Skip to main content
Erschienen in: BMC Musculoskeletal Disorders 1/2017

Open Access 01.12.2017 | Research article

Treatment of Charcot Neuroarthropathy and osteomyelitis of the same foot: a retrospective cohort study

verfasst von: Martin Berli, Lazaros Vlachopoulos, Sabra Leupi, Thomas Böni, Charlotte Baltin

Erschienen in: BMC Musculoskeletal Disorders | Ausgabe 1/2017

Abstract

Background

We evaluated treatment of osteomyelitis in the foot in the presence of Charcot neuroarthropathy, a devastating condition with progressive degeneration and joint destruction. We hypothesized that there was a difference in (1) amputation rate, (2) amputation level, (3) duration of antibiotic therapy, and (4) duration of immobilization for treatment of osteomyelitis within versus outside the Charcot zone.

Methods

Forty patients (43 ft) diagnosed with Charcot neuroarthropathy and osteomyelitis of the same foot were retrospectively analyzed. Some patients were successfully treated for osteomyelitis at different sites on the same foot at different times, thus 60 cases of osteomyelitis were identified in 40 treated patients. Cases were divided according to osteomyelitis localization: Group 1 had osteomyelitis outside the active Charcot region; Group 2 had osteomyelitis within the active Charcot region.

Results

Male patients (n = 29; mean age 58.2, range 40.1 to 77.5 years) were younger than female patients (n = 11; mean age 70.4, range 51.4 to 87.5, p = 0.02 years). Amputation rate was 52% overall (26/40 patients; 26/43 ft): 63% of 30 Group 1 cases and 40% of 30 Group 2 cases (p = 0.09). Amputation level (p = 0.009), duration of antibiotic treatment (p = 0.045) and duration of immobilization (p = 0.01) differed significantly between the groups.

Conclusions

Osteomyelitis within the Charcot region is associated with a higher level of amputation and longer durations of antibiotic therapy and immobilization. Osteomyelitis outside and within the Charcot affected region should be considered separately. If osteomyelitis occurs outside the active Charcot region, primary amputation may be preferred to internal resection.

Level of Evidence

Retrospective cohort chart review study.
Abkürzungen
CN
Charcot neuroarthropathy
IQR
interquartile range
MRI
magnetic resonance imaging

Background

Charcot neuroarthropathy (CN), or diabetic neuropathic osteoarthropathy with progressive degeneration and joint destruction as a consequence of any condition resulting in decreased peripheral sensation [1], is a rare but devastating complication. The most common cause of CN is diabetes mellitus; other causes include alcoholism, vitamin B12 or folic acid deficiency, intravenous drug use, late stage syphilis, syringomyelia, and multiple sclerosis. While the precise pathogenesis of CN remains controversial, it is undoubtedly multifactorial [2, 3]. The current theory of Charcot pathogenesis combines both neurotraumatic and neurovascular aspects [36].
Elements of osteopenia, bone hyperemia, instability, muscle weakness, and loss of protective sensation place the limb at risk for developing neuropathic bone and joint changes [7]. When the compromised foot experiences trauma and the injury remains unrecognized, the cascade of events that subsequently ensues will often result in neuropathic fractures, subluxation or osteoarthropathy [8], and severe foot deformity. If an ulcer is also present, and the bone can be palpated through the ulcer, osteomyelitis may be an aggravating complication. An infection can spread into the bone of the foot of a patient with diabetes and/or CN from any infection of adjacent soft tissue that is complicated by an ulcer [9]. Risk factors for osteomyelitis include peripheral neuropathy, vascular disease, limited joint mobility, foot deformities, abnormal foot pressures, minor trauma, a history of ulceration or amputation, and immunosuppression [912].
Treatment of early stage CN with the use of crutches and/or immobilization (i.e., total contact cast and/or orthosis) may stop the progression of deformity and reduce the occurrence of complications [1316]. However, if the diagnosis is initially missed, or if treatment is not initiated, the neuro-osteoarthropathy results in progressive deformities, consecutive ulcers and osteomyelitis, and is accompanied by a high risk of amputation [17].
Several studies have recently demonstrated that the location of diabetic foot ulcers or osteomyelitis affects prognosis and healing time [1824]. However, there is a paucity of data on healing outcomes of osteomyelitis in the presence of CN. Dalla Paola et al. [25] evaluated the rate of limb salvage and time to recovery in 33 patients affected by CN complicated by diffuse osteomyelitis. However, their study focused on outcomes of surgical treatment to stabilize and correct bone deformity, rather than on outcomes of treating the osteomyelitis. The purpose of this study was to evaluate the treatment of osteomyelitis of the foot in the presence of CN. We hypothesized that there was a difference in (1) amputation rate, (2) level of amputation, (3) duration of antibiotic therapy, and (4) duration of immobilization after treatment in a CN foot with osteomyelitis within versus outside the Charcot zone. The potential effects of the initial surgical treatment, duration of insulin dependency, and patient compliance with treatment on these outcomes were also evaluated.

