Trisomy 18: disparities of care and outcomes in the State of Texas between 2009 and 2019.
| dc.contributor.author | Mizrahi, Michelle | |
| dc.contributor.author | Well, Andrew | |
| dc.contributor.author | Gottlieb, Erin A | |
| dc.contributor.author | Stewart, Eileen | |
| dc.contributor.author | Lucke, Ashley | |
| dc.contributor.author | Fraser, Charles D | |
| dc.contributor.author | Mery, Carlos M | |
| dc.contributor.author | Beckerman, Ziv | |
| dc.date.accessioned | 2023-06-01T13:31:22Z | |
| dc.date.available | 2023-06-01T13:31:22Z | |
| dc.date.issued | 2023-02 | |
| dc.date.updated | 2023-06-01T13:31:22Z | |
| dc.description.abstract | ObjectiveTo perform a statewide characteristics and outcomes analysis of the Trisomy 18 (T18) population and explore the potential impact of associated congenital heart disease (CHD) and congenital heart surgery.Study designRetrospective review of the Texas Hospital Inpatient Discharge Public Use Data File between 2009 and 2019, analysing discharges of patients with T18 identified using ICD-9/10 codes. Discharges were linked to analyse patients. Demographic characteristics and available outcomes were evaluated. The population was divided into groups for comparison: patients with no documentation of CHD (T18NoCHD), patients with CHD without congenital heart surgery (T18CHD), and patients who underwent congenital heart surgery (T18CHS).ResultsOne thousand one hundred fifty-six eligible patients were identified: 443 (38%) T18NoCHD, 669 (58%) T18CHD, and 44 (4%) T18CHS. T18CHS had a lower proportion of Hispanic patients (n = 9 (20.45%)) compared to T18CHD (n = 315 (47.09%)), and T18NoCHD (n = 219 (49.44%)) (p < 0.001 for both). Patients with Medicare/Medicaid insurance had a 0.42 odds ratio (95%CI: 0.20-0.86, p = 0.020) of undergoing congenital heart surgery compared to private insurance. T18CHS had a higher median total days in-hospital (47.5 [IQR: 12.25-113.25] vs. 9 [IQR: 3-24] and 2 [IQR: 1-5], p < 0.001); and a higher median number of admissions (n = 2 [IQR: 1-4]) vs. 1 [IQR: 1-2] and 1 [IQR: 1-1], (p < 0.001 for both). However, the post-operative median number of admissions for T18CHS was 0 [IQR: 0-2]. After the first month of life, T18CHS had freedom from in-hospital mortality similar to T18NoCHD and superior to T18CHD.ConclusionsShort-term outcomes for T18CHS patients are encouraging, suggesting a freedom from in-hospital mortality that resembles the T18NoCHD. The highlighted socio-economic differences between the groups warrant further investigation. Development of a prospective registry for T18 patients should be a priority for better understanding of longer-term outcomes. | |
| dc.identifier | S1047951123000215 | |
| dc.identifier.issn | 1047-9511 | |
| dc.identifier.issn | 1467-1107 | |
| dc.identifier.uri | ||
| dc.language | eng | |
| dc.publisher | Cambridge University Press (CUP) | |
| dc.relation.ispartof | Cardiology in the young | |
| dc.relation.isversionof | 10.1017/s1047951123000215 | |
| dc.subject | CHD | |
| dc.subject | Edwards syndrome | |
| dc.subject | Health equity | |
| dc.subject | congenital heart surgery | |
| dc.title | Trisomy 18: disparities of care and outcomes in the State of Texas between 2009 and 2019. | |
| dc.type | Journal article | |
| duke.contributor.orcid | Beckerman, Ziv|0000-0001-8401-3279 | |
| pubs.begin-page | 1 | |
| pubs.end-page | 6 | |
| pubs.organisational-group | Duke | |
| pubs.organisational-group | School of Medicine | |
| pubs.organisational-group | Clinical Science Departments | |
| pubs.organisational-group | Surgery | |
| pubs.organisational-group | Surgery, Cardiovascular and Thoracic Surgery | |
| pubs.publication-status | Published |
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