File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1093/rheumatology/kem102
- Scopus: eid_2-s2.0-34547830793
- PMID: 17522097
- WOS: WOS:000248686800015
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: Recurrent major infections in juvenile-onset systemic lupus erythematosus - A close link with long-term disease damage
Title | Recurrent major infections in juvenile-onset systemic lupus erythematosus - A close link with long-term disease damage |
---|---|
Authors | |
Keywords | Children Infections SLE SlE Damage Index |
Issue Date | 2007 |
Publisher | Oxford University Press. The Journal's web site is located at http://rheumatology.oxfordjournals.org/ |
Citation | Rheumatology, 2007, v. 46 n. 8, p. 1290-1296 How to Cite? |
Abstract | Objectives. We postulate that patients with systemic lupus erythematosus (SLE) having recurrent infections are more likely to have poorer disease outcome. The aim of this study is to describe the pattern of infections and disease damage that occurred in a cohort of patients with juvenile-onset SLE, and to find out whether cumulative disease damage was associated with recurrent infections in these patients. Method. We retrospectively reviewed (1988-2004) the clinical characteristics, infective complications, and disease damage as measured by the Systemic Lupus International Collaborating Clinics/American College of Rheumatology (SLICC/ACR) Damage Index (SDI) in 47 juvenile-onset SLE patients. Potential risk factors for disease damage were evaluated by univariate analysis and logistic regression. The correlation between number of major infections and disease damage was determined. Results. Thirty-two (68.1%) patients had lupus nephropathy and 16 patients (34%) had neuropsychiatric lupus. Sixty-one episodes of major infections, defined as infections requiring more than 1 week of antimicrobial agents, occurred in 27 patients (57.4%), and 18 patients (31.4%) had recurrent major infections (≥ 2 episodes). Organ damage (SDI ≥ 1) was documented in 21 subjects (44.7%). By logistic regression, occurrence of major infections (P lt; 0.001) was the only significant risk factor for disease damage. There was a positive correlation between SDI score with the number of recurrent major infections (Spearman's correlation coefficient = 0.50, P lt; 0.001). Conclusion. Infections and disease damage are common co-morbidities in juvenile-onset SLE. Recurrent infections could predict poorer disease outcome and associated organ damage in SLE. © The Author 2007. |
Persistent Identifier | http://hdl.handle.net/10722/80023 |
ISSN | 2023 Impact Factor: 4.7 2023 SCImago Journal Rankings: 1.721 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Lee, PPW | en_HK |
dc.contributor.author | Lee, TL | en_HK |
dc.contributor.author | Ho, MHK | en_HK |
dc.contributor.author | Wong, WHS | en_HK |
dc.contributor.author | Lau, YL | en_HK |
dc.date.accessioned | 2010-09-06T08:01:29Z | - |
dc.date.available | 2010-09-06T08:01:29Z | - |
dc.date.issued | 2007 | en_HK |
dc.identifier.citation | Rheumatology, 2007, v. 46 n. 8, p. 1290-1296 | en_HK |
dc.identifier.issn | 1462-0324 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/80023 | - |
dc.description.abstract | Objectives. We postulate that patients with systemic lupus erythematosus (SLE) having recurrent infections are more likely to have poorer disease outcome. The aim of this study is to describe the pattern of infections and disease damage that occurred in a cohort of patients with juvenile-onset SLE, and to find out whether cumulative disease damage was associated with recurrent infections in these patients. Method. We retrospectively reviewed (1988-2004) the clinical characteristics, infective complications, and disease damage as measured by the Systemic Lupus International Collaborating Clinics/American College of Rheumatology (SLICC/ACR) Damage Index (SDI) in 47 juvenile-onset SLE patients. Potential risk factors for disease damage were evaluated by univariate analysis and logistic regression. The correlation between number of major infections and disease damage was determined. Results. Thirty-two (68.1%) patients had lupus nephropathy and 16 patients (34%) had neuropsychiatric lupus. Sixty-one episodes of major infections, defined as infections requiring more than 1 week of antimicrobial agents, occurred in 27 patients (57.4%), and 18 patients (31.4%) had recurrent major infections (≥ 2 episodes). Organ damage (SDI ≥ 1) was documented in 21 subjects (44.7%). By logistic regression, occurrence of major infections (P lt; 0.001) was the only significant risk factor for disease damage. There was a positive correlation between SDI score with the number of recurrent major infections (Spearman's correlation coefficient = 0.50, P lt; 0.001). Conclusion. Infections and disease damage are common co-morbidities in juvenile-onset SLE. Recurrent infections could predict poorer disease outcome and associated organ damage in SLE. © The Author 2007. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Oxford University Press. The Journal's web site is located at http://rheumatology.oxfordjournals.org/ | en_HK |
dc.relation.ispartof | Rheumatology | en_HK |
dc.rights | Rheumatology. Copyright © S Karger AG. | en_HK |
dc.subject | Children | en_HK |
dc.subject | Infections | en_HK |
dc.subject | SLE | en_HK |
dc.subject | SlE Damage Index | en_HK |
dc.title | Recurrent major infections in juvenile-onset systemic lupus erythematosus - A close link with long-term disease damage | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0080-2727&volume=46&issue=8&spage=1290&epage=1296&date=2007&atitle=Recurrent+major+infections+in+juvenile-onset+systemic+Lupus+erythematosus+-+a+close+link+with+long-term+disease+damage | en_HK |
dc.identifier.email | Lee, PPW:ppwlee@hku.hk | en_HK |
dc.identifier.email | Lau, YL:lauylung@hkucc.hku.hk | en_HK |
dc.identifier.authority | Lee, PPW=rp00462 | en_HK |
dc.identifier.authority | Lau, YL=rp00361 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1093/rheumatology/kem102 | en_HK |
dc.identifier.pmid | 17522097 | - |
dc.identifier.scopus | eid_2-s2.0-34547830793 | en_HK |
dc.identifier.hkuros | 128420 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-34547830793&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 46 | en_HK |
dc.identifier.issue | 8 | en_HK |
dc.identifier.spage | 1290 | en_HK |
dc.identifier.epage | 1296 | en_HK |
dc.identifier.isi | WOS:000248686800015 | - |
dc.publisher.place | United Kingdom | en_HK |
dc.identifier.scopusauthorid | Lee, PPW=14048822200 | en_HK |
dc.identifier.scopusauthorid | Lee, TL=24483772800 | en_HK |
dc.identifier.scopusauthorid | Ho, MHK=8925896400 | en_HK |
dc.identifier.scopusauthorid | Wong, WHS=13310222200 | en_HK |
dc.identifier.scopusauthorid | Lau, YL=7201403380 | en_HK |
dc.identifier.issnl | 1462-0324 | - |