3.8 Article

Pulmonary hypertension in late onset neonatal sepsis using functional echocardiography: a prospective study

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JOURNAL OF ULTRASOUND
卷 25, 期 2, 页码 233-239

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SPRINGER INT PUBL AG
DOI: 10.1007/s40477-021-00590-y

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Functional echocardiography; Neonatal sepsis; Pulmonary hypertension

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Pulmonary hypertension is associated with significant morbidity and mortality in newborns. Sepsis has been identified as an independent risk factor for pulmonary hypertension. This study found that nearly half of neonates with late onset sepsis had pulmonary hypertension.
Purpose Pulmonary hypertension (PH) in the newborn period is associated with significant morbidity and mortality. Sepsis has been identified as an independent risk factor for PH in newborns. Data on the proportion and severity of PH in association with neonatal sepsis are scarce. This study was aimed to measure the pulmonary artery systolic pressure (PASP) in neonates with late onset sepsis (LOS) and to estimate the proportion of PH in neonatal sepsis using functional echocardiography (FnECHO). Methods This prospective observational study was conducted at a tertiary neonatal intensive care unit (NICU). All neonates admitted in the NICU with suspected LOS underwent FnECHO within 6 hours of onset of clinical signs and PASP was recorded. Pulmonary hypertension was defined as PASP of > 35 mmHg. PASP of neonates with positive culture results (proven LOS) was compared with that of gestational age-matched stable controls without sepsis. Results Thirty three neonates with proven LOS were analysed (study group). Sixteen neonates (49%) in the study group had PH. Mean PASP of the study group was significantly higher than that of the control group (35.3 +/- 10.13 mmHg and 12.58 +/- 3.92 mmHg, respectively; P < 0.0001). None of the neonates in the control group had PH. Conclusion Pulmonary artery pressure was higher in neonates with late onset neonatal sepsis as compared to that of stable babies without sepsis. Pulmonary hypertension was seen in nearly half of term as well as preterm neonates with late onset sepsis.

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