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Case Report

Application of Dehydrated Amniotic Membrane Allografts in Advanced Diabetic Foot Ulceration: Case Report and Review of Literature

1
Regenative Labs, 1700 Main Street, Pensacola, FL 32502, USA
2
Ocean County Foot and Ankle Surgical Associates, 54 Bey Lea Road, Toms River, NJ 08753, USA
*
Author to whom correspondence should be addressed.
Reports 2022, 5(3), 28; https://doi.org/10.3390/reports5030028
Submission received: 30 June 2022 / Revised: 14 July 2022 / Accepted: 18 July 2022 / Published: 20 July 2022

Abstract

:
The management of diabetic foot ulcers (DFUs) presents challenges to even the most experienced wound-care providers. Because of the chronic, non-healing nature of many DFUs, advances in the treatment and care of this disease process are particularly relevant. This case study aims to report the efficacy of the application of dehydrated amniotic membrane allograft (DAMA) to a diabetic foot ulcer. The patient in this study is a 44-year-old male who presented with an aggressive infection on his right foot, which resulted in an open wound of 18-month duration. This patient received weekly applications of dual-layer DAMA over seven weeks. Upon examination at the initial application, the wound was classified as a Wagner grade 3 with necrosis of the underlying muscle. Upon inspection at the final visit, the wound was closed entirely. The results that were shown include improvements in the size, depth, edges, necrotic tissue amount, and epithelization of the wound. This case study demonstrates that the application of DAMA has the potential to augment the body’s natural DFU healing response; however, future nonrandomized and randomized controlled trials are needed to establish its efficacy further.

1. Introduction

Diabetic foot ulcers are foot lesions that may affect the foot’s skin, soft tissue, and bones. These lesions are caused by multifactorial etiologies as part of the microvascular complications of diabetes. As a result, an aggravated infection can occur in diabetic patients. Despite treatments, many DFUs remain active and unsuppressed. With approximately 37.3 million diabetic adults in the United States, physicians are faced with an epidemic of their own [1]. Given the projected increase of 1.4 million new diagnoses of diabetes mellitus each year, advancing knowledge and care for the disease and its related conditions is especially relevant [2].
In addition, many DFUs have a high recurrence rate, with 65% of the ulcers returning within five years [3]. The inability to heal DFUs presents a severe danger to patients as anywhere from 5 to 24% of untreated DFUs can lead to limb amputation within 6–18 months [4]. These infections can lead to long-term impairment and possible lower-limb amputation without timely and correct management.
With a median healing time of 12 weeks, complications of DFUs often result in amputation. The Centers for Disease Control Prevention (CDC) reported that in 2018 alone, 154,000 diabetic patients were discharged from hospitals with a recent lower-extremity amputation [5]. If the diabetic-related wounds were addressed promptly and efficiently, these amputations might have been preventable. The path to reducing limb amputation, in addition to the healthcare costs associated with amputation, must originate from the early and aggressive treatment of diabetic foot ulcerations. Since diabetic wounds heal slowly by nature, any process that promotes a quicker healing time ultimately improves a patient’s long-term quality of life. Despite typical treatment in a multi-disciplinary wound clinic, many patients with diabetic foot ulcers suffer from further wound complications or the severity of invasive amputations. The current standard of care for DFUs is debridement, followed by a moist dressing covering, wound off-loading, and a vascular assessment [6]. Understanding that necrotic tissue complicates and prolongs the healing process, the debridement of necrotic tissue is imperative to the initial treatment of DFUs. While these interventions are currently classified as the standard of care, one must consider the limitations of each of these regimens. The increased healing time and augmented risk of amputation associated with the standard of care only solidifies the need for new DFU treatment alternatives. Regenerative medicine is such an alternative.
The use of placental tissues in regenerative medicine has increased exponentially since the first use of amnion as a skin graft in 1910 [7]. The human amniotic membrane is a collagen-based extracellular matrix derived from the maternal placenta and is composed of two layers, the chorion and the amnion. The amnion, the innermost placental layer, protects against fluid loss and mechanical injury to the developing embryo. Consequently, the use of DAMA has excellent potential to decrease both the healing time and complications associated with treating diabetic wounds.
Despite the prevalence of diabetes-related ulcerations within the diabetic community and the severity of consequences they cause, DFUs and their management and treatment are a lesser-researched topic than other disease processes. Further education and research on improving the treatment for DFUs would indefinitely benefit the diabetic community.

2. Case Presentation Section

2.1. Dehydrated Human Amniotic Membrane Allografts

Following the standards established by the U.S. Food and Drug Administration (FDA) and the American Association of Tissue Banks (AATB), human amnions were obtained from consenting C-section donors. Amnions from natural deliveries were not accepted to avoid the risk of maternal–fetal blood cross-contamination. An independent certified laboratory tested all the donations for infectious disease in accordance with Clinical Laboratory Improvement Amendments (CLIA) of 1988, 42 CFR part 493, and FDA regulations. In addition, each birth mother was tested for Hepatitis B Core Antibody (HBcAb), Hepatitis B Surface Antigen (HbsAg), Hepatitis C Antibody (HCV), Human Immunodeficiency Virus Antibody (HIV1/HIV-2 Plus O), Human T-Lymphotropic Virus Antibody (HLTV-I/11), Syphilis (RPR), HIV1/HCV/HBV, NAT, and West Nile Virus (WNV). Each test was performed with an FDA-approved testing kit (see Appendix A). All test results were negative or non-reactive. The donated amnion was aseptically processed and did not involve the addition of cells, tissues, or articles other than the exceptions outlined in 21 CFR Part 1271.10(a)(3). The amnion was placed on a sterile drying tray and desiccated in a high-nitrogen-concentration drying chamber in a temperature-controlled area (10 °C–25 °C), with the air compressor set to 60–145 PSI. The patches were desiccated until the relative humidity reading was steady for one hour. The sterility of the final processed product was tested at an independent laboratory, Eurofins VRL Laboratories. In addition, the desiccated allografts were sterilized via electron beam irradiation before distribution.

2.2. Patient History

A 44-year-old male presented with a medical history of end-stage renal disease and Type 2 diabetes mellitus. The patient developed an aggressive infection of the right foot and underwent a trans-metatarsal amputation in 2019. The patient reported the occurrence of a large blister on the stump of his foot after the surgery. Due to the lack of health insurance, his wound remained open for 18 months. The patient reported numbness, tingling, and shooting sensations in the right foot. Severe pain was also noted when walking and removing shoe gear. The wound remained open despite the previous standard-of-care attempts, including using an off-loading pad in the shoe, dry sterile dressings, and sharp wound debridement with calcium alginate and betadine.
The patient received the first DAMA patch on 25 January 2022. Upon initial examination, the DFU measurement was 5.5 cm × 4.5 cm × 0.3 cm and classified as Wagner grade 3 with necrosis of the underlying muscle. Over seven weeks, the patient received weekly applications of dual-layer human amniotic membrane allografts directly on the wound. As the wound decreased in size, the sizes of the grafts that were applied also decreased. The first graft was 4 cm × 6 cm, and the last graft was 2 cm × 2 cm. The wound was noted as completely closed at the patient’s final appointment. The duration of the wound closure was 49 days from the initial allograft application. No adverse events or severe adverse effects from the amniotic membrane allograft application were reported.

3. Discussion

As observed in the present case study, treating chronic DFUs with dehydrated amniotic membrane allografts is an effective modality to afford a barrier layer over wounds and augment the body’s natural healing process. This is evident through the continual decrease in size over the seven amniotic membrane allograft applications. Each allograft was applied based on medical necessity. Weekly allograft applications were terminated upon wound closure, as is evident in Figure 1. The healing process of the DFU can be observed qualitatively in Figure 1 and quantitatively in Table 1.
The use of human amniotic membrane allografts as an effective method in DFU treatment is again supported by a 2016 randomized controlled trial (RCT) comparing the treatment standard of care to the utilization of dual-layer amniotic membrane allografts [8]. In this RCT, allograft reapplication occurred as often as once per week based upon the physician’s judgment, similar to our single-patient report. In this RCT, 45.5% of patients who received DFU standard of care (adhesive dressing and compression) and the amniotic membrane allograft achieved full closure of the DFU. In contrast, 0% of the patients who received only the standard-of-care procedure had complete wound closure. This RCT, along with our single-patient report, provides a foundation for future research in treating DFUs with DAMA.
While amniotic membrane allografts have proven to augment the body’s ability to regenerate the structural tissue defects associated with DFUs, they are also comparable in cost to the standard of care, which averages about USD 17,245 [9]. Not only is the standard of care for DFUs less effective, but it is also high in cost and typically relies on inpatient expenditures. Medicare recognizes the medical necessity of amniotic membrane allografts in the treatment of both DFUs and venous stasis ulcers. Consequently, many patients can rely on Medicare to assist with the costs associated with DFU treatment. This presents the opportunity for human amniotic membrane allografts to be utilized in rural and underserved communities where DFU treatment is typically delayed due to high costs and a lack of supplies. This could exponentially decrease the risk of amputations in diabetic patients in these rural and underserved communities. In the future, we plan to conduct a prospective study examining the efficacy of our products in underserved communities.

4. Results

Individual elements of the wound were examined during all seven allograft applications. These elements included the measurement of the wound size, depth, edges, necrotic tissue amount, and epithelization. All five elements decreased from the initial allograft application to the final wound closure (Figure 2 and Figure 3). Upon initial examination in January, the wound measured 5.5 cm × 4.5 cm × 0.3 cm (Table 1), with full-thickness skin loss involving damage or necrosis of the subcutaneous tissue. The edges of the wound were distinct and attached with a clearly visible outline. Necrotic tissue covered less than 25% of the wound bed. At the final examination in March, the wound was noted as being superficial, measuring 0.0 cm × 0.0 cm × 0.0 cm (Table 1), with intact skin and non-blanchable erythema. No edges or necrotic tissue were present. While improvements were seen in all five categories, perhaps the most notable of these elements was epithelialization. The DFU was classified as a 5 upon initial examination in January, correlating to less than 25% of the wound being covered. Over the 49 days, the epithelization of the wound increased from less than 25% to 100% wound coverage by the final patient visit (Table 2). This large-scale epithelization of the DFU provides the protective barrier essential to eliminating pathogens during the healing process. The patient experienced complete wound epithelization within seven weeks of weekly allograft applications. This is compared to the 18 months before application when the patient did not have any epithelization advancements. Evidently, the application of dehydrated amniotic membrane allografts was essential in augmenting the healing process of the DFU.
Our results are in accordance with other published studies demonstrating the potential of DAMA for treating DFU. Over the course of seven applications, our patient’s wound decreased drastically in each category of measurement. In comparison, a study displayed that the use of DAMA worked to help the body promote tissue reconstruction, which resulted in wound closure. The duration of each participant’s wound before joining the study spanned 24–84 months. Of the 14 individuals in the study who had an amniotic patch placed on their wound, all 14 patients experienced wound closure within 14–60 days [7].
Additionally, a retrospective case series examined the effects of DAMA on DFUs of eight patients. Each patient experienced wound closure in a mean time of 9.2 weeks after the initial DAMA application. Of the study group, four out of eight patients received three applications and each encountered wound closure in a mean time of 8.3 weeks [10].
Furthermore, in 2019, Joseph Caporusso demonstrated that the use of DAMA leads to successful wound closure in patients with diabetic foot ulcers greater than one year in duration, with the previous failure of prior conservative treatment [11]. The utilization of an amniotic membrane allograft in chronic DFUs resulted in the complete closure of the wound for patients with a median healing time of five weeks [11].
Each of these studies shows that DAMA has undeniable benefits relating to wound closure. The results gathered from each outside study are in accordance with the results analyzed in this case report. However, the patient in our single-patient study experienced quicker wound closure than several participants in the previously mentioned studies.

5. Conclusions

The utilization of amniotic membrane allografts in treating chronic DFUs produces favorable results and is consistent with the current medical literature. In the presented case study, the use of amniotic membrane allografts augmented the DFU healing process. The patient failed the standard-of-care methods for 18 months and achieved full closure within seven weeks of allograft application. Future applications for the early, preventative use of amniotic membrane allografts in addition to the current standard of care for DFUs present a novel opportunity to reduce long-term morbidity and amputation risk in diabetic patients.

Author Contributions

Conceptualization, C.B., S.M., and T.B.; methodology, C.B.; validation, C.B., M.R.; formal analysis, C.B.; investigation, C.B.; resources, C.B., S.M., and T.B.; data curation, C.B.; writing—original draft preparation, C.B.; writing—review and editing, M.R. and S.M.; visualization, C.B.; supervision, S.M. and T.B.; project administration, S.M. and T.B.; funding acquisition, T.B. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding. Regenative Labs is responsible for all APC charges.

Institutional Review Board Statement

The study was conducted in accordance with the Declaration of Helsinki, and approved by the Institutional Review Board of the Institute of Regenerative and Cellular Medicine (protocol code IRCM-2022-311 and approved on 12 January 2022).

Informed Consent Statement

Informed consent was obtained from all subjects involved in the study.

Data Availability Statement

Data can be found in Appendix A and Appendix B.

Acknowledgments

The authors would like to thank Keir Foot and Ankle Clinic for their collaboration in data collection. The authors would also like to thank Justine Davis for her collaboration in reviewing the manuscript.

Conflicts of Interest

Catherine Becker, Scott Martin, and Tyler Barrett are associated with Regenative Labs. Regenative Labs was involved in the design of the study, data analysis, and writing. An independent physician performed the treatment and data collection at Keir Foot and Ankle Clinic. Regenative Labs influenced the decision to publish.