Methods

A retrospective analysis of all medical records of patients treated for a diagnosis of CN and osteomyelitis of the same foot between 2002 and 2012 at the outpatient clinic of a large, urban, orthopedic, university-affiliated research hospital was performed. Inclusion criteria were: a diagnosis of CN according to the definition and diagnostic criteria of the French neurologist J.M. Charcot [26], radiographs of the affected foot, and osteomyelitis of the same side with radiological findings of osteomyelitis on MRI and/or positive bone biopsy cultures. Exclusion criteria were: primary treatment at another institution, or a previous fracture due to trauma of the same foot. This study was approved by the Research Ethics Committee of our institution.
Cases were divided into two groups according to whether the osteomyelitis was localized outside the active Charcot region of the foot (Group 1), or within the active Charcot region of the foot (Group 2). The region of the foot (i.e., forefoot, midfoot or hindfoot) where the osteomyelitis was localized was also recorded. To evaluate the effectiveness of the initial surgical treatment, the surgical management was divided into four categories: 1) “limited resection” was defined as resection of the infected bone, leaving the surrounding soft tissue in place, 2) “amputation” was defined as surgical removal of part of the lower limb (bone and soft tissue), 3) “arthrodesis” was defined as removal of the infected bone combined with external (Ilizarov fixateur) or internal fixation, and 4) “debridement” was defined as surgical removal of the infected or necrotic tissue around the wound with underlying osteomyelitis. Successful treatment was defined as the absence of clinical or radiological signs of a recurrence of osteomyelitis at the initially affected region. Duration of treatment was defined as the time from the first clinic visit to the last clinic visit for a single case of osteomyelitis. Antibiotic therapy was discontinued based on the recommendations of in-house infectious disease specialists, the elimination of clinical signs of infection (e.g. redness, warmth and swelling), C-reactive protein level and MRI results. The duration of antibiotic treatment, duration of immobilization, and duration of treatment were calculated in days, separately for each case of osteomyelitis. Other factors likely to influence outcome were recorded, including duration of diabetic treatment, insulin dependency, duration of surgery, smoking status, immunosuppressive therapy, peripheral arterial occlusive disease, obesity, age, gender, incidence of bilateral CN, and patient compliance.

Statistical analysis

Continuous data are reported as means and standard deviations. Categorical data are reported as numbers and percentages. Statistical analysis was performed using the software R (The R Foundation for Statistical Computing, Version 3.1.0, Vienna, Austria). Differences in categorical baseline characteristics were evaluated using the Mann-Whitney U test and the chi-square test. To address clustering of cases within patients, logistic regression analysis was performed, with amputation as the dependent variable and localization of osteomyelitis as the independent variable with robust standard error (patient identification as a cluster). Duration of antibiotic therapy and duration of immobilization were analyzed as logarithmic transformed dependent variables in linear regression with robust standard error (patient identification as a cluster). Categorical data (i.e., amputation level) were assessed using Fisher’s exact test. The significance level was set at p < 0.05. For graphical visualization, Tukey boxplots were depicted with whiskers maximum of 1.5 interquartile ranges (IQR).

Results

Study population

This retrospective chart review identified 70 patients diagnosed with CN and osteomyelitis of the same foot between 2002 and 2012. Thirty patients were excluded from the study due to incomplete medical reports (n = 26) or absence of reliable evidence of osteomyelitis (n = 4). Three patients (#7, #26, and #34) had bilateral osteomyelitis combined with CN. Thus, 40 patients (43 ft) were included in the study (Table 1).
Due to the progressive nature of CN, some patients were successfully treated for multiple episodes of osteomyelitis, which occurred independently of each other, at different sites on the same foot, or at different time points, months or years apart. One patient (#22) presented with osteomyelitis within the Charcot region, and then one month later presented with a separate case of osteomyelitis outside the Charcot region. Ten patients (#1, #4, #7 right foot, #11, #18, #25, #26 left foot, #27, #28, #39) had 2 separately treated and resolved cases of osteomyelitis on the same foot, months apart. Three patients (#6, #7 left foot, #21) had 3 separately treated and resolved cases of osteomyelitis on the same foot, months apart. The mean duration between independent cases of osteomyelitis in a single patient, measured as the date treatment ended for the first case to the date of diagnosis of the second case, was 16.3 months (range: 2.4 to 33.5 months).Thus, in total, we identified 60 cases of osteomyelitis for the 40 patients included in this study. The 60 cases were divided into two groups according to the localization of the osteomyelitis and CN, with 30 cases in Group 1 (i.e., osteomyelitis outside the active Charcot region), and 30 cases in Group 2 (i.e., osteomyelitis within the active Charcot region of the foot).
Patient demographic characteristics and individual treatments are summarized in Table 1. There were 29 (73%) male and 11 female patients; 44/60 (73%) cases of osteomyelitis were in male patients. Mean age was 61.6 ± 12.4 (range, 40.1 to 87.5) years. Male patients (mean age 58.2 ± 10.5; range, 40.1 to 77.5 years) were significantly younger than female patients (mean age 70.4 ± 13.4; range 51.4 to 87.5 years; p = 0.02). Twenty-three (58%) patients were between 50 and 70 years of age at initial diagnosis of CN; 8 (20%) were over 70 years of age, and 9 (23%) were under 50 years of age. No female patient was under 50 years of age at initial diagnosis of CN.
Twenty-five of 40 (63%) patients had insulin-dependent diabetes and 15 had non-insulin-dependent diabetes. The mean duration of treatment for diabetes at the time of initial treatment for osteomyelitis was 17.7 ± 13.2 (range: 0.2 to 52.9) years. The mean duration of treatment for diabetes at the time of initial diagnosis of CN was 15.5 ± 13.8 (range: 0.6 to 52.9) years. In Group 1, 16/30 (53%) cases were insulin-dependent; in Group 2, 19/30 (63%) cases were insulin-dependent.
There was no significant difference in age, gender, and duration of treatment for diabetes between the groups (p = 0.81, p = 0.82, and p = 0.30, respectively) (Table 2).

Amputation rate

An amputation was performed in 31/60 (52%) cases of osteomyelitis (26/40 patients; 26/43 ft). In the 44 male cases, 21 (48%) amputations were performed. In the 16 female cases, 10 (63%) amputations were performed.
The amputation rate was similar for Group 1 with osteomyelitis outside the Charcot region (19 amputations; 63%) and Group 2 with osteomyelitis within the Charcot region (12 amputations; 40%) (p = 0.09). Amputation rate did not differ significantly based on insulin dependency or compliance with treatment.

Level of amputation

The 31 amputations included 16 toe, 4 transmetatarsal, 1 Lisfranc, 1 Chopart, 8 transtibial and 1 transfemoral amputation. A major amputation (i.e., above the level of the ankle) was performed in 3/30 (10%) cases in Group 1 with osteomyelitis outside the active Charcot region and 6/30 (20%) cases in Group 2 with osteomyelitis within the active Charcot region (p = 0.009) (Fig. 1). The level of amputation did not differ significantly based on insulin dependency or compliance with treatment (Fig. 2).

