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Infections in Infants with SCID: Isolation, Infection Screening, and Prophylaxis in PIDTC Centers.
Dorsey, Morna J; Wright, Nicola A M; Chaimowitz, Natalia S; Dávila Saldaña, Blachy J; Miller, Holly; Keller, Michael D; Thakar, Monica S; Shah, Ami J; Abu-Arja, Rolla; Andolina, Jeffrey; Aquino, Victor; Barnum, J L; Bednarski, Jeffrey J; Bhatia, Monica; Bonilla, Francisco A; Butte, Manish J; Bunin, Nancy J; Chandra, Sharat; Chaudhury, Sonali; Chen, Karin; Chong, Hey; Cuvelier, Geoffrey D E; Dalal, Jignesh; DeFelice, Magee L; DeSantes, Kenneth B; Forbes, Lisa R; Gillio, Alfred; Goldman, Fred; Joshi, Avni Y; Kapoor, Neena; Knutsen, Alan P; Kobrynski, Lisa; Lieberman, Jay A; Leiding, Jennifer W; Oshrine, Benjamin; Patel, Kiran P; Prockop, Susan; Quigg, Troy C; Quinones, Ralph; Schultz, Kirk R; Seroogy, Christine; Shyr, David; Siegel, Subhadra; Smith, Angela R; Torgerson, Troy R; Vander Lugt, Mark T; Yu, Lolie C; Cowan, Morton J; Buckley, Rebecca H; Dvorak, Christopher C.
Afiliação
  • Dorsey MJ; Division of Pediatric Allergy, Immunology, & Bone Marrow Transplant, Benioff Children's Hospital, University of California San Francisco, San Francisco, CA, USA.
  • Wright NAM; Division of Hematology/Immunology, Department of Pediatrics, Alberta Children's Hospital, University of Calgary, Calgary, AB, Canada.
  • Chaimowitz NS; Section of Immunology, Allergy and Retrovirology, Department of Pediatrics, William T. Shearer Center for Human Immunobiology, Texas Children's Hospital, Baylor College of Medicine, Houston, TX, USA.
  • Dávila Saldaña BJ; Division of Blood and Marrow Transplantation, Children's National Medical Center, Washington, DC, USA.
  • Miller H; Department of Pediatrics, George Washington University, Washington, DC, USA.
  • Keller MD; Center for Cancer and Blood Disorders, Phoenix Children's Hospital, Phoenix, AZ, USA.
  • Thakar MS; Division of Allergy & Immunology, Children's National Health System, and Division of Pediatrics, George Washington University, Washington, DC, USA.
  • Shah AJ; Fred Hutchinson Cancer Research Center, University of Washington, Seattle, WA, USA.
  • Abu-Arja R; Division of Stem Cell Transplantation and Regenerative Medicine, Lucille Packard Children's Hospital, Stanford School of Medicine, Stanford, CA, USA.
  • Andolina J; Nationwide Children's Hospital, Columbus, OH, USA.
  • Aquino V; Department of Pediatrics, Golisano Children's Hospital, University of Rochester Medical Center, Rochester, NY, USA.
  • Barnum JL; University of Texas, Southwestern, Dallas, TX, USA.
  • Bednarski JJ; UPMC Children's Hospital of Pittsburgh, Pittsburgh, PA, USA.
  • Bhatia M; Department of Pediatrics, Washington University in St. Louis School of Medicine, St. Louis, MO, USA.
  • Bonilla FA; Pediatric Stem Cell Transplant Columbia, University Irving Medical Center, New York, NY, USA.
  • Butte MJ; Northeast Allergy, Asthma & Immunology (private practice), Leominster, MA, USA.
  • Bunin NJ; Division of Immunology, Allergy, and Rheumatology, Department of Pediatrics, University of California Los Angeles, Los Angeles, CA, USA.
  • Chandra S; Cellular Therapy and Transplant Section, Division of Oncology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Chaudhury S; Division of Bone Marrow Transplantation and Immune Deficiency, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
  • Chen K; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, USA.
  • Chong H; Division of Pediatric Hematology, Oncology, Stem Cell Transplantation, Ann & Robert H Lurie Children's Hospital of Chicago, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
  • Cuvelier GDE; Division of Allergy and Immunology, Department of Pediatrics, University of Utah School of Medicine, Salt Lake City, UT, USA.
  • Dalal J; UPMC Children's Hospital of Pittsburgh, Pittsburgh, PA, USA.
  • DeFelice ML; Pediatric Blood and Marrow Transplant Program, CancerCare Manitoba, Department of Pediatrics and Child Health, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, MB, Canada.
  • DeSantes KB; Pediatric Bone Marrow Transplant, Rainbow Babies and Children's Hospital, Cleveland, OH, USA.
  • Forbes LR; Division of Allergy and Immunology, Nemours/AI duPont Hospital for Children, Wilmington, DE, USA.
  • Gillio A; Division of Hematology, Oncology and Bone Marrow Transplant, Department of Pediatrics, University of Wisconsin School of Medicine, Madison, WI, USA.
  • Goldman F; William T Shearer Center for Human Immunobiology, Texas Children's Hospital, Baylor College of Medicine, Houston, TX, USA.
  • Joshi AY; Joseph M Sanzari's Childrens Hospital, Hackensack University Medical Center, Hackensack, NJ, USA.
  • Kapoor N; Department of Pediatrics, Division of Hematology Oncology, University of Alabama at Birmingham, Birmingham, AL, USA.
  • Knutsen AP; Pediatric and Adult Allergy/Immunology, Mayo Clinic, Rochester, MN, USA.
  • Kobrynski L; Section of Transplantation and Cellular Therapy, Children's Hospital Los Angeles Cancer and Blood Diseases Institute, USC Keck School of Medicine, Los Angeles, CA, USA.
  • Lieberman JA; Pediatric Allergy and Immunology, Cardinal Glennon Children's Hospital, St. Louis, MO, USA.
  • Leiding JW; Children's Healthcare of Atlanta, Emory University Department of Pediatrics, Allergy and Immunology, Atlanta, GA, USA.
  • Oshrine B; Department of Pediatrics, The University of Tennessee Health Science Center, Memphis, TN, USA.
  • Patel KP; Division of Allergy and Immunology, Department of Pediatrics, University of South Florida, St. Petersburg, FL, USA.
  • Prockop S; Johns Hopkins All Children's Hospital, Cancer and Blood Disorders Institute, St. Petersburg, FL, USA.
  • Quigg TC; Johns Hopkins All Children's Hospital, Cancer and Blood Disorders Institute, St. Petersburg, FL, USA.
  • Quinones R; Children's Healthcare of Atlanta, Atlanta, GA, USA.
  • Schultz KR; Department of Pediatrics, Bone Marrow Transplant Service, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Seroogy C; Pediatric Blood and Marrow Transplantation Program, Methodist Children's Hospital, San Antonio, TX, USA.
  • Shyr D; Pediatric Hematology, Oncology and Bone Marrow Transplant, Children's Hospital Colorado, Aurora, CO, USA.
  • Siegel S; Michael Cuccione Childhood Cancer Research Program, BC Children's Hospital and Research Institute, Vancouver, British Columbia, Canada.
  • Smith AR; University of Wisconsin School of Medicine and Public Health, Madison, WI, USA.
  • Torgerson TR; Division of Pediatric Hematology/Oncology, Department of Pediatrics, University of Utah School of Medicine, Primary Children's Hospital, Salt Lake City, UT, USA.
  • Vander Lugt MT; Division of Stem Cell Transplant, Department of Pediatrics, Stanford Medicine, Lucile Packard Children's Hospital, Palo Alto, CA, USA.
  • Yu LC; Division of Pediatric Pulmonology, Allergy and Immunology and Sleep Medicine, Westchester Medical Center, Valhalla, NY, USA.
  • Cowan MJ; Pediatric Blood and Marrow Transplantation, University of Minnesota, Minneapolis, MN, USA.
  • Buckley RH; Fred Hutchinson Cancer Research Center, University of Washington, Seattle, WA, USA.
  • Dvorak CC; Blood and Marrow Transplant Program, University of Michigan, Ann Arbor, MI, USA.
J Clin Immunol ; 41(1): 38-50, 2021 01.
Article em En | MEDLINE | ID: mdl-33006109
ABSTRACT

PURPOSE:

The Primary Immune Deficiency Treatment Consortium (PIDTC) enrolled children with severe combined immunodeficiency (SCID) in a prospective natural history study of hematopoietic stem cell transplant (HSCT) outcomes over the last decade. Despite newborn screening (NBS) for SCID, infections occurred prior to HSCT. This study's objectives were to define the types and timing of infection prior to HSCT in patients diagnosed via NBS or by family history (FH) and to understand the breadth of strategies employed at PIDTC centers for infection prevention.

METHODS:

We analyzed retrospective data on infections and pre-transplant management in patients with SCID diagnosed by NBS and/or FH and treated with HSCT between 2010 and 2014. PIDTC centers were surveyed in 2018 to understand their practices and protocols for pre-HSCT management.

RESULTS:

Infections were more common in patients diagnosed via NBS (55%) versus those diagnosed via FH (19%) (p = 0.012). Outpatient versus inpatient management did not impact infections (47% vs 35%, respectively; p = 0.423). There was no consensus among PIDTC survey respondents as to the best setting (inpatient vs outpatient) for pre-HSCT management. While isolation practices varied, immunoglobulin replacement and antimicrobial prophylaxis were more uniformly implemented.

CONCLUSION:

Infants with SCID diagnosed due to FH had lower rates of infection and proceeded to HSCT more quickly than did those diagnosed via NBS. Pre-HSCT management practices were highly variable between centers, although uses of prophylaxis and immunoglobulin support were more consistent. This study demonstrates a critical need for development of evidence-based guidelines for the pre-HSCT management of infants with SCID following an abnormal NBS. TRIAL REGISTRATION NCT01186913.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Imunodeficiência Combinada Severa / Controle de Infecções / Infecções Tipo de estudo: Diagnostic_studies / Guideline / Prognostic_studies / Qualitative_research / Screening_studies Limite: Female / Humans / Infant / Male / Newborn Idioma: En Revista: J Clin Immunol Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Imunodeficiência Combinada Severa / Controle de Infecções / Infecções Tipo de estudo: Diagnostic_studies / Guideline / Prognostic_studies / Qualitative_research / Screening_studies Limite: Female / Humans / Infant / Male / Newborn Idioma: En Revista: J Clin Immunol Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos