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. Author manuscript; available in PMC: 2015 Jan 1.
Published in final edited form as: Matern Child Health J. 2014 Jan;18(1):316–325. doi: 10.1007/s10995-013-1236-7

Development of a Linked Perinatal Data Resource From State Administrative and Community-Based Program Data

Eric S Hall 1,, Neera K Goyal 2, Robert T Ammerman 3, Megan M Miller 4, David E Jones 5, Jodie A Short 6, Judith B Van Ginkel 7
PMCID: PMC3936676  NIHMSID: NIHMS554610  PMID: 23420307

Abstract

To demonstrate a generalizable approach for developing maternal-child health data resources using state administrative records and community-based program data. We used a probabilistic and deterministic linking strategy to join vital records, hospital discharge records, and home visiting data for a population-based cohort of at-risk, first time mothers enrolled in a regional home visiting program in Southwestern Ohio and Northern Kentucky from 2007 to 2010. Because data sources shared no universal identifier, common identifying elements were selected and evaluated for discriminating power. Vital records then served as a hub to which other records were linked. Variables were recoded into clinically significant categories and a cross-set of composite analytic variables was constructed. Finally, individual-level data were linked to corresponding area-level measures by census tract using the American Communities Survey. The final data set represented 2,330 maternal-infant pairs with both home visiting and vital records data. Of these, 56 pairs (2.4 %) did not link to either maternal or infant hospital discharge records. In a 10 % validation subset (n = 233), 100 % of the reviewed matches between home visiting data and vital records were true matches. Combining multiple data sources provided more comprehensive details of perinatal health service utilization and demographic, clinical, psychosocial, and behavioral characteristics than available from a single data source. Our approach offers a template for leveraging disparate sources of data to support a platform of research that evaluates the timeliness and reach of home visiting as well as its association with key maternal-child health outcomes.

Keywords: Home visiting, Early childhood development, Data linking

Background and Motivation

Perinatal data resources, including state vital records, hospital discharge data, and records from community-based programs like home visiting, each contain unique elements important for maternal-child health research, and yet these data sets lack interoperability. Previous models of linked databases, such as the Massachusetts’s Pregnancy to Early Life Longitudinal (PELL) system and other statewide efforts in California and Pennsylvania, utilize a linked maternal-child data core. Core elements originating from vital statistics and hospital discharge records are generated for the entire population and include maternal and child demographics, diagnoses, and outcomes. These elements may serve as a core for linkage to subsequent data sets representing subpopulations with local program data [14]. While such linkages have enabled maternal-child health research for a range of state-level outcomes, additional research is needed to further leverage information collected by community-based programs like home visiting.

While the effectiveness of home visiting has been demonstrated for many outcomes, including infant development and parenting, the impact on preterm birth is currently not well understood. The utility of a maternal-child data core derived from administrative records can be enhanced by capturing detailed measures of prenatal program use including gestational age at enrollment, intensity of participation, and content of visits. Such further conceptualization and measurement of home visiting may be particularly important for preterm birth, where factors such as nutrition and health behaviors may only be amenable to intervention if exposure begins early and is sustained at a sufficiently high intensity.

The current aim is to demonstrate a generalizable approach to supplement state administrative records with local program data through the development of a maternal-child health resource. This paper outlines the process of linking data from home visiting to statewide records (birth and death vital records, hospital discharge records) and area-based measures of health. Our rationale is that linked data will expand the potential for evaluating population-level outcomes, enabling more detailed, hypothesis-driven analyses of perinatal outcomes in a real world setting. Given recent investments in home visiting through the Maternal, Infant, and Early Childhood Home Visiting (MIECHV) program, [5] population-based, linked systems are particularly relevant for evaluating the impact and timeliness of home visiting services provided to at-risk families.

Methods

Study Design and Population

This retrospective, descriptive analysis includes a population of women enrolled in Every Child Succeeds (ECS), an established, regional home visiting program serving Greater Cincinnati who gave birth at an Ohio hospital in 2007–2010. Since its inception in 1999, ECS has conducted over 400,000 home visits with 17,000 families in Southwestern Ohio and Northern Kentucky. Eligible participants must be first-time mothers with at least 1 of 4 risk characteristics: unmarried, low income (<300 % of poverty level, receipt of medicaid, or reported financial concerns), <18 years of age, or suboptimal prenatal care. Participants enroll during pregnancy or before their child reaches 3 months of age. Home visits are provided by social workers, child development specialists, nurses, or para-professionals, beginning weekly or more-frequent and tapering to fewer visits as the child ages until 3 years of age. A web-based data entry system is used to bill and document service provision data; home visitors collect detailed information for each maternal-infant pair, including content and frequency of home visits, household demographics, and screening instruments including the home observation for measurement of the environment (HOME), Kempe Family Stress Inventory, and Ages and Stages Questionnaires [69]. Participants enrolled in ECS have consented to data use for the purposes of quality assurance, benchmarking, and research. This study has resulted from collaboration and partnership between stakeholders including care providers, public health agencies, and local home visiting programs which have established common aims and data sharing agreements. The study was reviewed and approved by the Ohio Department of Health (ODH) and Cincinnati Children’s Hospital Medical Center Institutional Review Boards.

A maternal-child health data resource was generated by linking individual home visiting records with statewide vital and Ohio Hospital Association (OHA) records and census tract data from the American Community Survey (ACS) using established linkage strategies [1012]. Contributions of each data set are listed in Table 1. The process included the following steps, further detailed below: (a) Source data were consistently formatted in preparation for linking; (b) Variables from each source were prescreened and evaluated for “discriminating power” to identify the set best supporting individual-level record linkage; (c) Individual-level data sources were linked using a probabilistic and deterministic approach; (d) Unresolved links were manually resolved; (e) Variables were recoded into clinically significant categories; (f) Individual-level records were linked to corresponding area-level measures; (g) A cross-set of composite analytic variables was constructed.

Table 1.

Data categories and elements included in the linked data resource by each contributing source data set

Vital records Hospital discharge Home visiting program American Community Surveya
Demographics X X X
Maternal substance use X X X
Household and parental assessments X
Maternal comorbidities X
Complications of pregnancy X X
Complications of labor and delivery X X
Maternal body mass index X
Infant gestational age X
Infant birth weight X
Infant congenital anomalies X X
Postnatal complications X X
Infant mortality X X
Hospital charges and length of stay X
Home visiting program utilization X
Area-based measures by census tract X
a

Available as five-year estimates through the U.S. Census Bureau

Data Preparation

Vital records obtained from the ODH represented 597,000 live births within Ohio during 2007–2010. Approximately 6.5 million hospital discharges were represented by the OHA data for the corresponding time period. Newborn infants were identified by limiting OHA records to those with a birth date matching the date of hospital admission. In addition to 611,345 newborn records, 620,929 records representing maternal hospitalizations corresponding to birth events were identified by restricting the OHA set to records listing delivery related Diagnosis Related Group (DRG) codes (370–384). We identified 3,902 women enrolled in ECS who gave birth in 2007–2010. Of those, 2,476 (63.4 %) listed an Ohio residence while 1,426 (36.5 %) listed a Kentucky residence. Because a considerable number of mothers from Northern Kentucky give birth in Ohio hospitals and receive an Ohio birth certificate, all women included in the home visiting database were eligible for linkage.

Records shared no universal identifier for linking; instead, common identifying elements were selected and formatted to facilitate linkage. Formatting of names, dates, and zip codes was standardized and insurance status, infant gender, delivery route, and preterm birth status were consistently encoded across data—relevant OHA DRG codes indicated delivery route (370–375) and preterm birth status (386–391).

