TY - JOUR
T1 - Demographics, clinical characteristics and outcomes of neonates diagnosed with fetomaternal haemorrhage
AU - Stroustrup, Annemarie
AU - Trasande, Leonardo
PY - 2012/11
Y1 - 2012/11
N2 - Objective: To determine clinical characteristics, demographics and short-term outcomes of neonates diagnosed with fetomaternal haemorrhage (FMH). Design: The authors analysed the Nationwide Inpatient Sample, 1993 to 2008. Singleton births diagnosed with FMH were identifi ed by International Classifi cation of Diseases (ICD-9) code 762.3. Descriptive, univariate and multivariable regression analyses were performed to determine the national annual incidence of FMH over time as well as demographics and clinical characteristics of neonates with FMH. Results: FMH was identifi ed in 12 116 singleton births. Newborns with FMH required high intensity of care: 26.3% received mechanical ventilation, 22.4% received blood product transfusion and 27.8% underwent central line placement. Preterm birth (OR 3.7), placental abruption (OR 9.8) and umbilical cord anomaly (OR 11.4) were risk factors for FMH. Higher patient income was associated with increased likelihood of FMH diagnosis (OR 1.2), and Whites were more likely to be diagnosed than ethnic minorities (OR 1.9). There was reduced frequency of diagnosis in the Southern USA (OR 0.8 vs the Northeastern USA). Conclusions: Diagnosis of FMH is associated with signifi cant morbidity as well as regional, socioeconomic and racial disparity. Further study is needed to distinguish between diagnostic coding bias and true epidemiology of the disease. This is the fi rst report of socioeconomic and racial/ethnic disparities in FMH, which may represent disparities in detection that require national attention.
AB - Objective: To determine clinical characteristics, demographics and short-term outcomes of neonates diagnosed with fetomaternal haemorrhage (FMH). Design: The authors analysed the Nationwide Inpatient Sample, 1993 to 2008. Singleton births diagnosed with FMH were identifi ed by International Classifi cation of Diseases (ICD-9) code 762.3. Descriptive, univariate and multivariable regression analyses were performed to determine the national annual incidence of FMH over time as well as demographics and clinical characteristics of neonates with FMH. Results: FMH was identifi ed in 12 116 singleton births. Newborns with FMH required high intensity of care: 26.3% received mechanical ventilation, 22.4% received blood product transfusion and 27.8% underwent central line placement. Preterm birth (OR 3.7), placental abruption (OR 9.8) and umbilical cord anomaly (OR 11.4) were risk factors for FMH. Higher patient income was associated with increased likelihood of FMH diagnosis (OR 1.2), and Whites were more likely to be diagnosed than ethnic minorities (OR 1.9). There was reduced frequency of diagnosis in the Southern USA (OR 0.8 vs the Northeastern USA). Conclusions: Diagnosis of FMH is associated with signifi cant morbidity as well as regional, socioeconomic and racial disparity. Further study is needed to distinguish between diagnostic coding bias and true epidemiology of the disease. This is the fi rst report of socioeconomic and racial/ethnic disparities in FMH, which may represent disparities in detection that require national attention.
UR - https://www.scopus.com/pages/publications/84868199482
U2 - 10.1136/archdischild-2011-300820
DO - 10.1136/archdischild-2011-300820
M3 - Article
C2 - 22375020
AN - SCOPUS:84868199482
SN - 1359-2998
VL - 97
SP - F405-F410
JO - Archives of Disease in Childhood: Fetal and Neonatal Edition
JF - Archives of Disease in Childhood: Fetal and Neonatal Edition
IS - 6
ER -