- Open Access
Human amniotic membrane products for patients with diabetic foot ulcers. do they help? a systematic review and meta-analysis
Journal of Foot and Ankle Research volume 15, Article number: 71 (2022)
Diabetic foot ulcer (DFU) is one of the most serious diabetic complications. DFU is an open wound that usually occurs in the foot sole due to poor blood glucose control, peripheral neuropathy, and poor circulation. The human amniotic allograft membrane is a biological wound dressing derived from the amniotic membrane. It contains amino acids, nutrients, cytokines, and growth factors that make the growth process easier.
To compare dehydrated human amnion and chorion allograft (DHACA) plus the standard of wound care (SOC) with the SOC alone.
We searched for randomized clinical trials (RCTs) on PubMed, Scopus, Cochrane, and Web of Science till April 2021 using relevant keywords. All search results were screened for eligibility. We extracted the data from the included trials and pooled them as mean difference (MD) or risk ratio (RR) with the 95% confidence interval (CI) using Review Manager software (ver. 5.4).
The pooled effect estimate from 11 RCTs showed that DHACA was superior to SOC regarding the complete wound healing in both 6th and 12th week (RR = 3.78; 95% CI: [2.51, 5.70]; P < 0.00001) and (RR = 2.00; 95% CI: [1.67, 2.39], P < 0.00001 respectively). Also, the analysis favored the DHACA regarding the mean time to heal in the 12th-week (MD = -12.07, 95%CI: [-19.23, -4.91], P = 0.001). The wound size reduction was better with DHACA (MD = 1.18, 95%CI: [-0,10, 2.26], P = 0.03).
Using DHACA with SOC is safer and more effective than using SOC alone for DFU patients.
Diabetes mellitus (DM) is a worldwide epidemic disease. In 2019, the global diabetes prevalence was projected to be 9.3% (463 million people). The prevalence is estimated to rise to 10.2% (578 million) by 2030 and 10.9% (700 million) by 2045 . Diabetic foot ulcer (DFU) is one of the most serious and common complications of diabetes that itself can be complicated by wound infection, gangrene, and unfortunate amputation. Amputation can comprise a huge burden on the patients' quality of life and the health systems' economy . The global prevalence of DFU is 6.3%, affecting males more than females, and patients with type 2 DM more than type 1 . Diabetic foot ulcer is primarily caused by hyperglycemia that results from endothelial dysfunction, leading to vascular insufficiency and nerve injury [4, 5].
The current DFU standard of care (SOC) involves four principles; pressure relief, debridement, infection management, and revascularization when indicated. Preventative measures such as adequate glycemic control, periodic foot inspection, as well as patient and family education are always recommended [6, 7]. Sometimes the SOC is not enough for the management of DFUs, therefore, new trends have emerged to address this problem. These include negative pressure wound therapy, hyperbaric oxygen therapy, bioengineered skin substitutes, and shockwave therapy, among several other measures. These novel therapies have shown significant DFU clinical improvement in different subsets of DFU. However, much of the literature came from smaller trials with inconsistent patient selection and outcomes measurement, making it difficult to assess the exact clinical benefit of these treatments .
Although we associate regenerative medicine with the recent decades, amnion has been used in the medical field for over a century. The first known usage for amnion was in a skin transplant, in 1910 at John Hopkins Hospital . Dehydrated human amnion-chorion membranes and placenta possess marvelous features, from the pluripotent stem cells which can differentiate into all three germ layers, to the angiogenic anti-inflammatory properties coming from a wide variety and mixture of angio-modulatory cytokines, anti-bacterial peptides, and anti-inflammatory agents [9, 10]. These membranes are currently considered a new hope in regenerative medicine owing to their wide uses, low immunogenicity, and easy procurement from the placenta. As the placenta is a discarded tissue after parturition, the current controversies associated with the use of human embryonic stem cells are avoided .
