Key result
Conventional therapy for Eisenmenger syndrome is linked to a ~19% decrease in vWF:Ag at 18 months.
Why the study?
The long-term behavior of endothelial markers in patients with Eisenmenger syndrome under conventional therapy without vasodilators was not well characterized.
Does conventional therapy alter endothelial and coagulation markers over time in patients with Eisenmenger syndrome?
Cohort (n=17)
Does conventional therapy alter endothelial and coagulation markers over time in patients with Eisenmenger syndrome?
p-value: p=<0.0001
Conventional therapy in Eisenmenger syndrome may improve some markers of endothelial dysfunction, although residual abnormalities and increased thrombosis risk persist.
May indicate endothelial benefit from conventional therapy in Eisenmenger syndrome; leaves open effects on thrombosis risk and need for prospective confirmation.
The long-term behavior of endothelial markers was studied in patients with Eisenmenger syndrome who were subjected to conventional therapy (no vasodilators) and observed for 18 months. Biochemical markers were analyzed comparatively in patients with class II or III symptoms (group 1, n=10) and patients with class IV symptoms (group 2, n=7). Plasma von Willebrand factor antigen (vWF:Ag), thrombomodulin, tissue-type plasminogen activator (t-PA) and its inhibitor (PAI-1), and D-dimer were determined by immunoenzymatic assay at baseline, and at 6, 12, and 18 months. At baseline, the main clinical difference between groups was a decreased peripheral oxygen saturation in group 2 versus group 1 (77+/-5% and 86+/-4%, respectively, p=0.001). Basal vWF:Ag and t-PA were increased and thrombomodulin was decreased in both groups in comparison with controls (p<0.0001), while D-dimer was increased in group 2 only (p=0.0003). In response to treatment, there was a decrease in vWF:Ag in both groups (19% and 23%, respectively in groups 1 and 2, at 18 months vs. baseline, p<0.0001) and t-PA in group 1 (38% vs. baseline, p=0.0485). Plasma vWF:Ag tended to be higher in group 2 in comparison with group 1 during the whole follow-up. Levels of PAI-1 greater than 38.4 ng/mL (upper 90% limit for normals) and D-dimer greater than 500 ng/mL were detected in individual patients (both groups) during the follow-up period. Thrombomodulin remained decreased in both groups. Thus, severity of symptoms in the Eisenmenger syndrome appears to correlate with low oxygen saturation and higher vWF:Ag levels. Improvement of endothelial dysfunction may occur in response to treatment, although increased risk for thrombosis persists, in view of residual abnormalities.
No takes yet. Share an insight, caveat, or question.
Caramurú et al. (2006) conducted a cohort in Eisenmenger syndrome (n=17). Conventional therapy (no vasodilators) vs. Baseline was evaluated on Change in plasma von Willebrand factor antigen (vWF:Ag) at 18 months (p=<0.0001). Conventional therapy in patients with Eisenmenger syndrome was associated with a decrease in vWF:Ag at 18 months (19% in class II/III and 23% in class IV, p<0.0001).
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: