# Patient comorbidities, medication intake, and mortality in revision surgery for periprosthetic joint infection of the hip and knee: analysis of 346 patients

**Authors:** Filippo Migliorini, Christian David Weber, Andreas Bell, Marcel Betsch, Nicola Maffulli, Vanessa Poth, Michael Celik, Tommaso Bardazzi, Ulf Krister Hofmann, Frank Hildebrand, Arne Driessen

PMC · DOI: 10.1186/s13018-025-06209-w · Journal of Orthopaedic Surgery and Research · 2026-03-03

## TL;DR

This study found that patients with dementia, kidney issues, or a history of cancer have higher in-hospital mortality after hip or knee revision surgery for joint infections.

## Contribution

The study identifies specific comorbidities that increase mortality risk in revision surgery for joint infections.

## Key findings

- Dementia, renal insufficiency, and malignancy history significantly increase in-hospital mortality.
- Other conditions like diabetes or hypertension do not affect mortality in these surgeries.
- Medication intake does not influence in-hospital mortality for these patients.

## Abstract

Patient comorbidities and medication intake impact on the mortality rate in revision surgery for periprosthetic joint infection (PJI) of the lower limb. The present study collected data from patients who underwent revision surgery for PJI of total hip arthroplasty (THA) or total knee arthroplasty (TKA). Data regarding comorbidities and medication intake for each patient were collected to investigate whether comorbidities and medication intake influence in-hospital mortality in patients who underwent revision surgery for PJI of a THA or TKA.

The present study follows the STROBE Statement. Our institutional databases were searched using the OPS (operation and procedure codes) 5–823 and 5–821 in combination with the ICD (International Statistical Classification of Diseases and Related Health Problems) codes T84.5, T84.7 or T84.8. All patients with hip or knee implant infections who underwent revision surgery were retrospectively retrieved and included in the present study.

Data from 346 patients were collected (181 THAs and 165 TKAs). Patients with renal insufficiency demonstrated a statistically significant greater risk of in-hospital mortality (95% CI 0.0131 to 0.1132), as did patients with a history of malignancy (95% CI 0.1478 to 0.7497), and patients with dementia (95% CI 0.0398 to 0.3791). Nicotine and alcohol abuse, diabetes mellitus, arterial hypertension, hereditary thrombophilia, hereditary haemorrhages, cerebrovascular diseases, coronary heart diseases, chronic obstructive pulmonary disease osteoporosis, liver cirrhosis, rheumatoid arthritis, acute dental infection did not influence in the in-hospital mortality rate in patients who underwent revision surgery for PJI of a THA or TKA. Patient medication therapy did not impact the risk of in-hospital mortality in PJI.

Patients undergoing revision surgery for PJI after total hip and knee arthroplasty show an increased in-hospital mortality in the presence of the following comorbidities: dementia, renal insufficiency, and history of malignancy. Based on the present results, further infection prevention and geriatric co-management strategies should be evaluated for patients undergoing revision arthroplasty of the hip and knee for PJI.

## Linked entities

- **Diseases:** periprosthetic joint infection (MONDO:0800179), renal insufficiency (MONDO:0001106), malignancy (MONDO:0004992), dementia (MONDO:0001627), diabetes mellitus (MONDO:0005015), hereditary thrombophilia (MONDO:0100240), chronic obstructive pulmonary disease (MONDO:0005002), osteoporosis (MONDO:0005298), rheumatoid arthritis (MONDO:0008383)

## Full-text entities

- **Diseases:** Nicotine and alcohol abuse (MESH:D000437), coronary heart disease (MESH:D003327), skin and mucous membrane infections (MESH:D010390), pain (MESH:D010146), small cell lung cancer (MESH:D055752), peripheral vascular diseases (MESH:D016491), nicotine abuse (MESH:D014029), Trauma (MESH:D014947), bacteraemia (MESH:C531821), inflammation (MESH:D007249), chronic liver disease (MESH:D008107), swelling (MESH:D004487), acute dental infection (MESH:D010195), hereditary haemorrhages (MESH:D028243), liver cirrhosis (MESH:D008103), Diabetes mellitus (MESH:D003920), malignancies (MESH:D009369), substance abuse (MESH:D019966), kidney failure (MESH:D051437), hereditary thrombophilia (MESH:C540694), overweight (MESH:D050177), COPD (MESH:D029424), Hip (MESH:D025981), Obesity (MESH:D009765), rheumatoid diseases (MESH:D011695), PJI (MESH:D057068), healing (MESH:C563468), osteoarthritis (MESH:D010003), arterial hypertension (MESH:D000081029), hyperglycaemic blood sugar (MESH:D006402), died (MESH:D003643), rheumatoid arthritis (MESH:D001172), arthritis (MESH:D001168), Knee (MESH:D007718), osteoporosis (MESH:D010024), congenital heart defects (MESH:D006330), cerebrovascular diseases (MESH:D002561), UTI (MESH:D014552), coagulopathies (MESH:D001778), dental infection (MESH:D007239), dementia (MESH:D003704), diabetes mellitus type I or Type II (MESH:D003922), allergies (MESH:D004342), postoperative (MESH:D019106), implant (MESH:D057873), chronic pulmonary disease (MESH:D002908), bloodstream infections (MESH:D018805), fistula (MESH:D005402), ventricular fibrillation (MESH:D014693), septic shock (MESH:D012772)
- **Chemicals:** beta-lactam antibiotics (MESH:D008997), coumarin (MESH:C030123), Vancomycin (MESH:D014640), clindamycin (MESH:D002981), blood glucose (MESH:D001786), sulfamethoxazole (MESH:D013420), NOACs (-), nicotine (MESH:D009538), trimethoprim (MESH:D014295), cephalosporin (MESH:D002511), cefadroxil (MESH:D002434), creatinine (MESH:D003404), alcohol (MESH:D000438), heparins (MESH:D006493)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

15 references — full list in the complete paper: https://tomesphere.com/paper/PMC12954884/full.md

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Source: https://tomesphere.com/paper/PMC12954884