Duration of antibiotic treatment

The duration of antibiotic treatment was significantly shorter in Group 1 (mean 55.7 ± 48.9, range: 9 to 228 days) compared to Group 2 (mean 84.1 ± 51.2, range: 6 to 238 days, p = 0.045). Within Group 1, the mean duration of antibiotic treatment was 43.9 days shorter in cases initially treated with amputation compared to cases initially treated with internal resection (p = 0.02). Within Group 2, the duration of antibiotic treatment was similar across all initial surgical treatments (p = 0.09) (Fig. 3).

Duration of immobilization

The duration of immobilization was 61.4 days shorter in Group 1 where osteomyelitis outside the active Charcot region (mean 83.1 ± 70.5, range 19 to 304 days), compared to Group 2 with osteomyelitis within the active Charcot region (mean 144 ± 91.8, range 17 to 389 days, p = 0.01). There was no significant difference in the duration of immobilization between the different initial surgical treatments within each group (p = 0.40 and p = 0.90, respectively) (Fig. 4).

Discussion

Treatment of CN complicated by osteomyelitis is a complex, long-lasting procedure, demanding considerable perseverance from patients and physicians. Multiple surgical procedures, including a high rate of amputations, as well as prolonged antibiotic therapy and immobilization are often required [27]. This study demonstrated that patients treated for osteomyelitis within the Charcot region on the foot underwent more high level amputations and had longer durations of antibiotic treatment and immobilization than patients treated for osteomyelitis outside the Charcot region. However, the amputation rate was statistically similar for both groups.
Amputation was required during the course of treatment in 31/60 cases treated for CN and osteomyelitis of the same foot, whereas 29/60 cases were successfully treated with a combination of conservative surgery and antibiotic medication. The overall amputation rate did not differ significantly between the patients treated for osteomyelitis outside the Charcot region and those treated for osteomyelitis within the Charcot region. Wukich et al. [28] recently reported 16 of 43 patients (37.2%) with CN hospitalized for osteomyelitis underwent major amputation, but this rate can be expected to be lower in less severe cases that can be effectively managed in an outpatient setting such as ours. When considering the level of amputation, the 20% rate of major amputations we reported in cases of osteomyelitis within the Charcot region is comparable to the 23% rate of major amputations reported by Gazis et al. [29] in 47 patients with CN managed by a specialist diabetic foot clinic. However, our 10% amputation rate in cases of osteomyelitis outside the active Charcot region was significantly lower.
The mean duration of antibiotic treatment in this study ranged from 56 to 84 days, where patients with osteomyelitis within the active Charcot region required a longer duration of treatment. Two recent studies reported similar mean durations of antibiotic treatment of 76 days [30] and 77 days [31] for the nonsurgical management of diabetic foot osteomyelitis. Mutluoglu et al. [32] reported a mean of 47 days of antibiotic treatment in 37 patients with diabetic foot osteomyelitis, of whom 22 underwent minor amputation. In 2008, the International Working Group on the Diabetic Foot determined that there are no data to inform the optimal duration of antibiotic therapy [4].
In this study, the mean duration of immobilization ranged from 83 to 144 days, with patients with osteomyelitis within the active Charcot region requiring a longer period of immobilization. Several clinical trials evaluated different off-loading techniques for the treatment of diabetic foot ulcers and reported the duration of immobilization with a total contact cast ranged from 35 to 69 days [3336]. However, these trials excluded patients with osteomyelitis. In a study of 288 patients with acute Charcot foot that included 81 cases of ulceration and 20 cases of osteomyelitis, the median duration of immobilization for resolution of symptoms was 273 days [37]. Literature reporting specifically on immobilization of the Charcot foot with osteomyelitis is notably lacking.
The region of the foot on which the osteomyelitis was located likely contributed to the significant differences in the amputation level (p < 0.001), duration of antibiotic treatment (p = 0.045), and duration of immobilization (p = 0.01) observed between the groups who presented with osteomyelitis within the Charcot region versus outside the Charcot region. In the group with osteomyelitis within the Charcot region, a major amputation was performed in 3/8 cases with osteomyelitis in the hindfoot, 3/13 cases with osteomyelitis in the midfoot, and none of the cases with osteomyelitis in the forefoot. In the group with osteomyelitis outside the Charcot region, the osteomyelitis was almost exclusively (29/30 cases) located in the forefoot, thus elimination of infection by internal resection or amputation could be achieved more reliably. Diabetic foot ulcers and osteomyelitis located in the forefoot have been demonstrated to have a shorter healing time compared to those in the hindfoot [18, 2022, 24]. We therefore recommend that patients with osteomyelitis of the foot within versus outside the Charcot region should be analyzed separately in future research evaluating the outcome and treatment of CN and osteomyelitis.
The initial surgical treatment provided in this study did not affect the duration of antibiotic therapy or immobilization in the group with osteomyelitis in the Charcot region, but this may be due to the small sample sizes for each type of surgery. In the group with osteomyelitis outside the Charcot region, the duration of antibiotic therapy was 6 weeks shorter (p = 0.02) in those who initially underwent amputation compared to those who initially underwent internal resection, indicating that internal resection may not be sufficient to eliminate the infected tissue.
Four studies recently evaluated limb salvage procedures as alternatives to amputation in Charcot foot and ankle osteomyelitis. Farber et al. [38] reported that none of the 11 patients with midfoot CN and ulceration who underwent operative debridement and corrective osteotomy as a limb salvage procedure needed an amputation. Dalla Paola et al. [39] reported four (9%) major amputations for failed infection control in 43 patients who underwent arthrodesis [40] and external fixation as a limb salvage procedure for CN and ankle osteomyelitis. Pinzur et al. [41] reported 3 amputations (4.2%) in a cohort of 71 patients who underwent single-stage resection of infection and correction of deformity with a ring fixateur. Ramanujam et al. [42] reported one lower extremity amputation (3.7%) in 27 patients with diabetic CN and osteomyelitis who underwent surgical reconstruction using circular external fixation.
A long-standing history (>10 years) of diabetes at the time of initial diagnosis of CN is common [43, 44]. The mean duration of treatment for diabetes in our study was 15 (range: 0.6 to 53) years. No patient with insulin-dependent diabetes received the diagnosis of diabetes less than one year before the diagnosis of CN. However, two patients with non–insulin-dependent diabetes had an almost synchronous diagnosis of CN and diabetes, suggesting that the initial occurrence of Charcot may have guided the diagnosis of diabetes. There were less patients (62%) with insulin-dependent diabetes compared to the 75% previously reported in another study of CN [45]. However, insulin dependency did not appear to influence the amputation rate or amputation level.
In previous studies, noncompliance with treatment of CN was determined to be the strongest predictor for recurrence of CN, with an odds ratio of 19.7 [46, 47]. While the rate of noncompliance as recorded in patient charts was high in the present study (38%), noncompliance with treatment of the osteomyelitis did not appear to influence the amputation rate or level of amputation.
The large number of patients excluded from this study due to incomplete patient charts may have resulted in selection bias. Typically, CN patients do not come in for follow-up visits because they are poorly compliant with treatment (i.e., total contact cast) or they do not understand that they have a disease. The less complex cases are often followed for longer durations than the severe cases, to monitor their feet and their special shoes. Thus, to minimize the potential selection bias for more severe cases, we evaluated the effect of compliance with treatment on amputation rate and amputation level.
Limitations of this study include the retrospective study design, such that some pertinent factors that could potentially affect treatment outcomes may not have been recorded, and data collection at a single site, which limits the generalizability of the conclusions. Another limitation is the lack of recorded reasons for the initial surgical treatment that was elected. Finally, the heterogeneity of initial surgical treatments performed in Group 2 patients and the relatively small sample sizes did not allow further subgroup analysis.
Strengths of this study include the relatively large sample size compared to other studies of CN, and the detailed information available about the treatment regimens. However, the heterogeneity of patients with this disease and initial surgical treatment options limited may require prospective trials with larger samples to better elucidate the best treatment option for osteomyelitis in the presence of CN.

Conclusions

Patients treated for osteomyelitis within the Charcot region on the foot underwent more high level amputations and had longer durations of antibiotic treatment and immobilization than patients treated for osteomyelitis outside the Charcot region, although the amputation rate was similar for both groups. We recommend that. osteomyelitis outside and within the Charcot affected region should be regarded as separate entities when considering treatment protocols and in future research evaluating the outcome and treatment of CN and osteomyelitis. If osteomyelitis occurs outside the active Charcot region, primary amputation may be preferred to internal resection.

Acknowledgements

The authors thank Dagmar Gross for assistance with preparation of this manuscript.

Funding

The authors received no financial support for the research, authorship, and/or publication of this article.

Availability of data and materials

The datasets generated and/or analyzed during the current study are not publicly available in order to maintain individual privacy, but are available from the corresponding author on reasonable request.

Authors’ information

CB and SL are residents in orthopedic surgery; LV, TB, and MB are board-certified orthopedic surgeons; additionally, the senior authors TB and MB are specialized in the treatment of the diabetic foot.
This study was approved by the Ethics Committee of the Canton of Zurich, Switzerland (Amendment dt. 10.11.2016, positiv, BASEC 2016–00271). Written informed consent was obtained from all participants.
Not required, as there are no identifying data for any individual person.

Competing interests

The authors declare that they have no potential conflicts of interest or competing interests with respect to the research, authorship, and/or publication of this article.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://​creativecommons.​org/​licenses/​by/​4.​0/​), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://​creativecommons.​org/​publicdomain/​zero/​1.​0/​) applies to the data made available in this article, unless otherwise stated.
Literatur
1.
Zurück zum Zitat Frykberg RG, Bevilacqua NJ, Habershaw G. Surgical off-loading of the diabetic foot. J Vasc Surg. 2010;52(3 Suppl):44S–58S.CrossRefPubMed Frykberg RG, Bevilacqua NJ, Habershaw G. Surgical off-loading of the diabetic foot. J Vasc Surg. 2010;52(3 Suppl):44S–58S.CrossRefPubMed
2.
Zurück zum Zitat Wukich DK, Sung W. Charcot arthropathy of the foot and ankle: modern concepts and management review. J Diabetes Complicat. 2009;23(6):409–26.CrossRefPubMed Wukich DK, Sung W. Charcot arthropathy of the foot and ankle: modern concepts and management review. J Diabetes Complicat. 2009;23(6):409–26.CrossRefPubMed
3.
Zurück zum Zitat Strotman PK, Reif TJ, Pinzur MS. Charcot Arthropathy of the foot and ankle. Foot Ankle Int. 2016;37(11):1255–63.CrossRefPubMed Strotman PK, Reif TJ, Pinzur MS. Charcot Arthropathy of the foot and ankle. Foot Ankle Int. 2016;37(11):1255–63.CrossRefPubMed
4.
Zurück zum Zitat Berendt AR, Peters EJ, Bakker K, Embil JM, Eneroth M, Hinchliffe RJ, Jeffcoate WJ, Lipsky BA, Senneville E, Teh J, et al. Diabetic foot osteomyelitis: a progress report on diagnosis and a systematic review of treatment. Diabetes Metab Res Rev. 2008;24(Suppl 1):S145–61.CrossRefPubMed Berendt AR, Peters EJ, Bakker K, Embil JM, Eneroth M, Hinchliffe RJ, Jeffcoate WJ, Lipsky BA, Senneville E, Teh J, et al. Diabetic foot osteomyelitis: a progress report on diagnosis and a systematic review of treatment. Diabetes Metab Res Rev. 2008;24(Suppl 1):S145–61.CrossRefPubMed
5.
Zurück zum Zitat Rajbhandari SM, Jenkins RC, Davies C, Tesfaye S. Charcot neuroarthropathy in diabetes mellitus. Diabetologia. 2002;45(8):1085–96.CrossRefPubMed Rajbhandari SM, Jenkins RC, Davies C, Tesfaye S. Charcot neuroarthropathy in diabetes mellitus. Diabetologia. 2002;45(8):1085–96.CrossRefPubMed
6.
Zurück zum Zitat Chisholm KA, Gilchrist JM. The Charcot joint: a modern neurologic perspective. J Clin Neuromuscul Dis. 2011;13(1):1–13.CrossRefPubMed Chisholm KA, Gilchrist JM. The Charcot joint: a modern neurologic perspective. J Clin Neuromuscul Dis. 2011;13(1):1–13.CrossRefPubMed
7.
Zurück zum Zitat Herbst SA, Jones KB, Saltzman CL. Pattern of diabetic neuropathic arthropathy associated with the peripheral bone mineral density. J Bone Joint Surg Br. 2004;86(3):378–83.CrossRefPubMed Herbst SA, Jones KB, Saltzman CL. Pattern of diabetic neuropathic arthropathy associated with the peripheral bone mineral density. J Bone Joint Surg Br. 2004;86(3):378–83.CrossRefPubMed
8.
Zurück zum Zitat Frykberg RG, Mendeszoon E. Management of the diabetic Charcot foot. Diabetes Metab Res Rev. 2000;16(Suppl 1):S59–65.CrossRefPubMed Frykberg RG, Mendeszoon E. Management of the diabetic Charcot foot. Diabetes Metab Res Rev. 2000;16(Suppl 1):S59–65.CrossRefPubMed
9.
Zurück zum Zitat Game FL. Osteomyelitis in the diabetic foot: diagnosis and management. Med Clin North Am. 2013;97(5):947–56.CrossRefPubMed Game FL. Osteomyelitis in the diabetic foot: diagnosis and management. Med Clin North Am. 2013;97(5):947–56.CrossRefPubMed
10.
Zurück zum Zitat Boulton AJ, Kirsner RS, Vileikyte L. Clinical practice. Neuropathic diabetic foot ulcers. N Engl J Med. 2004;351(1):48–55.CrossRefPubMed Boulton AJ, Kirsner RS, Vileikyte L. Clinical practice. Neuropathic diabetic foot ulcers. N Engl J Med. 2004;351(1):48–55.CrossRefPubMed
11.
Zurück zum Zitat Ciampolini J, Harding KG. Pathophysiology of chronic bacterial osteomyelitis. Why do antibiotics fail so often? Postgrad Med J. 2000;76(898):479–83.CrossRefPubMedPubMedCentral Ciampolini J, Harding KG. Pathophysiology of chronic bacterial osteomyelitis. Why do antibiotics fail so often? Postgrad Med J. 2000;76(898):479–83.CrossRefPubMedPubMedCentral
12.
Zurück zum Zitat Frykberg RG. Diabetic foot ulcers: pathogenesis and management. Am Fam Physician. 2002;66(9):1655–62.PubMed Frykberg RG. Diabetic foot ulcers: pathogenesis and management. Am Fam Physician. 2002;66(9):1655–62.PubMed
13.
Zurück zum Zitat Chantelau E. The perils of procrastination: effects of early vs. delayed detection and treatment of incipient Charcot fracture. Diabet Med. 2005;22(12):1707–12.CrossRefPubMed Chantelau E. The perils of procrastination: effects of early vs. delayed detection and treatment of incipient Charcot fracture. Diabet Med. 2005;22(12):1707–12.CrossRefPubMed
14.
Zurück zum Zitat Sanders LJFR. Diabetic neuropathic osteoarthropathy: the Charcot foot. In: The high risk foot in diabetes mellitus; 1991. p. 325–33. Sanders LJFR. Diabetic neuropathic osteoarthropathy: the Charcot foot. In: The high risk foot in diabetes mellitus; 1991. p. 325–33.
15.
Zurück zum Zitat Petrova NL, Edmonds ME. Charcot neuro-osteoarthropathy-current standards. Diabetes Metab Res Rev. 2008;24(Suppl 1):S58–61.CrossRefPubMed Petrova NL, Edmonds ME. Charcot neuro-osteoarthropathy-current standards. Diabetes Metab Res Rev. 2008;24(Suppl 1):S58–61.CrossRefPubMed