Dehydrated human amniotic and chorionic allograft (DHACA) is easier for application and commercially available. This product can be applied directly to clean the debrided wounds where the infection has been controlled and adequate vasculature and perfusion state exist, to achieve wound healing as early as possible . Many studies have shown that DHACA as a treatment for diabetic foot ulcers is more effective than standard wound care alone. For further evaluation of the efficacy and time-sensitivity of DHACAs in patients suffering from DFU, we performed this systematic review and meta-analysis study. Our study compares using DHACA plus SOC versus SOC alone.
Material and methods
We performed a systematic review and meta-analysis for clinical trials on the use of dehydrated human amnion/chorion membrane for the treatment of DFU. We followed the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines in reporting our study .
We used four different databases for the literature search (PubMed, Scopus, Cochrane and Web of Science), and the search was conducted from their inception till October 2020. The following keywords were used (Diabetic foot ulcer, human amnion membrane, amniotic allograft, Grafix, AmnioBand, EpiFix), and MESH terms were used when applicable. We also did a manual screening of references in the included studies, searching for any relevant trials.
Inclusion and exclusion criteria
English-written human-based randomized clinical trials (RCTs) were included in our study. Diabetic patients with foot ulcers were the target population. The intervention was human amnion, chorion, placental membrane, or any brand using them like Grafix, GrafixPL PRIME, AmnioBand, Stravix, biological dressing, bio implant dressing, or EpiFix. The comparator was any effective measurement like SOC. We excluded conference abstracts, books, single-armed clinical trials, animal studies, and studies on non-diabetic patients.
We used EndNote X8 for citation management and duplicate removal for articles identified in the searches. We selected the included studies in a two-stage screening process. In the first stage, the titles and abstracts from the electronic searches were screened independently. The second stage of full-text screening was performed to determine the final decision on studies' eligibility. The assessment of each manuscript was performed independently by at least three authors, and any disagreements about inclusion were resolved by consultation with the principal investigator of the study.
The risk of bias was assessed according to the Cochrane risk of bias tool described in the Cochrane Handbook for Systematic Reviews of Interventions 5.1.0 . There are six domains in the tool: random sequence generation, allocation sequence concealment, blinding of study participants and personnel, blinding of outcome assessors, incomplete outcome data, selective outcomes reporting, and other potential sources of bias. We reported the quality of the included studies as low risk, high risk, or unclear risk of bias. In addition, we measured the publication bias through visualization of the funnel plot for any asymmetrical distribution .
Each author – independently – extracted data from all the included trials. Data extraction was performed in an excel sheet that included three sections. Firstly, general data included the year of publication, protocol registration, definition of ulcers, groups and sample size, and intervention. Then, baseline data included age, race, gender, Body Mass Index (BMI), mean glycated hemoglobin, smoking, duration of wound, initial wound surface area in cm2, and wound location.
Primary and secondary outcomes
The primary outcomes were the percentage of complete wound healing by the 6th and 12th week and the mean time to heal within the 1st, 6th, and 12th weeks. The secondary outcomes included the Kaplan–Meier plot of time to heal within the 1st, 6th, and 12th week, and wound size reduction. An adverse events analysis was performed, including any unfavorable outcome that occurred to patients in each group during the time of the trial like (Cellulitis, osteomyelitis and infection of the affected extremity, development of another ulcer, deep vein thrombosis, urinary tract infection and gastrointestinal bleed).
We conducted the meta-analyses using the Review Manager (RevMan) computer program (Version 5.4. Copenhagen: The Nordic Cochrane Centre, The Cochrane Collaboration, 2014). Regarding pooling of the study outcomes, risk ratio (RR) with the 95% confidence interval (CI) were used for dichotomous variables, while the mean difference (MD) and the 95% CI were presented for continuous variables. Cochrane's P values and the I2 were tested to examine heterogeneity among the included studies. High heterogeneity existed in some analyses most likely due to clinical and methodological factors, therefore, the random effect model was adopted in these analyses. Funnel plots and the Egger regression test were conducted and measured through visualization of the funnel plot. Besides, a sensitivity analysis was performed by sequentially deleting trials to check for the stability of the primary outcomes.
