Larva C.A. Vincent M.D.INTERNISTAManuel Galecio 1208 y Av. del Ejército (Centro Guayaquil)Bálsamos #629 ...
Advance Access Publication 5 May 2006                                                                                     ...
224          Maggot therapy: Part Iis also described and details of the nature of the potent            Maggot Therapy: Se...
eCAM 2006;3(2)             225upon emergence from the egg and undergo rigorous testing to            deep crevices that ma...
226            Maggot therapy: Part IFigure 1. Wound before maggot debridement therapy. This wound, covered           Figu...
eCAM 2006;3(2)                    227 9. Wollina U, Liebold K, Schmidt W-D, Hartmann M, Fassler D. Biosurgery       31. Sh...
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  1. 1. Larva C.A. Vincent M.D.INTERNISTAManuel Galecio 1208 y Av. del Ejército (Centro Guayaquil)Bálsamos #629 e/ Ficus y Las Monjas (Urdesa)Telf.: 2280008 / 2320936 Cel.: 0981137366 / 097226405Guayas - Ecuador
  2. 2. Advance Access Publication 5 May 2006 eCAM 2006;3(2)223–227 doi:10.1093/ecam/nel021ReviewMaggot Therapy: The Science and Implication for CAMPart I—History and Bacterial ResistanceYamni Nigam1, Alyson Bexfield1,2, Stephen Thomas3 and Norman Arthur Ratcliffe21 School of Health Science, University of Wales Swansea, Singleton Park, Swansea SA2 8PP, UK,2 Department of Biological Sciences, University of Wales Swansea, Singleton Park, Swansea SA2 8PP, UK and3 Biosurgical Research Unit (SMTL), Princess of Wales Hospital, Coity Road, Bridgend CF31 1RQ, UK It is now a universally acknowledged fact that maggot therapy can be used successfully to treat chronic, long-standing, infected wounds, which have previously failed to respond to conventional treatment. Such wounds are typically characterized by the presence of necrotic tissue, underlying infection and poor healing. Maggot therapy employs the use of freshly emerged, sterile larvae of the common green- bottle fly, Phaenicia (Lucilia) sericata, and is a form of artificially induced myiasis in a controlled clin- ical situation. In this review article, we will discuss the role of maggots and their preparation for clinical use. Maggot therapy has the following three core beneficial effects on a wound: debridement, disinfec- tion and enhanced healing. In part I we explore our current understanding of the mechanisms underlying these effects. Keywords: Maggot debridement therapy – MRSA – antimicrobial – Lucilia sericata – woundsIntroduction I—The Rise and Fall of made by many surgeons who followed, but it was WilliamMaggot Therapy Baer, Professor of Orthopaedic Surgery at the John Hopkins School of Medicine in Maryland, USA, who is believed to beNumerous clinical reports have been published that describe the founder of modern maggot therapy (14).the outstanding effects of maggot therapy, most notably on It was Baer who pioneered the use of sterile maggots as adebridement, cleansing, disinfection and healing of indolent reputable method of wound therapy, following observationswounds, many of which have previously failed to respond to he made about the value of maggots in traumatic wounds onconventional treatment (1–11). Current day maggot therapy, the battlefield in France during World War 1. Such was thewith its multi-action approach to wound cleansing and healing, success of Baer’s work that by the mid-1930s almost 1000is highly successful. North American surgeons employed maggot therapy (15) and Records of maggots in wounds, however, and the recogni- by the end of the decade it was in use in over 300 hospitalstion of improvement in the wound state as a consequence of in the US and Canada. However, by 1940, a new era was dawn-infestation, date back to the 16th century (12). In 1829, Baron ing. This era which saw the introduction and widespread use ofDominic Larrey, Napoleon’s battlefield surgeon, described antibiotics following the mass production of penicillin (16). Sohow men had arrived at his field hospital with healing despite the obvious success of maggot therapy, by themaggot-infested wounds (13). The wounds were sustained in mid-1940s it had practically disappeared from use. In Part 1battle, but, owing to the presence of maggots, were not infected of this review, we introduce the stages involved in the woundand showed accelerated healing. Such positive accounts were healing process, the advantages in the use of maggots for the cleaning (debridement) of infected wounds, and the possible mechanisms underlying the debridement of wounds by mag-For reprints and all correspondence: Yamni Nigam, University of WalesSwansea, Singleton Park, Swansea SA2 