The beneficial effects of maggots have been known for. The antimicrobial activity of maggots: in-vivo results RESEARCH PAPER

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97_101_JTV_Maggots 24/6/04 12:13pm Page 1 The antimicrobial activity of maggots: in-vivo results P Steenvoorde 1, GN Jukema 2 1 Section of Traumatology, Department of Surgery, Leiden University Medical Center, The Netherlands 2 Head, Section of Traumatology, Department of Surgery, Leiden University Medical Center, The Netherlands In the literature maggot therapy is discussed as a promising and potent form of debridement therapy. The number of maggots needed to debride a wound is estimated at 10 per cm 2, and more in case of a higher percentage of necrosis or slough. In the authors hospital, from March 1999 to May 2002, 16 patients were successfully treated with maggot therapy. The average maggot treatment time was 27 days, with an average of seven maggot changes. Most patients were treated for osteomyelitis, with trauma being the leading aetiological factor. In accordance with in-vitro findings, maggot therapy was found to be more effective in Gram-positive infected wounds. Gram-negative bacteria are cultured more often after maggot treatment than before it (p=0.001). The opposite effect was found for Gram-positive infected wounds (non-significant p=0.07). In vivo maggots seem to be less effective against Gram-negative infected wounds. The authors believe that a higher number of maggots is needed not only for a larger wound or a wound with a higher percentage covered with slough, but also for a wound infected with Gram-negative bacteria. Key words: maggot, wound, clinical, in vivo, bacteria The beneficial effects of maggots have been known for hundreds of years 1, however, maggots were only introduced to clinical practice in the late 1920s 2. Maggots were used extensively in hospitals during the 1930s and 1940s, especially in the United States. Problems with non-sterility of maggots, with consequent tetanus and infection, together with the introduction of penicillin in the 1940s and better aseptic wound dressings, almost completely removed maggots from the therapeutic arsenal 3,4. It was in the 1980s with the appearance of antibiotic-resistant bacteria, like methicillin-resistant Staphylococcus aureus (MRSA), that maggots made a comeback in the hospital setting 5 7. Clinical observations indicate that maggot therapy accelerates cleansing, Tissue Viability Society combats infection, hastens the removal of necrotic tissue without damaging the healthy tissue beneath and can prevent (further) amputation 8. Secretions of larvae of the common greenbottle (Lucilia sericata) have, in vitro, been shown to be most effective against Gram-positive bacteria, like streptococcus A and B and Staph. aureus. Gramnegative bacteria, especially Escherichia coli and Proteus spp., and to a lesser extent Pseudomonas spp., are more resistant to maggot secretions 9,10. This article reports the in-vivo results of the use of maggots (Lucilia sericata) to treat Gram-positive and Gramnegative infected wounds. Material and methods The protocol for maggot treatment in the authors hospital requires a wound swab of every treated wound on every maggot change. A swab is sent for culture (using Stuart medium) for aerobic and anaerobic organisms. Because all maggots in the hospital are sterile before application to the wound, new emerging bacteria in the wounds do not result from the application of the maggots. Antibiotic therapy is given when there are signs of systemic infection, which is always directed at the cultured micro-organism. Wound cultures are always taken as a superficial wound swab and never as a deep tissue biopsy culture. Although microbiological assessment of chronic diabetic patients is probably more sensitive 11, the (sometimes small) size of the wounds and the need to sedate non-diabetic patients for deep tissue cultures stopped the authors from using deep tissue biopsies. An analysis of all wound cultures taken 1 month before, during the whole maggot treatment period, and 1 month after treatment with maggots was undertaken. A wound culture can either be sterile, show growth of a Gram-positive or a Gram-negative bacteria, or both. If, for example, before maggot treatment three wound cultures were taken and two of these showed a Grampositive bacteria, the chance of culturing a Gram-positive bacteria is 0.66 (see Table 1, patient 1). These wound cultures were then analysed for Gram-positive (Table 1) and Gram-negative bacteria (Table 2) for 16 consecutive patients treated with maggots in the hospital from March 1999 until May 2002. JOURNAL OF TISSUE VIABILITY VOL 14 NO. 3 JULY 2004 97