Appendix A

Test Kits

  • HBcAb: Catalog number: 06P06, Abbott Laboratories, Abbott Park, IL, USA;
  • HbsAg: Catalog number: 06P02, Abbott Laboratories, Abbott Park, IL, USA;
  • HCV: Catalog number: 06P04, Abbott Laboratories, Abbott Park, IL, USA;
  • HIV1, HIV2, plus O: Catalog number: 06P01, Abbott Laboratories, Abbott Park, IL, USA;
  • HTLV-I/II: Catalog number: 06P07, Abbott Laboratories, Abbott Park, IL, USA;
  • RPR: Catalog number: 900025, Arlington Scientific, Springville, UT, USA;
  • HIV1, HCV, HBV, NAT: Catalog number: 303330, 303331, 303719, 303334, 303344;
  • WNV: Catalog number: 07001061190, Roche Diagnostics, Indianapolis, IN, USA.

Appendix B

Appendix B.1. Wound Size

  • Length × width less than 4 square cm;
  • Length × width between 4 and 16 square cm;
  • Length × width between 16.1 and 36 square cm;
  • Length × width between 36.1 and 80 square cm;
  • Length × width greater than 80 square cm.

Appendix B.2. Depth

  • Non-blanchable erythema on intact skin;
  • Partial-thickness skin loss involving epidermis and/or dermis;
  • Full-thickness skin loss involving damage or necrosis of subcutaneous tissue; may extend down to but not through underlying fascia; and/or mixed partial and full-thickness and/or tissue layers obscured by granulation tissue;
  • Obscured by necrosis;
  • Full-thickness skin loss with extensive destruction, tissue necrosis, or damage to muscle, bone, or supporting structures.

Appendix B.3. Edges

  • Instinct, diffuse, none clearly visible;
  • Distinct, outline clearly visible, attached, even with wound base;
  • Well-defined, not attached to wound base;
  • Well-defined, not attached to wound base, rolled under, thickened;
  • Well-defined, fibrotic, scarred, or hyperkeratotic.

Appendix B.4. Necrotic Tissue Amount

  • None visible;
  • <25% of wound bed covered;
  • 25% to 50% of wound covered;
  • >50% and <75% of wound covered;
  • 75% to 100% of wound covered.

Appendix B.5. Epithelialization

  • 100% wound covered, surface intact;
  • 75% to <100% wound covered and/or epithelial tissue extends >0.5 cm into wound bed;
  • 50% to <75% wound covered and/or epithelial tissue extends to <0.5 cm into wound bed;
  • 25% to <50% wound covered;
  • <25% wound covered.