16.
Zurück zum Zitat Ruotolo V, Di Pietro B, Giurato L, Masala S, Meloni M, Schillaci O, Bergamini A, Uccioli L. A new natural history of Charcot foot: clinical evolution and final outcome of stage 0 Charcot neuroarthropathy in a tertiary referral diabetic foot clinic. Clin Nucl Med. 2013;38(7):506–9.CrossRefPubMed Ruotolo V, Di Pietro B, Giurato L, Masala S, Meloni M, Schillaci O, Bergamini A, Uccioli L. A new natural history of Charcot foot: clinical evolution and final outcome of stage 0 Charcot neuroarthropathy in a tertiary referral diabetic foot clinic. Clin Nucl Med. 2013;38(7):506–9.CrossRefPubMed
17.
Zurück zum Zitat Illgner U, Podella M, Rummler M, Wuhr J, Busch HG, Wetz HH. Reconstructive surgery for Charcot foot. Long-term 5-year outcome. Orthopade. 2009;38(12):1180–6.CrossRefPubMed Illgner U, Podella M, Rummler M, Wuhr J, Busch HG, Wetz HH. Reconstructive surgery for Charcot foot. Long-term 5-year outcome. Orthopade. 2009;38(12):1180–6.CrossRefPubMed
18.
Zurück zum Zitat van Asten SA, Jupiter DC, Mithani M, La Fontaine J, Davis KE, Lavery LA. Erythrocyte sedimentation rate and C-reactive protein to monitor treatment outcomes in diabetic foot osteomyelitis. Int Wound J. 2017;14(1):142–8.CrossRefPubMed van Asten SA, Jupiter DC, Mithani M, La Fontaine J, Davis KE, Lavery LA. Erythrocyte sedimentation rate and C-reactive protein to monitor treatment outcomes in diabetic foot osteomyelitis. Int Wound J. 2017;14(1):142–8.CrossRefPubMed
19.
Zurück zum Zitat Aragon-Sanchez J, Lazaro-Martinez JL, Alvaro-Afonso FJ, Molines-Barroso R. Conservative surgery of diabetic forefoot osteomyelitis: how can I operate on this patient without amputation? Int J Low Extrem Wounds. 2015;14(2):108–31.CrossRefPubMed Aragon-Sanchez J, Lazaro-Martinez JL, Alvaro-Afonso FJ, Molines-Barroso R. Conservative surgery of diabetic forefoot osteomyelitis: how can I operate on this patient without amputation? Int J Low Extrem Wounds. 2015;14(2):108–31.CrossRefPubMed
20.
Zurück zum Zitat Vaseenon T, Thitiboonsuwan S, Cheewawattanachai C, Pimchoo P, Phanphaisarn A. Off-loading total contact cast in combination with hydrogel and foam dressing for management of diabetic plantar ulcer of the foot. J Med Assoc Thail. 2014;97(12):1319–24. Vaseenon T, Thitiboonsuwan S, Cheewawattanachai C, Pimchoo P, Phanphaisarn A. Off-loading total contact cast in combination with hydrogel and foam dressing for management of diabetic plantar ulcer of the foot. J Med Assoc Thail. 2014;97(12):1319–24.
21.
Zurück zum Zitat Cull DL, Manos G, Hartley MC, Taylor SM, Langan EM, Eidt JF, Johnson BL. An early validation of the Society for Vascular Surgery lower extremity threatened limb classification system. J Vasc Surg. 2014;60(6):1535–41.CrossRefPubMed Cull DL, Manos G, Hartley MC, Taylor SM, Langan EM, Eidt JF, Johnson BL. An early validation of the Society for Vascular Surgery lower extremity threatened limb classification system. J Vasc Surg. 2014;60(6):1535–41.CrossRefPubMed
22.
Zurück zum Zitat Wang A, Sun X, Wang W, Jiang K. A study of prognostic factors in Chinese patients with diabetic foot ulcers. Diabet Foot Ankle. 2014;5 Wang A, Sun X, Wang W, Jiang K. A study of prognostic factors in Chinese patients with diabetic foot ulcers. Diabet Foot Ankle. 2014;5
23.
Zurück zum Zitat Cecilia-Matilla A, Lazaro-Martinez JL, Aragon-Sanchez J, Garcia-Alvarez Y, Chana-Valero P, Beneit-Montesinos JV. Influence of the location of nonischemic diabetic forefoot osteomyelitis on time to healing after undergoing surgery. Int J Low Extrem Wounds. 2013;12(3):184–8.CrossRefPubMed Cecilia-Matilla A, Lazaro-Martinez JL, Aragon-Sanchez J, Garcia-Alvarez Y, Chana-Valero P, Beneit-Montesinos JV. Influence of the location of nonischemic diabetic forefoot osteomyelitis on time to healing after undergoing surgery. Int J Low Extrem Wounds. 2013;12(3):184–8.CrossRefPubMed
24.
Zurück zum Zitat Pickwell KM, Siersma VD, Kars M, Holstein PE, Schaper NC, Eurodiale c. Diabetic foot disease: impact of ulcer location on ulcer healing. Diabetes Metab Res Rev. 2013;29(5):377–83.CrossRefPubMed Pickwell KM, Siersma VD, Kars M, Holstein PE, Schaper NC, Eurodiale c. Diabetic foot disease: impact of ulcer location on ulcer healing. Diabetes Metab Res Rev. 2013;29(5):377–83.CrossRefPubMed
25.
Zurück zum Zitat Dalla Paola L, Carone A, Baglioni M, Boscarino G, Vasilache L. Extension and grading of osteomyelitis are not related to limb salvage in Charcot neuropathic osteoarthropathy: a cohort prospective study. J Diabetes Complicat. 2016;30(4):608–12.CrossRefPubMed Dalla Paola L, Carone A, Baglioni M, Boscarino G, Vasilache L. Extension and grading of osteomyelitis are not related to limb salvage in Charcot neuropathic osteoarthropathy: a cohort prospective study. J Diabetes Complicat. 2016;30(4):608–12.CrossRefPubMed
26.
Zurück zum Zitat Charcot J. Lectures on the diseases of the nervous system: delivered at la Salpêtrière. HC Lea. 1879; Charcot J. Lectures on the diseases of the nervous system: delivered at la Salpêtrière. HC Lea. 1879;
27.
