Evidence map›Paper›PMID 37220751›Full record

Trial reportClinical infectious diseases : an official publication of the Infectious Diseases Society of America2023

A Randomized Controlled Study Assessing Convalescent Immunoglobulins vs Convalescent Plasma for Hospitalized Patients With Coronavirus 2019.

Yasmin Maor, Eilat Shinar, Marina Izak, Galia Rahav, Tal Brosh-Nissimov, Asa Kessler, Naomi Rahimi-Levene, Odeda Benin-Goren, Dani Cohen, Iris Zohar and 3 more

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Article
  2. Review
  3. Hyperimmune Globulins in COVID-19.Current topics in microbiology and immunology · 2025
    Review
  4. Article
  5. COVID-19 therapeutics.Clinical microbiology reviews · 2024
    Review
  6. Review
  7. Review
  8. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Yasmin MaorInfectious Disease Unit, Wolfson Medical Center, Holon, Israel.ORCID 0000-0001-7258-3434
Eilat ShinarMagen David Adom, National Blood Services, Ramat Gan, Israel.
Marina IzakFaculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Galia RahavFaculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Tal Brosh-NissimovInfectious Diseases Unit, Samson Assuta Ashdod University Hospital, Ashdod, Israel.
Asa KesslerDepartment of Medicine, Hadassah Medical Center, Jerusalem, Israel.
Naomi Rahimi-LeveneBlood Bank, Shamir (Assaf Harofeh) Medical Center, Zerifin, Israel.
Odeda Benin-GorenGeneral Medical Directorate, Ministry of health, Jerusalem, Israel.
Dani CohenSchool of Public Health, Tel Aviv University, Tel Aviv, Israel.
Iris ZoharInfectious Disease Unit, Wolfson Medical Center, Holon, Israel.
Noga AlagemKAMADA, Rehovot, Israel.
Sharon CastroKAMADA, Rehovot, Israel.
Oren ZimhonyFaculty of Medicine, Hebrew University and Hadassah, Jerusalem, Israel.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIt is unknown whether convalescent immunoglobulins (cIgGs) are better than convalescent plasma (CP) for patients with coronavirus 2019 (COVID-19).

methodsIn this randomized controlled trial, we assigned high risk COVID-19 patients with ≤10 days of symptoms, to receive cIgGs or CP. The primary endpoint was improvement on day 14 according to the World Health Organization scale. Secondary endpoints were survival on day 14, and improvement, survival, and percent of ventilated patients on day 28, and treatment response in unvaccinated and vaccinated patients.

resultsA total of 319 patients were included: 166 received cIgGs and 153 CP. Median age was 64 to 66 years. A total of 112 patients (67.5%) in the cIgG group and 103 patients (67.3%) in the CP group reached the primary endpoint. Difference between groups was 0.1 (95% confidence interval, -10.1 to 10.4; P = .026), failing to reach noninferiority. More patients receiving cIgG improved by day 28 (136 patients [81.9%] and 108 patients [70.6%], respectively; 95% confidence interval, 1.9-20.7; P < .001; for superiority P = .018). Seventeen patients in the cIgG group (10.2%) and 25 patients (16.3%) in the CP group required mechanical ventilation (P = .136). Sixteen (9.6%) and 23 (15%) patients, respectively, died (P = .172). More unvaccinated patients improved by day 28 in the cIgG group (84.1% vs 66.1%; P = .024), and survival was better in the cIgG group (89.9% vs 77.4%; P = .066).

conclusionscIgGs failed to reach the primary noninferiority endpoint on day 14 but was superior to CP on day 28. Survival and improvement by day 28 in unvaccinated patients treated with cIgGs were better. In the face of new variants, cIgGs are a viable option for treating COVID-19. TRIAL REGISTRATION NUMBER: My Trials MOH_2021-01-14_009667.

Indexed as

COVID-19AgedCOVID-19 SerotherapyHumansImmunization, PassiveImmunoglobulinsMiddle AgedSARS-CoV-2Treatment OutcomeImmunoglobulinsCOVID-19immunoglobulinsplasma

Identifiers

PMID37220751
PMCPMC10552585

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.