Skip to main content
Deutsches Ärzteblatt International logoLink to Deutsches Ärzteblatt International
. 2017 Feb 24;114(8):130–136. doi: 10.3238/arztebl.2017.0130

Lower Limb Amputation in Germany

An Analysis of Data From the German Federal Statistical Office Between 2005 and 2014

Knut Kröger 1,*, Christian Berg 2, Frans Santosa 1, Nasser Malyar 3, Holger Reinecke 3
PMCID: PMC5374258  PMID: 28302263

Abstract

Background

Declining amputation rates have been reported in multiple countries in recent years. It is not yet known whether amputation rates have declined in Germany as well.

Methods

On the basis of DRG (diagnosis-related group) data, we received a list from the German Federal Statistical Office of all major and minor amputations documented in German hospitals from 2005 to 2014. Changes over this period were studied with linear regression.

Results

The absolute number of amputations per year in Germany rose slightly from 55 689 in 2005 to 57 637 (+3.5%) in 2014. After the exclusion of cases in which the main diagnosis was trauma, intoxication, musculoskeletal disease, diseases of the skin and subcutaneous tissue, or neoplasia, the corresponding numbers were 48 043 in 2005 and 48 561 in 2014 (+1.1%). The age-adjusted rate of major amputations per 100 000 persons per year fell from 23.3 to 16.1 (-30.9%), while the rate of minor amputations rose from 35.0 to 43.9 (+25.4%). The percentage of major amputations that took place in patients with diabetes mellitus as the main diagnosis or a side diagnosis declined from 70.2% to 63.7%. For all of these changes, p <0.0001.

Conclusion

From 2005 to 2014, the major amputation rate fell by 30.9% while the minor amputation rate rose by 25.4%. The goal of lowering amputation rates still further will be best served not only by applying the recognized preventive measures in patients with foot lesions, but also by further research into the causes of the recent changes in amputation numbers. Prospective registries will be needed.


In the Saint Vincent Declaration of 1989, representatives of governments, health authorities, and patients’ organizations from all European countries demanded, under the auspices of the World Health Organization (WHO), that the rate of amputations in diabetics be halved within 5 years (1). In the following years, however, it emerged that the goals could by no means be achieved as rapidly as originally assumed (2).

Nevertheless, the past 10 years have seen the publication of encouraging figures demonstrating decreases in the rate of major amputations in many European countries as well as the USA and Australia (313) (table 1). In this country too, studies have reported a downward trend in major amputations (1820). We therefore set out to ascertain whether amputation rates are also steadily decreasing in Germany.

Table 1. Recently published studies on trends in amputation over a number of years.

Study, country Population Study period Major amputations:change during study period Minor amputations:change during study period
USA
Rowe et al.,
2009 (4)
National sample, hospitalized patients
(age ≥ 18 years)
1996–2005 Decrease from 30.8% to 21.8% of all acute admissions with PAOD n.d.
Goodney et al.,
2009 (3)
Medicare population (age ≥ 67 years, disabled,
on dialysis)
1996–2006 Decrease from 263 to 188 per 100 000 insurees n.d.
UK
Vamos et al.,
2010 (6)
National hospital data
(age ≥ 16 years)
2004–2008 Decrease from 118 to 102 per 100 000 persons with DM Decrease from 157 to 149 per 100 000 persons with DM
Ireland
Buckley et al.,
2012 (14)
Survey of hospitalized patients
(age ≥ 16 years)
2005–2009 Increase from 47.9 to 48.0 per 100 000 persons with DM Increase from 96.2 to 127 per 100 000 persons with DM
Spain
Lopez-de-Andres et al.,
2015 (11)
National hospital discharge data 2001–2008 Increase from 7.12 to 7.47 per 100 000 persons with DM type 2 Increase from 9.23 to 10.97 per 100 000 persons with DM type 2
Italy
Lombardo et al.,
2014 (15)
National hospital discharge data 2001–2010 Decrease from 114.5 to 79.3 per 100 000 persons with DM Decrease from 168.8 to 161.1 per 100 000 persons with DM
Finland
Winell et al.,
2013 (16)
National hospital discharge data and dates of death 1997–2007 Decrease from 13.6 to 9.3 per 100 000 person-years in persons with DM Increase from 11.0 to 13.5 per 100 000 person-years in persons with DM

Author, country, population investigated, observation period, and details of major and minor amputations (based on [17]).