Zurück zum Zitat Dalla Paola L. Confronting a dramatic situation: the charcot foot complicated by osteomyelitis. Int J Low Extrem Wounds. 2014;13(4):247–62.CrossRefPubMed Dalla Paola L. Confronting a dramatic situation: the charcot foot complicated by osteomyelitis. Int J Low Extrem Wounds. 2014;13(4):247–62.CrossRefPubMed
28.
Zurück zum Zitat Wukich DK, Hobizal KB, Sambenedetto TL, Kirby K, Rosario BL. Outcomes of osteomyelitis in patients hospitalized with diabetic foot infections. Foot Ankle Int. 2016;37(12):1285–91.CrossRefPubMed Wukich DK, Hobizal KB, Sambenedetto TL, Kirby K, Rosario BL. Outcomes of osteomyelitis in patients hospitalized with diabetic foot infections. Foot Ankle Int. 2016;37(12):1285–91.CrossRefPubMed
29.
Zurück zum Zitat Gazis A, Pound N, Macfarlane R, Treece K, Game F, Jeffcoate W. Mortality in patients with diabetic neuropathic osteoarthropathy (Charcot foot). Diabet Med. 2004;21(11):1243–6.CrossRefPubMed Gazis A, Pound N, Macfarlane R, Treece K, Game F, Jeffcoate W. Mortality in patients with diabetic neuropathic osteoarthropathy (Charcot foot). Diabet Med. 2004;21(11):1243–6.CrossRefPubMed
30.
Zurück zum Zitat Zeun P, Gooday C, Nunney I, Dhatariya K. Predictors of outcomes in diabetic foot osteomyelitis treated initially with conservative (nonsurgical) medical management: a retrospective study. Int J Low Extrem Wounds. 2016;15(1):19–25.CrossRefPubMed Zeun P, Gooday C, Nunney I, Dhatariya K. Predictors of outcomes in diabetic foot osteomyelitis treated initially with conservative (nonsurgical) medical management: a retrospective study. Int J Low Extrem Wounds. 2016;15(1):19–25.CrossRefPubMed
31.
Zurück zum Zitat Lesens O, Desbiez F, Theis C, Ferry T, Bensalem M, Laurichesse H, Tauveron I, Beytout J, Aragon Sanchez J. Working group on diabetic O: Staphylococcus Aureus-related diabetic osteomyelitis: medical or surgical management? A French and Spanish retrospective cohort. Int J Low Extrem Wounds. 2015;14(3):284–90.CrossRefPubMed Lesens O, Desbiez F, Theis C, Ferry T, Bensalem M, Laurichesse H, Tauveron I, Beytout J, Aragon Sanchez J. Working group on diabetic O: Staphylococcus Aureus-related diabetic osteomyelitis: medical or surgical management? A French and Spanish retrospective cohort. Int J Low Extrem Wounds. 2015;14(3):284–90.CrossRefPubMed
32.
Zurück zum Zitat Mutluoglu M, Sivrioglu AK, Eroglu M, Uzun G, Turhan V, Ay H, Lipsky BA. The implications of the presence of osteomyelitis on outcomes of infected diabetic foot wounds. Scand J Infect Dis. 2013;45(7):497–503.CrossRefPubMed Mutluoglu M, Sivrioglu AK, Eroglu M, Uzun G, Turhan V, Ay H, Lipsky BA. The implications of the presence of osteomyelitis on outcomes of infected diabetic foot wounds. Scand J Infect Dis. 2013;45(7):497–503.CrossRefPubMed
33.
Zurück zum Zitat Faglia E, Caravaggi C, Clerici G, Sganzaroli A, Curci V, Vailati W, Simonetti D, Sommalvico F. Effectiveness of removable walker cast versus nonremovable fiberglass off-bearing cast in the healing of diabetic plantar foot ulcer: a randomized controlled trial. Diabetes Care. 2010;33(7):1419–23.CrossRefPubMedPubMedCentral Faglia E, Caravaggi C, Clerici G, Sganzaroli A, Curci V, Vailati W, Simonetti D, Sommalvico F. Effectiveness of removable walker cast versus nonremovable fiberglass off-bearing cast in the healing of diabetic plantar foot ulcer: a randomized controlled trial. Diabetes Care. 2010;33(7):1419–23.CrossRefPubMedPubMedCentral
34.
Zurück zum Zitat Lavery LA, Higgins KR, La Fontaine J, Zamorano RG, Constantinides GP, Kim PJ. Randomised clinical trial to compare total contact casts, healing sandals and a shear-reducing removable boot to heal diabetic foot ulcers. Int Wound J. 2015;12(6):710–5.CrossRefPubMed Lavery LA, Higgins KR, La Fontaine J, Zamorano RG, Constantinides GP, Kim PJ. Randomised clinical trial to compare total contact casts, healing sandals and a shear-reducing removable boot to heal diabetic foot ulcers. Int Wound J. 2015;12(6):710–5.CrossRefPubMed
35.
Zurück zum Zitat Armstrong DG, Lavery LA, Wu S, Boulton AJ. Evaluation of removable and irremovable cast walkers in the healing of diabetic foot wounds: a randomized controlled trial. Diabetes Care. 2005;28(3):551–4.CrossRefPubMed Armstrong DG, Lavery LA, Wu S, Boulton AJ. Evaluation of removable and irremovable cast walkers in the healing of diabetic foot wounds: a randomized controlled trial. Diabetes Care. 2005;28(3):551–4.CrossRefPubMed
36.
Zurück zum Zitat Ha Van G, Siney H, Hartmann-Heurtier A, Jacqueminet S, Greau F, Grimaldi A. Nonremovable, windowed, fiberglass cast boot in the treatment of diabetic plantar ulcers: efficacy, safety, and compliance. Diabetes Care. 2003;26(10):2848–52.CrossRefPubMed Ha Van G, Siney H, Hartmann-Heurtier A, Jacqueminet S, Greau F, Grimaldi A. Nonremovable, windowed, fiberglass cast boot in the treatment of diabetic plantar ulcers: efficacy, safety, and compliance. Diabetes Care. 2003;26(10):2848–52.CrossRefPubMed
37.
Zurück zum Zitat Game FL, Catlow R, Jones GR, Edmonds ME, Jude EB, Rayman G, Jeffcoate WJ. Audit of acute Charcot's disease in the UK: the CDUK study. Diabetologia. 2012;55(1):32–5.CrossRefPubMed Game FL, Catlow R, Jones GR, Edmonds ME, Jude EB, Rayman G, Jeffcoate WJ. Audit of acute Charcot's disease in the UK: the CDUK study. Diabetologia. 2012;55(1):32–5.CrossRefPubMed
38.