Prescreening

Elements in each set were evaluated for discrimination power—a calculated score indicating usefulness in distinguishing between records. For example, unique medical record numbers enable perfect discrimination among records. Conversely, a variable for which all records share the same value (e.g. birth state within a single state’s vital records) cannot be used to discriminate between records. Discrimination power was calculated using the LINKS record linkage package, a SAS (SAS Institute Inc., Cary, NC, USA) macro developed at the University of Manitoba [13]. Table 2 presents the variable combinations used in linking various individual-level data sets to the vital record (which served as a linkage hub to which all other records were matched) sorted in order of variable discriminating power.

Table 2.

List of data elements used in linking the various individual-level data sets, sorted in order of variable discriminating power

Rank based on discriminating power Description of variable Data sets containing the linkage variable (in addition to vital records)
1 Mother’s date of birth Home visiting program, hospital discharge—maternal
2 Street number of residence Home visiting program
3 Mother’s last name Home visiting program
4 Infant’s last name Home visiting program
5 Mother’s maiden name Home visiting program
6 Street name of residence Home visiting program
7 Infant’s date of birth Home visiting program, hospital discharge—maternal, hospital discharge—infant
8 Mother’s first name Home visiting program
9 Zip code of residence Home visiting program, hospital discharge—maternal, hospital discharge—infant
10 Birth hospital Hospital discharge—maternal, hospital discharge—infant
11 County of residence Home visiting program
12 Insurance status Home visiting program, hospital discharge—maternal, hospital discharge—infant
13 Infant gender Home visiting program, hospital discharge—infant
14 Delivery route Hospital discharge—maternal
15 Preterm birth status Hospital discharge—infant

Individual Records

The LINKS tool implemented probabilistic and deterministic linkage by evaluating common data elements to calculate likelihood of matches. Upon execution, variables with the greatest discriminating power were required to agree (deterministic) while other common elements contributed to a match likelihood score (probabilistic). Record pairs were deemed matched when a likelihood score threshold was exceeded. For linkage between home visiting and vital records, either maternal or infant birth date values were required to agree between all matched pairs. For linkage between vital and OHA records, birth hospital was required to agree. Additionally, infant birth date on the vital record was required to agree with birth date on the matched OHA newborn record and required to fall between the dates of admission and discharge on the matched OHA maternal record. A set of records with medium-to-high likelihood scores falling below the match threshold was produced for manual review. Frequent causes for inconclusive matches were inconsistent name spelling, address disagreement, and transposed numbers within dates. Under manual review such discrepancies were easily reconciled and comprised less than 2 % of the final data set.

The final mother-centric perinatal data resource represented each woman with a linked ECS-vital record pair. For multiple gestation pregnancies a single home visiting record potentially linked to multiple vital records. In these cases, data from all mothers were retained, but only data from the firstborn infant were included in the final set. For validation, a 10 % random sample of linked records (generated using SAS) was subjected to manual expert review to determine accuracy of matches by examining agreement between identifying elements.

Hospital Discharge Data

Indicator variables for relevant co-morbidities, risk factors, and complications were derived from the OHA data using International Classification of Diseases, 9th Revision, Clinical Modification (ICD-9-CM) diagnosis and procedure codes; categorization was modeled from previous studies utilizing similar data [14, 15]. Each hospital record contained a primary diagnosis, up to 14 additional diagnoses, a primary procedure, and up to 8 additional procedures. “Appendix” lists codes used to categorize hospital discharge variables.

Area-Level Measures

Geocoding ECS addresses produced latitude–longitude coordinate pairs for each observation. We linked individual records to five-year data estimates from the 2010 American Community Survey (ACS) containing aggregate sociodemographic measures by area of residence at the census tract level [16]. Area-level measures were selected on the basis of theoretical relevance for a range of maternal-child health outcomes and on the basis of previous empirical research [17].

