Why the study?
How do exercise-induced desaturation and gas-exchange responses during a 6-minute walk test differ between patients with idiopathic and congenital heart disease-related pulmonary hypertension?
Cross-Sectional (n=52)
How do exercise-induced desaturation and gas-exchange responses during a 6-minute walk test differ between patients with idiopathic and congenital heart disease-related pulmonary hypertension?
Patients with congenital heart disease-related pulmonary hypertension exhibit greater exercise-induced desaturation during a 6-minute walk test compared to idiopathic pulmonary hypertension, which correlates with an enhanced ventilatory response.
Greater desaturation in CHDPH may reflect unique ventilatory responses; leaves open targeted strategies pending prospective validation.
We measured pulmonary gas exchange during six minute walk test (6MWT) in patients with idiopathic (IPAH) and congenital heart disease-related pulmonary hypertension (CHDPH), and determined the relationship between the degree of desaturation and changes in minute ventilation to carbon dioxide production V˙EV˙CO2 and end-tidal partial pressure for carbon dioxide (PetCO2) in both groups. Fifty-two patients (IPAH, n = 28; CHDPH, n = 24) completed 6MWT with simultaneous pulmonary gas exchange. Whilst no significant difference in six minute walk distance was observed between groups (IPAH: 529 ± 89; CHDPH: 476 ± 119 m, p = 0.10), oxygen uptake, carbon dioxide production, and minute ventilation were higher in IPAH than CHDPH (p < 0.01). In addition, CHDPH desaturated to a greater extent than IPAH with a lower post-6MWT SPO2 (IPAH: 92.3 ± 7.9; CHDPH: 73.3 ± 14.9%, p < 0.01). The change in SpO2 correlated to the change in V˙E/V˙CO2 (r=−0.44, p = 0.02) and PetCO2 (r = 0.49, p < 0.01) for CHDPH, but not IPAH. The exercise-induced hypoxic stimulus during 6MWT in CHDPH may be associated with an enhanced ventilatory response.
No takes yet. Share an insight, caveat, or question.
Balmain et al. (2018) conducted a cross-sectional in Pulmonary hypertension (idiopathic and congenital heart disease-related) (n=52). Congenital heart disease-related pulmonary hypertension (CHDPH) vs. Idiopathic pulmonary arterial hypertension (IPAH) was evaluated on Post-6MWT SpO2 (p=< 0.01).
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: