A new study aiming to understand sarcoidosis-associated pulmonary hypertension symptoms and their impacts on patients’ lives determined that the Pulmonary Arterial Hypertension-Symptoms and Impact questionnaire could be used to suitably assess patients.
A new study determined that the Pulmonary Arterial Hypertension-Symptoms and Impact (PAH-SYMPACT) questionnaire is a suitable self-reporting instrument for assessing sarcoidosis-associated pulmonary hypertension (SAPH) symptoms and their impact on patients, according to findings published in BMC Pulmonary Medicine.
Patient-reported outcomes reported through the PAH-SYMPACT can be beneficial in understanding patients’ experience with SAPH and guiding disease management; currently no approved medicinal treatment for SAPH exists.
The PAH-SYMPACT assesses patients across 23 items: 11 on symptoms with 24-hour recall period, 11 on impacts with a 7-day recall period, and 1 item on oxygen use in the previous 24 hours. The symptom items are clustered into cardiopulmonary and cardiovascular domains, and the impact domains are clustered into physical and cognitive/emotional domains.
The study enrolled 11 patients diagnosed with SAPH, aged 18 to 85 years, who participated in qualitative 1-on-1 telephone interviews conducted in 2 parts: concept elicitation and cognitive debriefing. The concept elicitation portion of the interviews prompted participants to rate symptoms as “most bothersome or severe” and determine which impacts were “most difficult to cope with.”
After the interviews, participants were asked to complete the PAH-SYMPACT questionnaire and assess the comprehensibility, relevance, and clarity of the listed items. Participants were also asked to indicate the level of improvement they would consider to be meaningful.
Investigators used participants’ interview transcripts to understand SAPH symptoms, their impacts on patients’ lives, and determine the appropriateness of the PAH-SYMPACT for use in patients with SAPH.
Findings showed:
Although study findings indicate that the PAH-SYMPACT questionnaire is suitable for measuring symptoms and their impact in patients with SAPH, larger longitudinal studies are required to confirm the instrument’s suitability and ability to accurately detect symptom status among the patient population, the authors concluded.
Reference:
Currie BM, Davies EW, Beaudet A, Stassek L, Kleinman L, and Baughman RP. Symptoms, impacts, and suitability of the pulmonary arterial hypertension-symptoms and impact (PAH-SYMPACT) questionnaire in patients with sarcoidosis-associated pulmonary hypertension (SAPH): a qualitative interview study. BMC Pulm Med. Published online November 12, 2021. doi:10.1186/s12890-021-01694-1
Echocardiographic Assessment Shows Promise as Risk Predictor in PAH
August 29th 2025Close to 40% of patients with right heart failure and pulmonary arterial hypertension (PAH) who remain critically ill and require admittance to the intensive care unit die within 1 year of that hospitalization.
Read More
Tricuspid Regurgitation Reliable Prognostic Indicator of PAH Severity
August 13th 2025Despite knowledge of the benefits of right heart hemodynamic measures for evaluating patient prognosis in the setting of pulmonary arterial hypertension (PAH), gaps remain in a defined role for tricuspid regurgitation as it relates to echocardiographic phenotype.
Read More
Lung Transplant Referrals Lag for High-Risk Patients With PAH
July 18th 2025Despite recommendations on early referral for lung transplantation in cases of pulmonary arterial hypertension (PAH), there is a lack of in-depth understanding of this current landscape; in this analysis, clinical parameter data were used to compare outcomes between patients who were and were not referred for lung transplantation.
Read More