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Updated: Jun 14, 2026

A Simple Critical-sized Femoral Defect Model in Mice
Published on: March 15, 2015
Insufficient bone regenerate after intramedullary femoral lengthening: risk factors and classification system
Mohamed Kenawey1, Christian Krettek, Emmanouil Liodakis
1Trauma Department, Hannover Medical School, Carl-Neuberg-Str 1, 30625 Hannover, Germany. mohamed_kenawey@yahoo.com
Background:
Control of distraction rate with an intramedullary skeletal kinetic distractor (ISKD) may be problematic and a high distraction rate may result in insufficient bone regenerate.
Questions/Purposes:
Are distraction problems preventable when using the ISKD, and what are the risk factors for and radiologic types of insufficient bone regenerate during ISKD lengthening?
Patients And Methods:
We analyzed 37 consecutive ISKD femoral lengthening procedures in 35 patients with a mean age 33 ± 11 years and minimum followup of 12 months (average, 27 ± 9 months; range, 12-55 months). The average length gain was 42.8 ± 12.9 mm.
Results:
Eight patients had problems during distraction: seven had "runaway nails" and one had a nondistracting nail. Insufficient bone regenerate developed in eight patients. Important risk factors were a distraction rate greater than 1.5 mm/day (9.1 times higher risk), age 30 years or older, smoking, and lengthening greater than 4 cm. Less important risk factors identified were creation of the osteotomy at the site of previous trauma or surgery and acute correction of associated deformities. We proposed a radiologic classification for failure of bone regeneration: partial regenerate failure (Type I) or complete failure resulting in a segmental defect subdivided according to a length of 3 cm or less (Type IIa) or greater than 3 cm (Type IIb).
Conclusions:
Distraction problems with the ISKD were related mostly to internal malfunction of the lengthening mechanism. A distraction rate greater than 1.5 mm/day should be avoided in femoral intramedullary lengthening. Smoking should be a contraindication for femoral lengthening.
Level Of Evidence:
Level II, prognostic study. See Guidelines for Authors for a complete description of levels of evidence.
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