The literature search revealed 2477 results, 265 of them were duplicates. Therefore, we performed a title and abstract screening for 2212 results, of which only 43 results were judged relevant. These 43 studies were eligible for full-text screening which finally resulted in including only 11 studies in our review. We excluded 16 studies that were not RCTs, three studies because ulcers were not diabetic in origin, three studies because full-texts were not published (only abstracts available), two studies that were duplicates of already existed studies, two studies that were terminated, three studies that were in recruiting state, two studies for the different control group, and one study for reporting outcomes that were not of our interest. Fig. 1
Risk of bias
Overall, the included studies were of moderate quality. Regarding the selection bias, most of the studies reported appropriate randomization methods and were at low risk of bias. However, Lavery et al.  and NCT03547635 which did not report the method of randomization, and thus had an unclear risk of bias. Six studies [16,17,18,19,20,21] did not report the method of allocation concealment, and thus had an unclear risk of bias. However, one study NCT03547635 reported no allocation concealment, and thus was at high risk of bias. In terms of performance bias, eight studies reported an inability to blind the participants due to the nature of the intervention, however, blinding was possible in other two studies [22, 23]. Therefore, incomplete participants and personnel blinding were considered a high risk of bias. One study did not mention anything about the blinding, thus was considered unclear risk of bias . No missing data were detected, as all the studies reported using the intention to treat analysis. Regarding the detection bias, four studies reported that the analysis was performed by an unblinded statistician [16, 17]. Fig. 2
Finally, we considered the low sample size and the absence of protocol a high risk of other bias. Therefore, four studies [16,17,18, 20] were considered at high risk. None of the studies' authors had a conflict of interest with any of the suppliers of the amniotic membrane products. Publication bias was measured through visualization of the funnel plot and it was visually not symmetrical. Fig. 3
A total of 655 patients suffering from DFU were eligible for this review. From this total number, 328 patients underwent DHACA with SOC and 327 patients underwent SOC alone. Patients were followed up from six to 16 weeks. The majority of the trials followed the patients for 12 weeks. However, Snyder et al.  followed the patients for six weeks, while Serena et al.  followed them for 16 weeks. The summary of the eligible trials including NCT, sample size, follow-up duration, definition of ulcer, amniotic membrane products, and type of the applied intervention are presented in Table1. Baseline characteristics of the studies’ enrolled patients including study arms, the number of patients in each arm, age, gender, BMI, glycated hemoglobin, smoking status, initial wound area, and the wound location are presented in Table2.
Complete wound healing
The pooled results of the included studies showed a significant difference between DHACA plus SOC and the SOC alone, favoring the experimental group after the 6th and 12th weeks of follow-up (RR = 3.78; 95%CI: [2.51, 5.70], P < 0.00001) and (RR = 2.00; 95% CI: [1.67, 2.39], P < 0.00001) respectively. The pooled studies were homogenous in the 6th week while heterogenous in the 12th week (I2 = 0%, P = 0.61) and (I2 = 43%, P = 0.01) respectively. (Fig. 4a).
The analysis showed a significant difference between DHACA with SOC group and the SOC group favoring the experimental group (RR = 0.82, 95% CI: [0.70, 0.96], P = 0.01). The pooled studies' results were homogeneous (I2 = 29%, P = 0.19). (Fig. 4b).
Wound size reduction
The pooled analysis of wound size reduction significantly favored DHACA with SOC over the SOC alone (MD = 1.18; 95% CI: [0.10, 2.26], P = 0.03). The pooled studies were heterogeneous and the heterogeneity could not be resolved (I2 = 79%, P = 0.003). (Fig. 4c).
Time to heal
The analysis favored the DHACA group over the control group after the 1st week of follow-up (RR = 5.74; 95%CI: [2.04, 16.18], P = 0.0009) as well as after the 6th and 12th weeks (RR = 3.00; 95%CI: [2.26, 3.98], P = 0.00001), (RR = 1.82; 95%CI: [1.46, 2.27], P = 0.00001) respectively. The results were significant in the three durations of follow-up with no inter-heterogeneity among the studies in the 1st, 6th, and 12th weeks (I2 = 0%, P = 0.98), (I2 = 5%, P = 0.39), and (I2 = 17%, P = 0.31) respectively. (Fig. S.1).
