Maggot therapy (also known as larval therapy) is a type of biotherapy involving the introduction of live, disinfected maggots (fly larvae) into non-healing skin and soft-tissue wounds of a human or other animal for the purpose of cleaning out the necrotic (dead) tissue within a wound (debridement), and disinfection.
Maggot therapy | |
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Maggot debridement therapy on a wound from a diabetic foot | |
Other names | maggot debridement therapy (MDT), larval therapy, larva therapy, larvae therapy, biodebridement, biosurgery |
There is evidence that maggot therapy may help with wound healing.[1][2]
Medical uses
editMaggot therapy improves healing in chronic ulcers.[1] In diabetic foot ulcers there is tentative evidence of benefit.[3] A Cochrane review of methods for the debridement of venous leg ulcers found maggot therapy to be broadly as effective as most other methods, but the study also noted that the quality of data was poor.[4]
In 2003, the United States Food and Drug Administration (FDA) cleared maggots from common green bottle fly for use as a "medical device" in the US for the purpose of treatment of:[5]
- Non-healing necrotic skin and soft tissue wounds
- Pressure ulcers
- Venous stasis ulcers
- Neuropathic foot ulcers
- Non-healing traumatic or post-surgical wounds
Limitations
editThe wound must be of a type that can benefit from the application of maggot therapy. A moist, exudating wound with sufficient oxygen supply is a prerequisite. Not all wound-types are suitable: wounds which are dry, or open wounds of body cavities do not provide a good environment for maggots to feed. In some cases it may be possible to make a dry wound suitable for larval therapy by moistening it with saline soaks.[6]
Patients and doctors may find maggots distasteful, although studies have shown that this does not cause patients to refuse the offer of maggot therapy.[7] Maggots can be enclosed in opaque polymer bags to hide them from sight. Dressings must be designed to prevent any maggots from escaping, while allowing air to get to the maggots.[8] Dressings are also designed to minimize the uncomfortable tickling sensation that the maggots often cause.[9]
Mechanisms of action
editThe maggots have four principal actions:
- Debridement[10]
- Disinfection of the wound[11]
- Stimulation of healing[11]
- Biofilm inhibition and eradication[12]
Debridement
editIn maggot therapy, large numbers of small maggots consume necrotic tissue far more precisely than is possible in a normal surgical operation, and can debride a wound in a day or two. The area of a wound's surface is typically increased with the use of maggots due to the undebrided surface not revealing the actual underlying size of the wound. They derive nutrients through a process known as "extracorporeal digestion" by secreting a broad spectrum of proteolytic enzymes[13] that liquefy necrotic tissue, and absorb the semi-liquid result within a few days. In an optimum wound environment maggots molt twice, increasing in length from about 2 mm to about 10 mm, and in girth, within a period of 48–72 hours by ingesting necrotic tissue, leaving a clean wound free of necrotic tissue when they are removed.[14]
Disinfection
editSecretions from maggots believed to have broad-spectrum antimicrobial activity include allantoin, urea, phenylacetic acid, phenylacetaldehyde, calcium carbonate, proteolytic enzymes, and many others.[15] In vitro studies have shown that maggots inhibit and destroy a wide range of pathogenic bacteria including methicillin-resistant Staphylococcus aureus (MRSA), group A and B streptococci, and Gram-positive aerobic and anaerobic strains.[16] Other bacteria like Pseudomonas aeruginosa, E. coli or Proteus spp. are not attacked by maggots, and in case of Pseudomonas even the maggots are in danger.[17]
Biology of maggots
editThose flies whose larvae feed on dead animals will sometimes lay their eggs on the dead parts (necrotic or gangrenous tissue) of living animals. The infestation by maggots of live animals is called myiasis. Some maggots will feed only on dead tissue, some only on live tissue, and some on live or dead tissue. The flies used most often for the purpose of maggot therapy are blow flies of the Calliphoridae: the blow fly species used most commonly is Lucilia sericata, the common green bottle fly. Another important species, Protophormia terraenovae, is also notable for its feeding secretions, which combat infection by Streptococcus pyogenes and S. pneumoniae.[18]
History
editWritten records have documented that maggots have been used since antiquity as a wound treatment.[19] There are reports of the use of maggots for wound healing by Maya, Native Americans, and Aboriginal tribes in Australia. Maggot treatment was reported in Renaissance times. Military physicians observed that soldiers whose wounds had become colonized with maggots experienced significantly less morbidity and mortality than soldiers whose wounds had not become colonized. These physicians included Napoleon's general surgeon, Baron Dominique Larrey. Larrey reported during the French campaign in Egypt and Syria (1798–1801) that certain species of fly consumed only dead tissue and helped wounds to heal.[18]
Joseph Jones, a ranking Confederate medical officer during the American Civil War, stated:
I have frequently seen neglected wounds ... filled with maggots ... as far as my experience extends, these worms eat only dead tissues, and do not injure specifically the well parts."