8PP, UK. E-mail: gots. The antimicrobial activity of maggots to treat resistant Staphylococcus aureus (MRSA)-infected woundsÓ The Author (2006). Published by Oxford University Press. All rights reserved.The online version of this article has been published under an open access model. Users are entitled to use, reproduce, disseminate, or display the open accessversion of this article for non-commercial purposes provided that: the original authorship is properly and fully attributed; the Journal and Oxford UniversityPress are attributed as the original place of publication with the correct citation details given; if an article is subsequently reproduced or disseminated not in itsentirety but only in part or as a derivative work this must be clearly indicated. For commercial re-use, please contact
  3. 3. 224 Maggot therapy: Part Iis also described and details of the nature of the potent Maggot Therapy: Selection of the Fliesantibacterial activity of maggot secretions are then consideredin Part II of this review. Many dipteran species are capable of infesting living verte- brate hosts (a condition termed myiasis). Maggot therapy isReview of Wounds and Events during Healing essentially artificially induced myiasis, performed in a con- trolled environment by experienced medical practitioners.A wound is a breach in the skin, which may allow the entry of Myiasis-causing flies may be grouped into two categories asmicroorganisms, possibly leading to infection. Wound tissue follows: obligate and facultative parasites. Obligate parasitesprovides the rich environment necessary for the proliferation require the ingestion of living tissue in order to complete theirof microbes. It is characterized by hypoxia, necrosis and often lifecycles (22). Larvae of obligate parasites can cause severean accompanying impaired immune response owing to subop- damage to healthy tissue and are therefore unsuitable for usetimal delivery of immune effector molecules through damaged in maggot therapy. Facultative parasites are able to parasitizeblood vessels (17). This compromised, necrotic, sloughy tissue living hosts if conditions are favorable, but more commonlyprovides a warm, moist and nutritive environment, perfect for develop on carrion and therefore have greater potential forreplication of colonizing bacteria. Bacterial species which therapeutic use.were previously harmless commensals of the human body, Selection of a suitable fly species for use in maggot therapymost commonly on the skin, may become pathogenic in a is of paramount importance, determining both the safety andwound environment (18). In order for a wound to heal, it success of the treatment. It is imperative to select a speciesmust progress through the following four main stages of the that feeds almost exclusively on necrotic tissue. Williamhealing process (19): (i) the inflammatory phase where hemo- Baer chose the larvae of Phaenicia sericata, the commonstasis occurs and numerous inflammatory mediators are green-bottle, as the most appropriate species for this applica-released. Leukocytes migrate into the wound, and the bacterial tion and this is the species still used by practitioners today.burden of the wound is decreased. (ii) The destructive phase Phaenicia larvae are facultative parasites, unable to ingest orwhich sees the phagocytosis of necrotic tissue and killing of significantly damage healthy human tissue (2). Infestationsingested microbes and foreign particles. Numerous growth fac- of living hosts by Phaenicia do, however, occur, most com-tors are released during this phase. (iii) The proliferative phase monly in sheep to induce an often fatal condition known asinvolves the formation of new capillary loops and granulation sheep strike. Exactly why Phaenicia attack the healthy tissuetissue (angiogenesis), fibroplasia and the synthesis of new of sheep and appear unable to do the same to human tissue ismatrix and collagen. (iv) The maturation phase occurs when as yet unknown.wound collagen is remodeled and reorganized. The woundcontracts and epithelialization occurs. These events often hap-pens during wound healing using adaptogens (20) (natural herb Female Flies, Eggs, Larvae andproducts that increase the body’s resistance to physical, chem- Preparation for Clinical Useical or biological stresses). There is considerable overlap In the wild, adult female Phaenicia lay a large number of eggsbetween the various stages, and the entire healing process (2000–3000) over the course of a few weeks, a necessity ascan take months to complete, with full maturation often not relatively few will survive to adults. The eggs are laid inachieved until a year after the wound was initiated. clusters directly onto the chosen food source, upon which the emerging larvae will feed. Larval development requires aTypes of Wounds moist environment to prevent desiccation, so larvae are gener-Wounds can be broadly divided into two types, acute and ally found in nutritious, damp places such as decaying animalchronic, which exhibit significant differences in the healing corpses or moist, necrotic wounds (22). Eggs hatch withinprocess. An acute wound is one which is usually instigated 18–24 h, depending on optimal conditions, into first instarby a sudden, solitary insult, such as a traumatic injury. Such larvae (maggots), 1–2 mm in length, which immediatelywounds generally proceed through the healing process in an and actively begin to feed. It is this vigorous feeding activity,orderly manner. In contrast, a chronic wound, such as a leg which is beneficial to an infected or necrotic wound. Maggotsulcer, is usually owing to an underlying pathological process, feed by the extracorporeal secretion of a wide spectrum ofsuch as diabetes or vascular insufficiency, which produces a proteolytic enzymes that liquefy the host tissue (23–26). Thisrepeated and prolonged insult to the tissue, resulting in severe semi-digested liquid material is then ingested as a sourcedamage. The chronic wound does not normally progress of nutrients. The maturing first instar larvae continue to feedthrough the healing process, often remaining in the inflammat- for 4–5 days, molting twice as they increase in size toory, infected phase and causing much discomfort and distress 8–10 mm, at which point they stop feeding and leave theto the patient. Although maggots can be used for any kind of wound or corpse to search for a dry place in the ground wherepurulent, sloughy wound on the skin, independent of the they pupate (25). Following metamorphosis, an adult flyunderlying disease or the location on the body (21), it is in emerges from the pupa. In preparation for clinical use, fliesthe cleansing and healing of such chronic wounds that maggot typically oviposit onto porcine liver, and the eggs are separatedtherapy becomes an invaluable tool. and chemically sterilized. Resultant (L1) larvae are sterile
  4. 4. eCAM 2006;3(2) 225upon emergence from the egg and undergo rigorous testing to deep crevices that may be beyond the reach of a surgeon’sensure their microbiological status (3). Larvae are then main- scalpel. Reports have been published marveling at the benefitstained under aseptic conditions prior to wound application. of maggot debridement therapy (MDT) in all sorts of wounds, including abscesses, burns, gangrenous wounds, arterial and venous ulcers, osteomyelitis, diabetic foot ulcers and pressureDebridement (Wound Clearing) sores (7,9,31–33). One such study compared MDT with con-Maggot therapy has the following three core beneficial effects servative debridement therapy for the treatment of pressureon a wound: debridement, disinfection and enhanced healing. sores (34). Here, 80% of maggot-treated wounds (n ¼ 43)Debridement is the removal of cellular debris and non-viable were completely debrided, while only 48% of conventionallynecrotic tissue from the wound bed. This is a first, essential treated wounds (n ¼ 49) were completely debrided. Also, bystep before healing can commence. Removal of necrotic tissue using maggots, total wound surface area decreased, whereasabolishes many of the associated bacteria and also reduces during conventional debridement therapy, the total woundwound odor. The removal of necrotic tissue, which acts as a area had increased (p ¼ 0.001) (34). The report concludedmicrobial substrate, may also reduce the risk of infection. Dur- that maggot therapy was a more effective and efficient waying the inflammatory stage of wound healing host leucocytes of debriding chronic pressure sores than the conventionalplay an important role in debridement of wound sites, degrad- treatments damaged extracellular matrix (ECM) components throughthe release of proteases. The injury is initially filled with a pro- Mechanisms of MDTvisional wound matrix consisting predominantly of fibrin andfibronectin. Key proteases are involved in ECM degradation How exactly maggots remove devitalized, necrotic tissue from(see below). These are released from neutrophils, macro- the wound is currently actively being investigated. Researchphages, fibroblasts, epithelial and endothelial cells. As healing into the debridement mechanisms underlying maggot therapyproceeds, and new ECM constituents such as collagen, elastin has revealed that maggots secrete a rich soup of digestiveand proteoglycans are