References

  1. Centers for Disease Control and Prevention. National Diabetes Statistics Report. 2019. Available online: https://www.cdc.gov/diabetes/data/statistics-report/index.html (accessed on 15 April 2022).
  2. Centers for Disease Control and Prevention. Incidence of Newly Diagnosed Diabetes. 2020. Available online: https://www.cdc.gov/diabetes/data/statistics-report/newly-diagnosed-diabetes.html (accessed on 15 April 2022).
  3. Everett, E.; Mathioudakis, N. Update on Management of Diabetic Foot Ulcers. Ann. N. Y. Acad. Sci. 2018, 1411, 153–165. [Google Scholar] [CrossRef] [PubMed]
  4. Neville, R.F.; Kayssi, A.; Buescher, T.; Stempel, M.S. The Diabetic Foot. Curr. Probl. Surg. 2016, 53, 408–437. [Google Scholar] [CrossRef] [PubMed]
  5. Centers for Disease Control and Prevention. Coexisting Conditions and Complications. 2021. Available online: https://www.cdc.gov/diabetes/data/statistics-report/coexisting-conditions-complications.html (accessed on 18 April 2022).
  6. Frykberg, R.G.; Banks, J. Challenges in the Treatment of Chronic Wounds. Adv. Wound Care 2015, 4, 560–582. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  7. ElHeneidy, H.; Omran, E.; Halwagy, A.; Al-Inany, H.; Al-Ansary, M.; Gad, A. Amniotic Membrane Can Be a Valid Source for Wound Healing. Int. J. Women’s Health 2016, 8, 225–231. [Google Scholar] [CrossRef] [Green Version]
  8. Snyder, R.J.; Shimozaki, K.; Tallis, A.; Kerzner, M.; Reyzelman, A.; Lintzeris, D.; Bell, D.; Rutan, R.L.; Rosenblum, B. 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 Ulcers. Wounds Compend. Clin. Res. Pract. 2016, 28, 70–77. Available online: https://www.hmpgloballearningnetwork.com/site/wounds/article/prospective-randomizedmulticenter-controlled-evaluation-use-dehydrated-amniotic-membrane (accessed on 14 April 2022).
  9. Driver, V.R.; Fabbi, M.; Lavery, L.A.; Gibbons, G. The Costs of Diabetic Foot: The Economic Case for the Limb Salvage Team. J. Vasc. Surg. 2010, 52, 17S–22S. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  10. Rosenblum, B.I. A Retrospective Case Series of a Dehydrated Amniotic Membrane Allograft for Treatment of Unresolved Diabetic Foot Ulcers. J. Am. Podiatr. Med. Assoc. 2016, 106, 328–333. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  11. Caporusso, J.; Abdo, R.; Karr, J.; Smith, M.; Anaim, A. Clinical Experience Using a Dehydrated Amnion/Chorion Membrane Construct for the Management of Wounds. Wounds Compend. Clin. Res. Pract. 2019, 31, S19–S27. Available online: https://www.researchgate.net/publication/332624695_Clinical_experience_using_a_dehydrated_amnionchorion_membrane_construct_for_the_management_of_wounds (accessed on 15 April 2022).
Figure 1. Progression of the diabetic foot ulcer throughout amniotic membrane allograft applications. (A) Date of exam: 1 February 2022; DFU measurements: 5.3 cm × 4.3 cm × 0.1 cm. (B) Date of exam: 22 February 2022; DFU measurements: 4.2 cm × 3.5 cm × 0.1 cm. (C) Date of exam: 15 March 2022; DFU measurements: DFU is now closed.
Figure 1. Progression of the diabetic foot ulcer throughout amniotic membrane allograft applications. (A) Date of exam: 1 February 2022; DFU measurements: 5.3 cm × 4.3 cm × 0.1 cm. (B) Date of exam: 22 February 2022; DFU measurements: 4.2 cm × 3.5 cm × 0.1 cm. (C) Date of exam: 15 March 2022; DFU measurements: DFU is now closed.
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Figure 2. Progression of size, depth, and necrotic tissue amount in DFU over 49 days. Reference Appendix B for the key correlated to each value.
Figure 2. Progression of size, depth, and necrotic tissue amount in DFU over 49 days. Reference Appendix B for the key correlated to each value.
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Figure 3. Progression of edges and epithelization in DFU over 49 days. Reference Appendix B for the key correlated to each value.
Figure 3. Progression of edges and epithelization in DFU over 49 days. Reference Appendix B for the key correlated to each value.
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Table 1. Measurements of the DFU at each time point.
Table 1. Measurements of the DFU at each time point.
Date of Examination DFU Measurements
25 January 2022 5.5 cm × 4.5 cm × 0.3 cm
1 February 2022 5.3 cm × 4.3 cm × 0.1 cm
8 February 2022 5.1 cm × 4.4 cm × 0.1 cm
15 February 2022 5.0 cm × 3.9 cm × 0.1 cm
22 February 2022 4.2cm × 3.5 cm × 0.1 cm
1 March 2022 3.1 cm × 1.8 cm × 0.1 cm
8 March 2022 0.9 cm × 0.8 cm × superficial
15 March 2022 0.0 cm × 0.0 cm × superficial
Table 2. Progression of size, depth, edges, necrotic tissue amount, and epithelization in DFU over 49 days.
Table 2. Progression of size, depth, edges, necrotic tissue amount, and epithelization in DFU over 49 days.
Application #1Application #2Application #3Application #4Application #5Application #6Application #7Final Visit
Size33322211
Depth33333331
Edges22222221
Necrotic Tissue Amount22111111
Epithelization55544441
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MDPI and ACS Style

Becker, C.; Regulski, M.; Martin, S.; Barrett, T. Application of Dehydrated Amniotic Membrane Allografts in Advanced Diabetic Foot Ulceration: Case Report and Review of Literature. Reports 2022, 5, 28. https://doi.org/10.3390/reports5030028

AMA Style

Becker C, Regulski M, Martin S, Barrett T. Application of Dehydrated Amniotic Membrane Allografts in Advanced Diabetic Foot Ulceration: Case Report and Review of Literature. Reports. 2022; 5(3):28. https://doi.org/10.3390/reports5030028

Chicago/Turabian Style

Becker, Catherine, Matthew Regulski, Scott Martin, and Tyler Barrett. 2022. "Application of Dehydrated Amniotic Membrane Allografts in Advanced Diabetic Foot Ulceration: Case Report and Review of Literature" Reports 5, no. 3: 28. https://doi.org/10.3390/reports5030028

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