Kaplan–meier plot of time to heal
The pooled effect estimate of the included studies showed no significant difference between the two groups in the 4th week (MD = -3.42; 95%CI: [-8.82, 1.97], P = 0.21), and the 6th week (MD = -2.92; 95% CI: [-6.10, 0.26], P = 0.07). On the other hand, the analysis favored the experimental group in the 12th week of follow-up (MD = -12.07; 95% CI: [-19.23, -4.91], P = 0.001). The results of pooled studies were heterogenous in the analyses of the 4th, 6th, and 12th weeks (I2 = 92%, P < 0.00001), (I2 = 66%, P = 0.01), and (I2 = 71%, P = 0.004) respectively. (Fig. S.2).
This systematic review and meta-analysis is based on ten published RCTs [12, 17, 18, 20,21,22,23,24,25,26] and one unpublished RCT (NCT03547635) that compared DHACA with SOC versus SOC alone in the treatment of DFUs. A total of 655 patients suffering from DFU were included in this systematic review. The meta-analysis findings showed that using DHACA with SOC is more effective and safer than the SOC alone for treating chronic DFUs. The pooled effect estimate of the 11 RCTs showed the superiority of the DHACA regarding complete wound healing in both the 6th and 12th weeks. The mean time for healing was not significantly different between the two groups at the 4th and 6th weeks, while a significant reduction in healing time was observed in the 12th week favoring DHACA. Kaplan–Meier's plot of time to heal was significantly better in DHACA with SOC than SOC alone in the 1st, 6th, and 12th weeks. Moreover, the current meta-analysis results revealed that DHACA can significantly reduce the wound size with a low risk of adverse events compared to SOC alone.
Similar to our findings, a previous meta-analysis  reported that the incomplete wound healing outcomes are less associated with DHACA plus SOC group than SOC only group at the 4th, 6th, and 12th weeks with significant P values of < 0.0001, < 0.0001, and < 0.0001 respectively. This meta-analysis was conducted on seven studies with a total sample size of 347 patients and was limited by assessing a single outcome (wound healing). Contrary to the previous meta-analysis , our meta-analysis evaluated five outcomes: the percentage of complete wound healing, mean time to heal, Kaplan–Meier plot of time to heal, wound size reduction, and adverse events.
The human amniotic membrane is structured from three types of material: active cells, collagen fibers, extracellular matrix, and regenerative molecules. The amniotic membrane has been studied to investigate its effects on the wound healing process . DiDomenico et al. 2016  demonstrated that the mean and median time for wound healing is 12 weeks in the DHACA group, which was faster than most of the other cellular and/or tissue-based products (CTPs) reported in other RCTs [21, 25, 28,29,30,31,32,33,34,35]. In the multicenter trial Reyzelman et al. , 69.6% of the allograft has healed. While in Niezgoda et al.  49% of small intestine submucosal CTP has healed. These findings reflect that DHACA might be promising and the most effective CTPs available.
Wound infections developed in DFU patients have 56 times the risk of requiring hospitalization and 155 times the risk of requiring amputation when compared to other wounds  . Once the patient’s foot or leg is amputated, an increase in the risk of repeated infections and ulcers arises . To achieve wound healing, a 100% epithelialization must occur without drainage or need for dressing . The main goal of DFU treatment is to enhance and facilitate complete wound healing; therefore, reducing the risk of complications such as infection, amputation, and delayed wound healing .
For our included studies, Zelen et al.  reported that complete wound healing occurred in 73%, 97%, and 51% of patients treated with bioengineered skin substitutes (BSS), dHACM, and SOC alone within 12 weeks, respectively. DiDomenico et al. 2016  & DiDomenico et al. 2018  showed that at the 12th week, 85% of the DHACA-treated DFUs healed compared with 25% and 33% when treated with SOC alone, respectively. The mean time to heal ranged between 36 and 70 days in DiDomenico et al. 2016  and between 37 and 67 days in DiDomenico et al. 2018 . In addition, they concluded that the DHACA graft might have a sufficient clinical effect to be used in patients with more complex deep wounds that reach tendon and bone.
