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Complete Versus Staged Repair for Neonates With Tetralogy of Fallot

Establishment and Validation of a Cohort of 2235 Patients Using Detailed Surgery Sequence Review of Health Care Administrative Data

Bibliographic Data

ID9102238
AuthorsJill J Savla (0000-0001-5639-9119, Children’s Hospital of Philadelphia, Division of Cardiology, corresponding author), Brian T Fisher (0000-0002-8224-4281, Children’s Hospital of Philadelphia, Division of Infectious Diseases), Jennifer A Faerber (Children's Hospital of Philadelphia), Jennifer Faerber (Children's Hospital of Philadelphia), Yuan-Shung V Huang (Children’s Hospital of Philadelphia, Center for Pediatric Clinical Effectiveness, Philadelphia, PA), Yuan‐Shung Huang (0000-0002-1942-6197, Children's Hospital of Philadelphia), Laura Mercer-Rosa (Children’s Hospital of Philadelphia, Division of Cardiology), Laura Mercer‐Rosa (Children's Hospital of Philadelphia, corresponding author)
Year2018
Volume56
Issue11
Pagese76-e82
Publication date2018-11-01
Peer ReviewedYes
Open AccessNo
TypeARTICLE
VenueMedical Care (JOURNAL)
Journal identifiersISSN: 0025-7079 • E-ISSN: 1537-1948
PublisherOvid Technologies (Wolters Kluwer Health) (PUBLISHER)
DOI10.1097/mlr.0000000000000846
PMID29240000
OpenAlexW2773754917
LanguageEN
References cited18

BACKGROUND: The surgical strategy for neonates with tetralogy of Fallot (TOF) consists of complete or staged repair. Assessing the comparative effectiveness of these approaches is facilitated by a large multicenter cohort. We propose a novel process for cohort assembly using the Pediatric Health Information System (PHIS), an administrative database that contains clinical and billing data for inpatient and emergency department stays from tertiary children's hospitals. METHODS: A 4-step process was used to identify neonates with TOF: (1) screen neonates in PHIS with International Classification of Diseases-9 (ICD-9) diagnosis or procedure codes for TOF; (2) include patients with TOF procedures before 30 days of age; (3) exclude patients with missing 2-year follow-up data; (4) analyze patients' 2-year surgery sequence patterns, exclude patients inconsistent with a treatment strategy for TOF, and designate patients as complete or staged repair. Manual chart review at 1 PHIS center was performed to validate this process. RESULTS: Between January 2004 and March 2015, 5862 patients were identified in step 1. Step 2 of cohort assembly excluded 3425 patients (58%); step 3 excluded 148 patients (3%); and step 4 excluded 54 patients (1%). The final cohort consisted of 2235 neonates with TOF from 45 hospitals. Manual chart review of 336 patients showed a positive predictive value for accurate PHIS identification of 44% after step 1 and 97% after step 4. CONCLUSIONS: This systematic cohort identification algorithm resulted in a high positive predictive value to appropriately categorize patients. This carefully assembled cohort offers a unique opportunity for future studies in neonatal TOF outcomes

Cohort · Cohort study · Diagnosis code · Heart disease · Population · Retrospective cohort study · Tetralogy of Fallot · Congenital Diaphragmatic Hernia Studies · Congenital Heart Disease Studies · Internal Medicine · Medicine · Surgery · Tracheal and airway disorders · Pediatrics

  • Establishment of an 11-Year Cohort of 8733 Pediatric Patients Hospitalized at United States Free-standing Children’s Hospitals With De Novo Acute Lymphoblastic Leukemia From Health Care Administrative Data

    Brian T Fisher, Tracey Harris et al.•Medical Care•2014

Citation velocityhistorical
Highly citedNo

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