The first documented therapeutic use of maggots in the United States is credited to a second Confederate medical officer Dr. J.F. Zacharias, who reported during the American Civil War that:
"Maggots in a single day would clean a wound much better than any agents we had at our command ... I am sure I saved many lives by their use."
He recorded a high survival rate in patients he treated with maggots.[20]
During World War I, orthopedic surgeon William S. Baer recorded the case of a soldier left for several days on the battlefield who had sustained compound fractures of the femur and large flesh wounds. The soldier arrived at the hospital with maggots infesting his wounds but had no fever or other signs of infection and survived his injuries, which would normally have been fatal. After the war, Baer began using maggot therapy at Boston Children's Hospital in Massachusetts.[21][22]: 169–71
There were reports that American prisoners of war of the Japanese in World War II resorted to maggot therapy to treat severe wounds.[23][24]
A survey of US Army doctors published in 2013 found that 10% of them had used maggot therapy.[25]
Regulation
editIn January 2004, the FDA granted permission to produce and market maggots for use in humans or animals as a prescription-only medical device for the following indications: "For debriding non-healing necrotic skin and soft tissue wounds, including pressure ulcers, venous stasis ulcers, neuropathic foot ulcers, and non-healing traumatic or post-surgical wounds."[26][27]
Veterinary use
editThe use of maggots to clean dead tissue from animal wounds is part of folk medicine in many parts of the world.[28] It is particularly helpful with chronic osteomyelitis, chronic ulcers, and other pus-producing infections that are frequently caused by chafing due to work equipment.[citation needed] Maggot therapy for horses in the United States was re-introduced after a study published in 2003 by veterinarian Dr. Scott Morrison. This therapy is used in horses for conditions such as osteomyelitis secondary to laminitis, sub-solar abscesses leading to osteomyelitis, post-surgical treatment of street-nail procedure for puncture wounds infecting the navicular bursa, canker, non-healing ulcers on the frog, and post-surgical site cleaning for keratoma removal.[29]
However, there have not been many case studies done with maggot debridement therapy on animals, and as such it can be difficult to accurately assess how successful it is.[30]
References
edit- ^ a b Sun, Xinjuan; Jiang, Kechun; Chen, Jingan; et al. (2014). "A systematic review of maggot debridement therapy for chronically infected wounds and ulcers". International Journal of Infectious Diseases. 25: 32–7. doi:10.1016/j.ijid.2014.03.1397. PMID 24841930.
- ^ Nasoori, A.; Hoomand, R. (December 2017). "Maggot debridement therapy for an electrical burn injury with instructions for the use of Lucilia sericata larvae". Journal of Wound Care. 26 (12): 734–41. doi:10.12968/jowc.2017.26.12.734. PMID 29244970.
- ^ Tian, X; Liang, XM; Song, GM; et al. (September 2013). "Maggot debridement therapy for the treatment of diabetic foot ulcers: a meta-analysis". Journal of Wound Care. 22 (9): 462–9. doi:10.12968/jowc.2013.22.9.462. PMID 24005780.
- ^ Gethin, Georgina; Cowman, Seamus; Kolbach, Dinanda N. (14 September 2015). "Debridement for venous leg ulcers". Cochrane Database of Systematic Reviews. 2015 (9): CD008599. doi:10.1002/14651858.CD008599.pub2. PMC 6486053. PMID 26368002.
- ^ "Product Classification: Maggots, Medical". fda.gov. US: Food and Drug Administration.
- ^ Gottrup, Finn; Jørgensen, Bo (2011). "Maggot Debridement: An Alternative Method for Debridement". ePlasty. 11 (33). Copenhagen: 290–302. PMC 3136394. PMID 21776326.
- ^ Parnés, A.; Lagan, K. M. (2007). "Larval therapy in wound management: A review" (PDF). International Journal of Clinical Practice. 61 (3): 488–93. doi:10.1111/j.1742-1241.2006.01238.x. PMID 17313618. S2CID 34169406.
