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Group A included patients with group 1 pulmonary arterial hypertension (PAH), group B consisted of patients with PH from groups 2 to 5, and group C comprised patients with no PH during RHC.

We measured the transannular plane systolic excursion; basal, mid, and longitudinal right ventricular dimensions; right ventricular end-systolic and end-diastolic surface areas; right atrial surface area; left ventricular end-systolic and end-diastolic surface area, as well as left atrial surface area [8].For the present analysis, the diagnosis of PH is suggestive if an estimated RVSP by echocardiography of more than or equal to 40 mm Hg using simplified Bernoulli equation in one hand and TRV of 2.8–3.4 m/s with more than or equal to one echocardiographic sign of PH or TRV more than 3.4 m/s, according the recommendations of the recent ECS/ERS 2015 PH guidelines recommendation on the other hand.All echocardiographic determinations were performed by investigators blinded to the results of the RHC.Egypt J Chest Dis Tuberc 2019;3-8How to cite this URL: Ahmed MK, Elshinawy OM, Agmy GM, Shaban LH, Dweik RA, Tonelli AR.Egypt J Chest Dis Tuberc [serial online] 2019 [cited 2019 Sep 1];3-8. 2019/68/2/203/258432Pulmonary hypertension (PH) is a chronic debilitating cardiopulmonary disease in which early diagnosis and treatment can improve outcomes [1],[2].

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