DM, diabetes mellitus; n.d., no data; PAOD, peripheral arterial occlusive disease

Patient selection and methods

The national diagnosis-related groups (DRG) statistics from the German Federal Statistical Office include data from all hospitals in Germany that use the DRG system. More than 99% of inpatient treatments are covered. All hospitals are legally obliged to transmit comprehensive information on hospital treatments, including patient demographic data, diagnoses, comorbidities, complications, and procedures, to the Institut für das Entgeltsystem im Krankenhaus (InEK; Institute for Hospital Fees). InEK uses the data for an annual adjustment of the DRG system and passes them on to the Federal Statistical Office. All diagnoses from the years 2005 to 2014 were coded according to the German version of the International Classification of Diseases and Related Health Problems, 10th Edition (GM ICD-10).

Detailed lists of all major and minor amputations (coded 5-864 and 5-865, respectively, in the German procedure classification OPS) were provided by the Federal Statistical Office following submission of an analysis plan. In addition, age-adjusted amputation rates per 100 000 inhabitants were calculated. The term major amputation is used to mean any amputation above the ankle region, up to and including hemipelvectomy. All amputations distal to the ankle are designated minor. This includes the Syme procedure, in which the calcaneum, talus, and mortise are removed.

In the attempt to ensure that only amputations indicated by peripheral arterial occlusive disease (PAOD) and/or diabetes mellitus (diabetic foot syndrome, DFS) were included, we excluded amputations in patients with the principal diagnosis of tumor (C00–D48), cutaneous or subcutaneous disease (L00–L99), musculoskeletal disease (M00–M99), or injury/poisoning (S00–T98). Hereinafter, these diagnoses are referred to as CLMS, from their ICD codes.

To encompass diabetes mellitus (DM) as risk factor for amputation, following exclusion of CLMS diagnoses all amputations with the diagnosis DM (E10–E14), whether main or secondary, were included in analysis.

Linear regression analysis was used for statistical evaluation of trends over the 10-year study period.

Results

The absolute number of amputations in Germany rose slightly from 55 689 in 2005 to 57 637 (+3.5%) in 2014. After exclusion of patients with CLMS main diagnoses, the figures were 48 043 and 48 561 (+1.1%).

The number of non-CLMS major amputations went down from 19 189 in 2005 to 13 048 in 2014 (table 2). The age-adjusted rate of amputations per 100 000 inhabitants dropped from 23.3 in 2005 to 16.1 in 2014, a decrease of 30.9%. The number of minor amputations rose from 28 854 in 2005 to 35 513 in 2014. The age-adjusted rate of amputations per 100 000 inhabitants went up from 35.0 to 43.9, an increase of 25.4%. As shown in Figure 1, the number of major amputations in patients with CLMS main diagnoses did not decrease over the 10-year observation period.

Table 2. Total number of amputations, number of amputations after exclusion of cases with the ICD main diagnoses C00–D48, L00–L99, M00–M99, and SOO–T98 (CLMS), and age-standardized rates of amputations per 100 000 inhabitants after exclusion of CLMS: major and minor amputations.

Year Major amputations (ICD 5-864) Minor amputations (ICD 5-865)
Total After exclusion of CLMS Per
100 000
Total After exclusion of
CLMS
Per
100 000
2005 22 619 19 189 23.3 33 070 28 854 35.0
2006 22 003 18 590 22.6 33 702 29 715 36.1
2007 21 246 17 928 21.8 34 021 30 081 36.6
2008 20 744 17 272 21.0 35 465 31 315 38.1
2009 20 009 16 323 19.9 36 604 32 143 39.3
2010 18 758 15 193 18.6 37 717 33 148 40.5
2011 18 071 14 509 18.1 38 580 33 719 42.0
2012 17 295 13 795 17.2 38 809 33 847 42.1
2013 17 151 13 535 16.8 40 575 35 099 43.5
2014 16 645 13 048 16.1 40 992 35 513 43.9
Difference between
2005 and 2014
–5974 –6141 –7.2 +7922 +6659 +8.9
Relative change
2005 to 2014
–26.4% –32.0% –30.9% +24.0% +23.1% +25.4%
p-value <0.0001 <0.0001 <0.0001 <0.0001 <0.0001 <0.0001

ICD, International Classification of Diseases and Related Health Problems

Figure 1.

