Pulmonary Hypertension
Pulmonary hypertension (PH) is defined by a mean pulmonary artery pressure (mPAP) >25 mmHg at rest or >30 mmHg with exercise [26]. A large case-control study, including 3,349 HIV-infected patients over a period of 5.5 years found a cumulative incidence of PH of 0.57%, resulting in an annual incidence of 0.1%, whereas its incidence in the general population is only 1-2 per 1 million people [27].
PH carries a poor and comparable prognosis in HIV-positive and seronegative patients. Mesa et al. [28] found that half of the patients died during the median follow-up of 8 months with a median time interval from the diagnosis of PH to death of 6 months. Comparing 20 HIV and PH to 93 HIV seronegative patients, Petitprez et al. [29] found a similar mortality rate. The major causes of death are right-sided heart failure, cardiogenic shock, sudden death and respiratory failure [29]. PH occurs in all stages of HIV infection without any clear relation to immune deficiency. Histologically, plexogenic pulmonary arteriopathy is the most frequent finding [29]. The pathogenesis of PH remains unclear. It has been advocated that PH might result from a genetic predisposition. An indirect role of HIV that can stimulate the production of endothelin 1, tumor necrosis factor, proteolytic enzyme and platelet derived factor has been also suggested [30, 31].Echocardiography is a reliable tool to screen PH, rule out secondary forms and refine prognostic stratification. Echocardiography allows the estimation of pulmonary arterial systolic pressure (PASP) (Fig. 3) and provides additional information regarding the cause, consequences and prognosis of PH. A high correlation was found between transthoracic echocardiography findings and right heart catheterisation measurements [26]. Age, body mass index, systemic hypertension have been shown to increase PASP and should be taken into account when a PASP level is interpreted at an individual level [26].
Echocardiography also allows diagnosis of secondary causes of PH. It can easily recognize left heart valvular and myocardial diseases responsible for pulmonary venous hypertension, and congenital heart diseases with systemic-pulmonary shunts. The examination includes venous injection of agitated saline contrast medium to rule out atrial septal defect or patent Foramen ovale.
In the pre-HAART era and among 131 cases, the most frequent echocardiographic findings were a dilatation of right heart chambers (98%), tricuspid regurgitation (64%), and paradoxical septal motion (40%) [32]. Zuber et al. [33] suggested an indirect link between HIV, HAART and the incidence of PH. They found, in a retrospective study, an improvement of hemodynamic parameters in patients treated with HAART. In a group of 35 patients who had serial Doppler echocardiography, RV systolic pressure increased by a median of 25 mm Hg in nine patients who were not treated with HAART, decreased by a median of 3 mm Hg in nine patients who were not treated with NRTI and decreased by a median of 21 mm Hg in 14 patients who received HAART (ppatients with HIV infection, Kaposi sarcoma and lymphoma occur more commonly than in immunocompetent subjects. In the pre-HAART period, the cardiac Kaposi sarcoma prevalence varies from 12-8% in retrospective autopsies studies [44]. Echocardiographic findings in this setting found pericardial tamponade or pericardial constriction.
Malignant Lymphoma
Lymphomas are observed in 5-10% of patients with AIDS, which is 25-60 times higher than expected in the general population [45]. Primary cardiac lymphoma is rare [46]. Clinical presentation and echocardiographic findings include congestive heart failure, pericardial effusion or tamponade with nodular or polypoid masses involving the pericardium with variable myocardial infiltration and of the right atria. Malignant lymphoma is infrequent in HIV patients; the lesions predominantly involve the pericardium with myocardial infiltration [46].The introduction of HAART led to the reduction in the incidence of cardiac involvement by Kaposi sarcoma and non-Hodgkin’s lymphoma [8].
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