Introduction
The majority of trauma-associated limb fractures in children can be treated with cast immobilization [
1]. Fracture reduction and subsequent surgical fixation might be necessary if casting results in insufficient immobilization or inadequate reduction. A variety of fixation methods and materials can be used, depending on the fracture type and location. Once the fracture has healed, the metal implants can be removed.
Several studies have discussed the pros and cons of implant removal in children [
2‐
13]. Whether metal implants in children should be removed routinely is controversial [
2,
3,
5,
6,
10,
11,
13]. Up to 60% of the surgeons routinely remove hardware after bone healing [
5,
10]. Operation-related complications due to implant removal play a key role in this discussion and no general agreement among surgeons exists about the need of hardware removal in children that are free of material-associated complaints [
2‐
7,
10,
11,
13].
The aim of this study was to analyze the number and type of complications due to hardware removal in children with a (healed) limb fracture after trauma.
Patients and methods
In this retrospective analysis, all children under the age of 16 years with limb fractures due to trauma, who were admitted to our trauma center and were treated operatively with Kirschner wires (K-wires), elastic stable intramedullary nails (ESIN), or screw fixation between 1st January 2000 and 1st January 2007, were included. Excluded from the study were all children with refractures, pathological fractures, fractures of the hands or feet, and polytrauma patients (Injury Severity Score [ISS] > 15). The medical records from the Trauma Database of the Trauma Centre West of the Leiden University Medical Centre (LUMC) were used to collect patient data for analysis. If the postoperative follow-up was done in another hospital, the patient was categorized as lost to follow-up. The follow-up period of the children after the implant removal was 1 year. If the implant was not removed, the follow-up was continued until outpatient discharge. Data collected from the medical records were: diagnosis, comorbidity, information about the primary operation, complications with the material in situ, information about the implant removal operation, and complications after implant removal. Complications as described in the patient records during the follow-up were specified as minor or major. Minor complications were pain, irritation of the soft tissue or skin, superficial infection, unintentional protrusion or prominence of material, neurapraxia, and wound dehiscence. Prominence was defined as a combination of palpable material with pain, irritation, or an uncomfortable feeling. Major complications were deep infection, refracture, epiphysiodesis, nonunion, and malunion.
A database was constructed in Microsoft Access (Microsoft, Redmond, WA) and statistical analyses were performed using SPSS 17.0 (SPSS Inc., Chicago, IL). Fisher’s exact test was used to investigate differences in the complication rate between groups. A p-value of <0.05 was considered to be significant for the statistical test.
Discussion
Analyzing the number and type of complications that occurred after implant removal, we aimed to determine whether hardware removal in children could be performed safely and as a routine procedure. The study population existed of children with fractures treated with K-wires, ESIN, or screw fixation. In the groups treated with K-wires or ESIN, removal surgery was performed routinely, unlike the group treated with screw fixation. No significant differences in the complication rates could be found between the three groups after removal surgery (17/173, 7/96, and 4/19) or between hardware removal (4/19) and retention (4/21) in the case of screw fixation.
Our results showed, overall, 28 complications after 288 hardware removal operations: nine major, 18 minor, and one other material-related complication. Of these nine major complications, four epiphysiodesis were due to the trauma mechanism and one deep infection was already present when the material was in situ. In the case of the four refractures, all materials were removed according protocol after a sufficient time of being in situ. This low number of four refractures, after 288 removal surgeries (1%), rather reinforces the arguments pro removal of implants, than providing arguments not to remove the material. All minor complications and one material-related complication were temporary, except for one case of neurapraxia. Given these results on complications that occurred after implant removal and the fact that only two complications occurred during the removal procedure itself, implant removal surgery of K-wires, ESIN, and screws can be put forward as a safe intervention.
Although a standard procedure in many hospitals, routine hardware removal in children remains controversial. Currently, no evidence-based guideline exists on the topic of hardware removal in children. Arguments against removal would be the potential for complications from the surgery, the repeated anesthesia, and increased medical costs. Since pins and K-wires can be removed in an outpatient situation under local anesthesia, these arguments do apply to a lesser extent for percutaneously inserted and removed metal wires.
Four previous studies investigated complications after hardware removal in children. It remains unclear in these studies whether these fractures were all due to trauma or also included pathological fractures [
4,
12‐
14]. Rosson and Shearer [
12] investigated the incidence of refractures after plate removal from the forearm in children. No refractures were reported after the removal of 43 plates in 29 patients. Also, Kim et al. [
13] investigated complications after forearm plate removal. One superficial wound infection and three refractures were reported, two in the same child, after the removal of 44 plates in 43 children. The removal of K-wires in 119 fractures was studied by Symons et al. [
14]. They primarily investigated complaints of pain after the removal of K-wires. They also documented one ulnar nerve neurapraxia, four superficial wound infections, and 11 overgranulations of the wound after removal of the K-wires. Simanovsky et al. [
4] studied the removal of flexible titanium nails in 143 children after femur or forearm fracture fixation. No postoperative infections or neurovascular injuries associated with nail removal were registered. Two refractures were documented, both in the forearm group. In comparison, the current study has not been restricted to one fracture location, or outcome parameter, and, therefore, relates the results in a wider perspective.
We also looked into the consequences of material retention after fracture consolidation in children, a topic that has not been widely investigated. The only results published on the topic showed higher numbers of treatments in which the primary decision for metal retention was reconsidered [
3]. But they all concerned femoral fractures treated with ESIN, in children between 6.5 and 13 years of age. In our study, ESIN was routinely removed.
A limitation of our study is the retrospective follow-up design. Children, who experienced complaints or a refracture, may also have presented elsewhere and were lost to follow-up.
In conclusion, hardware removal of K-wires, ESIN, or screws in children is considered to be a safe procedure. The removal of K-wires or ESIN is, by definition, indicated after fracture healing in children.