2015
DOI: 10.2340/00015555-2176
|View full text |Cite
|
Sign up to set email alerts
|

Hidradenitis Suppurativa Disproportionately Affects African Americans: A Single-center Retrospective Analysis

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

5
64
1

Year Published

2017
2017
2024
2024

Publication Types

Select...
7

Relationship

0
7

Authors

Journals

citations
Cited by 63 publications
(70 citation statements)
references
References 7 publications
5
64
1
Order By: Relevance
“…1,2,5,9-14 This data justifies its late diagnosis and in more advanced stages, as found in our study, with a mean time of 9 years for diagnosis and most patients presenting Hurley stage II or III.…”
Section: Discussionsupporting
confidence: 86%
See 2 more Smart Citations
“…1,2,5,9-14 This data justifies its late diagnosis and in more advanced stages, as found in our study, with a mean time of 9 years for diagnosis and most patients presenting Hurley stage II or III.…”
Section: Discussionsupporting
confidence: 86%
“…1-7 It is characterized by recurrent nodules, bridge scars and suppuration in intertriginous areas. 1,2,8,9 The disease severely affects patients' quality of life.…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…A Danish trial did not report race for any participants [36]. Two trials did have cohorts containing 19–20% AA; however, this still contrasts with results from studies reporting that AA make up to 65% of patients with HS in the USA, have a 1-year incidence of HS more than double that of Caucasians, and have the highest 1-year incidence of HS across all age groups [4, 5, 34, 35]. Furthermore, none of the trials reported the percentage of patients that were Hispanic or stratified the responses to adalimumab by race.…”
Section: Treatment Response In Socmentioning
confidence: 71%
“…Although the prevalence of HS varies (from 0.00033 to 4.1%), studies have reported an increased prevalence in African and Hispanic populations, as well as in women [4, 5]. The disease burden of HS is largely due to a profound physical and psychological impact, which leads to depression and impaired quality of life (QoL) [6, 7].…”
Section: Introductionmentioning
confidence: 99%