- ^ Scavée, V; Polis, X; Schoevaerdts, J. C. (2003). "Maggot therapy: Many hands make light work" (PDF). Acta Chirurgica Belgica. 103 (4): 405–7. doi:10.1080/00015458.2003.11679453. PMID 14524161. S2CID 28650392. Archived from the original (PDF) on 2016-03-10. Retrieved 2015-03-04.
- ^ Morgan, Rosemary (2002). "Larval therapy". Student BMJ. 10: 259–302. doi:10.1136/sbmj.0208271. S2CID 220099046.
- ^ Chan, Dominic CW; Fong, Daniel HF; Leung, June YY; Patil, NG; Leung, Gilberto KK (October 2007). "Maggot debridement therapy in chronic wound care". Hong Kong Medical Journal. 13 (5): 382–6. PMID 17914145.
- ^ a b Sherman, R. A. (2014). "Mechanisms of Maggot-Induced Wound Healing: What Do We Know, and Where Do We Go from Here?". Evidence-Based Complementary and Alternative Medicine. 2014: 1–13. doi:10.1155/2014/592419. PMC 3976885. PMID 24744812.
- ^ Sherman, R. A. (2009). "Maggot Therapy Takes Us Back to the Future of Wound Care: New and Improved Maggot Therapy for the 21st Century". Journal of Diabetes Science and Technology. 3 (2): 336–44. doi:10.1177/193229680900300215. PMC 2771513. PMID 20144365.
- ^ Reames, Mark K.; Christensen, Chris; Luce, Edward A. (1988). "The Use of Maggots in Wound Debridement". Annals of Plastic Surgery. 21 (4): 388–91. doi:10.1097/00000637-198810000-00017. PMID 3232928.
- ^ Jordan, Ashley; Khiyani, Neeraj; Bowers, Steven R.; Lukaszczyk, John J.; Stawicki, Stanislaw P. (2018). "Maggot debridement therapy: A practical review". International Journal of Academic Medicine. 4 (1): 21–34. doi:10.4103/IJAM.IJAM_6_18. S2CID 88155109.
- ^ Heuer, Heike; Heuer, Lutz (2011). "Blowfly Strike and Maggot Therapy: From Parasitology to Medical Treatment". In Mehlhorn, Heinz (ed.). Nature Helps. Parasitology Research Monographs. pp. 301–23. ISBN 978-3-642-19381-1.
- ^ Bowling, Frank L.; Salgami, Eleanna V.; Boulton, Andrew J.M. (February 2007). "Larval Therapy: A Novel Treatment in Eliminating Methicillin-Resistant Staphylococcus aureus From Diabetic Foot Ulcers". Diabetes Care. 30 (2): 370–371. doi:10.2337/dc06-2348. PMID 17259512.
- ^ Andersen, A. S.; Joergensen, B.; Bjarnsholt, T.; Johansen, H.; Karlsmark, T.; Givskov, M.; Krogfelt, K. A. (2009). "Quorum-sensing-regulated virulence factors in Pseudomonas aeruginosa are toxic to Lucilia sericata maggots". Microbiology. 156 (2): 400–7. doi:10.1099/mic.0.032730-0. PMC 2885677. PMID 19892758.
- ^ a b Sherman, R. A.; Hall, M. J. R.; Thomas, S. (2000). "Medicinal Maggots: An Ancient Remedy for Some Contemporary Afflictions". Annual Review of Entomology. 45: 55–81. doi:10.1146/annurev.ento.45.1.55. PMID 10761570.
- ^ Whitaker, I. S.; Twine, C; Whitaker, M. J.; et al. (2007). "Larval therapy from antiquity to the present day: Mechanisms of action, clinical applications and future potential". Postgraduate Medical Journal. 83 (980): 409–13. doi:10.1136/pgmj.2006.055905. PMC 2600045. PMID 17551073.
- ^ Donnelly, J. (1998). "Wound healing--from poultices to maggots. (a short synopsis of wound healing throughout the ages)". The Ulster Medical Journal. 67 (Suppl 1): 47–51. PMC 2448900. PMID 9807955.
- ^ Baer, William S. (1931). "The treatment of chronic osteomyelitis with the maggot (larva of the blow fly)". The Journal of Bone and Joint Surgery. 13 (3): 438–75. Archived from the original on 2016-01-07. Retrieved 2015-03-03.
- ^ Roach, Mary (2016-06-07). Grunt: The Curious Science of Humans at War (1 ed.). W. W. Norton & Company. ISBN 9780393245448.
- ^ Nimmons, Don Stewart (2003). Treasures of War. Xulon Press. p. 105. ISBN 9781591604600.
