What did survey results from the BOOM meeting reveal about the use of DAIR-based procedures?
This worldwide survey of 272 surgeons revealed striking variability; 62% of surgeons routinely perform radical soft tissue debridement when managing PJIs, and approximately 55% believe DAIR works most of the time, but 20% think it doesn’t work. Time thresholds for implementation of these DAIR-[based] procedures varied as well. A total of 32% [of surgeons] will [perform the procedure] within 3 weeks of the inciting infection, 29% within 6 weeks, and only 19% 12 weeks or [after] presentation of the infection. Antibiotic duration ranged broadly from one-third favoring 3 months or more [to approximately] 40% favoring up to 6 weeks. There’s great heterogeneity there, which reflects a gap in knowledge as well as a systems gap. Surgeons are compelled to adapt to patient complexity [and] limited biologic reserve, and this can have catastrophic consequences.
Could DAIR have a role in oncologic reconstruction? What factors might predict its success?
A major insight from this study is that DAIR does have a role in oncologic reconstruction, but its success depends heavily on context. Early infections fare better than chronic infections. Aggressive debridement remains the strongest predictor of DAIR success. Polyethylene-only exchanges, which we see often in the arthroplasty literature, may underperform compared with modular component exchanges because of the massive nature of these prostheses. The biggest limitation is the absence of comparative data across these major sarcoma centers, leaving surgeons to rely on experience rather than evidence.
What next steps are needed to achieve consensus on the definition of PJIs and DAIR procedures?
Standardization is essential. Without unified definitions, multicenter trials and meta-analyses are impossible. BOOM proposed nomenclature as a critical step toward global coherence. We need to stratify our patients in reconstructions. We need to look at the reconstruction type, specifically biologic vs these mega-prostheses, infection timing, acute vs chronic, host physiology, accounting for systemic treatments, immunosuppression, and other oncologic variables, in addition to organism types such as staph, which is the most common, gram negative, and maybe fungal.
Doing this will allow us to have a prospective collaborative effort, because these are uncommon procedures, but the relative infection rate compared with the arthroplasty literature is high. We need to be able to get beyond individual institutional data sets. We need BOOM and the Musculoskeletal Tumor Society in the United States and then the European societies and the Asian Pacific groups to coordinate their data sets. This will allow us to improve our outcomes by being able to understand better the soft tissue management, the antibiotic const, the antibiotic latent constructs, and be able to potentially even recognize infections earlier based upon risk factor.
What are the most common secondary infections seen after limb salvage surgery, and what risk factors should medical oncologists be most aware of?
[Staphylococcus] aureus is by far the most common infection we see; sometimes S epidermidis and other skin flora, but mucosal bugs are also an issue. There are talks about nasal swabs and things of that sort in terms of what medical oncologists need to be aware of. They’re not responsible for [managing] the wounds, but [they should be prepared to ask] cursory questions, if not evaluate the area in question, to determine whether there’s any warmth, new swelling, or redness, and then alert the orthopedic oncologist as to that finding.
How do prior or ongoing cancer therapies affect infection risk, presentation, and healing following limb salvage procedures?
If patients are on cytotoxic chemotherapy, that can create an immunocompromised situation. Immunomodulation therapies, by definition, can potentially increase the risk of infection. Coordination of these modalities with the orthopedic oncologist, factoring in comorbidities such as diabetes and other conditions that might affect the immune system, is important when the medical and orthopedic oncologists are deciding what the best course of action is for the reconstruction.
What early clinical or imaging signs should prompt oncologists to suspect a secondary infection and refer patients back to orthopedic surgery promptly?
If the patient is post operative, they should ask, “How is the surgical area? How is it feeling? [Is there] any warmth, [have you had] any fevers?” Most of these [infections] would be picked up in a standard review of systems by the medical oncologist. [It’s important to have] that added finesse and question the [patient about the] surgical site for warmth, swelling, or increasing tenderness, and then any fevers.
How do secondary infections affect long-term functional outcomes in limb preservation? When does infection shift the risk-benefit ratio toward a more aggressive intervention?
That’s the crux of what we’re trying to figure out. These are big defects with artificial components, or sometimes biologic components put in place of the area where we have to do the resection, [so] to have to explant these devices or constructs is a huge source of morbidity for these patients and puts the limb at risk. Because these infections can be so extensive, they can also put the patient at risk because of the systemic sequelae of an immunocompromised host. [Infections can also] delay additional therapy, which can be limb, life, and oncologically threatening.
What best practices for multidisciplinary coordination can help prevent and manage secondary infections more effectively?
We’re trying to tease out best practices given what we outlined at the BOOM meeting, but orthopedic oncologists remain vigilant in doing scrub down techniques for the patient ahead of surgery, nasal swabbing, and things of that sort to check for abnormal bacterial counts in a variety of sites that put the host at risk. Fervent communication with the medical oncologist and the orthopedic oncologist needs to happen in real time if there are concerns about an emerging secondary infection.
What take-home message would you like to share with colleagues?
PJI after tumor reconstruction for bone sarcomas is completely different from that in routine arthroplasty. The BOOM global study shows that widespread practice variations exist. Although there’s a lack of consensus, there’s a shared willingness among surgeons to unify definitions and work toward evidence-based practices. Establishing a consistent conceptual and procedural framework for DAIR and DAIR plus in modular exchange is the most important next step in improving outcomes for our patients.
With respect to medical oncologists who we partner with to take care of patients with bone sarcomas, this [process] can influence the timing of chemotherapy, immunotherapy, and targeted agents, so there needs to be increased awareness from both the medical oncologists as well as the sarcoma surgeons to be able to stratify for infection risk, wound biology, and the viability of limb salvage reconstructions. When we understand DAIR strategies more stringently, we’re likely to succeed or fail in a much more precise way, a much more predictive way, and this will help medical oncologists coordinate systemic therapy, anticipate complications, and advocate for earlier surgical reevaluations when they’re starting to suspect that there might be an infection and potentially avoid a catastrophic reconstruction failure, which would be a huge impact to not only the patient’s quality of life, but potentially their overall survival.
References
- Jeys L, Botello E, Boyle RA, et al. A modified Delphi consensus on periprosthetic infection in orthopaedic oncology: a report from the Birmingham Orthopaedic Oncology Meeting (BOOM). Bone Jone J. 2025;107-B(12):1352-1359. doi:10.1302/0301-620X.107B12.BJJ-2024-1039.R4
- Khan Z, Khan ZA, Zamora T, et al. What is debridement, antibiotics, and implant retention in orthopaedic oncology? Bone Jt Open. 2025;6(11):1495-1503. doi:10.1302/2633-1462.611.BJO-2025-0114.R2