synthesized, damaged ECM is removed enzymes while feeding, including carboxypeptidases A and Bby these proteases (27). (35), leucine aminopeptidase (35), collagenase (23,36) and serine proteases (trypsin-like and chymotrypsin-like enzymes) (35,37). Recently, workers in Nottingham, UK, demonstratedChronic Wounds in vitro a range of enzymes secreted by P. sericata larvaeChronic wounds do not proceed through the normal healing (26). Four proteolytic enzymes, comprising two serine pro-process and are typically characterized by prolonged inflam- teases, a metalloproteinase and an aspartyl proteinase, weremation, inhibition of cell proliferation (28,29), incomplete detected, with molecular weights ranging from 20 to 40 kDa,ECM remodeling and a failure to epithelialize (30). Over with activity across a wide pH range. A chymotrypsin-likeexpression and inefficient debridement of temporary ECM serine proteinase exhibited excellent degradation of ECMcomponents, e.g. fibronectin and fibrin, contribute to the fail- components laminin, fibronectin, and collagen types I and IIIure of chronic wounds to heal. The entire environment of a (26), and may therefore play a significant role in the digestionchronic wound must be rebalanced for wound repair to proceed of wound matrix and effective completion, an undertaking which is unlikely to occur The mechanical action of numerous wriggling maggots in awithout extraneous intervention and one of the explanations necrotic debris-filled wound has also been suggested in aidingas to why chronic wounds may persist for many years. wound debridement. Maggots possess a pair of mandibles There are a number of existing methods for the debridement (hooks) which assist with locomotion and attachment to tissue.of chronic wounds as described by Schultz et al. (27). These This probing and maceration of wound tissue with maggotinclude surgical and sharp debridement (using scalpel or mouthhooks may enhance debridement (38), but these hooksscissors to remove debris and necrotic tissue), mechanical are used during feeding to disrupt membranes and thus facilit-debridement using methods such as wet-to-dry dressings, ate the penetration of proteolytic enzymes (3). Together, thiswound irrigation and whirlpool techniques, enzymatic debri- mechanical action and the secretion of powerful, proteolyticdement using the application of exogenous enzymes, and enzymes may be the secret of efficient tissue debridement.autolytic debridement using hydrogels and hydrocolloids.Each of these techniques has associated disadvantages such Disinfection (Introduction toas extended treatment times, pain and mechanical damage to Antibiotic Activity)underlying healthy tissue. For wounds to heal, and progress through stages of destruc- tion and proliferation onto maturation, infection needs to beMaggot Debridement Therapy eliminated. The majority of wounds are polymicrobial, hostingThe alternative is maggot therapy. Maggots debride wounds a range of both anaerobic and aerobic bacteria (18,39).quickly and effectively, without damage to viable tissue. Antimicrobial treatment of clinically infected and non-healingMaggots are photophobic and will naturally move into the wounds, should, therefore, encompass broad-spectrum anti-
  5. 5. 226 Maggot therapy: Part IFigure 1. Wound before maggot debridement therapy. This wound, covered Figure 2. Wound following three applications of maggots. The wound is com-with a thick layer of slough, failed to respond to conventional treatment over pletely free of slough and rich with granulation tissue.18 months.microbials in order to cleanse the wound effectively. The kill clinical isolates of MRSA (51,52). As an example, Fig. 1application of maggots to an infected wound results in shows a wound 5 cm in diameter and totally covered with athe rapid elimination of such infecting microorganisms thick layer of viscous slough. One pot of larvae was applied(2,6,40,41). The most frequently isolated pathogen from acute and left for 48 h, after which there was an immediate andand chronic wounds is Staphylococcus aureus. S. aureus is marked improvement to the wound. Two further applicationscarried innocuously by 30% of the general population (42) of larvae were made. At this point, only 6 days after maggot[40–70% of hospital staff (43,44)], usually on the moist skin therapy had commenced, the wound, which had not respondedin the nose, axillae (armpits) and perineum (groin), but can to conventional treatment over 18 months, was now com-become pathogenic when able to enter damaged skin. S. aureus pletely free from slough. It was filling rapidly with healthyhas caused great concern owing to its ability to acquire granulation tissue and a swab failed to detect any presenceresistance to a range of antimicrobials. of MRSA (Fig. 2). Larval therapy was now discontinued and the wound continued to progress normally and healed uneventfully (6).Penicillin Methicillin Resistance and MRSAIn 1948, 4 years after the widespread introduction of penicillin, Acknowledgmentsover 50% of nosocomial S. aureus were penicillin-resistant(45) owing to the production of penicillinase (b-lactamase), We wish to thank Bro Morgannwg and Action Medicalan enzyme which inactivates b-lactam antibiotics (46). Research (grant number AP1010) for financial support. TheCurrently, the majority (80–90%) of S. aureus are penicillin- work was partly funded by the Bro Morgannwg NHS Trust.resistant. In 1960, a structural modification of penicillin sawthe synthetic production of methicillin, which was activeagainst penicillin-resistant strains of S. aureus. The launch Referencesof methicillin, however, failed to control the proliferation of 1. Baer WS. The treatment of chronic osteomyelitis with the maggot (larva of the blow fly). J Bone Joint Surg 1931;13:438–75.resistant strains of bacteria and the first clinical isolate of 2. Weil GC, Simon RJ, Sweadner WR. A biological bacteriological andMRSA was reported in 1961 (47). Since then, MRSA has con- clinical study of larval or maggot therapy in the treatment of acute andtinued to disseminate rapidly, causing serious hospital and chronic pyogenic infections. Am J Surg 1933;19:36–48. 3. Thomas S, Jones M, Shutler S, Jones S. Using larvae in modern woundcommunity infections all over the world, with global increases management. J Wound Care 1996;5:60– both the numbers of infected patients and mortality. The 4. Johnson S. Larval therapy in the treatment of wounds: case history.recent isolation of vancomycin-resistant strains of S. aureus Br J Community Nurs 1999;4:293–5. 5. Mumcuoglu KY, Ingber A, Gilead L, Stessman J, Friedman R,(VRSA) in Japan (48) severely reduces the repetoire of drugs Schulman H, et al. Maggot therapy for the treatment of intractableavailable to treat infections caused by resistant strains of wounds. Int J Dermatol 1999;38:623–7.S. aureus. 6. Thomas S, Jones M. Maggots can benefit patients with MRSA. Pract Nurse 2000;20:101–4. In the literature, there is an ever increasing trend supporting 7. Graninger M, Grassberger M, Galehr E, Huemer F, Gruschina E, Minar E,the clinical use of maggots for treating wounds infected with et al. Biosurgical debridement facilitates healing of chronic skin ulcers.MRSA (6,40,49,50). This support, initially anecdotal, was Arch Int Med 2002;162:1906–7. 8. Jukema GN, Menon AG, Bernards AT, Steenvoorde P, Taheri Rastegar A,strengthened by case studies and most recently, strong laborat- Van Dissel JT. Amputation-sparing treatment by nature: ‘‘surgical’’ory evidence indicates that maggots do possess the ability to maggots revisited. Clin Infect Dis 2002;35:1566–71.
  6. 6. eCAM 2006;3(2) 227 9. Wollina U, Liebold K, Schmidt W-D, Hartmann M, Fassler D. Biosurgery 31. Sherman RA, Tran JM-T, Sullivan R. Maggot therapy for venous stasis supports granulation and debridement in chronic wounds—clinical ulcers. Arch Dermatol 1996;132:254–6. data and remittance spectroscopy measurement. Int J Dermatol 2002;41: 32. Mumcuoglu KY, Lipo M, Ioffe-Uspensky I, Miller J, Galun R. Maggot 635–9. therapy for gangrene and osteomyelitis. Harefuah 1997;132:323–5.10. Sherman RA. Maggot therapy for treating diabetic foot ulcers 33. Namias N, Varela JE, Varas RP, Quintana O, Ward CG. Biodebridement: unresponsive to conventional therapy. Diabetes Care 2003;26:446–51. a case report of maggot therapy for limb salvage after forth degree burns.11. Sherman RA, Shimoda KJ. Presurgical maggot debridement of soft J Burn Care Rehabil 2000;21:254–7. tissue wounds is associated with decreased rates of postoperative 34. Sherman RA. 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Detection and partial chronic wound fluid. Wound Repair Regen 1993;1:181–6. characterisation of two antibacterial factors from the excretions/secretions29. Agren MS, Steenfos HH, Dabelsteen S, Hansen JB, Dabelsteen E. Prolif- of the medicinal maggot Lucilia sericata and their activity against eration and mitogenic response to PDGF-BB of fibroblasts isolated from methicillin-resistant Staphylococcus aureus (MRSA). Microbes Infect chronic leg ulcers is ulcer-dependent. J Invest Dermatol 1999;112:463–9. 2004;6:1297–304.30. Tarnuzzer RW, Shultz GS. Biochemical analysis of acute and chronic wound environments. Wound Repair Regen 1996;4:321–5. Received September 13, 2005; accepted March 23, 2006