- ^ Congressional Record. Pt 6. Vol. 152. 8 May 2006. pp. 7, 908.
- ^ Heitkamp, Rae A.; Peck, George W.; Kirkup, Benjamin C. (2013-11-14). "Maggot Debridement Therapy in Modern Army Medicine: Perceptions and Prevalence". Military Medicine. 177 (11): 1, 411–16. doi:10.7205/milmed-d-12-00200. PMID 23198524.
- ^ Carrie Arnold for Scientific American. April 1, 2013 New Science Shows How Maggots Heal Wounds
- ^ FDA CDRH 510(k) summary
- ^ Root-Bernstein, Robert; Root-Bernstein, Michèle M. (1998). Honey, Mud, Maggots, and Other Medical Marvels. Houghton Mifflin. ISBN 978-0-395-92492-1.[unreliable medical source?][page needed]
- ^ Sherman, Ronald A.; Morrison, Scott; Ng, David (2007). "Maggot debridement therapy for serious horse wounds – A survey of practitioners". The Veterinary Journal. 174 (1): 86–91. doi:10.1016/j.tvjl.2006.05.012. PMID 16831562.
- ^ Jones, Gemma; Wall, Richard (2008). "Maggot-therapy in veterinary medicine". Research in Veterinary Science. 85 (2): 394–8. doi:10.1016/j.rvsc.2007.12.006. PMID 18237754.
Further reading
edit- Sherman, R. A. (2003). "Maggot Therapy for Treating Diabetic Foot Ulcers Unresponsive to Conventional Therapy". Diabetes Care. 26 (2): 446–51. doi:10.2337/diacare.26.2.446. PMID 12547878.
- Van Der Plas, M. J. A.; Jukema, G. N.; Wai, S.-W.; Dogterom-Ballering, H. C. M.; Lagendijk, E. L.; Van Gulpen, C.; Van Dissel, J. T.; Bloemberg, G. V.; Nibbering, P. H. (2007). "Maggot excretions/secretions are differentially effective against biofilms of Staphylococcus aureus and Pseudomonas aeruginosa". Journal of Antimicrobial Chemotherapy. 61 (1): 117–22. doi:10.1093/jac/dkm407. PMID 17965032.
- Cazander, G.; Van Veen, K.E.B.; Bernards, A.T.; Jukema, G.N. (2009). "Do maggots have an influence on bacterial growth? A study on the susceptibility of strains of six different bacterial species to maggots of Lucilia sericata and their excretions/secretions". Journal of Tissue Viability. 18 (3): 80–7. doi:10.1016/j.jtv.2009.02.005. PMID 19362001.
- Cazander, Gwendolyn; Schreurs, Marco W. J.; Renwarin, Lennaert; Dorresteijn, Corry; Hamann, Dörte; Jukema, Gerrolt. N. (2012). "Maggot excretions affect the human complement system". Wound Repair and Regeneration. 20 (6): 879–86. doi:10.1111/j.1524-475X.2012.00850.x. PMID 23110586. S2CID 24568980.
- Mumcuoglu, Kosta Y.; Ingber, Arieh; Gilead, Leon; Stessman, Jochanan; Friedmann, Reuven; Schulman, Haim; Bichucher, Hellen; Ioffe-Uspensky, I; Miller, J; Galun, R; Raz, I (1999). "Maggot therapy for the treatment of intractable wounds". International Journal of Dermatology. 38 (8): 623–7. doi:10.1046/j.1365-4362.1999.00770.x. PMID 10487456. S2CID 45118935.
- Bowler, P. G.; Duerden, B. I.; Armstrong, D. G. (2001). "Wound Microbiology and Associated Approaches to Wound Management". Clinical Microbiology Reviews. 14 (2): 244–69. doi:10.1128/CMR.14.2.244-269.2001. PMC 88973. PMID 11292638.
- Sherman, R. A.; Hall, M. J. R.; Thomas, S. (2000). "Medicinal Maggots: An Ancient Remedy for Some Contemporary Afflictions". Annual Review of Entomology. 45: 55–81. doi:10.1146/annurev.ento.45.1.55. PMID 10761570.
- Nigam, Yamni; Bexfield, Alyson; Thomas, Stephen; Ratcliffe, Norman Arthur (2006). "Maggot Therapy: The Science and Implication for CAM Part I—History and Bacterial Resistance". Evidence-Based Complementary and Alternative Medicine. 3 (2): 223–7. doi:10.1093/ecam/nel021. PMC 1475942. PMID 16786052.