CLINICAL RESEARCH
Intraosseous Vancomycin for Acute Periprosthetic
Knee Infection: A Retrospective Study
Walter F. Martínez,*
Eduardo J. Bochatey,** Fernando
A. Lopreite#
*Clínica Privada Hispano
Argentina, Tres Arroyos, Buenos Aires, Argentina
**Instituto Argentino de
Diagnóstico y Tratamiento, Autonomous City of Buenos Aires, Argentina
#Orthopedics and
Traumatology Service, Hospital Británico de Buenos
Aires, Autonomous City of Buenos Aires, Argentina
ABSTRACT
Introduction: Periprosthetic joint infection (PJI) is an uncommon but
serious complication after total knee arthroplasty (TKA), with significant
clinical and healthcare implications. This study evaluated the effectiveness of
the debridement, antibiotics, and implant retention (DAIR) protocol combined
with intraosseous vancomycin administration and modular component exchange in
controlling acute infection and improving functional outcomes. Materials and Methods: We conducted a
retrospective study across three institutions, including 12 patients (7 women,
5 men; mean age, 72.4 ± 6.3 years) with acute PJI treated with DAIR between
February 2022 and June 2023. The mean interval between primary TKA and the DAIR
procedure was 12.3 days. A standardized protocol was applied,
consisting of intraosseous vancomycin delivery, modular component exchange, and
pathogen-directed antibiotic therapy. Results: The mean
surgical time was 95 ± 10 minutes. Infection control was
achieved in 11 of 12 cases (91.6%), with one reinfection requiring
two-stage revision. The Knee Society Score improved significantly from 42.5 ±
5.8 preoperatively to 88.6 ± 6.3 at 1 year (p < 0.001). Conclusion: The DAIR protocol with intraosseous
vancomycin and modular component exchange appears to be a promising strategy
for managing acute periprosthetic knee infection.
Larger studies are needed to confirm these preliminary
results.
Keywords: Periprosthetic joint infection; knee; intraosseous
vancomycin; debridement; implant retention.
Level of Evidence: IV
Vancomicina intraósea para la
infección periprotésica aguda de rodilla. Estudio retrospectivo
RESUMEN
Introducción: La infección periprotésica es una
complicación poco frecuente, pero grave, tras la artroplastia total de rodilla,
tiene un alto impacto clínico y sanitario. Este estudio evalúa la eficacia del
protocolo de desbridamiento, antibióticos y retención del implante (debridement, antibiotics, and implant
retention, DAIR), combinado con la administración intraósea de vancomicina
y el recambio de componentes modulares, para controlar la infección aguda y
mejorar los resultados funcionales. Materiales y Métodos: Estudio retrospectivo en 3
instituciones, que incluyó a 12 pacientes (7 mujeres, 5 hombres; edad media
72.4 ± 6.3 años) con infección periprotésica aguda tratados con DAIR entre febrero
de 2022 y junio de 2023. El tiempo promedio desde la artroplastia total de
rodilla hasta la cirugía DAIR fue de 12.3 días. Se aplicó un protocolo uniforme
con administración intraósea de vancomicina, recambio de componentes modulares
y antibioterapia dirigida. Resultados: El tiempo quirúrgico medio fue de 95 ± 10 minutos. Se logró el control de la infección en
el 91,6%, hubo una reinfección que requirió revisión en dos tiempos. El Knee Society Score mejoró de 42,5 ± 5,8
a 88,6 ± 6,3 al año (p <0,001). Conclusión: El protocolo DAIR
con vancomicina intraósea y recambio
modular es prometedor en el manejo de la infección periprotésica aguda de
rodilla. Se requieren estudios más amplios.
Palabras clave: Infección periprotésica de rodilla;
vancomicina intraósea; desbridamiento; retención de implantes.
Nivel de Evidencia: IV
INTRODUCTION
Total knee arthroplasty
(TKA) is a proven and increasingly common procedure. According to the 2023 American Joint Replacement Registry
report, 194,695 TKAs were performed in the United
States.1 Periprosthetic
joint infection (PJI) is the leading
cause of knee revision, accounting for 29.5% of all revisions and 50.3% of
early revisions.1
The use of debridement,
antibiotics, and implant retention (DAIR) to treat acute PJI after TKA remains
a matter of debate.2,3 Variable
definitions and diagnostic criteria for PJI, pathogen heterogeneity,
differences in host immunocompetence, and evolving
success criteria partly explain the inconsistent outcomes reported.4 Strategies such as modular component exchange5 and intraosseous antibiotic administration6 have been proposed to improve the effectiveness
of DAIR by targeting bacterial biofilms at concentrations unattainable with
systemic intravenous therapy.
The aim of this study was
to evaluate the efficacy and safety of DAIR supplemented with intraosseous
vancomycin and modular component exchange in patients with acute knee PJI,
compared with conventional infection-management methods.
MATERIALS AND
METHODS
Study Design
We conducted a retrospective,
multicenter, observational study at three
institutions in Argentina, including patients with acute knee PJI who underwent
a DAIR protocol between February 2022 and June 2023. Clinical, radiological,
and functional follow-ups lasted at least 12 months. Intraoperative and
postoperative adverse events related to intraosseous vancomycin were recorded.
Patient
Selection and Inclusion Process
To mitigate selection bias,
we systematically searched electronic and paper medical records at each
institution to identify all patients presenting with symptoms or signs
suggestive of acute PJI (severe pain, erythema, edema,
persistent drainage, limited mobility) during the study period. An orthopedic surgeon, an infectious
disease specialist, and a radiologist jointly reviewed the cases and confirmed
PJI based on the following clinical and laboratory criteria: (1) severe or
persistent knee pain; (2) erythema, edema, or wound
drainage for at least 7 days; (3) C-reactive protein >100 mg/L; and (4)
arthrocentesis with >10,000 cells/mL and >90% polymorphonuclear
cells, or two positive cultures with phenotypically identical organisms.
Patients with chronic
infection (>6 weeks after primary TKA), an unstable implant, or serious
medical conditions contraindicating surgery were excluded.
Fifteen potential cases
were identified; three were excluded (two chronic infections >6 weeks and
one unstable prosthesis). Thus, 12 patients (7 women, 5 men; mean age 72.4 ±
6.3 years) were included. The mean interval between the index TKA and DAIR was
12.3 days (range, 8–31).
The study adhered to the
principles of the Declaration of Helsinki. Informed consent was
obtained from all participants.
Data
Collection and Bias Management
Data were
extracted and coded by an independent investigator not involved in the surgery
or postoperative care. A unified database captured demographics,
comorbidities, culture results, operative time, blood loss, complications,
follow-up duration, and joint function scores.
Reducing
Measurement Variability
Knee Society
Score (KSS)
assessment was standardized across institutions by
training evaluators on the same scale. Uniform protocols were
followed for sampling and for the DAIR surgical technique to minimize
method-related variability.
Interpretation
Bias Control
Antibiotic regimens were
determined by the Infectious Diseases Service according to pathogen
susceptibility and local guidelines.
We recognize the inherent
limitations of retrospective designs; documentation is not always standardized.
However, all data were double-checked (medical records, operative notes, laboratory reports) to limit omissions of relevant
information.
Surgical
procedure: standardized DAIR protocol
Intraosseous vancomycin was
administered per the protocol of Young et al.6 Five hundred milligrams of vancomycin were
dissolved in 10 mL of normal saline, then diluted in 140 mL of saline (total
150 mL). An incision was made in the adhesive field
and skin (Figure 1), cancellous bone was
accessed medial to the tibial tubercle using a Jamshidi needle (Figure 2),
and the 150 mL preparation was injected (Figure 3).
A tourniquet was used in all cases.
The knee was
approached through a standard medial parapatellar
incision. Five representative periprosthetic
tissue samples were obtained for culture in enriched media. Extensive
debridement of infected tissue and removal of the tibial
polyethylene were performed. Exposed metal components were scrubbed with a sterile brush soaked in 0.36% povidoneiodine.
Irrigation followed a
five-step protocol based on Kildow et al.:
1. Low-pressure irrigation
with 3 L of saline.
2. Irrigation with 100 mL of
3% hydrogen peroxide (H2O2) plus 100 mL of sterile water for 2 minutes.
3. Irrigation with 2 L of
saline.
4. Irrigation with 1 L of
sterile diluted 0.36% povidone-iodine, left in the wound for 3 minutes.
5. Low-pressure irrigation
with 3 L of normal saline.
Gauze soaked in diluted
povidone-iodine was placed between prosthetic
components, the skin was closed, and instruments, gowns, and drapes were
changed. The skin was reprepped
with povidone-iodine, the sutures were removed, and the joint was reirrigated with diluted povidone-iodine and 1 L of saline.
Finally, a new tibial polyethylene insert was
implanted.
Microorganisms
and Antibiotic Regimens
Isolates among the 12 infections
were: methicillin-resistant Staphylococcus aureus (MRSA, n=3), methicillin-resistant
coagulase-negative Staphylococcus
(n=1), methicillin-susceptible S. aureus
(MSSA, n=2), methi-cillin-susceptible
coagulase-negative Staphylococcus
(n=2), Streptococcus agalactiae
(n=1), Enterobacterales (n=2), and culture-negative
(n=1).
All patients received
intravenous antibiotics for at least one week after surgery, followed by oral
antibiotics for at least three months, provided clinical status was stable and infection
markers improved (decreasing/normalized ESR and CRP, satisfactory wound
appearance, and appropriate clinical course).
Study
Variables
Variables included
demographics (age, sex); surgical data (operative time, intraoperative blood
loss); intra-and perioperative complications; time to ambulation; knee function
(e.g., KSS); and infection control (resolution of clinical signs and
normalization of CRP and ESR).
Treatment success was
defined by the criteria of Diaz-Ledezma et al.,7 which were
developed through a consensus reached using the Delphi method. These criteria are based on the eradication of infection, the absence of
subsequent surgical interventions, and the absence of deaths associated with
prosthesis infection.
Statistical
Analysis
Descriptive statistics
characterized the cohort (means ± SD or median and interquartile range, as
appropriate). Categorical variables are reported as
frequencies and percentages. Paired t-tests compared pre- and postoperative KSS
values. Significance was set at p < 0.05.
RESULTS
Population
Characteristics
Twelve patients (7 women, 5
men; mean age 72.4 ± 6.3 years) were included. Six had at least one comorbidity (Table 1).
Intraoperative and Postoperative Data
Mean operative time was 95
± 10 min (range, 80-110). Mean intraoperative blood loss was 180 ± 30 mL
(range, 140-220).
No cases of hypotension or
bradycardia were observed during intraosseous
vancomycin infusion or upon tourniquet release. No histamine-related cutaneous
events were recorded.
Perioperative
Complications
One patient (8.3%) had
wound drainage during the first 72 hours, which resolved with conservative
management. Two patients with type 2 diabetes had hyperglycemic
events managed by Endocrinology. No other major immediate postoperative complications
were observed.
Control of
the Infectious Process
Infection control was achieved in 11 of 12 patients (91.6%). There was one
recurrence (reinfection). In that case, pre- and intraoperative cultures
(arthrocentesis fluid and tissue) were negative; the patient underwent
two-stage revision, and intraoperative cultures grew Pseudomonas aeruginosa. Imipenem 2 g/day plus ciprofloxacin 1 g/day
were given intravenously for 7 days, followed by oral
ciprofloxacin 1 g/day during the spacer phase (12 weeks).
Clinical and
Functional Outcomes
Patients began weight-bearing on the operated limb at 24 hours
postoperatively with a walker. KSS improved significantly in all
cases (Table 2).
Statistical analysis showed
a significant improvement in the KSS (p < 0.001) between the preoperative
period and the 6- and 12-month follow-ups.
Paired Student’s t-tests were used to compare preoperative and postoperative KSS
scores, with a significance level set at p < 0.05. Improvements in KSS
scores were statistically significant, indicating significant functional
improvement in all patients treated with the DAIR protocol, intraosseous
vancomycin, and modular component exchange.
DISCUSSION
Our findings suggest that
DAIR supplemented with intraosseous vancomycin, chemical debridement, and
modular component exchange is effective and safe for managing acute knee PJI.
