Differences between adult and pediatric onset Henoch‐Schonlein purpura from North India. (8th November 2017)
- Record Type:
- Journal Article
- Title:
- Differences between adult and pediatric onset Henoch‐Schonlein purpura from North India. (8th November 2017)
- Main Title:
- Differences between adult and pediatric onset Henoch‐Schonlein purpura from North India
- Authors:
- Gupta, Vikas
Aggarwal, Amita
Gupta, Ranjan
Chandra Chowdhury, Abhra
Agarwal, Vikas
Lawrence, Able
Misra, Ramnath - Abstract:
- Abstract: Aim: Henoch‐Schönlein purpura (HSP), a primary vasculitis, characterized by purpura, abdominal pain, arthritis and renal involvement, is predominantly a disease of childhood. However, rarely it can occur in adults in whom it is believed to be a more severe form with poor renal outcomes. We aimed to answer if the age of onset affected the clinical spectrum and renal outcomes of the disease in a north Indian population. Hence, we studied the differences in clinical spectrum and renal outcomes between adult‐onset HSP and childhood‐onset HSP. Methods: Case records of all adult patients diagnosed with HSP (onset ≥ 18 years) over the last 25 years in our department (1992–2017) were retrieved. Data on clinical features, lab abnormalities and outcomes were extracted and compared with that in pediatric HSP patients (onset < 18 years) seen during the same period. Results: A total of 87 patients, including 30 adults and 57 children, were seen during this period. Compared to children, most of the adults had purpura as the first clinical manifestation (86.7% vs . 56.1%, P < 0.01) whereas abdominal pain was only rarely the initial symptom in adults (10.0% vs . 36.8%, P < 0.02). During the disease course, adults had a higher frequency of joint involvement as compared to children (90.0% vs . 43.9%, P < 0.001). There was no significant difference in the frequency of renal involvement (60.0% vs . 50.9%, P = NS) and gastrointestinal involvement (66.7% vs . 84.2%, P = NS) betweenAbstract: Aim: Henoch‐Schönlein purpura (HSP), a primary vasculitis, characterized by purpura, abdominal pain, arthritis and renal involvement, is predominantly a disease of childhood. However, rarely it can occur in adults in whom it is believed to be a more severe form with poor renal outcomes. We aimed to answer if the age of onset affected the clinical spectrum and renal outcomes of the disease in a north Indian population. Hence, we studied the differences in clinical spectrum and renal outcomes between adult‐onset HSP and childhood‐onset HSP. Methods: Case records of all adult patients diagnosed with HSP (onset ≥ 18 years) over the last 25 years in our department (1992–2017) were retrieved. Data on clinical features, lab abnormalities and outcomes were extracted and compared with that in pediatric HSP patients (onset < 18 years) seen during the same period. Results: A total of 87 patients, including 30 adults and 57 children, were seen during this period. Compared to children, most of the adults had purpura as the first clinical manifestation (86.7% vs . 56.1%, P < 0.01) whereas abdominal pain was only rarely the initial symptom in adults (10.0% vs . 36.8%, P < 0.02). During the disease course, adults had a higher frequency of joint involvement as compared to children (90.0% vs . 43.9%, P < 0.001). There was no significant difference in the frequency of renal involvement (60.0% vs . 50.9%, P = NS) and gastrointestinal involvement (66.7% vs . 84.2%, P = NS) between adults and children. Outcomes were good in both groups and most adults and children achieved complete recovery (83.3% and 86.0%, respectively). There was no difference in the frequency of immunosuppressive treatment required by the two groups. None of the patients developed renal insufficiency on follow‐up. Conclusion: Compared to children, adults with HSP seldom have abdominal pain as the first clinical manifestation while joint involvement is seen more commonly in them during the disease course. … (more)
- Is Part Of:
- International journal of rheumatic diseases. Volume 21:Number 1(2018)
- Journal:
- International journal of rheumatic diseases
- Issue:
- Volume 21:Number 1(2018)
- Issue Display:
- Volume 21, Issue 1 (2018)
- Year:
- 2018
- Volume:
- 21
- Issue:
- 1
- Issue Sort Value:
- 2018-0021-0001-0000
- Page Start:
- 292
- Page End:
- 298
- Publication Date:
- 2017-11-08
- Subjects:
- adults -- children -- Henoch‐Schönlein purpura -- IgA vasculitis -- renal outcomes
Rheumatology -- Periodicals
Rheumatology -- Asia -- Periodicals
Rheumatology -- Pacific Area -- Periodicals
Rheumatic Diseases -- Periodicals
Connective Tissue Diseases -- Periodicals
Immune System Diseases -- Periodicals
616.723 - Journal URLs:
- http://ejournals.ebsco.com/direct.asp?JournalID=715072 ↗
http://www.blackwell-synergy.com/loi/ijrd ↗
http://www.blackwellpublishing.com/aims.asp?ref=1756-1841&site=1 ↗
http://www3.interscience.wiley.com/journal/120118343/grouphome/home.html ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1756-185X ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/1756-185X.13221 ↗
- Languages:
- English
- ISSNs:
- 1756-1841
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