File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
  • Find via Find It@HKUL
Supplementary

Conference Paper: Ustekinumab increases risk of herpes zoster in patients with spondyloarthritis

TitleUstekinumab increases risk of herpes zoster in patients with spondyloarthritis
Authors
Issue Date2018
PublisherWiley-Blackwell Publishing Asia. The Journal's web site is located at http://www.blackwell-synergy.com/loi/ijrd
Citation
The 20th Asia Pacific League of Associations for Rheumatology Congress (APLAR 2018), Kaohsiung, Taiwan, 6-9 September 2018. In International Journal of Rheumatic Diseases, 2018, v. 21 n. S1, p. 64, abstract no. SU144 How to Cite?
AbstractObjective: To report the risk factors of herpes zoster (HZ) in patients with spondyloarthritis (SpA). Method: Three hundred and forty four patients with an expert diagnosis of SpA were identified retrospectively from 3 rheumatology centers in Hong Kong. Medical records from 1998 to 2018 were reviewed for incidence of HZ and demographic parameters. This included age, sex, duration of follow‐up, co‐morbidities, and smoking and drinking status. We identified all disease modifying anti‐rheumatic drugs (DMARDs) used, including sulphasalazine, methotrexate, leflunomide, cyclosporin, steroids, etanercept, infliximab, adalimumab, golimumab, secukinumab and ustekinumab. Cox regression models were used to evaluate hazard ratios (HRs) of HZ in SpA patients on different immunosuppressants. Result: Among 344 patients with SpA, the male‐to‐female ratio was 6.1:3.9. Mean age was 47.6 years. Mean disease duration was 8.2 years. Sixty‐nine patients were diagnosed with psoriatic arthritis (PsA). Sixteen patients suffered from HZ during the period of study. The incident was 5.68 per 1000 patient‐years. Univariate cox regression showed sulphalazine (HR 0.31, P = 0.07), ustekinumab (HR 11.20, P = 0.03), diabetes (HR 4.11, P = 0.01), renal impairment (HR 4.30, P = 0.01) and thyroid disease (HR 5.67, P = 0.02) were associated with HZ. Multivariate cox regression model showed an increased risk of HZ with use of ustekinumab (HR 14.46, 95% CI 1.65; 126.49, P = 0.02), renal impairment (HR 3.35. 95% CI 0.97; 11.54, P = 0.06) and thyroid disease (HR 6.83, 95% CI 1.47; 31.71, P = 0.01). Conclusion: Use of ustekinumab was associated with HZ in patients with SpA. Other identified risks factors were renal impairment and thyroid disease.
DescriptionPoster presentation no. 144
Persistent Identifierhttp://hdl.handle.net/10722/256454
ISSN
2023 Impact Factor: 2.4
2023 SCImago Journal Rankings: 0.653

 

DC FieldValueLanguage
dc.contributor.authorChung, HY-
dc.contributor.authorYuen, KKL-
dc.contributor.authorLau, WCS-
dc.date.accessioned2018-07-20T06:34:55Z-
dc.date.available2018-07-20T06:34:55Z-
dc.date.issued2018-
dc.identifier.citationThe 20th Asia Pacific League of Associations for Rheumatology Congress (APLAR 2018), Kaohsiung, Taiwan, 6-9 September 2018. In International Journal of Rheumatic Diseases, 2018, v. 21 n. S1, p. 64, abstract no. SU144-
dc.identifier.issn1756-1841-
dc.identifier.urihttp://hdl.handle.net/10722/256454-
dc.descriptionPoster presentation no. 144-
dc.description.abstractObjective: To report the risk factors of herpes zoster (HZ) in patients with spondyloarthritis (SpA). Method: Three hundred and forty four patients with an expert diagnosis of SpA were identified retrospectively from 3 rheumatology centers in Hong Kong. Medical records from 1998 to 2018 were reviewed for incidence of HZ and demographic parameters. This included age, sex, duration of follow‐up, co‐morbidities, and smoking and drinking status. We identified all disease modifying anti‐rheumatic drugs (DMARDs) used, including sulphasalazine, methotrexate, leflunomide, cyclosporin, steroids, etanercept, infliximab, adalimumab, golimumab, secukinumab and ustekinumab. Cox regression models were used to evaluate hazard ratios (HRs) of HZ in SpA patients on different immunosuppressants. Result: Among 344 patients with SpA, the male‐to‐female ratio was 6.1:3.9. Mean age was 47.6 years. Mean disease duration was 8.2 years. Sixty‐nine patients were diagnosed with psoriatic arthritis (PsA). Sixteen patients suffered from HZ during the period of study. The incident was 5.68 per 1000 patient‐years. Univariate cox regression showed sulphalazine (HR 0.31, P = 0.07), ustekinumab (HR 11.20, P = 0.03), diabetes (HR 4.11, P = 0.01), renal impairment (HR 4.30, P = 0.01) and thyroid disease (HR 5.67, P = 0.02) were associated with HZ. Multivariate cox regression model showed an increased risk of HZ with use of ustekinumab (HR 14.46, 95% CI 1.65; 126.49, P = 0.02), renal impairment (HR 3.35. 95% CI 0.97; 11.54, P = 0.06) and thyroid disease (HR 6.83, 95% CI 1.47; 31.71, P = 0.01). Conclusion: Use of ustekinumab was associated with HZ in patients with SpA. Other identified risks factors were renal impairment and thyroid disease.-
dc.languageeng-
dc.publisherWiley-Blackwell Publishing Asia. The Journal's web site is located at http://www.blackwell-synergy.com/loi/ijrd-
dc.relation.ispartofInternational Journal of Rheumatic Diseases-
dc.relation.ispartofAsia Pacific League of Associations for Rheumatology Congress (APLAR 2018)-
dc.titleUstekinumab increases risk of herpes zoster in patients with spondyloarthritis-
dc.typeConference_Paper-
dc.identifier.emailChung, HY: jameschy@hku.hk-
dc.identifier.emailLau, WCS: cslau@hku.hk-
dc.identifier.authorityChung, HY=rp02330-
dc.identifier.authorityLau, WCS=rp01348-
dc.identifier.hkuros286165-
dc.identifier.volume21-
dc.identifier.issueS1-
dc.identifier.spage64-
dc.identifier.epage64-
dc.publisher.placeAustralia-
dc.identifier.issnl1756-1841-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats