Evidence map›Paper›PMID 35415922›Full record

ArticleBritish journal of haematology2022

International guidelines regarding the role of IVIG in the management of Rh- and ABO-mediated haemolytic disease of the newborn.

Lani Lieberman, Enrico Lopriore, Jillian M Baker, Rachel S Bercovitz, Robert D Christensen, Gemma Crighton, Meghan Delaney, Ruchika Goel, Jeanne E Hendrickson, Amy Keir and 12 more

Open access · hybridAbstract read
In one paragraph

Article in British journal of haematology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
9.5field-weighted citation impact, top 2% of its field
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

11 citing papers in PubMed, 26 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

22 authors at 19 institutions in 10 countries.

Lani LiebermanDepartment of Clinical Pathology, University Health Network, Toronto, Ontario, Canada.ORCID 0000-0002-3633-0728
Enrico LoprioreDivision of Neonatology, Department of Pediatrics, Leiden University Medical Center, Leiden, The Netherlands.
Jillian M BakerDepartment of Pediatrics, Unity Health Toronto (St. Michael's Hospital), Toronto, Ontario, Canada.
Rachel S BercovitzDivision of Hematology, Oncology, and Stem Cell Transplant, Department of Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Robert D ChristensenDivisions of Neonatology and Hematology/Oncology, University of Utah Health, Salt Lake City, UT, USA.
Gemma CrightonDepartment of Haematology, Royal Children's Hospital, Melbourne, Australia.
Meghan DelaneyDivision of Pathology & Laboratory Medicine, Children's National Hospital, Washington, District of Columbia, USA.
Ruchika GoelDivision of Transfusion Medicine, Department of Pathology, School of Medicine, Johns Hopkins University, Baltimore, Maryland, USA.
Jeanne E HendricksonDepartments of Laboratory Medicine and Pediatrics, Yale University, New Haven, Connecticut, USA.ORCID 0000-0002-7928-3132
Amy KeirSAHMRI Women and Kids, South Australian Health and Medical Institute, North Adelaide, South Australia, Australia.
Denise LandryCanadian Blood Services, Ottawa, Ontario, Canada.
Ursula La RoccaDepartment of Translational and Precision Medicine, Sapienza University, Rome, Italy.
Brigitte LemyreDepartment of Pediatrics, University of Ottawa, Ottawa, Ontario, Canada.
Rolf F MaierChildren's Hospital, University Hospital, Philipps University, Marburg, Germany.
Eduardo Muniz-DiazDepartment of Immunohematology, Blood and Tissue Bank of Catalonia, Barcelona, Spain.
Susan NahirniakAlberta Precision Laboratories and Department of Laboratory Medicine and Pathology, University of Alberta, Edmonton, Alberta, Canada.
Helen V NewClinical Directorate, NHS Blood and Transplant, London, UK.ORCID 0000-0001-6290-8004
Katerina PavenskiDepartment of Laboratory Medicine and Pathology, Unity Health Toronto (St. Michael's Hospital), Toronto, Ontario, Canada.
Maria Cristina Pessoa Dos SantosIFF/Fundação Oswaldo Cruz, Rio de Janeiro, Brazil.
Glenn RamseyDepartment of Pathology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.
Nadine ShehataDepartments of Medicine, Laboratory Medicine and Pathobiology, Institute of Health, Policy Management and Evaluation, University of Toronto, Mount Sinai Hospital, Toronto, Ontario, Canada.
International Collaboration for Transfusion Medicine Guidelines (ICTMG)
Northwestern University · USSt. Michael's Hospital · CABanc de Sang i Teixits · ESCanadian Blood Services · CAChildren's National · USFundação Oswaldo Cruz · BRIntermountain Healthcare · USJohns Hopkins University · USLeiden University Medical Center · NLMount Sinai Hospital · CANHS Blood and Transplant · GBPhilipps University of Marburg · DERoyal Children's Hospital · AUSapienza University of Rome · ITSouth Australian Health and Medical Research Institute · AUSunnybrook Health Science Centre · CAUniversity of Alberta · CAUniversity of Ottawa · CAYale University · US

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
NCATS NIH HHS UL1 TR001863
6 · The paper itself

Abstract

Haemolytic disease of the newborn (HDN) can be associated with significant morbidity. Prompt treatment with intensive phototherapy (PT) and exchange transfusions (ETs) can dramatically improve outcomes. ET is invasive and associated with risks. Intravenous immunoglobulin (IVIG) may be an alternative therapy to prevent use of ET. An international panel of experts was convened to develop evidence-based recommendations regarding the effectiveness and safety of IVIG to reduce the need for ETs, improve neurocognitive outcomes, reduce bilirubin level, reduce the frequency of red blood cell (RBC) transfusions and severity of anaemia, and/or reduce duration of hospitalization for neonates with Rh or ABO-mediated HDN. We used a systematic approach to search and review the literature and then develop recommendations from published data. These recommendations conclude that IVIG should not be routinely used to treat Rh or ABO antibody-mediated HDN. In situations where hyperbilirubinaemia is severe (and ET is imminent), or when ET is not readily available, the role of IVIG is unclear. High-quality studies are urgently needed to assess the optimal use of IVIG in patients with HDN.

Indexed as

Erythroblastosis, FetalImmunoglobulins, IntravenousBlood Group IncompatibilityExchange Transfusion, Whole BloodFemaleHumansInfant, NewbornPhototherapyImmunoglobulins, Intravenousalloimmunizationevidence-based guidelineshaemolytic disease of the newbornintravenous immunoglobulinpregnancy

Identifiers

PMID35415922
PMCPMC9324942
OpenAlexW4223450106

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.