Lavery et al.  reported that the incidence of adverse events was 44% in Grafix group versus 66% in the SOC group, and the wound-related infections were fewer in the Grafix group (18%) than in the SOC group (36.2%). Similar to these findings, Zelen et al. 2013  findings demonstrated that of patients who experienced DFU-related complications, 92% have healed with dehydrated human amniotic membrane allografts (EpiFix), while only 8% have healed with SOC alone. Zelen et al. 2015  compared the median time to wound healing in DFPs using EpiFix, Apligraf, and SOC, they found that the healing time was significantly faster in EpiFix (13 days) compared to Apligraf (49 days) or standard care (49 days).
This meta-analysis is based on RCTs, which is considered a point of strength, the findings should be cautiously interpreted due to several concerns. The first concern is that dietary factors that could vary in other populations might have affected the generalizability of the studies' results. The second concern is about the possibility of patients' overlap in included studies. The third concern is the high heterogeneity in some outcomes that could not be resolved. Including English studies only could be considered a limitation of the current review. In addition, a possible concern can arise in studies by Zelen et al. 2013 , Zelen et al. 2015 , and Zelen et al. 2016 , also in DiDomenico et al. 2016  and DiDomenico et al. 2018  since these studies were conducted by the same authors. Therefore, future studies from different countries/populations are necessary to explore the effect of DHACA in treating DFUs in other populations.
The current review results support that DHACA with SOC has better efficacy than SOC alone in enhancing wound healing, reducing the mean time to wound healing, and diminishing the risk of adverse events. All these findings are in turn beneficial for treating DFUs patients.
Availability of data and material
All data are available upon reasonable request from the corresponding author.
Saeedi P, Petersohn I, Salpea P, Malanda B, Karuranga S, Unwin N, et al. Global and regional diabetes prevalence estimates for 2019 and projections for 2030 and 2045: Results from the International Diabetes Federation Diabetes Atlas, 9th edition. Diabetes Res Clin Pract. 2019;157:107843.
Woods TJ, Tesfay F, Speck P, Kaambwa B. Economic evaluations considering costs and outcomes of diabetic foot ulcer infections: A systematic review. PLoS ONE. 2020;15(4): e0232395.
Zhang P, Lu J, Jing Y, Tang S, Zhu D, Bi Y. Global epidemiology of diabetic foot ulceration: a systematic review and meta-analysis†. Ann Med. 2017;49(2):106–16.
Noor S, Zubair M, Ahmad J. Diabetic foot ulcer - A review on pathophysiology, classification and microbial etiology. Diabetes Metab Syndr Clin Res Rev. 2015;9(3):192–9.
Kolluru GK, Bir SC, Kevil CG. Endothelial dysfunction and diabetes: Effects on angiogenesis, vascular remodeling, and wound healing. Int J Vasc Med. 2012;2012:918267.
Hingorani A, Lamuraglia GM, Henke P, Meissner MH, Loretz L, Zinszer KM, et al. The management of diabetic foot: A clinical practice guideline by the Society for Vascular Surgery in collaboration with the American Podiatric Medical Association and the Society for Vascular Medicine. J Vasc Surg. 2016;63(2):3S-21S.
Aldana PC, Khachemoune A. Diabetic Foot Ulcers: Appraising Standard of Care and Reviewing New Trends in Management. Am J Clin Dermatol. 2020;21(2):255–64.
Moy AM. The History and Future of Amniotic Membrane Use in Medicine. J Dry Eye Dis. 2019;2(1):e7-9.
Burgos H. Angiogenic and growth factors in human amnio-chorion and placenta. Eur J Clin Invest. 1983;13(4):289–96.
Farhadihosseinabadi B, Farahani M, Tayebi T, Jafari A, Biniazan F, Modaresifar K, et al. Amniotic membrane and its epithelial and mesenchymal stem cells as an appropriate source for skin tissue engineering and regenerative medicine. Artif Cells, Nanomedicine Biotechnol. 2018;46(sup2):431–40.
Insausti CL, Blanquer M, Bleda P, Iniesta P, Majado MJ, Castellanos G, et al. The amniotic membrane as a source of stem cells. Histol Histopathol. 2010;25(1):91–8.
