Key result
Children with PAH-CHD had significantly elevated mean platelet volume (10.19 vs 8.80 FL, p<0.001) compared to those with CHD alone, which correlated with disease severity and poor prognosis.
Why the study?
The study aimed to evaluate platelet activation markers (MPV, PDW, and platecrit) in children with PAH-CHD, assess their predictive value for adverse outcomes, and correlate their levels with clinical data.
Do platelet activation markers (MPV, PDW, platecrit) predict adverse outcomes (death or readmission) in children with PAH-CHD?
Cohort (n=180)
No
Do platelet activation markers (MPV, PDW, platecrit) predict adverse outcomes (death or readmission) in children with PAH-CHD?
Platelet activation markers, particularly MPV and platecrit, are elevated in children with PAH-CHD and serve as strong predictors of poor prognosis at 6 months.
Answers are grounded in this paper and cite their sources.
Platelet markers may aid risk stratification in pediatric PAH-CHD; hypothesis-generating and requires validation before clinical use.
The study aimed to evaluate mean platelet volume (MPV), platelet distribution width (PDW), and platecrit in children with pulmonary arterial hypertension associated with congenital heart disease (PAH-CHD), to assess the predictive value of these platelet activation markers for adverse outcomes, and to correlate their levels with various data in these patients. This prospective cohort study included 60 children with PAH-CHD as group I and 60 children with CHD and no PAH as group II. Another 60 healthy children of matched age and sex served as the control group. All included children were evaluated by echocardiography. MPV, PDW, and platecrit were also measured using an automated blood counter. All patients were followed up for death or readmission for 6 months. MPV, PDW, and platecrit were significantly higher in group I compared to group II and the control group and they correlated well with increasing severity of PAH. MPV, PDW, and platecrit positively correlated with right ventricular diameter and mean pulmonary artery pressure, however they correlated negatively with right ventricular systolic and diastolic function. The best cut-off of platelet activation markers levels to predict poor prognosis in group I was > 11.2 FL with 75% sensitivity and 96.6% specificity for MPV, > 12.7 FL with 75% sensitivity and 61.5% specificity for PDW, and > 0.505% with 75% sensitivity and 93.2% specificity for platecrit. MPV, PDW, and platecrit were elevated in children with PAH-CHD and found to be good predictive markers for poor prognosis in these children.
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Awad et al. (2022) conducted a cohort in Pulmonary arterial hypertension associated with congenital heart disease (PAH-CHD) (n=180). Pulmonary arterial hypertension associated with congenital heart disease (PAH-CHD) vs. Congenital heart disease without PAH and healthy controls was evaluated on Mean platelet volume (MPV) (p=<0.001). Children with PAH-CHD had significantly elevated mean platelet volume (10.19 vs 8.80 FL, p<0.001) compared to those with CHD alone, which correlated with disease severity and poor prognosis.
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