# Perioperative Management of Biologic and Targeted Synthetic DMARDs in Orthopedic Surgery: Balancing Infection Risk and Disease Control

**Authors:** Francesco Mancuso, Jacopo Angelini, Alen Zabotti, Francesco Russiani, Massimo Baraldo, Luca Quartuccio, Hemant Pandit, Paolo Di Benedetto, Araldo Causero

PMC · DOI: 10.3390/microorganisms14020398 · Microorganisms · 2026-02-07

## TL;DR

This paper discusses managing biologic drugs before orthopedic surgery to balance infection risk and disease control.

## Contribution

It provides updated guidelines for individualized drug management based on drug type, surgery, and patient factors.

## Key findings

- Withholding biologics before surgery reduces infection risk but may increase disease flare-ups.
- Pharmacokinetics and surgery type are critical in deciding drug discontinuation timing.
- Multidisciplinary coordination is essential to optimize patient outcomes.

## Abstract

The perioperative management of biologic and immunomodulatory therapies in patients undergoing orthopedic surgery poses a clinical challenge, primarily due to the increased risk of postoperative infections. Biologic agents, particularly TNF inhibitors and interleukin-targeting drugs, may impair host immune responses, potentially increasing the risk of surgical site infections (SSIs), delayed wound healing, and systemic infections. However, abrupt discontinuation of these therapies can lead to disease flare-ups, which themselves may complicate recovery and rehabilitation. In addition, discontinuation of biologics can lead to drug tolerance and unresponsiveness when they are restarted and thereby need switching to another biologic. Recent studies suggest that the infection risk is particularly elevated with ongoing biologic therapy during major surgeries, especially in procedures involving prosthetic implants. Guidelines generally recommend withholding biological disease-modifying antirheumatic drugs (bDMARDs) for at least one dosing cycle prior to surgery, when feasible, while maintaining non-biologic DMARDs in most cases. The decision must be individualized, taking into account the pharmacokinetics of each drug, the type of surgery, the patient’s comorbidities, and the activity of the underlying disease. Close coordination among rheumatologists, orthopedic surgeons, and infectious disease specialists is essential to minimize perioperative complications and optimize patient outcomes.

## Linked entities

- **Proteins:** TNF (tumor necrosis factor)

## Full-text entities

- **Genes:** IL1A (interleukin 1 alpha) [NCBI Gene 3552] {aka IL-1 alpha, IL-1A, IL1, IL1-ALPHA, IL1F1}, FGB (fibrinogen beta chain) [NCBI Gene 2244] {aka HEL-S-78p}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, THBD (thrombomodulin) [NCBI Gene 7056] {aka AHUS6, BDCA-3, BDCA3, CD141, THPH12, THRM}, SAA [NCBI Gene 6287], IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, IL17A (interleukin 17A) [NCBI Gene 3605] {aka CTLA-8, CTLA8, IL-17, IL-17A, IL17, ILA17}, IL23A (interleukin 23 subunit alpha) [NCBI Gene 51561] {aka IL-23, IL-23A, IL23P19, P19, SGRF}, F3 (coagulation factor III, tissue factor) [NCBI Gene 2152] {aka CD142, TF, TFA}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}
- **Diseases:** diabetes (MESH:D003920), inflammatory complications (MESH:D018746), prosthetic failure (MESH:D051437), inflammatory rheumatic and musculoskeletal diseases (MESH:D012213), edema (MESH:D004487), chronic kidney disease (MESH:D051436), hyperglycemia (MESH:D006943), Chronic inflammation (MESH:D007249), Respiratory infections (MESH:D012141), degenerative joint disease (MESH:D019636), injury to (MESH:D014947), pyogenic bacteria (MESH:C000719206), pain (MESH:D010146), fracture (MESH:D050723), pulmonary embolism (MESH:D011655), fever (MESH:D005334), arthritic (MESH:D015535), frailty (MESH:D000073496), PJI (MESH:D057068), damage (MESH:D020263), obesity (MESH:D009765), febrile (MESH:D000071072), autoimmune diseases (MESH:D001327), rheumatoid (MESH:D011695), pneumonia (MESH:D011014), overweight (MESH:D050177), ankylosing spondylitis (MESH:D013167), hip (MESH:D025981), postoperative complications (MESH:D011183), gastrointestinal infections (MESH:D005767), end-stage arthritis (MESH:D007676), synovitis (MESH:D013585), Infection (MESH:D007239), MACE (MESH:D002318), effusions (MESH:D000080324), rheumatic (MESH:D012216), joint (MESH:D007592), DVT (MESH:D020246), thrombotic (MESH:D013927), RA (MESH:D001172), arthritis (MESH:D001168), Anemia (MESH:D000740), malnutrition (MESH:D044342), Venous thromboembolic (MESH:D054556), stiffness (MESH:C566112), erythema (MESH:D004890), immune dysregulation (OMIM:614878), Infectious Complications (MESH:D003141), sepsis (MESH:D018805), disability (MESH:D009069), MRSA colonization (MESH:D003108), CoNS (MESH:D064726), inflammatory bowel disease (MESH:D015212), RMDs (MESH:D009140), bacterial infection (MESH:D001424), TDM (MESH:D000081015), granuloma (MESH:D006099), postoperative (MESH:D019106), thromboembolic (MESH:D013923), SSI (MESH:D013530)
- **Chemicals:** tofacitinib (MESH:C479163), Risankizumab (MESH:C000601773), Tocilizumab (MESH:C502936), oxazolidinones (MESH:D023303), chlorhexidine (MESH:D002710), Secukinumab (MESH:C555450), Infliximab (MESH:D000069285), Adalimumab (MESH:D000068879), methotrexate (MESH:D008727), carbapenems (MESH:D015780), vancomycin (MESH:D014640), Rituximab (MESH:D000069283), Ixekizumab (MESH:C549079), cephalosporins (MESH:D002511), rifampicin (MESH:D012293), dalbavancin (MESH:C469289), leflunomide (MESH:D000077339), Golimumab (MESH:C529000), fluoroquinolones (MESH:D024841), sulfasalazine (MESH:D012460), Janus (-), Canakinumab (MESH:C541220), penicillins (MESH:D010406), Guselkumab (MESH:C000588857), alcohol (MESH:D000438), oritavancin (MESH:C100708), glucose (MESH:D005947), Prednisone (MESH:D011241), steroid (MESH:D013256), daptomycin (MESH:D017576), Bimekizumab (MESH:C000625981), cefazolin (MESH:D002437)
- **Species:** Pseudomonas aeruginosa (species) [taxon 287], Cutibacterium acnes (species) [taxon 1747], Nocardia (genus) [taxon 1817], Escherichia coli (E. coli, species) [taxon 562], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Mycobacterium tuberculosis (species) [taxon 1773], Staphylococcus aureus (species) [taxon 1280], Homo sapiens (human, species) [taxon 9606], Staphylococcus epidermidis (species) [taxon 1282], Listeria monocytogenes (species) [taxon 1639]

## Full text

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## Figures

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## References

96 references — full list in the complete paper: https://tomesphere.com/paper/PMC12943139/full.md

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Source: https://tomesphere.com/paper/PMC12943139