Table 3.
Univariable | ||||
---|---|---|---|---|
All cases | Implant failure | Odds ratio | p | |
Total number of breasts | 542 | 33 | ||
Age (years) at IBR | ||||
< 50 | 319 | 21 | 1.00 (reference) | |
50–60 | 163 | 10 | 0.93 (0.43–2.02) | 0.850 |
> 60 | 60 | 2 | 0.49 (0.11–2.14) | 0.343 |
Missing | 0 | 0 | ||
Histopathological tumour stage | ||||
Tis (in situ only) | 135 | 11 | 1.00 (reference) | |
T1 (≤ 20 mm) | 55 | 1 | 0.21 (0.03–1.66) | 0.138 |
T2 (21–50 mm) | 112 | 4 | 0.42 (0.13–1.35) | 0.144 |
T3/T4 (> 50 mm) | 86 | 5 | 0.70 (0.23–2.08 | 0.516 |
Missing | 154 | 12 | ||
Histopathological nodal stage | ||||
Node negative | 407 | 17 | 1.00 (reference) | |
Node positive | 111 | 14 | 3.31 (1.58–6.95) | 0.002 |
Missing | 24 | 2 | ||
Axillary clearance | ||||
No | 290 | 7 | 1.00 (reference) | |
Yes | 240 | 26 | 4.91 (2.09–11.53) | < 0.001 |
Missing | 12 | 0 | ||
Type of implant | ||||
Temporary expander | 33 | 1 | 1.00 (reference) | |
Permanent expander | 434 | 29 | 2.29 (0.30–17.37) | 0.422 |
Fixed-volume implant | 68 | 2 | 0.97 (0.09–11.10) | 0.980 |
Missing | 7 | 1 | ||
Final implant volume* | ||||
< 300 cc | 151 | 8 | 1.00 (reference) | |
300–400 cc | 265 | 12 | 0.85 (0.34–2.12) | 0.724 |
> 400 cc | 118 | 10 | 1.66 (0.63–4.33) | 0.305 |
Missing | 8 | 3 | ||
Radiotherapy | ||||
None | 288 | 9 | 1.00 (reference) | |
Yes, prior to IBR | 24 | 2 | 2.82 (0.57–13.85) | 0.202 |
Yes, after IBR | 223 | 22 | 3.39 (1.53–7.53) | 0.003 |
Missing | 7 | 0 | ||
Type of adjuvant radiotherapy** | ||||
Local | 82 | 3 | 1.00 (reference) | |
Locoregional | 141 | 19 | 4.10 (1.18–14.32) | 0.027 |
Missing | 0 | 0 | ||
Radiotherapy dose/fractions** | ||||
46 Gy/23 fractions | 18 | 2 | 1.00 (reference) | |
50 Gy/25 fractions | 198 | 20 | 0.90 (0.19–4.20) | 0.892 |
Missing/other | 7 | 0 | ||
Months from end of radiotherapy to first surgical revision | ||||
> 9 months | 163 | 13 | 1.00 (reference) | |
6–9 months | 50 | 3 | 3.17 (0.78–12.80) | 0.106 |
< 6 months | 14 | 3 | 0.74 (0.20–2.71) | 0.651 |
Missing | 20 | 5 | ||
Postoperative infection within 30 days after IBR | ||||
No infection | 398 | 10 | 1.00 (reference) | |
Clinical signs of infection, oral antibiotic treatment | 72 | 7 | 4.18 (1.54–11.37) | 0.005 |
Confirmed infection, oral antibiotic treatmenta | 14 | 4 | 15.52 (4.15–58.01) | < 0.001 |
Confirmed infection, intravenous antibiotic treatmenta | 12 | 3 | 12.93 (3.04–55.12) | 0.001 |
Missing | 46 | 9 | ||
Postoperative complication with return to theatre (within 30 days) after IBR | ||||
No | 489 | 24 | 1.00 (reference) | |
Yes | 11 | 1 | 1.94 (0.24–15.76) | 0.536 |
Missing | 42 | 8 | ||
Postoperative complication without return to theatre after IBR | ||||
None | 464 | 23 | 1.00 (reference) | |
Seroma | 44 | 4 | 1.92 (0.63–5.82) | 0.250 |
Infection | 5 | 2 | 12.78 (2.04–80.30 | 0.007 |
Bleeding | 8 | 1 | 2.74 (0.32–23.21) | 0.355 |
Skin necrosis | 7 | 1 | 3.20 (0.37–27.66) | 0.291 |
≥ 2 complications | 14 | 2 | 3.20 (0.68–15.13) | 0.143 |
Missing | 0 | 0 | ||
Previous revision surgery performed | ||||
No | 395 | 22 | 1.00 (reference) | |
Yes | 147 | 11 | 1.37 (0.65–2.90) | 0.409 |
Missing | 0 | 0 | ||
BMIc | ||||
Normal (18.5–30) | 438 | 18 | 1.00 (reference) | |
Underweight (< 18.5) | 8 | 1 | 3.33 (0.39–28.55) | 0.272 |
Overweight (> 30) | 23 | 3 | 3.50 (0.95–12–87) | 0.059 |
Missing | 73 | 11 | ||
Smokingc | ||||
Never smoked | 383 | 19 | 1.00 (reference) | |
Currently smoking | 65 | 11 | 3.90 (1.76–8.65) | 0.001 |
Former smoker | 73 | 2 | 0.54 (0.12–2.37) | 0.414 |
Missing | 21 | 1 | ||
Immunosuppressive treatmentc | ||||
No | 498 | 31 | 1.00 (reference) | |
Yes | 9 | 2 | 3.57 (0.74–17.24) | 0.113 |
Missing | 35 | 0 | ||
Antihypertensive medicationc | ||||
No | 454 | 26 | 1.00 (reference) | |
Yes | 42 | 5 | 2.08 (0.76–5.70) | 0.155 |
Missing | 46 | 2 | ||
Diabetesc | ||||
No | 502 | 31 | 1.00 (reference) | |
Yes, with medicationb | 6 | 2 | 5.40 (1.05–27.85) | 0.044 |
Missing | 34 | 0 |
Each case represents one operated breast
IBR immediate implant-based breast reconstruction
*Final expander volume or fixed-volume implant size
**Reporting only patients who had received RT after IBR
aConfirmed by positive bacterial cultures and/or elevated C-reactive protein
bIncluding oral medication and/or insulin
cRegistered at the time of IBR, not at implant revision surgery