Results

The final data set represented 2,330 women with linked home visiting and vital record pairs. Basic demographics and enrolment timing are described in Table 3. Although birth certificates belonging to Ohio residents delivering out-of-state were unavailable for linkage; the final set contained 2,183 records listing an Ohio residence representing 88.2 % of the Ohio-based (ECS) population during the study period. For each of the 2,330 linked home visiting and vital record pairs, an attempt was made for linkage to two OHA records—one representing maternal hospitalization and one representing infant hospitalization. Of these linked pairs, 88.9 % were able to be linked to a maternal OHA discharge record; 85.9 %of the linked pairs were able to be linked to an infant OHA discharge record; 2.4 %were not linked to either OHA discharge record. In the 10 % validation subset (n = 233), 100 % of the reviewed matches between home visiting and vital records were determined to be true matches.

Table 3.

Demographic characteristics and enrollment timing of women with linked home visiting and vital records data

Among total population (N = 2,330) %
Ohio residence 2,183 93.7
Kentucky residence 147 6.3
Prenatal enrollment 1,128 48.4
 Enrolled during 1st trimester of pregnancy 134 5.8
 Enrolled during 2nd trimester of pregnancy 521 22.4
Maternal age (years)
 < 18 580 24.9
 18–25 1,493 64.1
 25–35 231 9.9
Maternal race
 African American 1,330 57.1
 White 928 39.8
Hispanic ethnicity 173 7.4
Unmarried 2,163 92.8
Maternal education
 < High school diploma or equivalent 1,066 45.8
 High school completion 638 27.4
 Some college 502 21.6
Medicaid or other public insurance 1,737 74.5
Enrolled in WIC 1,790 76.8

Analytic Variables

Table 4 presents final analytic variables as constructed through a combination of data derived from home visiting, vital records, and OHA data sets. The final linked set represented a broad range of measures including demographics, clinical and psychosocial indicators, behavioral risk factors, measures of home environment and program utilization, and birth outcomes.

Table 4.

Select variables, origin data sources, and percent missingness in the final combined data resource

Description of variable Data source Percent missing (%)
Birth weight Vital Statistics 0.26
Cervical abnormalities Hospital Discharge Data 0.00
Chorioamnionitis Vital Records
Hospital Discharge Data
0.00
Cleft lip or palate Vital Records
Hospital Discharge Data
0.00
Congenital cardiac anomaly Vital Records
Hospital Discharge Data
0.00
Congenital pulmonary anomaly Vital Records
Hospital Discharge Data
0.00
Congenital spinal anomaly Vital Records
Hospital Discharge Data
0.00
Maternal diabetes Vital Records
Hospital Discharge Data
0.00
Fetal Distress Vital Records
Hospital Discharge Data
0.00
Gestational age at birth Vital Records 0.05
Gestational age at enrollment Vital Records
Home Visiting Program
0.00
Home visiting agency Home Visiting Program 0.00
Home visit frequency Home Visiting Program 0.00
Home visiting referral source Home Visiting Program 0.00
Household income Home Visiting Program 15.46
Human immunodeficiency virus Hospital Discharge Data 0.00
Induction of labor Vital Records
Hospital Discharge Data
0.00
Infant age at death Hospital Discharge Data
Vital Records
0.00
Infant length of stay Hospital Discharge Data 14.27
Infant mechanical ventilation Vital Records
Hospital Discharge Data
0.00
Insurance type Vital Records
Hospital Discharge Data
0.31
Intrauterine growth retardation Hospital Discharge Data 0.00
Intraventricular hemorrhage Hospital Discharge Data 0.00
Living arrangement Home Visiting Program 8.12
Marital status Vital Records
Home Visiting Program
0.21
Maternal age Vital Records 0.00
Maternal body mass index Vital Records 7.96
Maternal contact with baby’s father Home Visiting Program 9.88
Maternal education Vital Records
Home Visiting Program
0.26
Maternal ethnicity Vital Records
Home Visiting Program
0.00
Maternal hypertension Vital Records
Hospital Discharge Data
0.00
Maternal hypothyroidism Hospital Discharge Data 0.00
Maternal race Vital Records
Home Visiting Program
0.00
Method of delivery Vital Records
Hospital Discharge Data
0.00
Multiple gestation pregnancy Vital Records 0.00
Necrotizing enterocolitis Hospital Discharge Data 0.00
NICU admission Vital Records 0.00
Oligohydramnios Hospital Discharge Data 0.00
Percent below poverty level, by census tracta American Community Survey 0.00
Placental disorders Hospital Discharge Data 0.00
Preeclampsia Hospital Discharge Data 0.00
Preterm labor Hospital Discharge Data 0.00
Previous fetal loss, stillbirth or neonatal death Vital Records
Hospital Discharge Data
0.00
Premature rupture of membranes Vital Records
Hospital Discharge Data
0.00
Retinopathy of prematurity Hospital Discharge Data 0.00
Sexually transmitted infections Vital Records
Hospital Discharge Data
0.00
Substance use—alcohol Home Visiting Program
Hospital Discharge Data
0.00
Substance use—cigarettes Home Visiting Program
Vital Records
Hospital Discharge Data
0.00
Substance use—other drugs Home Visiting Program
Hospital Discharge Data
0.00
Total infant hospital charges Hospital Discharge Data 15.05
Townsend index scorea,b American Community Survey 0.00

Clinical variables from hospital discharge and/or vital records data were constructed as binary indicator variables based on the presence of available data to confirm the diagnosis

a

Available as five-year estimates through the U.S. Census Bureau

b

The Townsend Index score is calculated as a sum of the standardized scores for four census tract-level variables: (1) percentage unemployed, (2) percentage of households without access to a car, (3) percentage of all households renting, and (4) percentage of households with crowded housing. Higher Townsend Index scores reflect higher levels of deprivation and social disadvantage

Discussion

Home visiting represents an early opportunity to improve pregnancy and child health outcomes through care coordination, education, and social support in at-risk populations [1820]. A particular focus for investment in home visiting through the MIECHV program is prenatal care management and risk reduction for preterm birth, which occurs with profound sociodemographic and geographic disparity [5, 21, 22]. Research focused on community-based prevention of preterm birth remains challenging due to the complexity of biological, cultural, and socioeconomic risk factors associated with this outcome [23]. Our study demonstrates how combining data obtained through home visiting with a core of data from vital and hospital discharge records provides a data platform supporting perinatal epidemiologic research. These methods can serve as a template for developing similar regional data resources as states and communities implement or expand home visiting.

Previous strategies linking vital records using sociodemographic variables have similarly found match rates above 80 % [24]. Other statewide linked resources have enabled investigations for a range of maternal-child outcomes [3, 4, 2527]. The PELL system, which uses the same LINKS tool utilized in the current study, has demonstrated the utility of linked maternal-child data in Early Intervention program evaluation [1, 2, 27]. The current study builds upon previously established capabilities by supplementing population-level data with maternal information obtained through home visiting and with area-based measures of health. This detailed data resource integrates previously disparate measures enabling innovative epidemiological research involving clinical, social, and community factors which contribute to adverse perinatal outcomes.

An example of the enhanced utility of this data resource is the ability to evaluate of the effect of engagement level, or treatment dosage, in prenatal home visiting. Specifically, we will test the hypothesis that preterm birth and birth weight are associated with both timing of prenatal enrollment by weeks of gestation and frequency of home visits, adjusting for maternal risk factors. This dataset will also enable inclusion of covariates such as the percent living below poverty level by census tract, an important area-level measure associated with health outcomes including preterm birth [28]. Further applications of area-level measures may include the use of an ecological framework to test the effect of community characteristics on program retention, level of engagement, and program effectiveness [29].