97_101_JTV_Maggots 24/6/04 12:13pm Page 2 The data were analysed using Spearman s rho, which is a measure of association between two variables measured on at least an ordinal scale. An association of p=0.05 was considered a significant effect. Results Maggot therapy was first used in the Netherlands in the authors hospital in 1999. Between then and May 2002, 16 patients have been successfully treated with maggots (Table 3). All wounds eventually responded to the therapy and healed within 6 months of commencing TABLE 1. The chance of culturing a Gram-positive bacteria Before maggots Maggot After maggots Patient no. (1 month) therapy (1 month) 1 0.66 (3) 0.62 (13) 0.38 (13) 2 0.8 (5) 1 (2) 1 (1) 3 1 (3) 1 (4) 4 0.5 (2) 0.3 (23) 0 (7) 5 0.75 (8) 0 (8) 0.66 (3) 6 0 (1) 0 (3) 7 0 (1) 0.2 (10) 0.2 (5) 8 2 (1) 0.5 (4) 0 (1) 9 1 (2) 0.33 (15) 0 (1) 10 0.6 (5) 0.1 (29) 2 (1) 11 0 (4) 0 (9) 12 0 (2) 0.17 (6) 1.25 (4) 13 0.55 (11) 0.33 (9) 14 0.8 (5) 0.1 (10) 0 (5) 15 1 (2) 1.5 (2) 16 0 (4) 0 (13) 0 (2) Median 0.66 0.20 0.20 Average 0.54 0.36* 0.41 *Non-significant Spearman s rho (p=0.07); figure in brackets is the number of wound cultures; = missing value. Sometimes in one wound culture more than one bacterial species can be found. The average number of cultured bacterial species can therefore be higher than one maggot therapy. Three patients died, one as a result of an accident, and two as a result of underlying disease (progression of cancer and a haematological disorder). There were two methods for applying maggots to the wound. Initially, with the first three patients, maggots were put freely on the wound covered by a net, but after 3 4 days, when maggots grow up to 8 10 mm, the treatment can become painful. Therefore the last 13 patients of this group were treated with the biobag technique. The larvae are incorporated in a small polyvinylalcohol (PVA) biobag (Polymedics Bioproducts, TABLE 2. The chance of culturing a Gram-negative bacteria Before maggots Maggot After maggots Patient no. (1 month) therapy (1 month) 1 1 (3) 1.38 (13) 1.53 (13) 2 0.2 (5) 0.5 (2) 0 (1) 3 0 (3) 0 (4) 4 0 (2) 0 (23) 0.14 (7) 5 0.38 (8) 1.25 (8) 0.33 (3) 6 0 (1) 0 (3) 7 1 (1) 0.9 (10) 1 (5) 8 0 (1) 0 (4) 0 (1) 9 0 (2) 0.6 (15) 2 (1) 10 0.8 (5) 1.38 (29) 1 (1) 11 0 (4) 0.77 (9) 12 0 (2) 0 (6) 0 (4) 13 0 (11) 0.11 (9) 14 1 (5) 0.9 (10) 0.4 (5) 15 0 (2) 0 (2) 16 0.25 (4) 0.38 (13) 0 (2) Median 0.25 0.60 0.33 Average 0.29 0.51* 0.4 *Significant Spearman s rho (p=0.001); figure in brackets is the number of wound cultures; = missing value. Sometimes in one wound culture more than one bacterial species can be found. The average number of cultured bacterial species can therefore be higher than one 98 JOURNAL OF TISSUE VIABILITY VOL 14 NO. 3 JULY 2004

97_101_JTV_Maggots 24/6/04 12:13pm Page 3 Peer, Belgium). Incorporated in this bag they still act as necrophages, but this is less painful. Average treatment time with maggots was 27 days (range 12 83 days), with an average of seven dressings applied (range 3 21 dressings). In total almost 15 000 maggots were used (average per patient 925 maggots, range 100 2900). Most patients were treated for osteomyelitis (Table 3). Trauma was the cause in 50% of the cases, TABLE 3. Characteristics of patients treated with sterile maggots Period of Total number Number of Age Underlying maggot Dressing of maggots maggot No. Sex (yrs) Diagnosis Region condition(s) therapy (days) used* applied changes 1 M 50 Osteomyelitis Lower leg Vascular insufficiency 32 Biobag 800 9 2 M 60 Osteomyelitis Knee joint Vascular/DM 12 Net 1000 4 3 M 41 Osteomyelitis Both feet Trauma 28 Net 2900 7 4 M 81 Osteomyelitis Femur Trauma/steroid/DM/ 28 Biobag 550 8 vascular insufficiency 5 F 62 Osteomyelitis Lower leg Trauma/vascular 20 Biobag 360 6 6 M 70 Osteomyelitis Lower leg Trauma/DM 25 Biobag 260 6 7 M 33 Osteomyelitis Lower leg Trauma 37 Biobag 500 10 8 M 59 Osteomyelitis Elbow Trauma 24 Biobag 240 6 9 M 38 Osteomyelitis Heel DM 83 Biobag 780 21 10 M 50 Fasciitis Neck and RA/trauma 13 Biobag 560 4 necroticans head 11 M 46 Fasciitis Abdomen Scrotal abscess 19 Biobag 1200 5 necroticans and perineal region 12 F 88 Soft tissue Upper leg Trauma 27 Biobag 450 8 infection 13 M 51 Soft tissue Upper leg Trauma/vascular 13 Biobag 100 4 infection insufficiency 14 M 54 Gangrene Stump Vascular 11 Net 2000 3 lower limb insufficiency/dm 15 M 16 Gangrene Both hands Meningococcal 27 Biobag 2100 8 and feet sepsis 16 M 61 Ulcus cruris Lower leg Venous insufficiency/ 34 Biobag 1000 10 DM/RA/steroid treatment Average 54 27 925 7 DM = diabetes mellitus; F = female; M = male; RA = rheumatoid arthritis; * net = a loose nylon mesh wound dressing over free maggots; biobags = porous, polyvinylalcohol bags containing maggots JOURNAL OF TISSUE VIABILITY VOL 14 NO. 3 JULY 2004 99

97_101_JTV_Maggots 24/6/04 12:13pm Page 4 followed by diabetes mellitus (38%), arterial vascular insufficiency (38%), rheumatoid arthritis (13%), steroid use (13%), fasciitis necroticans (13%), venous insufficiency (6%) and meningococcal sepsis (6%). In Table 1 the result for Gram-positive cultures are presented. Gram-positive bacteria are cultured less often after maggot treatment than before. Using Spearman s rho this is a non-significant effect (p=0.07). Gramnegative bacteria (Table 2), on the other hand, are cultured more often after maggot treatment than before (p=0.001). Discussion It is still not clear how maggot therapy works. It is probably more complicated than the mere washing out of bacteria by the serous exudate or than the simple crawling of the larvae in the wound. Maggots move over the surface of the wound, secreting proteolytic enzymes that break down dead tissue, turning it into a soup, which they then ingest 12. Maggots are capable of destroying bacteria in their alimentary tract. They also produce substances with healing properties, such as allantoin and urea. There is also a change in the wound ph, from acidic to alkaline, as a result of the ammonia and calcium carbonate excreted by the maggots 13. In the 1930s Robinson and Norwood were able to show that Gram-positive bacteria (β-haemolytic Streptococcus and Staph. aureus) are ingested and killed completely as they pass through the gut of the larvae 14,15. More recently the direct killing of Gram-negative bacteria (E. coli) by maggots was studied. Most of the bacteria were killed, but 17.8% of the hindgut still harboured live bacteria 16.In vitro, maggot secretions were found to adequately kill Gram-positive bacteria but Gram-negative bacteria were killed less effectively 10. Gram-negative bacteria appeared to grow faster in the presence of maggots, possibly as a result of an increase in the ph of the wound. This retrospective study showed that the chance of culturing a Gram-positive bacteria is higher before than after treatment with maggot therapy (p=0.07), and found the opposite effect for Gram-negative cultures (p=0.001). Looking at a subgroup of these 16 patients, namely the four patients in which the chance of culturing a Gram-negative bacteria after treatment with maggots increases (patient 1, 4, 9 and 12), shows an interesting effect. The only difference between this subgroup and the other 12 patients is that fewer maggots were applied (645 in the subgroup vs 1020 in the other group). Looking at another subgroup, namely the patients who were treated with a minimum of 1000 maggots in total (patients 2, 3, 11, 14, 15 and 16), the chance of culturing a Gram-negative bacteria decreased after treatment with maggots. The number of maggots needed to debride a wound is estimated at 10 larvae per cm 2 of wound, but there seems to be no maximum number of larvae per cm 2 of wound 17. Special calculators have been developed to calculate the number of maggots needed to debride a wound, based on size and percentage of wound area covered with slough 18. In accordance with in-vitro findings 10,14 16, maggot therapy appears to be more effective against Gram-positive bacteria. Reasons for faster growing of Gram-negative bacteria during maggot treatment could be because of a result of an increase in the ph of the growth medium. Another reason could be that endotoxins produced by Gram-negative bacteria are capable of destroying secretions produced by maggots. Although the methodological limitations of the present open label, non-comparative cohort study precludes a definite conclusion concerning the effectiveness of maggots against Gram-positive and Gram-negative infected wounds, the authors believe that, for these patients, Gram-positive bacteria are digested and killed more easily than Gram-negative bacteria. The authors believe that a higher number of maggots is not only needed for a larger wound, or for a wound covered with a higher percentage of slough, but also for a Gram-negative infected wound. A limitation of the present study was that all patients who were septic or had a severe wound infection were treated with antibiotics directed at the causative agent which would probably have influenced the subsequent cultures. Address for correspondence Dr P Steenvoorde, Department of Surgery, K6-R, Leiden University Medical Center, P.O. Box 9600, 2300 RC Leiden, The Netherlands, tel: +31 71 526 3610, fax: +31 71 526 6750, e-mail: p.steenvoorde@lumc.nl Received: 27 October 2003; revised: 10 December 2003; accepted: 8 March 2004 References 1 Grassberger M. Ein historischer Ruckblick auf den therapeutischen einsatz von fliegenlarven. NTM 2002; 10: 13 24. 