Snyder RJ, Shimozaki K, Tallis A, Kerzner M, Reyzelman A, Lintzeris D, et al. A Prospective, Randomized, Multicenter, Controlled Evaluation of the Use of Dehydrated Amniotic Membrane Allograft Compared to Standard of Care for the Closure of Chronic Diabetic Foot Ulcer. Wounds. 2016;28(3):70–7.
Liberati A, Altman DG, Tetzlaff J, Mulrow C, Gøtzsche PC, Ioannidis JPA, et al. The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate healthcare interventions: explanation and elaboration. BMJ. 2009;339.
O’Connor D, Green S, Higgins PTJ. Cochrane Handbook: General Methods For Cochrane Reviews: Ch 5: Defining the review question and developing criteria for including studies. Cochrane Handb Syst Rev Interv [Internet]. 2011;6(5):81–94.
Egger M, Smith GD, Schneider M, Minder C. Bias in meta-analysis detected by a simple, graphical test. Br Med J. 1997;315(7109):629–34.
Lavery LA, Fulmer J, Shebetka KA, Regulski M, Vayser D, Fried D, et al. The efficacy and safety of Grafix® for the treatment of chronic diabetic foot ulcers: Results of a multi-centre, controlled, randomised, blinded, clinical trial. Int Wound J. 2014;11(5):554–60.
Zelen CM, Serena TE, Denoziere G, Fetterolf DE. A prospective randomised comparative parallel study of amniotic membrane wound graft in the management of diabetic foot ulcers. Int Wound J. 2013;10(5):502–7.
Serena TE, Yaakov R, Moore S, Cole W, Coe S, Snyder R, et al. A randomized controlled clinical trial of a hypothermically stored amniotic membrane for use in diabetic foot ulcers. J Comp Eff Res. 2020;9(1):23–34.
Beach NM, Wound P, Foot A, Specialists A, Wound WM, Deaconess BI. Pl At At. 2016;28(3):70–7.
Thompson P, Hanson DS, Langemo D, Anderson J. Comparing Human Amniotic Allograft and Standard Wound Care When Using Total Contact Casting in the Treatment of Patients with Diabetic Foot Ulcers. Adv Ski Wound Care. 2019;32(6):272–7.
Zelen CM, Serena TE, Gould L, Le L, Carter MJ, Keller J, et al. Treatment of chronic diabetic lower extremity ulcers with advanced therapies: A prospective, randomised, controlled, multi-centre comparative study examining clinical efficacy and cost. Int Wound J. 2016;13(2):272–82.
DiDomenico LA, Orgill DP, Galiano RD, Serena TE, Carter MJ, Kaufman JP, et al. Use of an aseptically processed, dehydrated human amnion and chorion membrane improves likelihood and rate of healing in chronic diabetic foot ulcers: A prospective, randomised, multi-centre clinical trial in 80 patients. Int Wound J. 2018;15(6):950–7.
DiDomenico LA, Orgill DP, Galiano RD, Serena TE, Carter MJ, Kaufman JP, et al. Aseptically processed placental membrane improves healing of diabetic foot ulcerations: Prospective, randomized clinical trial. Plast Reconstr Surg - Glob Open. 2016;4(10):1–9.
Zelen CM, Gould L, Serena TE, Carter MJ, Keller J, Li WW. A prospective, randomised, controlled, multi-centre comparative effectiveness study of healing using dehydrated human amnion/chorion membrane allograft, bioengineered skin substitute or standard of care for treatment of chronic lower extremity diabetic ul. Int Wound J. 2015;12(6):724–32.
Lavery LA, Fulmer J, Shebetka KA, Regulski M, Vayser D, Fried D, et al. The efficacy and safety of Grafix ® for the treatment of chronic diabetic foot ulcers: results of a multi-centre, controlled, randomised, blinded, clinical trial. Int Wound J. 2014;11(5):554–60.
Tettelbach W, Cazzell S, Reyzelman AM, Sigal F, Caporusso JM, Agnew PS. A confirmatory study on the efficacy of dehydrated human amnion/chorion membrane dHACM allograft in the management of diabetic foot ulcers: A prospective, multicentre, randomised, controlled study of 110 patients from 14 wound clinics. Int Wound J. 2019;16(1):19–29.