Figure 1

Age-standardized rates of all major and minor amputations per 100 000 inhabitants and all major and minor amputations after exclusion of cases with the ICD main diagnoses C00–D48, L00–L99, M00–M99, and SOO–T98 (CLMS)

The decrease in major amputations was seen both in men and in women. In contrast, the increase in minor amputations was much greater in men (etable). Looking at the age-group figures and just comparing 2005 with 2014, the curves for age-adjusted major amputation rate begin to diverge in the sixth decade of life for men and in the seventh decade for women. For minor amputations men show a distinct increase from the middle of the seventh decade of life onward, in contrast to women (efigure).

eTable. Age-standardized rates of major and minor amputations per 100 000 inhabitants after exclusion of cases with the ICD main diagnoses C00–D48, L00–L99, M00–M99, and SOO–T98 (CMLS): men and women.

Major amputations
(ICD 5–864)
Minor amputations
(ICD 5–865)
Year Men Women Men Women
2005 27.0 19.7 47.4 23.1
2006 26.6 18.7 49.5 23.2
2007 25.6 18.2 50.6 23.1
2008 25.1 17.1 53.7 23.2
2009 24.2 15.9 55.6 23.5
2010 22.9 14.4 57.8 23.9
2011 22.6 13.7 61.0 23.9
2012 21.6 12.9 60.9 24.1
2013 20.9 12.8 63.4 24.5
2014 20.8 11.6 64.4 24.1
Difference between
2005 and 2014
–6.2 –8.1 +17.0 +1.0
Relative change
2005 to 2014
–23.0% –41.1% +35.9% +4.3%
p-value <0.0001 <0.0001 <0.0001 <0.0001

ICD, International Classification of Diseases and Related Health Problems

eFigure.

eFigure

Rate of major and minor amputations per 100 000 from the fourth decade of life onward for the years 2005 and 2014 after exclusion of cases with the ICD main diagnoses C00–D48, L00–L99, M00–M99, and SOO–T98 (CLMS) (top, men; bottom, women);

ICD, International Classification of Diseases and Related Health Problems

The proportion of major amputations in which the diagnosis DM had been coded dropped from 70.2% in 2005 to 63.7% in 2014. The equivalent figures for minor amputations were 93.9% and 85.6%. Separation of main and secondary diagnoses shows that this fall is due to a decrease in coding of DM as principal diagnosis. The proportion of major amputations with the main diagnosis DM went down from 29.7% to 22.8% (p <0.0001), and the proportion of minor amputations with the main diagnosis DM fell from 55.8% to 50% (p <0.0001) (figure 2). In contrast, the proportions of both major and minor amputations with DM as secondary diagnosis fluctuated slightly over the observation period but essentially remained unchanged.

Figure 2.

Figure 2

Proportion of all major and minor amputations with diabetes mellitus (E10–E14) coded as main or secondary diagnosis, after exclusion of cases with the ICD main diagnoses C00–D48, L00–L99, M00–M99, and SOO–T98 (CLMS)

Discussion

The data presented here show that there was a marked decrease in the number of major amputations carried out each year in Germany between 2005 and 2014. The annual number of minor amputations increased over the same 10-year period.

Owing to the style of documentation in the German DRG system we cannot distinguish amputations performed primarily because of a diabetes-related problem from those attributable primarily to PAOD, particularly since the two diseases frequently occur together and precise classification is often impossible. Almost half (49.7%) of patients with PAOD have DM (21), and over one quarter (26.3%) of patients aged 65 years or more have PAOD (22). We thus focused not on these underlying diseases, but on the amputations performed. The annual total of amputations in patients with CLMS main diagnoses was fairly stable over the observation period. A decrease could be shown only for patients with non-CLMS diagnoses. In this group, 63.7% of the cases of major amputation and 85.6% of the cases of minor amputation were in patients with the coded diagnosis DM. This disease is therefore of great etiological importance.

According to the German Health Interview and Examination Survey for Adults (DEGS) 2012, the prevalence of known DM has reached 7.2%, an increase of 2% over the previous German National Health Interview and Examination Survey in 1998 (23). DM is usually incurable and has a lasting influence on DFS. In contrast to DM, coding of the diagnosis PAOD gives no information as to whether arterial perfusion was still restricted at the time of amputation or whether PAOD was an old diagnosis coded along with the current diagnosis. We view only DM as a lasting risk factor. However, the coded diagnosis DM says nothing about whether or not an advanced Wagner–Armstrong stage of DFS was actually the reason for the clinical decision to amputate. Our data merely show that despite a general increase in the number of people with DM (23), the proportion of amputations in which DM was coded decreased slightly over the observation period. This trend is attributable particularly to falls in the number of cases with amputation and in the proportion of all amputations with DM as main diagnosis. If the proportion of amputations with a secondary diagnosis of DM had increased to the same extent, a change in coding behavior could have been suspected. Since that is not the case, however, it can be assumed that among the risk factors for amputation DM has slightly decreased and other factors such as confinement to bed and decubitus ulcers have increased in importance (24, 25). Thus, in the period 2008 to 2011 around every fifth patient with a major amputation had a secondary diagnosis of dementia (26). In bedridden demented patients with advanced tissue destruction, primary major amputation makes more sense than revascularization (27, 28).

Overall, the decrease in major amputations in Germany is in line with developments in other countries (table 1). Direct comparisons, however, are hampered by the heterogeneity of the study populations. According to an analysis of Medicare data in the USA, the rate of amputations went down by 45% between 1996 and 2011, but the population was restricted to persons over 67 years of age, persons with disabilities, and patients who required dialysis. A fall in the number of major amputations was mainly responsible for the decrease (3). In Australia, analysis of data from the Western Australian Data Linkage System for the period 2000 to 2010 revealed decreases in the rate of major amputations of 6.2% per year in diabetics and 6.9% per year in persons without DM (10). The rates of minor amputations fell by 0.6% and 1.4% per annum, respectively. In England, Vamos et al. analyzed the National Health Service data of all patients over 16 years of age with nontraumatic amputation in the period 2004 to 2008 (6). During this time the incidence of diabetes-related amputations went down by 9.1% from 27.5 to 25.0 per 10 000 diabetics (p >0.2). In Spain, national hospital discharge data for the years 2001 to 2012 were evaluated (11). The authors found a decrease of 9.84% in minor amputations between 2001 and 2008, with the rate remaining constant thereafter. Major amputations in type 2 diabetics increased by 4.29% between 2001 and 2004, but then decreased by 1.85% from 2004 to 2012.

Although major amputation represents a greater detriment to physical integrity, minor amputations should also be prevented. The data on minor amputations in German hospitals are an underestimate of the true situation. An unknown but probably high number of patients with foot lesions are nowadays treated out of hospital, and the treatment includes amputation of gangrenous of mummified toes. In view of the rising prevalence of DM, the rate of minor amputations may reflect the burden placed on the healthcare system by the increasing number of DM patients, while the rate of major amputations affords insight into the efficacy of treatment strategies. The lack of a decrease—or indeed the presence of an increase—in minor amputations could indicate that in Germany, in comparison with other countries, primary prevention of foot lesions is insufficiently effective or that the available treatment options are either not offered early enough or fail to take effect. On the other hand, the increase in minor amputations is found above all in elderly men, raising the question of whether sex-specific changes in behavior of the elderly might be responsible. In the EURODIALE Study, which investigated foot lesions in a cohort of 1088 patients at 14 European centers, a multivariable model identified male sex as an independent predictor of lack of healing (29).

It is not clear what precise changes in the healthcare system underlie the decrease in major amputations. Increased awareness of DFS among office-based physicians or general improvement of care structures may be responsible. An analysis carried out by our group showed a possible link between major amputations and, in particular, percutaneous transluminal angioplasty (PTA) of the crural arteries and the number of referrals for podological treatment (30). This seems logical, because PTA of the crural arteries is indicated only in patients with foot wounds and prescription of podological treatment is restricted to patients with DM and DFS. However, the findings do not show whether PTA and podology in themselves prevent amputation in individual patients or whether they are just markers of basic improvements in care structures with earlier escalation of treatment. This needs to be investigated further in care evaluation studies.

