Evidence map›Paper›PMID 39449355›Full record

ArticleInternational journal of neonatal screening2024

A Novel Newborn Screening Program for Sickle Cell Disease in Nigeria.

Aisha A Galadanci, Umma A Ibrahim, Yvonne Carroll, Yusuf D Jobbi, Zubaida L Farouk, Aisha Mukaddas, Nafiu Hussaini, Bilya Sani Musa, Lauren J Klein, Michael R DeBaun

Abstract read
In one paragraph

Article in International journal of neonatal screening, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
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

10 authors.

Aisha A GaladanciDepartment of Hematology, Bayero University/Aminu Kano Teaching Hospital, Kano 700233, Nigeria.
Umma A IbrahimDepartment of Pediatrics, Bayero University/Aminu Kano Teaching Hospital, Kano 700233, Nigeria.ORCID 0009-0005-0742-3123
Yvonne CarrollDepartment of Hematology, St Jude Children's Research Hospital, Memphis, TN 38105, USA.
Yusuf D JobbiDepartment of Hematology, Bayero University/Aminu Kano Teaching Hospital, Kano 700233, Nigeria.
Zubaida L FaroukDepartment of Pediatrics, Bayero University/Aminu Kano Teaching Hospital, Kano 700233, Nigeria.ORCID 0000-0003-3984-9354
Aisha MukaddasDepartment of Hematology, Bayero University/Aminu Kano Teaching Hospital, Kano 700233, Nigeria.
Nafiu HussainiDepartment of Mathematical Sciences, Bayero University Kano, Kano 700233, Nigeria.
Bilya Sani MusaDepartment of Administration, Aminu Kano Teaching Hospital, Kano 700233, Nigeria.ORCID 0000-0001-9780-5507
Lauren J KleinD. Brent Polk Division of Pediatric Gastroenterology, Department of Pediatrics, Hepatology, and Nutrition, Monroe Carell Jr. Children's Hospital at Vanderbilt, Nashville, TN 37232, USA.ORCID 0000-0003-1076-8518
Michael R DeBaunVanderbilt Institute for Global Health, Nashville, TN 37232, USA.ORCID 0000-0002-0574-1604

Funding

St. Jude Children's Research Hospital 181090010
6 · The paper itself

Abstract

Newborn screening for sickle cell disease (SCD) is sparse in sub-Saharan Africa. The leadership of the Aminu Kano Teaching Hospital (AKTH) in Kano, Nigeria, with the support of local religious authorities, established a groundbreaking SCD newborn screening program that has become the standard of care for pregnant women and their newborns. Our program includes (1) prenatal genetic counseling for all pregnant women in the antenatal clinic, (2) newborn screening, (3) postnatal genetic counseling for parents of newborns diagnosed with SCD and SCT, and (4) referral of newborns with SCD for follow-up in the SCD Comprehensive Care Clinic by 3 months of age. From September 2020 to December 2023, the team screened 7530 infants for SCD at the AKTH, identifying 126 (1.7%) infants with SCD and 1546 (20.5%) with SCT. Of these, 93 (73.8%) newborns with SCD received individualized genetic counseling, and 43 (46%) were referred to the SCD Comprehensive Care Clinic before 3 months. Group genetic counseling was provided to the parents of 778 (50.3%) of newborns identified with SCT. The SCD newborn screening at the AKTH is now standard care, indicating the viability of sustaining an SCD newborn screening program that provides pre- and postnatal genetic counseling and comprehensive SCD care within a low-income setting.

Indexed as

Africagenetic counselingnewborn screeningsickle cell disease

Identifiers

PMID39449355
PMCPMC11503303

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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.