98%
921
2 minutes
20
Background: Individuals with sarcoidosis face many sources of illness uncertainty, including diagnostic delays, unpredictable therapeutic efficacy and toxicity, and disease-associated morbidity and mortality. Patient perspectives on illness uncertainty in sarcoidosis have not been evaluated critically and offer an opportunity for providers to contextualize and prioritize gaps in care and patient support.
Research Question: How do patients with sarcoidosis describe their lived experiences with the disease and challenges they face in receiving care?
Study Design And Methods: We conducted semistructured qualitative interviews with patients with biopsy-proven pulmonary sarcoidosis receiving treatment for the disease who were seen at a tertiary sarcoidosis center of excellence. Interviews examined patient experiences of living with sarcoidosis, including their journey with diagnosis, treatment, and monitoring of disease activity. Transcripts were coded and categorized into themes and subthemes. Saturation was defined as at least 3 interviews without new information.
Results: Twenty-five participants completed semistructured interviews. The median age was 60 years, with 64% of the participants being female and 68% identifying as Black. The impact of illness uncertainty was a shared component of their care journeys. Key themes that emerged were (1) the burden of limited disease awareness, (2) uncertainty about sarcoidosis management, and (3) the unpredictability of disease progression. Uncertainty emerged as a major challenge that contributed to delays in care, poor disease control, psychological distress, or a combination thereof.
Interpretation: Our findings are the first, to our knowledge, to highlight the impact of patient illness uncertainty on sarcoidosis disease outcomes and psychological distress. Individuals living with sarcoidosis may benefit by addressing the psychosocial impact of uncertainty. Individuals living with sarcoidosis may benefit significantly from targeted interventions to mitigate the impact of illness uncertainty.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1016/j.chest.2025.06.025 | DOI Listing |
PLoS One
September 2025
Department of Safety and Quality of Meat, Max Rubner-Institute, Federal Research Institute of Nutrition and Food, Kulmbach, Bavaria, Germany.
Background: According to surveillance data, Campylobacter enteritis (CE) has been the most frequently notified bacterial gastrointestinal disease in Germany and Europe for many years. Presumably, the total number of cases is underestimated because an unknown number of cases is not diagnosed and some diagnosed cases are not reported in the surveillance system. The aim of this study was to estimate the disease and economic burden of CE and its related sequelae in Germany.
View Article and Find Full Text PDFAnn Med Surg (Lond)
September 2025
Department of Hematology/Oncology, Danbury Hospital, Danbury/Nuvance Health, Connecticut, USA.
Introduction: "Comfort care" is a holistic approach for patients with terminal conditions, such as cancer, who are not expected to recover. It focuses on managing pain, among other end-of-life symptoms, and providing support to both the patient and their family during the dying process, which can last unpredictably from hours to days. End-of-life care concepts are often shaped by personal judgment and culture and thus lack a single consensus.
View Article and Find Full Text PDFInt J Qual Stud Health Well-being
December 2025
Department of Community Medicine, UiT The Arctic University of Norway, Tromsø, Norway.
Background: Chronic musculoskeletal pain (CMP) is a prevalent condition often lacking clear biomedical explanations, leading to frustration for both clinicians and patients. The uncertainty surrounding CMP deeply affects the dynamics of clinical consultations.
Aim: This study investigates how clinicians and patients navigate expectations and uncertainty in CMP consultations, focusing on the interplay between hope and acceptance.
Ann Neurosci
August 2025
School of Pharmaceutical and Population Health Informatics, DIT University, Dehradun, Uttarakhand, India.
Background: Memory, learning, language and decision-making are just some of the cognitive abilities that may be negatively impacted by neurological illnesses such as dementia, anxiety and depression.
Purpose: This research aims to examine the influence of demographic variables on the prevalence of dementia, anxiety and depression in patients recovering from COVID-19.
Methods: This research looks at those who are at risk of developing dementia, anxiety or depression after being exposed to COVID-19.
PLoS One
September 2025
Ethiopian Public Health Institute, Addis Ababa, Ethiopia.
Background: Tuberculosis (TB), despite being a preventable and curable disease, remains a leading infectious cause of death. In Eastern Africa, TB poses a significant public health challenge. This study examined TB incidence, prevalence, mortality, and disability-adjusted life years (DALYs) from 1990 to 2021.
View Article and Find Full Text PDF