Individuals affected by eosinophilic gastrointestinal disorders have complex unmet needs and frequently experience unique barriers to care

被引:40
作者
Hiremath, Girish [1 ]
Kodroff, Ellyn [2 ]
Strobel, Mary J. [3 ]
Scott, Melissa [4 ]
Book, Wendy [3 ]
Reidy, Cathy [4 ]
Kyle, Shay [2 ]
Mack, Denise [3 ]
Sable, Kathleen [3 ]
Abonia, Pablo [5 ]
Spergel, Jonathan [6 ]
Gupta, Sandeep K. [7 ]
Furuta, T. Glenn [8 ]
Rothenberg, Marc E. [5 ]
Dellon, Evan S. [9 ]
机构
[1] Monroe Carell Jr Childrens Hosp Vanderbilt, Div Pediat Gastroenterol Hepatol & Nutr, DOT Suite 10226,2200 Childrens Way, Nashville, TN 37232 USA
[2] Campaign Urging Res Eosinophil Dis, Lincolnshire, IL USA
[3] Amer Partnership Eosinophil Disorders, Atlanta, GA USA
[4] Eosinophil Family Coalit, Cincinnati, OH USA
[5] Cincinnati Childrens Hosp & Med Ctr, Div Allergy & Immunol, Cincinnati, OH USA
[6] Univ Penn, Dept Pediat, Perelman Sch Med, Div Allergy & Immunol, Philadelphia, PA 19104 USA
[7] Univ Illinois, Coll Med, Div Pediat Gastroenterol Hepatol & Nutr, Peoria, IL 61656 USA
[8] Childrens Hosp Colorado, Digest Hlth Inst, Gastrointestinal Eosinophil Dis Program, Aurora, CO USA
[9] Univ N Carolina, Sch Med, Ctr Esophageal Dis & Swallowing, Div Gastroenterol & Hepatol, Chapel Hill, NC 27515 USA
关键词
Rare diseases; Eosinophitic; Eosiriophilic esophagitis; Eosinophilic gastritis; Eosinophilic gastroenteritis; Unmet needs; Survey; Healthcare barriers; Health services research; Health promotion; ESOPHAGITIS; PREVALENCE;
D O I
10.1016/j.clinre.2018.03.003
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Introduction: Eosinophilic gastrointestinal disorders (EGIDs) are a rare but emerging healthcare problem. Patient advocacy groups (PAGs) have an important role in representing the EGID community, and serve as valuable research partners. By leveraging the partnership between medical researchers and PAGs, we examined the unmet needs and barriers to care perceived by individuals affected by EGIDs. Next, we examined if these varied between adult EGID patients and adult caregivers of children with EGID. Methods: Adult EGID patients and adult caregivers of children (<18 years) with EGIDs participated in this study. PAGs conducted focus groups comprised of individuals affected by EGIDs to identify domains and questions meaningful to the EGID community and this information was used to develop an online REDCap survey. The survey consisted of 58 questions across medical, healthcare, social, and emotional impact domains. It was distributed via the PAGs' web-based platforms. Demographic data, and responses to questions on a six-point Likert scale were collected and analyzed. Results: Of the 361 responses analyzed, 90 (25%) were from adult EGID patients and 271 (75%) were from adult caregivers. Of the applicable responses, in the medical domain only 19% of participants indicated that repeated endoscopies to monitor response to treatment was convenient. In the healthcare domain, 67% indicated that lack of insurance coverage for elemental formula was a barrier. In the social domain, only 5% of respondents reported adequate awareness of EGIDs in schools. In the emotional domain, 64% had experienced significant stress due to EGID related out-of-pocket costs. Multivariate logistic regression revealed that some of these responses varied between adult EGID patients and adult caregivers of children with EGID. The respondents indicated highest priority for improvement in the medical domain compared to other domains. Conclusions: Individuals affected by EGIDs have a constellation of complex unmet needs and perceived barriers across medical, healthcare, social and emotional domains. Addressing unmet needs in the medical domain is relatively more important for the EGID community. Understanding unmet needs and barriers will likely help design improved patient-centered EGID care paradigms. (C) 2018 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:483 / 493
页数:11
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