Diabetes mellitus is a risk factor for complications after operative management of ankle fractures. Generally, diabetic sequelae such as neuropathy and nephropathy portend greater risk; however, the degree of risk resulting from these patient factors is poorly defined. We sought to evaluate the effects of the diabetic sequelae of neuropathy, chronic kidney disease (CKD), and peripheral vascular disease (PVD) on the risk of complications following operative management of ankle fractures.

Using a national claims-based database we analyzed patients who had undergone operative management of an ankle fracture and who remained active in the database for at least two years thereafter. Patients were divided into two cohorts, those with a diagnosis of diabetes and those without. Each cohort was further stratified into five groups: neuropathy, CKD, PVD, multiple sequelae, and no sequelae. The multiple sequelae group included patients with more than one of the three sequelae of interest: CKD, PVD and neuropathy. Postoperative complications were queried for two years following surgery. The main complications of interested were: deep vein thrombosis (DVT), surgical site infection, hospital readmission within 90 days, revision internal fixation, conversion to ankle fusion, and below knee amputation (BKA).

We identified 210,069 patients who underwent operative ankle fracture treatment; 174,803 had no history of diabetes, and 35,266 were diabetic. The diabetic cohort was subdivided as follows: 7,506 without identified sequelae, 8,994 neuropathy, 4,961 CKD, 1,498 PVD, and 12,307 with multiple sequelae.

Compared to non-diabetics, diabetics without sequelae had significantly higher odds of DVT, infection, readmission, revision internal fixation and conversion to ankle fusion (OR range 1.21 – 1.58, p values range Compared to uncomplicated diabetics, diabetics with neuropathy alone and diabetics with multiple sequelae were found to have significantly higher odds of all complications (OR range 1.18 – 31.94, p values range < 0.001 - 0.034). Diabetics with CKD were found to have significantly higher odds of DVT, readmission, and BKA (OR range 1.34 – 4.28, p values range < 0.001 - 0.002). Finally, diabetics with PVD were found to have significantly higher odds of DVT, readmission, conversion to ankle fusion, and BKA (OR range 1.62 - 9.69, p values range < 0.001 - 0.039).

Diabetic patients with sequelae of neuropathy, CKD or PVD generally had higher complication rates than diabetic patients without these diagnoses. Unsurprisingly, diabetic patients with multiple sequalae are at the highest risk of complications and had the highest odds ratios of all complications. While neuropathy is known to be associated with postoperative complications, our analysis demonstrates that CKD represents a significant risk factor for multiple complications following the operative management of ankle fractures and has rarely been discussed in prior studies.

Introduction

Different subclinical neurological dysfunction has been reported in adolescent idiopathic scoliosis (AIS), including poor postural control and asymmetric otolith vestibulo-ocular responses when compared with normal controls. The objective of this pilot study is to establish whether abnormal MRI morphoanatomical changes arise in the CNS (brain and vestibular system), among left-thoracic versus right-thoracic AIS when compared with normal adolescent controls, with use of advanced computerised statistical morphometry techniques.

Observation of sub-clinical neurological abnormalities has led to the proposal of a neuro-developmental etiologic model for AIS. Our research group have demonstrated longer latency in somatosensory–evoked potential (SSEP) and impaired balance control in AIS subjects. A previous pilot study compared the regional brain volume between right thoracic AIS subjects and normal controls. Significant regional brain differences were found relating to corpus callosum, premotor cortex, proprioceptive and visual centers. Most of these regions involved the brain unilaterally, indicating there might be abnormal asymmetrical development in the brain in right thoracic AIS. In this pilot study, we investigated whether similar changes are present in left thoracic AIS patients who differ from matched control subjects. Nine AIS female patients with atypical left thoracic AIS (mean age 14.8, mean Cobb angle 19°) and 11 matched controls as well as 20 right thoracic AIS (mean Cobb angle 33.8°) and 17 matched controls, underwent three-dimensional isotropic magnetization prepared rapid acquisition gradient echo (3D_MPRAGE) magnetic resonance (MR) imaging of the brain. Fully automatic morphometric analysis was used to analyse the MR images; it included brain-tissue classification into grey matter (GM), white matter (WM) and cerebrospinal fluid (CSF). and non-linear registration to a template brain. Tissue densities were compared between AIS subjects and controls. There was no significant difference between AIS subjects and normal controls when comparing absolute and relative (i.e. brain-size adjusted) volumes of grey and white matter. Using voxel-based morphometry, significant group differences (controls > left AIS) were found in the density of WM in the genu of the corpus callosum, the left internal capsule (anterior arm) and WM underlying the orbitofrontal cortex of the left hemisphere. The above differences were not observed in the right AIS group. This first controlled study of regional tissue density showed that corpus callosum, which is the major commissural fiber tract, was different in the atypical left thoracic scoliosis while significant regional brain changes have not yet been found in those with typical right thoracic scoliosis. Further investigation is warranted to see whether the above discrepancy is related to laterality of the scoliotic curves and infratentorial neuroanatomical abnormalities. A larger sample and a longitudinal study is required to establish whether the brain abnormalities are predictive of curve progression.