Laurent I, Astère M, Wang KR, Cheng Q feng, Li QF. Efficacy and Time Sensitivity of Amniotic Membrane treatment in Patients with Diabetic Foot Ulcers: A Systematic Review and Meta-analysis. Diabetes Ther. 2017;8:967–79.
Schmidt W. The amniotic fluid compartment: the fetal habitat. Adv Anat Embryol Cell Biol. 1992;127:1–100.
Cazzell SM, Lange DL, Dickerson JE, Slade HB. The Management of Diabetic Foot Ulcers with Porcine Small Intestine Submucosa Tri-Layer Matrix: A Randomized Controlled Trial. Adv wound care. 2015;4(12):711–8.
Driver VR, Lavery LA, Reyzelman AM, Dutra TG, Dove CR, Kotsis S V, et al. A clinical trial of Integra Template for diabetic foot ulcer treatment. Wound Repair Regen. 2015;23(6):891–900.
Reyzelman A, Crews RT, Moore JC, Moore L, Mukker JS, Offutt S, et al. Clinical effectiveness of an acellular dermal regenerative tissue matrix compared to standard wound management in healing diabetic foot ulcers: a prospective, randomised, multicentre study. Int Wound J. 2009;6(3):196–208.
Veves A, Falanga V, Armstrong DG, Sabolinski ML. Apligraf Diabetic Foot Ulcer Study. Graftskin, a human skin equivalent, is effective in the management of noninfected neuropathic diabetic foot ulcers: a prospective randomized multicenter clinical trial. Diabetes Care. 2001;24(2):290–5.
Marston WA, Hanft J, Norwood P, Pollak R. Dermagraft Diabetic Foot Ulcer Study Group. The efficacy and safety of Dermagraft in improving the healing of chronic diabetic foot ulcers: results of a prospective randomized trial. Diabetes Care. 2003;26(6):1701–5.
Niezgoda JA, Van Gils CC, Frykberg RG, Hodde JP. Randomized clinical trial comparing OASIS Wound Matrix to Regranex Gel for diabetic ulcers. Adv Skin Wound Care. 2005;18(5 Pt 1):258–66.
DiDomenico L, Landsman AR, Emch KJ, Landsman A. A prospective comparison of diabetic foot ulcers treated with either a cryopreserved skin allograft or a bioengineered skin substitute. Wounds a Compend Clin Res Pract. 2011;23(7):184–9.
Lavery LA, Armstrong DG, Wunderlich RP, Mohler MJ, Wendel CS, Lipsky BA. Risk factors for foot infections in individuals with diabetes. Diabetes Care. 2006;29(6):1288–93.
Lavery LA, Peters EJG, Williams JR, Murdoch DP, Hudson A, Lavery DC, et al. Reevaluating the way we classify the diabetic foot: restructuring the diabetic foot risk classification system of the International Working Group on the Diabetic Foot. Diabetes Care. 2008;31(1):154–6.
Open access funding provided by The Science, Technology & Innovation Funding Authority (STDF) in cooperation with The Egyptian Knowledge Bank (EKB). No funding received to this work.
Ethics approval and consent to participate
Consent for publication
None to declare.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Figure S.1. Forest plot of risk ratio (RR) in time to heal after 4th, 6th, 12th follow-up, between (DHACA)+(SOC) group and the (SOC) alone group. Figure S.2. Forest plot of mean difference (MD) in Kaplan–Meier plot of time to heal within 1st, 6th, and 12th weeks follow-up, between (DHACA)+(SOC) group and the (SOC) alone group.
About this article
Cite this article
Mohammed, Y.A., Farouk, H.K., Gbreel, M.I. et al. Human amniotic membrane products for patients with diabetic foot ulcers. do they help? a systematic review and meta-analysis. J Foot Ankle Res 15, 71 (2022). https://doi.org/10.1186/s13047-022-00575-y
- Diabetic foot ulcer
- Human amnion membrane
- Amniotic allograft