There appears to be room for further reduction in the rate of amputations. For instance, analysis of a German health insurance fund’s data for the period 2009 to 2011, which permitted case-related evaluation, showed that in 37% of inpatients with chronic critical ischemia treated with amputation, neither angiography nor attempted revascularization was documented in the 24 months before surgery (31, 32). There is thus an urgent need for clarification of how, and on what basis, the decision to amputate is arrived at in each individual patient.

Limitations

Although routinely recorded data contained in electronic medical records are often used for secondary purposes, no systematic analysis of coding quality in Germany has yet been carried out (33, 34). Controlled studies are needed to determine whether coding as a precondition for further use of the data in medicine and in healthcare policy corresponds to reality. It can be assumed, however, that—in contrast to subjective parameters and comorbidities—hard clinical endpoints such as amputation and death are affected very little or not at all by coding errors and are an accurate reflection of medical practice.

Also deserving of mention is the fact that the data are procedure related, not patient related. Therefore, it is unknown how many patients underwent amputation of more than one limb or first had a minor amputation and later a major amputation of the same limb. The decrease in amputations may therefore be even greater in terms of the number of persons affected.

Summary

Despite the aging of society and the increasing number of persons with DM, the data show a pronounced drop of 30.9% in the annual number of major amputations in Germany between 2005 and 2014. However, the rate of minor amputations rose over the same period. The precise reasons for these developments are unclear. Together with targeted implementation of the existing strategies for prevention of foot lesions, prospective registries are necessary to clarify the effect of changes in behavior among the elderly and of medical treatment methods.

Key Messages.

  • The total annual number of major amputations carried out in German hospitals fell by 26.4% between 2005 and 2014 (from 22 619 to 16 645). After exclusion of cases with the main diagnoses trauma or intoxication, musculoskeletal disease, diseases of the skin or subcutaneous tissue, and neoplasia, the decrease was 32% (from 19 189 to 13 048).

  • In the same period, the total annual number of minor amputations performed in hospital rose by 24%, from 33 070 to 40 992. After exclusion of the above-mentioned main diagnoses, the increase was 23.1% (from 28 854 to 35 513).

  • The marked rise in the overall number of minor amputations is due principally to an increased amputation rate in men above 70 years of age.

  • Focusing on amputations without the above-mentioned main diagnoses, the proportion of cases with a coded diagnosis of diabetes mellitus fell from 70.2% in 2005 to 63.7% in 2014 for major amputations and from 93.9% to 85.6% for minor amputations.

Acknowledgments

We are grateful to the staff of Section VIII A 1 of the Federal Statistical Office for extracting and providing data from the DRG statistics.

Translated from the original German by David Roseveare

Footnotes

Conflict of interest statement

Prof. Kröger has received reimbursement of conference attendance fees and travel costs as well as payments for lectures from UCB Pharma, Sanofi, and Bayer.

Prof. Reinecke has received payments for consultancy from Bristol-Myers, Pfizer, and Pluristem. Study support (third-party funding) was provided to him by Pluristem, Bard, Bayer, and Biotronik.

The remaining authors declare that no conflict of interest exists.

