Mortality From Primary Pulmonary Hypertension in the United States, 1979–1996

CHEST Journal ◽  
2000 ◽  
Vol 117 (3) ◽  
pp. 796-800 ◽  
Author(s):  
David E. Lilienfeld ◽  
Lewis J. Rubin
1999 ◽  
Vol 123 (6) ◽  
pp. 539-540 ◽  
Author(s):  
Jennifer Strother ◽  
Peter Fedullo ◽  
Eunhee S. Yi ◽  
Eliezer Masliah

Abstract Anorectic agents, such as aminorex and fenfluramine derivatives, have been associated previously with the development of primary pulmonary hypertension. The combination diet drug phentermine-fenfluramine (or “phen-fen”) was recently marketed in the United States. We describe a case of a 39-year-old woman with rapidly progressing, fatal pulmonary hypertension following administration of phentermine-fenfluramine. Autopsy was remarkable for complex pulmonary vascular lesions most consistent with thrombotic arteriopathy.


2015 ◽  
Vol 13 (4) ◽  
pp. 172-173
Author(s):  
Diane Ramirez ◽  
Laura Hoyt D'Anna

In 1987, after three years of being treated aggressively for asthma and then a prolapsed mitral valve, I was finally diagnosed with primary pulmonary hypertension (PPH). I was told I would be lucky if I lived 2 years without having a heart/double lung transplant and that I didn't have much time to get my affairs in order. There were fewer than 200 patients in the United States at the time. There were no treatment centers, support groups, or even an advocacy group like the Pulmonary Hypertension Association (PHA). I struggled with the loneliness of this diagnosis and the lack of information available.


2018 ◽  
Vol 37 (4) ◽  
pp. S205
Author(s):  
H. Farber ◽  
J. Badlam ◽  
A. Frost ◽  
R. Benza ◽  
E. Austin ◽  
...  

2020 ◽  
Vol 10 (4) ◽  
pp. 204589402091183
Author(s):  
John W. McConnell ◽  
Yuen Tsang ◽  
Janis Pruett ◽  
William Drake III

Two oral medications targeting the prostacyclin pathway are available to treat pulmonary arterial hypertension in the United States: oral treprostinil and selexipag. We compared real-world hospitalization in patients receiving these medications. A retrospective administrative claims study was conducted using the Optum® Clinformatics® Data Mart database. Patients with pulmonary hypertension were identified using diagnostic codes. Cohort inclusion required age ≥ 18 years, first oral treprostinil or selexipag prescription between 1 January 2015 and 30 September 2017 (index date), and continuous enrollment in the prior ≥6 months. Patients who switched index drug were excluded. Follow-up was from index date until the first of end of index drug exposure, end of continuous enrollment, death, or 31 December 2017. Multivariable Cox proportional hazard and Poisson regression were used to compare risk and rate, respectively, of hospitalization associated with oral treprostinil vs. selexipag, adjusting for potential confounders. The study cohort included 99 patients receiving oral treprostinil and 123 receiving selexipag. Mean age was 61 years, and most patients were females (71%). Compared with oral treprostinil, selexipag was associated with a 46% lower risk of all-cause hospitalization (hazard ratio 0.54, 95% confidence interval 0.31, 0.92; P = 0.02), a 47% lower risk of pulmonary hypertension-related hospitalization (hazard ratio 0.53, 95% confidence interval 0.31, 0.93; P = 0.03), a 42% lower all-cause hospitalization rate (rate ratio 0.58, 95% confidence interval 0.39, 0.87; P = 0.01), and a 46% lower pulmonary hypertension-related hospitalization rate (rate ratio 0.54, 95% confidence interval 0.35, 0.82; P = 0.004). This study suggests that selexipag is associated with lower hospitalization risk and rate than oral treprostinil.


CHEST Journal ◽  
2000 ◽  
Vol 117 (3) ◽  
pp. 870-874 ◽  
Author(s):  
Stuart Rich ◽  
Lewis Rubin ◽  
Alexander M. Walker ◽  
Sebastian Schneeweiss ◽  
Lucien Abenhaim

Sign in / Sign up

Export Citation Format

Share Document