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Living with pulmonary hypertension: unique insights from an international ethnographic study
  1. Martha Kingman1,
  2. Barbara Hinzmann2,
  3. Oliver Sweet3,
  4. Jean-Luc Vachiéry4
  1. 1Pulmonary Hypertension Program, UT Southwestern Medical Center, Dallas, Texas, USA
  2. 2Department of Global Market Research, Market Research Cardiology, Bayer HealthCare Pharmaceuticals, Berlin, Germany
  3. 3Ethnography Centre of Excellence, Ipsos MORI, London, UK
  4. 4Département de Cardiologie, Cliniques Universitaires de Bruxelles, Hôpital Erasme, Brussels, Belgium
  1. Correspondence to Dr Martha Kingman, Martha.Kingman{at}UTSouthwestern.edu

Abstract

Objectives To better understand the patient's perspective of pulmonary hypertension (PH), including the impact of living with PH, disease management and treatment.

Design This qualitative ethnographic study collected observational video footage, supplemented by field notes and patient diaries to assess the impact of PH on the patient's life.

Setting Patients were observed and filmed in their home for up to 6 h, capturing the environment, interactions and activities of everyday life.

Participants Patients with pulmonary arterial hypertension (PAH) or chronic thromboembolic PH who were receiving PAH-specific medication were recruited through healthcare professionals (HCPs) and patient associations in seven countries across four continents. Sampling was purposive and subgroup analysis was not intended.

Results Overall, 39 patients with PH were enrolled. Many patients had a poor understanding of PH and found their ‘invisible’ disease difficult to explain to others. An important finding was the secrecy surrounding PH. Feelings of insecurity and isolation were regularly reported, and many patients admitted to hiding their symptoms. The marked improvement in symptoms after therapy initiation made assessment of disease progression more difficult as patients compared their quality of life (QoL) against pretreatment levels. Extensive planning and adherence to daily routines were required in patients’ everyday life.

Conclusions Ethnography was used for the first time, in several countries, to evaluate the patient's perception of living with PH. This approach revealed key findings that would not typically be uncovered using other qualitative techniques, including the secrecy surrounding PH, the difficulties in describing the disease and the challenges in assessing disease progression. A more tailored dissemination of information from HCPs and development of a simple and understandable PH definition may be beneficial in alleviating the secrecy reported by patients. A greater appreciation of how patients perceive their disease and QoL has the potential to improve PH management.

  • pulmonary arterial hypertension
  • chronic thromboembolic pulmonary hypertension
  • qualitative
  • quality of life
  • ethnography

This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 3.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/3.0/.

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