Objectives. To identify patients with hyperthyroidism and coincidental
pulmonary hypertension and to document reversibility of pulmonary hyp
ertension after treatment of hyperthyroidism. Design. Patients with hy
perthyroidism referred for transthoracal echocardiography for any reas
on that showed elevated pulmonary arterial pressures were collected. A
fter therapy for the thyreotoxic state with documented normalization o
f thyroid hormone (fT4), pulmonary arterial pressure was measured agai
n noninvasively. Setting. An out-patient tertiary referral centre. Sub
jects. The medical records were used to identify, retrospectively pati
ents with hyperthyroidism and pulmonary hypertension over a three-year
period (April 1993 to April 1996). Interventions and main outcome mea
sures. Systolic pulmonary artery pressure (PAPs) was determined by add
ing up right ventricular systolic pressure (RVSP) and mean right atria
l pressure (RAP) measured by continuous-wave Doppler echocardiography
according to standard techniques. All patients were treated for hypert
hyroidism to normal fT4 levels. After successful therapy, Doppler echo
cardiography was repeated. Results. Four patients with pulmonary hyper
tension showing elevated PAPs of 40 +/- 11 mmHg were identified. After
therapy, PAPs decreased in all patients to a mean of 25 +/- 6 mmHg. C
onclusion. The observation of four patients with pulmonary hypertensio
n and hyperthyroidism is striking and suggests a possible pathogenetic
link of these disorders.