of patients with severe Covid-19 received treatment with remdesivir under a compassionate-use protocol. Improvement in oxygen-support status was observed in 68% of patients, and overall mortality was 13% over a median follow-up of 18 days.
Jun 11See Also Chinese Translation in NEJM 医学前沿
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Original Article
Compassionate-Use Remdesivir for Severe Covid-19
J. Grein and Others
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Medicine and Society
Tribal Truce
L. Rosenbaum
Since human behavior — including wearing or shunning masks — will determine the ultimate toll of the Covid-19 pandemic, communication strategies that bridge our partisan divide over science may prove as important as any novel therapeutic.
Sep 23 -
Perspective
Facial Masking for Covid-19
M. Gandhi and G.W. Rutherford
Increasing the proportion of SARS-CoV-2 infections that are asymptomatic with the simple public health measure of universal masking might help make the infection less deadly and increase population-level immunity without severe illnesses and deaths.
Sep 08Correspondence Facial Masking for Covid-19
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Medicine and Society
Tribal Truce
L. Rosenbaum
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Videos in Clinical Medicine
Personal Protective Equipment and Covid-19
R. Ortega and Others
This video demonstrates a procedure for donning and doffing one type of PPE recommended by the CDC for use in hospitals to minimize the risk of exposure to infectious material during the care of patients with Covid-19.
Jun 25Correspondence Personal Protective Equipment and Covid-19
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Correspondence
Universal Masking in the Covid-19 Era
M. Klompas, C.A. Morris, and E.S. Shenoy
Klompas and colleagues write that they understand that some people are citing their Perspective article (published on April 1) as support for discrediting widespread masking. In truth, the intent of their article was to push for more masking, not less.
Jul 09Perspective Universal Masking in Hospitals in the Covid-19 Era
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Correspondence
Universal Masking in the Covid-19 Era
M. Klompas, C.A. Morris, and E.S. Shenoy
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Sounding Board
Allocating Scarce Medical Resources for Covid-19
E.J. Emanuel and Others
The Covid-19 pandemic has already stressed health care systems throughout the world, requiring rationing of medical equipment and care. The authors discuss the ethical values relevant to health care rationing and provide six recommendations to guide fair allocation of scarce medical resources during the pandemic.
May 21Perspective The Toughest Triage — Allocating Ventilators in a Pandemic
Correspondence Allocating Medical Resources in the Time of Covid-19
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Sounding Board
Allocating Scarce Medical Resources for Covid-19
E.J. Emanuel and Others
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Original Article
The mRNA-1273 Vaccine in Adolescents
K. Ali and Others
In a trial of mRNA-1273 or placebo involving 3700 adolescents 12 to 17 years of age, two doses of vaccine stimulated high levels of neutralizing antibodies, with a side-effect profile similar to that seen in other age groups. The incidence of Covid-19 in the unvaccinated group was too low to gauge protection, but Covid-19 did not develop in any vaccinated participants.
Aug 11
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Original Article
The mRNA-1273 Vaccine in Adolescents
K. Ali and Others
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Original Article
BNT162b2 Vaccination against Covid-19 in 12-to-15-Year-Old Adolescents
R.W. Frenck, Jr., and Others
This randomized trial of the BNT162b2 vaccine involved 2260 adolescents 12 to 15 years of age. Similar levels of antibody to SARS-CoV-2 were elicited in the 12-to-15-year-old participants and in 16-to-25-year-old participants in a parallel trial. Among participants with no evidence of previous infection, no cases of Covid-19 were diagnosed in vaccine recipients, as compared with 16 cases in placebo recipients.
Jul 15Letters responding to this article are now published: BNT162b2 Covid-19 Vaccine in Adolescents
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Original Article
BNT162b2 Vaccination against Covid-19 in 12-to-15-Year-Old Adolescents
R.W. Frenck, Jr., and Others

