BOSTON — Among patients with interstitial lung disease, 30% had pulmonary arterial hypertension and 20% had right ventricular hypertrophy, according to data presented at the CHEST Annual Meeting.
“Clinicians should evaluate symptoms of ILD along with ECG and ECHO findings right at the time of first consultation — we would get indirect evidence of chronicity too,” Radha Munje, MBBS, DTCD, MD, FICS, professor and head of the department of respiratory medicine at Indira Gandhi Government Medical College and Hospital Nagpur, told Healio.
In this cross-sectional study utilizing electrocardiography (ECG) and 2D echocardiography, Munje and colleagues evaluated 150 patients with ILD to determine cardiac abnormality prevalence in this population.
During the assessment of ECG data, researchers reported that 60 patients (40%) had right axis deviation, and 30 patients (20%) had signs of right ventricular hypertrophy, totaling 90 patients with ECG abnormalities.
Switching to findings from echocardiography, the same number of patients with signs of right ventricular hypertrophy had this condition (n = 30), and nearly one-third of patients (n = 45; 30%) had pulmonary arterial hypertension (mean pulmonary artery pressure, 25 mmHg), according to the abstract.
Researchers reported smaller proportions of patients with diastolic dysfunction (n = 22; 14.67%) and left ventricular hypertrophy (n = 15; 10%) on echocardiography.
Lastly, the abstract indicated that two factors — longer ILD symptom duration and an idiopathic pulmonary fibrosis diagnosis — had correlation to greater PAH and right ventricular hypertrophy prevalence in this patient population.
“Now we need to see whether an equation can be developed, at what time duration there is cardiac involvement, plus is it multifactorial like exacerbations, etiology, duration of symptoms and treatment ongoing,” Munje told Healio.