DAIR is
commonly used in the early postoperative period for acute postoperative
or hematogenous infections. While early intervention is generally assumed to improve control, reported success
rates for open irrigation and debridement with component retention in acute
infection vary widely from 16% to 100% (mean ~50%).8,9
Recent studies indicate that
host factors, causative microorganism, the timing of intervention, modular
component exchange, and symptom duration can influence the outcomes of the DAIR
protocol. Duque et al. reported an 80% failure rate in methicillin-resistant Staphylococcus aureus infections treated
with debridement,10
while Bradbury et al. reported an 84% failure rate in patients with acute MRSA
knee PJI treated with DAIR.11
To address the modest
outcomes of DAIR in acute PJI, several adjunctive strategies have
been proposed. Riesgo et al. combined
vancomycin powder and diluted povidone-iodine lavage with DAIR and modular exchange
for Staphylococcus infections, achieving an 83% eradication rate versus 63% in
controls at ≥1-year follow-up.12 McQuivey et al. described a two-stage debridement using
high-dose antibiotic-loaded cement microspheres between stages plus modular
exchange for acute PJI, with 87% eradication in both primary and revision TKA.13
Another strategy to improve
the results of the DAIR protocol is prolonged oral antibiotic therapy. Siqueira et al. reported higher 5-year survival with
suppressive therapy after S. aureus
infection versus no suppression (57.4% and 40.1%, respectively, p = 0.047).14 A recent systematic review concluded
suppressive therapy after DAIR may benefit S.
aureus PJI.15
Methods to achieve higher
tissue antibiotic concentrations via intraosseous administration have also been
described.16 Such
levels are otherwise unattainable without systemic toxicity. Low-dose
intraosseous delivery has achieved 10–20-fold higher tissue concentrations
compared with systemic intravenous administration.6,17
Despite these elevated concentrations, we observed no significant complications
with intraosseous vancomycin, consistent with prior reports.18 Kildow et al. reported a 92.3% control
rate in acute knee PJI treated with DAIR, modular exchange, and intraosseous vancomycin
at a mean 16.5-month follow-up.19
In our study, we expanded
the series to 12 cases, including the successful management of infections
caused by methicillin-resistant Staphylococcus
aureus, methicillin-sensitive Staphylococcus
aureus, coagulase-negative Staphylococcus,
Streptococcus, and even two cases of enterobacterales, under appropriate antibiotic regimens. Nevertheless, small sample size,
retrospective design, and lack of a control group limit generalizability. Prospective
studies with larger cohorts are needed to confirm and
refine these findings.
CONCLUSIONS
Intraosseous vancomycin,
combined with modular component exchange and aggressive debridement (DAIR),
appears to be an effective strategy for improving control of acute knee PJI
without increasing vancomycin-related adverse events. Although our results are
encouraging, prospective, larger studies are required to confirm these
observations and to better define selection criteria, optimal timing, and
long-term follow-up protocols.
Statement on generative AI and
AI-assisted technologies in the writing process
During
manuscript preparation, the authors used ChatGPT (OpenAI) to improve readability and language. After using
this tool, the authors reviewed and edited the content as necessary and assume
full responsibility for the publication’s content.
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E. J. Bochatey ORCID
ID: https://orcid.org/0000-0003-3645-6563
F. A. Lopreite ORCID
ID: https://orcid.org/0000-0002-2065-8649
Received on May 6th, 2025. Accepted after evaluation
on July 21st, 2025 • Dr. Walter F. Martínez • wfm5252@gmail.com • https://orcid.org/0009-0004-7249-1563
How to cite this article: Martínez WF, Bochatey EJ, Lopreite
FA. Intraosseous Vancomycin for Acute Periprosthetic
Knee Infection: A Retrospective Study. Rev
Asoc Argent Ortop Traumatol 2025;90(5):438-445. https://doi.org/10.15417/issn.1852-7434.2025.90.5.2164
Article Info
Identification: https://doi.org/10.15417/issn.1852-7434.2025.90.5.2164
Published: October, 2025
Conflict of interests: The authors declare no conflicts of
interest.
Copyright: © 2025, Revista de la
Asociación Argentina de Ortopedia y Traumatología.
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