Limitations

Previous analyses have identified deficiencies in the completeness, accuracy, and content of research data containing administrative codes such as ICD-9-CM codes [30]. Limitations in the number of coded diagnoses and procedures may crowd out relevant codes among highly complicated patients or may be biased toward maximizing financial reimbursement [3134]. We attempted to mitigate the impact of undercoding by generating, whenever possible, composite variables from multiple sources. Future use of this data may require validation of measures like maternal complications and congenital anomalies using length of stay, procedures, and co-diagnoses to minimize misclassification. Previous vital record validation efforts have demonstrated that such data elements, when reported, are highly accurate and concordant with independently generated clinical data [3538]. As an example of preliminary validation in our dataset, of 108 maternal-infant pairs identified as having chorioamnionitis, over 75 % were associated with a co-diagnosis of maternal or infant infection, treatment with maternal antibiotics, labor induction in the setting of fetal distress, or prolonged hospitalization and neonatal intensive care use.

The final data set also reflects some limitations of source data. Although composite variables reduced the effects of missing source data, missingness was highest among variables originating from a single data set, including body mass index (7.96 %missing in vital records), household income(15.46 % missing in home visiting data), and infant length of stay (14.27 % missing based on hospital discharge data). Finally, an important consideration in development of community-based, locally-linked data is the limitation of population and program size that may impact generalizability.

Conclusions

Population-based, linked data systems are essential for evaluating the impact and reach of home visiting to at-risk families, a relevant topic given federal investments through MIECHV. The current study demonstrates a generalizable approach for integrating community-based program data with state data including vital and hospital discharge records to enable hypothesis-driven analysis pertinent to perinatal outcomes. Following this model, researchers elsewhere may develop similar resources that leverage available data and inform stakeholders as they tailor policies to local maternal-child populations.

Acknowledgments

Dr. Goyal was supported by the BIRCWH K12 program, co-funded by the Office of Research on Women’s Health and the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), Award Number 5K12HD051953-07. Dr. Ammerman was supported by Grant R01MH087499 from the National Institute of Mental Health. The content is solely the responsibility of the authors and does not represent the official views of the NICHD, the NIMH, or the NIH. The authors acknowledge support of the United Way of Greater Cincinnati, Kentucky H.A.N.D.S., and Ohio Help Me Grow, and technical assistance from Ted Folger.

Appendix

See Table 5.

Table 5.

International classification of diseases, 9th revision, clinical modification (ICD-9-CM) codes used to categorize hospital discharge diagnoses