References

  • 1.The Saint Vincent Declaration on diabetes care and research in Europe. Acta Diabetol. 1989;(10):143–144. [Google Scholar]
  • 2.Nickolaus B. Diabetes mellitus - Gutachten identifiziert Mängel. Dtsch Arzteblatt. 2012;109 [Google Scholar]
  • 3.Goodney PP, Beck AW, Nagle J, Welch HG, Zwolak RM. National trends in lower extremity bypass surgery, endovascular interventions, and major amputations. J Vasc Surg. 2009;50:54–60. doi: 10.1016/j.jvs.2009.01.035. [DOI] [PubMed] [Google Scholar]
  • 4.Rowe VL, Lee W, Weaver FA, Etzioni D. Patterns of treatment for peripheral arterial disease in the United States: 1996-2005. J Vasc Surg. 2009;49:910–917. doi: 10.1016/j.jvs.2008.11.054. [DOI] [PubMed] [Google Scholar]
  • 5.Li Y, Burrows NR, Gregg EW, Albright A, Geiss LS. Declining rates of hospitalization for nontraumatic lower-extremity amputation in the diabetic population aged 40 years or older: US., 1988-2008. Diabetes Care. 2012;35:273–277. doi: 10.2337/dc11-1360. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Vamos EP, Bottle A, Edmonds ME, Valabhji J, Majeed A, Millett C. Changes in the incidence of lower extremity amputations in individuals with and without diabetes in England between 2004 and 2008. Diabetes Care. 2010;33:2592–2597. doi: 10.2337/dc10-0989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Goodney PP, Tarulli M, Faerber AE, Schanzer A, Zwolak RM. Fifteen-year trends in lower limb amputation, revascularization, and preventive measures among medicare patients. JAMA Surg. 2015;150:84–86. doi: 10.1001/jamasurg.2014.1007. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Heyer K, Debus ES, Mayerhoff L, Augustin M. Prevalence and regional distribution of lower limb amputations from 2006 to 2012 in Germany: a population based study. Eur J Vasc Endovasc Surg. 2015;50:761–766. doi: 10.1016/j.ejvs.2015.07.033. [DOI] [PubMed] [Google Scholar]
  • 9.Lazzarini PA, O’Rourke SR, Russell AW, Derhy PH, Kamp MC. Reduced incidence of foot-related hospitalisation and amputation amongst persons with diabetes in Queensland, Australia. PLoS One. 2015;10 doi: 10.1371/journal.pone.0130609. e0130609. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Kurowski JR, Nedkoff L, Schoen DE, Knuiman M, Norman PE, Briffa TG. Temporal trends in initial and recurrent lower extremity amputations in people with and without diabetes in Western Australia from 2000 to 2010. Diabetes Res Clin Pract. 2015;108:280–287. doi: 10.1016/j.diabres.2015.02.008. [DOI] [PubMed] [Google Scholar]
  • 11.Lopez-de-Andres A, Jiménez-García R, Aragón-Sánchez J, et al. National trends in incidence and outcomes in lower extremity amputations in people with and without diabetes in Spain, 2001-2012. Diabetes Res Clin Pract. 2015;108:499–507. doi: 10.1016/j.diabres.2015.01.010. [DOI] [PubMed] [Google Scholar]
  • 12.Jørgensen ME, Almdal TP, Faerch K. Reduced incidence of lower-extremity amputations in a Danish diabetes population from 2000 to 2011. Diabet Med. 2014;31:443–447. doi: 10.1111/dme.12320. [DOI] [PubMed] [Google Scholar]
  • 13.Carmona GA, Lacraz A, Hoffmeyer P, Assal M. Incidence of major lower limb amputation in Geneva: twenty-one years of observation. Rev Med Suisse. 2014;10:1997–1998. [PubMed] [Google Scholar]
  • 14.Buckley CM, O’Farrell A, Canavan RJ, et al. Trends in the incidence of lower extremity amputations in people with and without diabetes over a five-year period in the Republic of Ireland. PLoS One. 2012;7 doi: 10.1371/journal.pone.0041492. e41492. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Lombardo FL, Maggini M, De Bellis A, Seghieri G, Anichini R. Lower extremity amputations in persons with and without diabetes in Italy: 2001-2010. PLoS One. 2014;9 doi: 10.1371/journal.pone.0086405. e86405. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Winell K, Venermo M, Ikonen T, Sund R. Indicators for comparing the incidence of diabetic amputations: a nationwide population-based register study. Eur J Vasc Endovasc Surg. 2013;46:569–574. doi: 10.1016/j.ejvs.2013.07.010. [DOI] [PubMed] [Google Scholar]