Zurück zum Zitat Farber DC, Juliano PJ, Cavanagh PR, Ulbrecht J, Caputo G. Single stage correction with external fixation of the ulcerated foot in individuals with Charcot neuroarthropathy. Foot Ankle Int. 2002;23(2):130–4.CrossRefPubMed Farber DC, Juliano PJ, Cavanagh PR, Ulbrecht J, Caputo G. Single stage correction with external fixation of the ulcerated foot in individuals with Charcot neuroarthropathy. Foot Ankle Int. 2002;23(2):130–4.CrossRefPubMed
39.
Zurück zum Zitat Dalla Paola L, Brocco E, Ceccacci T, Ninkovic S, Sorgentone S, Marinescu MG, Volpe A. Limb salvage in Charcot foot and ankle osteomyelitis: combined use single stage/double stage of arthrodesis and external fixation. Foot Ankle Int. 2009;30(11):1065–70.CrossRefPubMed Dalla Paola L, Brocco E, Ceccacci T, Ninkovic S, Sorgentone S, Marinescu MG, Volpe A. Limb salvage in Charcot foot and ankle osteomyelitis: combined use single stage/double stage of arthrodesis and external fixation. Foot Ankle Int. 2009;30(11):1065–70.CrossRefPubMed
40.
Zurück zum Zitat Biz C, Hoxhaj B, Aldegheri R, Iacobellis C. Minimally invasive surgery for Tibiotalocalcaneal arthrodesis using a retrograde intramedullary nail: preliminary results of an innovative modified technique. J Foot Ankle Surg. 2016;55(6):1130–8.CrossRefPubMed Biz C, Hoxhaj B, Aldegheri R, Iacobellis C. Minimally invasive surgery for Tibiotalocalcaneal arthrodesis using a retrograde intramedullary nail: preliminary results of an innovative modified technique. J Foot Ankle Surg. 2016;55(6):1130–8.CrossRefPubMed
41.
Zurück zum Zitat Pinzur MS, Gil J, Belmares J. Treatment of osteomyelitis in charcot foot with single-stage resection of infection, correction of deformity, and maintenance with ring fixation. Foot Ankle Int. 2012;33(12):1069–74.CrossRefPubMed Pinzur MS, Gil J, Belmares J. Treatment of osteomyelitis in charcot foot with single-stage resection of infection, correction of deformity, and maintenance with ring fixation. Foot Ankle Int. 2012;33(12):1069–74.CrossRefPubMed
42.
Zurück zum Zitat Ramanujam CL, Han D, Zgonis T. Lower extremity amputation and mortality rates in the reconstructed diabetic Charcot foot and ankle with external fixation: data analysis of 116 patients. Foot Ankle Spec. 2016;9(2):113–26.CrossRefPubMed Ramanujam CL, Han D, Zgonis T. Lower extremity amputation and mortality rates in the reconstructed diabetic Charcot foot and ankle with external fixation: data analysis of 116 patients. Foot Ankle Spec. 2016;9(2):113–26.CrossRefPubMed
43.
Zurück zum Zitat Fabrin J, Larsen K, Holstein PE. Long-term follow-up in diabetic Charcot feet with spontaneous onset. Diabetes Care. 2000;23(6):796–800.CrossRefPubMed Fabrin J, Larsen K, Holstein PE. Long-term follow-up in diabetic Charcot feet with spontaneous onset. Diabetes Care. 2000;23(6):796–800.CrossRefPubMed
44.
Zurück zum Zitat Pakarinen TK, Laine HJ, Honkonen SE, Peltonen J, Oksala H, Lahtela J. Charcot arthropathy of the diabetic foot. Current concepts and review of 36 cases. Scand J Surg. 2002;91(2):195–201.CrossRefPubMed Pakarinen TK, Laine HJ, Honkonen SE, Peltonen J, Oksala H, Lahtela J. Charcot arthropathy of the diabetic foot. Current concepts and review of 36 cases. Scand J Surg. 2002;91(2):195–201.CrossRefPubMed
45.
Zurück zum Zitat Myerson MS, Henderson MR, Saxby T, Short KW. Management of midfoot diabetic neuroarthropathy. Foot Ankle Int. 1994;15(5):233–41.CrossRefPubMed Myerson MS, Henderson MR, Saxby T, Short KW. Management of midfoot diabetic neuroarthropathy. Foot Ankle Int. 1994;15(5):233–41.CrossRefPubMed
46.
Zurück zum Zitat Osterhoff G, Boni T, Berli M. Recurrence of acute Charcot neuropathic osteoarthropathy after conservative treatment. Foot Ankle Int. 2013;34(3):359–64.CrossRefPubMed Osterhoff G, Boni T, Berli M. Recurrence of acute Charcot neuropathic osteoarthropathy after conservative treatment. Foot Ankle Int. 2013;34(3):359–64.CrossRefPubMed
47.
Zurück zum Zitat Renner N, Wirth SH, Osterhoff G, Boni T, Berli M. Outcome after protected full weightbearing treatment in an orthopedic device in diabetic neuropathic arthropathy (Charcot arthropathy): a comparison of unilaterally and bilaterally affected patients. BMC Musculoskelet Disord. 2016;17(1):504.CrossRefPubMedPubMedCentral Renner N, Wirth SH, Osterhoff G, Boni T, Berli M. Outcome after protected full weightbearing treatment in an orthopedic device in diabetic neuropathic arthropathy (Charcot arthropathy): a comparison of unilaterally and bilaterally affected patients. BMC Musculoskelet Disord. 2016;17(1):504.CrossRefPubMedPubMedCentral
Metadaten
Titel
Treatment of Charcot Neuroarthropathy and osteomyelitis of the same foot: a retrospective cohort study
verfasst von
Martin Berli
Lazaros Vlachopoulos
Sabra Leupi
Thomas Böni
Charlotte Baltin
Publikationsdatum
01.12.2017
Verlag
BioMed Central
Erschienen in
BMC Musculoskeletal Disorders / Ausgabe 1/2017
Elektronische ISSN: 1471-2474
DOI
https://doi.org/10.1186/s12891-017-1818-4

Weitere Artikel der Ausgabe 1/2017

BMC Musculoskeletal Disorders 1/2017 Zur Ausgabe

Arthropedia

Grundlagenwissen der Arthroskopie und Gelenkchirurgie. Erweitert durch Fallbeispiele, Videos und Abbildungen. 
» Jetzt entdecken

Update Orthopädie und Unfallchirurgie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.