Life with a Primary Immune Deficiency: a Systematic Synthesis of the Literature and Proposed Research Agenda
- PMID: 26873708
- PMCID: PMC11090044
- DOI: 10.1007/s10875-016-0241-1
Life with a Primary Immune Deficiency: a Systematic Synthesis of the Literature and Proposed Research Agenda
Abstract
Purpose: The clinical immunology literature is punctuated with research on psychosocial dimensions of illness. Studies investigating the lived experiences and stated needs of patients with primary immune deficiencies and their families are essential to improving clinical management and determining the research questions that matter to patients and other stakeholders. Yet, to move the field forward, a systematic review of literature and proposed agenda is needed.
Methods: A systematic review was conducted via PubMed and Scopus to include original research on psychological, social, or behavioral aspects of primary immune deficiencies published between 1999 and 2015. A Title/Abstract keyword search was conducted, 317 candidate article abstracts were manually reviewed, and forward/backward reference searches were completed.
Results: Twenty-nine studies met inclusion criteria. These illuminate the complex psychological, social, and emotional experiences of primary immune deficiency. Themes included the potential for negative psychosocial impact from disease; adaptation over time; the multi-dimensional assessments of quality of life; familial impact; the important roles of hope, developing a sense of control, social support; and addressing anxiety/depression in our patients and their families. Methodological considerations and areas for improvement are discussed.
Conclusion: We propose the research agenda focus on study creativity and rigor, with improved engagement with existing literature and critical study design (e.g., methodology with adequate statistical power, careful variable selection, etc.). This review highlights opportunities to advance psychosocial research and bring a brighter future to clinicians, researchers, and families affected by primary immune deficiency.
Keywords: Quality of life; patient-centered; primary immune deficiency; psychosocial.
Conflict of interest statement
References
-
- Schwartz MD, Peshkin BN, Hughes C, Main D, Isaacs C, Lerman C. Impact of BRCA1/BRCA2 mutation testing on psychologic distress in a clinic-based sample. J Clin Oncol. 2002;20:514–20. - PubMed
-
- van Dijk S, Timmermans DR, Meijers-Heijboer H, Tibben A, van Asperen CJ, Otten W. Clinical characteristics affect the impact of an uninformative DNA test result: the course of worry and distress experienced by women who apply for genetic testing for breast cancer. J Clin Oncol. 2006;24(22):3672–7. - PubMed
-
- Cukier YR, Thompson HS, Sussner K, Forman A, Jandorf L, Edwards T, et al. Factors associated with psychological distress among women of African descent at high risk for BRCA mutations. J Genet Couns. 2013;22(1):101–7. - PubMed
-
- Wang JH, Schwartz MD, Brown RL, Maxwell AE, Lee MM, Adams IF, et al. Results of a randomized controlled trial testing the efficacy of a culturally targeted and a generic video on mammography screening among chinese-american immigrants. Cancer Epidemiol Biomarkers Prev. 2012;21(11):1923–32. - PMC - PubMed
Publication types
MeSH terms
Supplementary concepts
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Miscellaneous