  • 17.Kröger K. Major and minor amputation rates: what do they tell us? EWMA Journal. 2015;15:65–67. [Google Scholar]
  • 18.Kröger K, Moysidis T, Feghaly M, Schäfer E, Bufe A. On behalf of the Initiative Chronische Wunden e V., Germany. Association of diabetic foot care and amputation rates in Germany. Int Wound J. 2016,;13:686–691. doi: 10.1111/iwj.12347. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Santosa F, Moysidis T, Kanya S, Babadagi-Hardt Z, Luther B, Kröger K. Decrease in major amputations in Germany. Int Wound J. 2015;12:276–279. doi: 10.1111/iwj.12096. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Moysidis T, Nowack T, Eickmeyer F, et al. Trends in amputations in people with hospital admissions for peripheral arterial disease in Germany. Vasa. 2011;40:289–295. doi: 10.1024/0301-1526/a000117. [DOI] [PubMed] [Google Scholar]
  • 21.Silbernagel G, Rein P, Saely CH, et al. Prevalence of type 2 diabetes is higher in peripheral artery disease than in coronary artery disease patients. Diab Vasc Dis Res. 2015;12:146–149. doi: 10.1177/1479164114560342. [DOI] [PubMed] [Google Scholar]
  • 22.Lange S, Diehm C, Darius H, et al. High prevalence of peripheral arterial disease but low antiplatelet treatment rates in elderly primary care patients with diabetes. Diabetes Care. 2003;26:3357–3358. doi: 10.2337/diacare.26.12.3357. [DOI] [PubMed] [Google Scholar]
  • 23.Richter-Kuhlmann E. Gesundheitssurvey des Robert-Koch-Instituts Zivilisationskrankheiten nehmen zu. Dtsch Arzteblatt. 2012;109 A-1376-7. [Google Scholar]
  • 24.Twilley H, Jones S. Heel ulcers—pressure ulcers or symptoms of peripheral arterial disease? An exploratory matched case control study. J Tissue Viability. 2016;25:150–156. doi: 10.1016/j.jtv.2016.02.007. [DOI] [PubMed] [Google Scholar]
  • 25.McGinnis E, Greenwood DC, Nelson EA, Nixon J. A prospective cohort study of prognostic factors for the healing of heel pressure ulcers. Age Ageing. 2014;43:267–271. doi: 10.1093/ageing/aft187. [DOI] [PubMed] [Google Scholar]
  • 26.Schuch V, Moysidis T, Weiland D, Santosa F, Kröger K. Dementia and amputation. Interv Med Appl Sci. 2012;4:175–180. doi: 10.1556/IMAS.4.2012.4.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Bosanquet DC, Wright AM, White RD, Williams IM. A review of the surgical management of heel pressure ulcers in the 21st century. Int Wound J. 2016;13:9–16. doi: 10.1111/iwj.12416. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Lawall H. S3-Leitlinie zur Diagnostik, Therapie und Nachsorge der peripheren arteriellen Verschlusskrankheit AWMF-Registernummer 065-003 [Google Scholar]
  • 29.Prompers L, Schaper N, Apelqvist J, et al. Prediction of outcome in individuals with diabetic foot ulcers: focus on the differences between individuals with and without peripheral arterial disease. The EURODIALE Study. Diabetologia. 2008;51:747–755. doi: 10.1007/s00125-008-0940-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Pütter C, Stausberg J, von Beckerath O, Reinecke H, Schäfer E, Kröger K. Determinants of decreasing major amputation rates in Germany. Vasa. 2016;45:311–315. doi: 10.1024/0301-1526/a000543. [DOI] [PubMed] [Google Scholar]
  • 31.Reinecke H, Unrath M, Freisinger E, et al. Peripheral arterial disease and critical limb ischaemia: still poor outcomes and lack of guideline adherence. Eur Heart J. 2015;36:932–938. doi: 10.1093/eurheartj/ehv006. [DOI] [PubMed] [Google Scholar]
  • 32.Malyar NM, Freisinger E, Meyborg M, et al. Low rates of revascularization and high In-hospital mortality in patients with ischemic lower limb amputation: morbidity and mortality of ischemic amputation. Angiology. 2016;67:860–869. doi: 10.1177/0003319715626849. [DOI] [PubMed] [Google Scholar]
  • 33.Statistisches Bundesamt. Fachserie 12, Reihe 6.4, 2005. Fallpauschalenbezogene Krankenhausstatistik (DRG-Statistik) [Google Scholar]
  • 34.Stausberg J. Quality of coding in acute inpatient care Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2007;50:1039–1046. doi: 10.1007/s00103-007-0296-5. [DOI] [PubMed] [Google Scholar]

Articles from Deutsches Ärzteblatt International are provided here courtesy of Deutscher Arzte-Verlag GmbH

RESOURCES