Prevalence of Pulmonary Hypertension in Elderly Patients with Diastolic Heart Failure

2007 ◽  
Vol 13 (6) ◽  
pp. S93
Author(s):  
Timothy P. Fitzgibbons ◽  
Joseph L. Bouchard ◽  
Theo E. Meyer ◽  
Gerard P. Aurigemma
2003 ◽  
Vol 41 (6) ◽  
pp. 168
Author(s):  
Erik J. Kouba ◽  
Gregory Hundley ◽  
Peter Brubaker ◽  
Barbara Nicklas ◽  
Dalane W. Kitzman

2013 ◽  
Vol 12 (3) ◽  
pp. 122-126
Author(s):  
Sonja Bartolome

Patients with chronic obstructive pulmonary disease (COPD) often present with mild pulmonary hypertension (PH). This finding has been attributed to hypoxic pulmonary vasoconstriction. However, a small proportion of COPD patients will present with moderate or severe elevations in their pulmonary artery pressure (PAP), and these patients appear to have worsened symptoms and survival when compared to patients with milder elevations in PAP. The diagnosis of PH in COPD may be difficult, due to inaccuracies in the echocardiographic estimates of PAP in these patients. Additionally, many patients with COPD will also have comorbid conditions such as diastolic heart failure, systolic heart failure, or obstructive sleep apnea, which may cause increased pulmonary pressures through other mechanisms. Clinical trials investigating the effect of PH-specific therapy for patients with PH and COPD have been small, with mixed results. A careful evaluation for other causes of PH and hemodynamic evaluation will help guide medical therapy for this group of patients.


2016 ◽  
Vol 43 (4) ◽  
pp. 350-353 ◽  
Author(s):  
Loheetha Ragupathi ◽  
Drew Johnson ◽  
Gregary D. Marhefka

Surgically created arteriovenous fistulae (AVF) for hemodialysis can contribute to hemodynamic changes. We describe the cases of 2 male patients in whom new right ventricular enlargement developed after an AVF was created for hemodialysis. Patient 1 sustained high-output heart failure solely attributable to the AVF. After AVF banding and subsequent ligation, his heart failure and right ventricular enlargement resolved. In Patient 2, the AVF contributed to new-onset right ventricular enlargement, heart failure, and ascites. His severe pulmonary hypertension was caused by diastolic heart failure, diabetes mellitus, and obstructive sleep apnea. His right ventricular enlargement and heart failure symptoms did not improve after AVF ligation. We think that our report is the first to specifically correlate the echocardiographic finding of right ventricular enlargement with AVF sequelae. Clinicians who treat end-stage renal disease patients should be aware of this potential sequela of AVF creation, particularly in the upper arm. We recommend obtaining preoperative echocardiograms in all patients who will undergo upper-arm AVF creation, so that comparisons can be made postoperatively. Alternative consideration should be given to creating the AVF in the radial artery, because of less shunting and therefore less potential for right-sided heart failure and pulmonary hypertension. A multidisciplinary approach is optimal when selecting patients for AVF banding or ligation.


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