Why the study?
Can serial NT-proBNP monitoring guide the management of pulmonary arterial hypertension in a preterm infant with chronic lung disease?
Can serial NT-proBNP monitoring guide the management of pulmonary arterial hypertension in a preterm infant with chronic lung disease?
Serial NT-proBNP monitoring may serve as a useful surrogate marker to guide therapy and predict prognosis in infants with PAH associated with CLD.
Serial NT-proBNP trends in infant CLD-PAH are described; leaves open validation before guiding therapy.
We measured the serial changes in N-terminal probrain natriuretic peptide (NT-proBNP) levels in a 6-month-old male infant with chronic lung disease (CLD) complicated by pulmonary arterial hypertension (PAH). The patient was born at the 24th week of gestation weighing 695 g. At 1 month after birth, an echocardiogram confirmed the diagnosis of CLD with PAH. He was treated with inhaled nitric oxide (iNO) and oral sildenafil and discharged from the hospital. At 190 days of age, the patient was readmitted to our department because of a viral upper respiratory infection. At 195 days of age, his respiratory condition worsened with pulmonary edema and his NT-proBNP level was determined to be 10,117 pg/mL. The patient was immediately administered iNO, and his respiratory condition improved, and NT-proBNP levels decreased. However, he experienced repeated severe cyanosis attacks. Before the attacks, his NT-proBNP level was > 1,000 pg/mL. Therefore, we continuously administered iNO until his NT-proBNP level decreased to < 1,000 pg/mL. We safely discontinued iNO administration at 473 days of age. In conclusion, serial change in NT-proBNP is a surrogate marker with prognostic value in patients with PAH associated with CLD.
No takes yet. Share an insight, caveat, or question.
Seki et al. (2019) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: