Preoperative risk factors in joint replacement surgery - A prospective risk calculating model to estimate postoperative medical complications and IMC/ICU transmission

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00012529

Enrollment

649

Registered

2017-06-07

Start date

2013-09-02

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

All patients that needed primary or revision implantation of knee endoprosthesis (multiple health conditions, i.e. neoplasia, haemophilia, trauma, septic arthritis, infected knee endoprosthesis, secondary gonarthrosis etc.) M17.1

Interventions

Group 1: Single-arm observational study: All patients treated with primary or revision total knee arthroplasty in the clinic for orthopedic and trauma surgery of the University Hospital Bonn from 200

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: All patients treated with primary or revision total knee arthroplasty in the clinic for orthopedic and trauma surgery of the University Hospital Bonn from 01/01/2008 until 31/12/2012.

Exclusion criteria

Exclusion criteria: Deficient or missing amount of data in our institutional database (ORBIS)

Design outcomes

Primary

Measure	Time frame
Occurrence of postoperative complications (defined as unexpected adverse events (myocardial infarction, deep vein thrombosis, pulmonary embolism, systemic inflammatory response syndrome (SIRS), postoperative artificial respiration, postoperative demand for catecholamines and/or resuscitation), demand for postoperative blood transfusion and necessary transfer to Intermediate Care- (IMC) or Intensive Care Unit (ICU) is retrospectively anonymized evaluated through institutional database (ORBIS).	—

Measure

Time frame

Occurrence of postoperative complications (defined as unexpected adverse events (myocardial infarction, deep vein thrombosis, pulmonary embolism, systemic inflammatory response syndrome (SIRS), postoperative artificial respiration, postoperative demand for catecholamines and/or resuscitation), demand for postoperative blood transfusion and necessary transfer to Intermediate Care- (IMC) or Intensive Care Unit (ICU) is retrospectively anonymized evaluated through institutional database (ORBIS).

—

Countries

Germany

Contacts

Public ContactAnne Klausing

Universitätsklinikum Bonn Klinik für Mund-, Kiefer- und Plastische Gesichtschirurgie

anne.klausing@ukbonn.de+49 176 832 819 16

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026