Optimizing the AKI definition during first postnatal week using Assessment of Worldwide Acute Kidney Injury Epidemiology in Neonates (AWAKEN) cohort.


Journal

Pediatric research
ISSN: 1530-0447
Titre abrégé: Pediatr Res
Pays: United States
ID NLM: 0100714

Informations de publication

Date de publication:
02 2019
Historique:
received: 28 06 2018
accepted: 24 11 2018
revised: 06 11 2018
pubmed: 16 1 2019
medline: 9 6 2020
entrez: 16 1 2019
Statut: ppublish

Résumé

Neonates with serum creatinine (SCr) rise ≥0.3 mg/dL and/or ≥50% SCr rise are more likely to die, even when controlling for confounders. These thresholds have not been tested in newborns. We hypothesized that different gestational age (GA) groups require different SCr thresholds. Neonates in Assessment of Worldwide Acute Kidney Epidemiology in Neonates (AWAKEN) with ≥1 SCr on postnatal days 1-2 and ≥1 SCr on postnatal days 3-8 were assessed. We compared the mortality predictability of SCr absolute (≥0.3 mg/dL) vs percent (≥50%) rise. Next, we determine usefulness of combining absolute with percent rise. Finally, we determined the optimal absolute, percent, and maximum SCr thresholds that provide the highest mortality area under curve (AUC) and specificity for different GA groups. The ≥0.3 mg/dL rise outperformed ≥50% SCr rise. Addition of percent rise did not improve mortality predictability. The optimal SCr thresholds to predict AUC and specificity were ≥0.3 and ≥0.6 mg/dL for ≤29 weeks GA, and ≥0.1 and ≥0.3 mg/dL for >29 week GA. The maximum SCr value provides great specificity. Unique SCr rise cutoffs for different GA improves outcome prediction. Percent SCr rise does not add value to the neonatal AKI definition.

Sections du résumé

BACKGROUND
Neonates with serum creatinine (SCr) rise ≥0.3 mg/dL and/or ≥50% SCr rise are more likely to die, even when controlling for confounders. These thresholds have not been tested in newborns. We hypothesized that different gestational age (GA) groups require different SCr thresholds.
METHODS
Neonates in Assessment of Worldwide Acute Kidney Epidemiology in Neonates (AWAKEN) with ≥1 SCr on postnatal days 1-2 and ≥1 SCr on postnatal days 3-8 were assessed. We compared the mortality predictability of SCr absolute (≥0.3 mg/dL) vs percent (≥50%) rise. Next, we determine usefulness of combining absolute with percent rise. Finally, we determined the optimal absolute, percent, and maximum SCr thresholds that provide the highest mortality area under curve (AUC) and specificity for different GA groups.
RESULTS
The ≥0.3 mg/dL rise outperformed ≥50% SCr rise. Addition of percent rise did not improve mortality predictability. The optimal SCr thresholds to predict AUC and specificity were ≥0.3 and ≥0.6 mg/dL for ≤29 weeks GA, and ≥0.1 and ≥0.3 mg/dL for >29 week GA. The maximum SCr value provides great specificity.
CONCLUSION
Unique SCr rise cutoffs for different GA improves outcome prediction. Percent SCr rise does not add value to the neonatal AKI definition.

Identifiants

pubmed: 30643188
doi: 10.1038/s41390-018-0249-8
pii: 10.1038/s41390-018-0249-8
pmc: PMC6377843
mid: NIHMS1515823
doi:

Substances chimiques

Biomarkers 0
Creatinine AYI8EX34EU

Types de publication

Journal Article Observational Study Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

329-338

Subventions

Organisme : NCATS NIH HHS
ID : UL1 TR003096
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR001449
Pays : United States
Organisme : NCATS NIH HHS
ID : U54 TR001356
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR001417
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK103608
Pays : United States
Organisme : FDA HHS
ID : R01 FD005092
Pays : United States
Organisme : NCRR NIH HHS
ID : KL2 RR025776
Pays : United States

Investigateurs

David T Selewski (DT)
Subrata Sarkar (S)
Alison Kent (A)
Jeffery Fletcher (J)
Shahnaz Duara (S)
Jennifer R Charlton (JR)
Jonathan R Swanson (JR)
Ronnie Guillet (R)
Carl D'Angio (C)
Ayesa Mian (A)
Deepak Kumar (D)
Jennifer G Jetton (JG)
Patrick D Brophy (PD)
Tarah T Colaizy (TT)
Jonathan M Klein (JM)
Ayse Akcan Arikan (AA)
Christopher J Rhee (CJ)
Stuart L Goldstein (SL)
Amy T Nathan (AT)
Juan C Kupferman (JC)
Alok Bhutada (A)
Shantanu Rastogi (S)
Elizabeth Bonachea (E)
John Mahan (J)
Alexandra Smith (A)
Mamta Fuloria (M)
Kimberly Reidy (K)
Frederick J Kaskel (FJ)
Danielle E Soranno (DE)
Jason Gien (J)
Katja M Gist (KM)
Aftab S Chishti (AS)
Mina H Hanna (MH)
Sangeeta Hingorani (S)
Michelle Starr (M)
Sunny Juul (S)
Craig S Wong (CS)
Catherine Joseph (C)
Tara DuPont (T)
Robin Ohls (R)
Amy Staples (A)
Surender Khokhar (S)
Mary Revenis (M)
Sidharth K Sethi (SK)
Smriri Rohatgi (S)
Cherry Mammen (C)
Anne Synnes (A)
Sanjay Wazir (S)
Pia Wintermark (P)
Robert Woroniecki (R)
Shanty Sridhar (S)
Susan Ingraham (S)
Arwa Nada (A)

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Auteurs

David Askenazi (D)

Children's of Alabama, University of Alabama at Birmingham, Birmingham, AL, USA. daskenazi@peds.uab.edu.

Carolyn Abitbol (C)

Holtz Children's Hospital, University of Miami, Miami, FL, USA.

Louis Boohaker (L)

Children's of Alabama, University of Alabama at Birmingham, Birmingham, AL, USA.

Russell Griffin (R)

University of Alabama at Birmingham, Birmingham, AL, USA.

Rupesh Raina (R)

MetroHealth Medical Center, Case Western Reserve University, Cleveland, OH, USA.

Joshua Dower (J)

Tufts Medical Center, Tufts University School of Medicine, Boston, MA, USA.

T Keefe Davis (TK)

Washington University, St. Louis, MO, USA.

Patricio E Ray (PE)

Children's National Medical Center, George Washington University School of Medicine and the Health Sciences, Washington, DC, USA.

Sofia Perazzo (S)

Children's National Medical Center, George Washington University School of Medicine and the Health Sciences, Washington, DC, USA.

Marissa DeFreitas (M)

Holtz Children's Hospital, University of Miami, Miami, FL, USA.

Lawrence Milner (L)

Tufts Medical Center, Tufts University School of Medicine, Boston, MA, USA.

Namasivayam Ambalavanan (N)

Children's of Alabama, University of Alabama at Birmingham, Birmingham, AL, USA.

F Sessions Cole (FS)

Washington University, St. Louis, MO, USA.

Erin Rademacher (E)

Golisano Children's Hospital, University of Rochester, Rochester, NY, USA.

Michael Zappitelli (M)

Toronto Hospital for Sick Children, University of Toronto, Toronto, Canada.

Maroun Mhanna (M)

MetroHealth Medical Center, Case Western Reserve University, Cleveland, OH, USA.

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