2 Baer WS. The treatment of chronic osteomyelitis with the maggot (larva of the blow fly). Journal of Bone and Joint Surgery 1931; 13: 438 475. 3 Vistnes LM, Lee R, Ksander GA. Proteolytic activity of blowfly larvae secretions in experimental burns. Surgery 1981; 90: 835 841. 4 Courtenay M, Church JC, Ryan TJ. Larva therapy in wound management. Journal of the Royal Society of Medicine 2000; 93: 72 74. 5 Teich S, Myers RA. Maggot therapy for severe skin infections. Southern Medical Journal 1986; 79: 1153 1155. 6 Sherman RA, Pechter EA. Maggot therapy: a review of the therapeutic applications of fly larvae in human medicine, especially for treating osteomyelitis. Medical and Veterinary Entomology 1988; 2: 225 230. 100 JOURNAL OF TISSUE VIABILITY VOL 14 NO. 3 JULY 2004

97_101_JTV_Maggots 24/6/04 12:13pm Page 5 7 Thomas S, Andrews A, Jones M. The use of larval therapy in wound management. Journal of Wound Care 1998; 7: 521 524. 8 Jukema GN, Menon AG, Bernards AT, Steenvoorde P, Rastegar AT, Van Dissel JT. Amputation-sparing treatment by nature: "Surgical" maggots revisited. Clinical and Infectious Diseases 2002; 35: 1566 1571. 9 Simmons SW. The bactericidal properties of excretions of the maggot of Lucilia sericata. Bulletin of Entomological Research 1935; 26: 559 563. 10 Thomas S, Andrews AM, Hay NP, Bourgoise S. The antimicrobial activity of maggot secretions: results of a preliminary study. Journal of Tissue Viability 1999; 9: 127 132. 11 Pellizzer G, Strazzabosco M, Presi S et al. Deep tissue biopsy vs. superficial swab culture monitoring in the microbiological assessment of limb-threatening diabetic foot infection. Diabetic Medicine 2001; 18: 822 827. 12 Bonn D. Maggot therapy: an alternative for wound infection. Lancet 2000; 356: 1174. 13 Mumcuoglu KY, Ingber A, Gilead L et al. Maggot therapy for the treatment of diabetic foot ulcers. Diabetes Care 1998; 21: 2030 2031. 14 Robinson W, Norwood VH. The role of surgical maggots in the disinfection of osteomyelitis and other infected wounds. Journal of Bone and Joint Surgery 1933; 15: 409 412. 15 Robinson W, Norwood VH. Destruction of pyogenic bacteria in the alimentary tract of surgical maggots implanted in infected wounds. The Journal of Laboratory and Clinical Medicine 1933; 19: 581 585. 16 Mumcuoglu KY, Miller J, Mumcuoglu M, Friger M, Tarshis M. Destruction of bacteria in the digestive tract of the maggot of Lucilia sericata (Diptera: Calliphoridae). Journal of Medical Entomology 2001; 38: 161 166. 17 Fitzpatrick M. Tiny "surgeons" prove surprisingly effective. JAMA 2000; 284: 2306 2307. 18 Thomas S, Jones M, Wynn K, Fowler T. The current status of maggot therapy in wound healing. British Journal of Nursing 2001; 10: S5 12. QUAY BOOKS MA HEALTHCARE LTD Fundamental Aspects of Tissue Viability Fundamental Aspects of Nursing series by Cheryl Dunford and Bridgit Günnewicht ISBN: 1 85642 260 7; 216 x 138 mm; p/back; 144 pages; publication April 2004; 24.99 This book provides a sound foundation in the field of tissue viability, particularly for those who are becoming involved in this aspect of nursing for the first time as a student or newly qualified nurse. the text is both patient-centred and research-based. Each chapter includes patient scenarios, reflective activities and time-out sections. These allow the reader to focus directly on the patient. The chapters cover: How wounds heal; Assessing wounds; Wound healing therapies; Specific wound types; Advanced therapies; and Ensuring quality of patient care. Cheryl Dunford is Lecturer at the School of Nursing and Midwifery, Southampton University. Bridget Günnewicht is Consultant Nurse, Integumentary health, South Birmingham PCT. To order your copy please contact: Quay Books Division, MA Healthcare Limited, Jesses Farm, Snow Hill, Dinton, Salisbury, Wiltshire, SP3 5HN, UK Tel: 01722 716998 Fax: 01722 716887 e-mail: quaybooks@markallengroup.com web: www.quaybooks.com Quay Books JOURNAL OF TISSUE VIABILITY VOL 14 NO. 3 JULY 2004 101