Intensive versus conventional glycaemic control for treating diabetic foot ulcers

被引:35
作者
Fernando, Malindu E. [1 ,2 ]
Seneviratne, Ridmee M. [1 ]
Tan, Yong Mong [3 ]
Lazzarini, Peter A. [4 ,5 ]
Sangla, Kunwarjit S. [3 ]
Cunningham, Margaret [6 ]
Buttner, Petra G. [7 ]
Golledge, Jonathan [1 ,8 ]
机构
[1] James Cook Univ, Coll Med & Dent, Queensland Res Ctr Peripheral Vasc Dis, Vasc Biol Unit, Townsville, Qld 4811, Australia
[2] Podiatry Serv, Kirwan Community Hlth Campus, Townsville, Qld, Australia
[3] Townsville Hosp, Dept Diabet & Endocrinol, Townsville, Qld, Australia
[4] Queensland Hlth, Allied Hlth Res Collaborat, Brisbane, Qld, Australia
[5] Queensland Univ Technol, Sch Clin Sci, Brisbane, Qld 4001, Australia
[6] Univ Stirling, NMAHP RU, Stirling FK9 4LA, Scotland
[7] Trop Hlth Solut Pty Ltd, Townsville, Qld, Australia
[8] Townsville Hosp, Dept Vasc & Endovasc Surg, Townsville, Qld, Australia
来源
COCHRANE DATABASE OF SYSTEMATIC REVIEWS | 2016年 / 01期
关键词
CONTROLLED-TRIAL; GLUCOSE CONTROL; CLINICAL-TRIAL; MULTIFACTORIAL INTERVENTION; CARDIOVASCULAR OUTCOMES; CLASSIFICATION-SYSTEM; MANAGEMENT; COMPLICATIONS; DISEASE; CARE;
D O I
10.1002/14651858.CD010764.pub2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background The estimated likelihood of lower limb amputation is 10 to 30 times higher amongst people with diabetes compared to those without diabetes. Of all non-traumatic amputations in people with diabetes, 85% are preceded by a foot ulcer. Foot ulceration associated with diabetes (diabetic foot ulcers) is caused by the interplay of several factors, most notably diabetic peripheral neuropathy (DPN), peripheral arterial disease (PAD) and changes in foot structure. These factors have been linked to chronic hyperglycaemia (high levels of glucose in the blood) and the altered metabolic state of diabetes. Control of hyperglycaemia may be important in the healing of ulcers. Objectives To assess the effects of intensive glycaemic control compared to conventional control on the outcome of foot ulcers in people with type 1 and type 2 diabetes. Search methods In December 2015 we searched: The Cochrane Wounds Specialised Register; The Cochrane Central Register of Controlled Trials (CENTRAL) (The Cochrane Library); Ovid MEDLINE; Ovid MEDLINE (In-Process & Other Non-Indexed Citations); Ovid EM-BASE; EBSCO CINAHL; Elsevier SCOPUS; ISI Web of Knowledge Web of Science; BioMed Central and LILACS. We also searched clinical trial databases, pharmaceutical trial databases and current international and national clinical guidelines on diabetes foot management for relevant published, non-published, ongoing and terminated clinical trials. There were no restrictions based on language or date of publication or study setting. Selection criteria Published, unpublished and ongoing randomised controlled trials (RCTs) were considered for inclusion where they investigated the effects of intensive glycaemic control on the outcome of active foot ulcers in people with diabetes. Non randomised and quasi-randomised trials were excluded. In order to be included the trial had to have: 1) attempted to maintain or control blood glucose levels and measured changes in markers of glycaemic control (HbA1c or fasting, random, mean, home capillary or urine glucose), and 2) documented the effect of these interventions on active foot ulcer outcomes. Glycaemic interventions included subcutaneous insulin administration, continuous insulin infusion, oral anti-diabetes agents, lifestyle interventions or a combination of these interventions. The definition of the interventional (intensive) group was that it should have a lower glycaemic target than the comparison (conventional) group. Data collection and analysis All review authors independently evaluated the papers identified by the search strategy against the inclusion criteria. Two review authors then independently reviewed all potential full-text articles and trials registry results for inclusion. Main results We only identified one trial that met the inclusion criteria but this trial did not have any results so we could not perform the planned subgroup and sensitivity analyses in the absence of data. Two ongoing trials were identified which may provide data for analyses in a later version of this review. The completion date of these trials is currently unknown.
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