Diagnosis ICD-9-CM codes
Cigarette use 649.01, V15.82
Alcohol use 305.00, 305.03
Marijuana use 305.20, 305.21, 305.23, 305.31
Other drugs of abuse 304.00, 305.50, 305.90, 304.71, 648.31, 304.01, 304.21, 305.60, 304.23, 305.61
Maternal mental health diagnosis 311.0, 300.4, 296.20, 296.50, 296.80, 296.90, 300.00, 300.11, 309.81, 313.81, 648.41, 648.42, V62.84, 307.51, 295.30, 295.90, 296.7, 295.32, 300.01
Previous poor birth outcome V23.49, V23.5
HIV V08
Sexually transmitted infection 647.11, 098.0, 098.15, 647.01, 054.9, 054.10, 054.19, 131.9, 614.9, 616.0, 131.01, 646.61, 647.21, 131.00, V08, 090.2, 090.9
Hypertension 401.9, 642.01, 642.31, 642.71, 642.91, 642.32, 642.21, 760
Obesity 278.00, 278.01, 649.11, V85.34, V85.37, V85.4, V85.36, V85.54, V85.32, V85.39
Hypothyroidism 244.1, 244.9, 648.11, 244.0, 244.8
Asthma 493.20, 493.90
Maternal transfusion 99.04, 99.07
Maternal cardiac complications 413, 414, 410.1, 410.2, 410.4, 421.0, 424.0, 426.0, 427.89, 648.61, 648.62, V12.53, V45.01, 426.7, 438.89, 412, 427.9
Maternal anemia 280.0, 280.9, 285.9, 648.21, 648.22, 282.41, 282.49
Maternal sickle cell disease 282.60, 282.63
Epilepsy 345.90, 649.41, 345.2
Disorders of placentation 656.71, 641.21, 641.01, 656.91
Cervical abnormalities 649.71, 654.51, 654.61
Uterine abnormalities 218.9, 615.0, 615.9, 617.9, 621.8, 654.01, 654.11, 654.41, 752.34, 654.12, 665.22, 752.2
Fetal malpresentation 652.21, 652.31, 652.61, 652.71, 652.81, 660.01, 652.91
Cephalopelvic disproportion or dystocia 653.01, 653.11, 653.41, 660.11, 660.21, 660.31, 660.41, 660.71, 660.81, 653.51
Cord abnormality 663.11, 663.21, 663.31, 663.41, 663.81, 663.01
Maternal hemorrhage or shock 285.1, 666.12, 666.22, 669.12, 669.21, 666.02, 669.22
Group B streptococcus carrier V02.51
Preeclampsia or eclampsia 642.41, 642.42, 642.51, 642.61
Preterm Labor 644.21
Oligohydramnios 658.01, 761.2
Intrauterine growth retardation 656.51, 764.93, 764.07, 764.08, 764.09
Maternal diabetes 250.00, 648.01, 648.81, 790.21, 249.00, 250.01, V58.67, 775
Induction of labor 73.01, 73.1, 73.4
Chorioamnionitis 658.41, 670.12, 670.02, 670.82, 762.7
Meconium stained amniotic fluid 770.12, 779.84, 770.11
Fetal distress 656.31, 659.71
Vacuum or forceps instrumentation 72, 72.1, 72.21, 72.4, 72.71, 72.79, 73.3, 72.29, 72.6, 72.9
Premature rupture of membranes 658.11, 658.21
Birth injury 767.2, 767.3, 767.6, 767.8
Congenital spinal anomaly 756.1, 756.19
Congenital pulmonary anomaly 748.4, 277, 748.69, 748.3
Congenital gastrointestinal anomaly 751.3, 751.69, 756.73, 756.79
Cleft palate or lip 749.04
Congenital renal condition 593.89, 753.15, 753.29, 753.3
Congenital cardiac anomaly 416.8, 423.9, 745.4, 745.5, 747, 746.89, 427.9, 745.11, 747.49, 747.83, 745.1, 747.3
Metabolic, genetic, or chromosomal disorders V29.3, 758, 759.81
Intraventricular hemorrhage 772.11, 772.14, 772.12
Necrotizing enterocolitis 777.5, 777.53
Neonatal infection 771.81, 041.04, 771.89, 322.9, 041.1, 041.19, 041.85, 482, V29.0, 041.01, 482.32, 770, 771.1, 771.82, 771.83, 008.45, 995.92
Retinopathy of prematurity 362.23, 362.2, 362.22

Contributor Information

Eric S. Hall, Email: eric.hall@cchmc.org, Perinatal Institute and Biomedical Informatics, Cincinnati Children’s Hospital, Cincinnati, OH, USA

Neera K. Goyal, Email: neera.goyal@cchmc.org, Perinatal Institute, Cincinnati Children’s Hospital, Cincinnati, OH, USA

Robert T. Ammerman, Email: robert.ammerman@cchmc.org, Every Child Succeeds, Cincinnati Children’s Hospital, Cincinnati, OH, USA

Megan M. Miller, Email: megan.miller_2@cchmc.org, Perinatal Institute, Cincinnati Children’s Hospital, Cincinnati, OH, USA

David E. Jones, Email: david.jones@cchmc.org, Biostatistics and Epidemiology, Cincinnati Children’s Hospital, Cincinnati, OH, USA

Jodie A. Short, Email: Jodie.Short@cchmc.org, Every Child Succeeds, Cincinnati Children’s Hospital, Cincinnati, OH, USA

Judith B. Van Ginkel, Email: judith.vanginkel@cchmc.org, Every Child Succeeds, Cincinnati Children’s Hospital, Cincinnati, OH, USA

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