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A Detailed Study of Infection Following Custom-Made Porous Hydroxyapatite Cranioplasty: Risk Factors and How to Possibly Avoid Device Explantation

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Background/Objectives: Postoperative infection is a significant complication following cranioplasty procedures. This study aimed to assess infection risk factors and clinical outcomes in patients undergoing cranioplasty with custom-made porous hydroxyapatite (PHA) implants, with a particular focus on treatment strategies used to manage infections and avoid implant explantation. Methods: This retrospective multicenter analysis included 984 patients who underwent PHA cranioplasty as part of a post-market clinical follow-up. Clinical data included demographics, surgical characteristics, infection features, microbiological results, infection management strategies, and outcomes. Associations with infection risk and implant explantation were assessed using chi-square tests. Results: Seventy-six patients (7.7%) developed postoperative infections. Infection risk was significantly associated with second-line procedures (p = 0.011) and implant location (p = 0.037). Most infections were superficial (92.1%) and early-onset (≤2 months from the surgery, 61.9%), with Staphylococcus spp. as the predominant pathogens. Explantation occurred in 77.6% of infected cases. The infection management strategy—whether initial conservative treatment with antibiotics alone (n = 18 of which 11.1% explanted) or surgical reoperation (n = 58 of which 93.8% explanted)—along with surgical cleaning and local (in situ) antibiotic use alone, was significantly associated with explantation outcomes (all p < 0.001). Among 18 patients treated with systemic antibiotics alone, 88.9% retained their implants. Notably, all successful cases had received broad-spectrum antibiotics for at least 4 weeks. Local antibiotic therapy was administered in 13 patients; no explants occurred among those who also received prolonged systemic treatment. Pathogen type was not significantly associated with the risk of explantation. Conclusions: Prolonged systemic antibiotic therapy, especially when combined with local treatment, may allow implant retention in selected infections, supporting individualized, conservative management strategies.
Title: A Detailed Study of Infection Following Custom-Made Porous Hydroxyapatite Cranioplasty: Risk Factors and How to Possibly Avoid Device Explantation
Description:
Background/Objectives: Postoperative infection is a significant complication following cranioplasty procedures.
This study aimed to assess infection risk factors and clinical outcomes in patients undergoing cranioplasty with custom-made porous hydroxyapatite (PHA) implants, with a particular focus on treatment strategies used to manage infections and avoid implant explantation.
Methods: This retrospective multicenter analysis included 984 patients who underwent PHA cranioplasty as part of a post-market clinical follow-up.
Clinical data included demographics, surgical characteristics, infection features, microbiological results, infection management strategies, and outcomes.
Associations with infection risk and implant explantation were assessed using chi-square tests.
Results: Seventy-six patients (7.
7%) developed postoperative infections.
Infection risk was significantly associated with second-line procedures (p = 0.
011) and implant location (p = 0.
037).
Most infections were superficial (92.
1%) and early-onset (≤2 months from the surgery, 61.
9%), with Staphylococcus spp.
as the predominant pathogens.
Explantation occurred in 77.
6% of infected cases.
The infection management strategy—whether initial conservative treatment with antibiotics alone (n = 18 of which 11.
1% explanted) or surgical reoperation (n = 58 of which 93.
8% explanted)—along with surgical cleaning and local (in situ) antibiotic use alone, was significantly associated with explantation outcomes (all p < 0.
001).
Among 18 patients treated with systemic antibiotics alone, 88.
9% retained their implants.
Notably, all successful cases had received broad-spectrum antibiotics for at least 4 weeks.
Local antibiotic therapy was administered in 13 patients; no explants occurred among those who also received prolonged systemic treatment.
Pathogen type was not significantly associated with the risk of explantation.
Conclusions: Prolonged systemic antibiotic therapy, especially when combined with local treatment, may allow implant retention in selected infections, supporting individualized, conservative management strategies.

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