Multicenter cohort study on the perioperative adverse events with orthopedic surgery associated with abatacept

Multicenter cohort study on the perioperative adverse events with orthopedic surgery associated with abatacept - Perioperative complications with abatacept

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000023088

Enrollment

200

Registered

2016-07-11

Start date

2016-08-01

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

rheumatoid arthritis

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1) rheumatoid arthritis patients diagnosed by the classification criteria of ACR 1987 or ACR/EULAR 2010 2) patients who received abatacept for rheumatoid arthritis, underwent orthopedic surgery during April 2011 to March 2014, and were followed-up for 12 months

Exclusion criteria

Exclusion criteria: 1) patients who received bDMARD other than abatacept within 6 months before the operation 2) patients who have history of infection on the operated joint 3) operation other than orthopedic surgery 4) follow-up period less than 12 months 5) missing or insufficient data 6) patients who did not show consent for this study

Design outcomes

Primary

Measure	Time frame
the occurrence ratio of surgical site infection	—

Countries

Japan

Contacts

Public ContactHiromu Hiromu

Kyoto University Hospital Orthopaedic Surgery

hiromu@kuhp.kyoto-u.ac.jp075-751-3366

Outcome results