| Literature DB >> 30007467 |
Susan V Jennings1, Valerie M Slee2, Rachel M Zack2, Srdan Verstovsek3, Tracy I George4, Hongliang Shi5, Philina Lee5, Mariana C Castells6.
Abstract
Understanding experiences, perceptions, and perspectives of patients with a mast cell disorder (MCD), including cutaneous mastocytosis, systemic mastocytosis, mast cell activation syndromes, and hereditary α-tryptasemia, is an important aspect of successful care, treatment, and informed development of novel therapies. This article reviews existing studies and presents new data on MCD patient perceptions regarding medical care, symptoms, allergies/sensitivities, triggers, future health/disease progression, treatment, impact on daily living, quality of life, support needs, and concerns regarding possible familial disease. Discussion includes aspects affecting the MCD community that require further consideration and development.Entities:
Keywords: Anaphylaxis; Disability; Mast cell activation; Mast cell disorder; Patient perceptions and experiences; Quality of life; Support; The Mastocytosis Society
Mesh:
Year: 2018 PMID: 30007467 DOI: 10.1016/j.iac.2018.04.006
Source DB: PubMed Journal: Immunol Allergy Clin North Am ISSN: 0889-8561 Impact factor: 3.479