Evidence map›Paper›PMID 38972510›Full record

ArticleTransplantation and cellular therapy2024

Reproductive Health Assessment and Reports of Fertility Counseling in Pediatric and Adolescent Patients with Sickle Cell Disease After Hematopoietic Cell Transplantation.

Sobenna A George, Anirudh Veludhandi, Yijin Xiang, Katie Liu, Elizabeth Stenger, Staci D Arnold, Akanksha Mehta, David A Schirmer, Jessica B Spencer, Gregory M T Guilcher and 5 more

Abstract read
In one paragraph

Article in Transplantation and cellular therapy, 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. Trial
  2. Article
  3. Article
  4. Review
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

15 authors.

Sobenna A GeorgeDepartment of Pediatrics, Division of Endocrinology, Emory+ Children's Pediatric Institute, Atlanta, Georgia. Electronic address: sgeorg4@emory.edu.
Anirudh VeludhandiAflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta, Atlanta, Georgia.
Yijin XiangDepartment of Pediatrics, Pediatrics Biostatistics Core, Children's Healthcare of Atlanta, Emory University, Atlanta, Georgia.
Katie LiuDepartment of Pediatrics, Pediatrics Biostatistics Core, Children's Healthcare of Atlanta, Emory University, Atlanta, Georgia.
Elizabeth StengerAflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta, Atlanta, Georgia.
Staci D ArnoldAflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta, Atlanta, Georgia.
Akanksha MehtaDepartment of Urology, Emory University School of Medicine, Atlanta, Georgia.
David A SchirmerDepartment of Gynecology and Obstetrics, Division of Reproductive Endocrinology & Infertility, Emory University School of Medicine, Atlanta, Georgia.
Jessica B SpencerDepartment of Gynecology and Obstetrics, Division of Reproductive Endocrinology & Infertility, Emory University School of Medicine, Atlanta, Georgia.
Gregory M T GuilcherDepartment of Oncology and Pediatrics, Section of Oncology/Cellular Therapy, Alberta Children's Hospital, University of Calgary, Calgary, Alberta, Canada.
Monica BhatiaPediatric Stem Cell Transplant, Irving Medical Center, Columbia University, New York, New York.
Allistair AbrahamCenter for Cancer and Immunology Research, Children's National Hospital, George Washington University School of Medicine and Health Sciences, Washington, District of Columbia.
Veronica Gomez-LoboPediatric and Adolescent Gynecology, NICHD, Bethesda, Maryland.
Lakshmanan KrishnamurtiSection of Pediatric Hematology/Oncology/BMT, Yale School of Medicine, New Haven, Connecticut.
Lillian R MeachamDepartment of Pediatrics, Division of Endocrinology, Emory+ Children's Pediatric Institute, Atlanta, Georgia; Department of Pediatrics, Division of Hematology Oncology and BMT, Emory + Children's Pediatric Institute, Atlanta, Georgia.

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
Pediatric and Adolescent Gynecology Training ProgramZIEHD008985 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI GOMEZ-LOBO, VERONICA · 2022 to 2025
$9.3M
Pediatric and Adolescent Gynecology Training ProgramZIAHD008985 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI GOMEZ-LOBO, VERONICA · 2019 to 2021
$5.3M
Ovarian tissue for fertility preservation-which will involve 2 IRB approved protocols: 000106 and 000715ZIAHD009005 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI GOMEZ-LOBO, VERONICA · 2022 to 2025
$2.4M
Long-term health-related quality of life and cost of allogeneic hematopoietic cell transplantation for children with sickle cell diseaseK23HL143164 · NHLBI · EMORY UNIVERSITY · PI ARNOLD, STACI D. · 2018 to 2022
$837k
Sickle Cell post Transplantation Long Term and Late Effects Registry ( STELLAR)OT2HL152762 · NHLBI · EMORY UNIVERSITY · PI KRISHNAMURTI, LAKSHMANAN · 2019 to 2019
$750k
Intramural NIH HHS ZIA HD008985Intramural NIH HHS ZIA HD009005NCATS NIH HHS UL1 TR001863NHLBI NIH HHS K23 HL143164NHLBI NIH HHS OT2 HL152762
6 · The paper itself

Abstract

Conditioning regimens for hematopoietic cell transplant (HCT) in patients with sickle cell disease (SCD) place patients at risk for reproductive health issues. The purpose of this study was to assess reproductive health and reports of fertility counseling in patients with SCD who received a transplant. This was a secondary analysis of gonadal hormone production, future infertility risk assessment, and parent-proxy/patient reports of fertility counseling in SCD transplant recipients who are currently pubertal and were enrolled in the Atlanta sites of the Sickle Cell Transplant Evaluation of Long-term and Late Effects Registry (STELLAR) between May 2017 and October 2023. Clinical information was abstracted from medical records and reproductive health survey data from the STELLAR database. Descriptive statistics were reported as median (interquartile range [IQR]) or percentages. There were 20 females and 12 males in the study population. Females were median (IQR) 19.6 (9.4) years old and males 20.8 (11.4) years old at the time of the study. Transplants most commonly occurred in the decade 2010 to 2019 at 10.7 (4.8) years old for females and 11.1 (4.1) years old for males. Most participants received bone marrow stem cells (95.0% females, 100.0% males) from matched sibling donors (90.0% females, 100.0% males). Participants received one of seven HCT conditioning regimens with cyclophosphamide equivalent doses ranging from 3388 to 9706 mg/m

Indexed as

Anemia, Sickle CellCounselingFertilityHematopoietic Stem Cell TransplantationReproductive HealthAdolescentAdultChildFemaleHumansMaleTransplantation ConditioningYoung AdultFertility counselingInfertility riskOvarian damageSickle cell diseaseTesticular damageTransplant

Identifiers

PMID38972510
PMCPMC11344653

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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.