This article has Open Peer Review reports available.
Multi-drug resistant A cinetobacterinfections in critically injured Canadian forces soldiers
- Homer C Tien1, 2Email author,
- Anthony Battad†2,
- Elizabeth A Bryce†3,
- Jeffrey Fuller†4,
- Michael Mulvey†5,
- Kathy Bernard†5,
- Ronald Brisebois†2, 6,
- Jay J Doucet†2, 7,
- Sandro B Rizoli†1, 8,
- Robert Fowler†8 and
- Andrew Simor†9
© Tien et al; licensee BioMed Central Ltd. 2007
Received: 04 June 2007
Accepted: 14 August 2007
Published: 14 August 2007
Military members, injured in Afghanistan or Iraq, have returned home with multi-drug resistant Acinetobacter baumannii infections. The source of these infections is unknown.
Retrospective study of all Canadian soldiers who were injured in Afghanistan and who required mechanical ventilation from January 1 2006 to September 1 2006. Patients who developed A. baumannii ventilator associated pneumonia (VAP) were identified. All A. baumannii isolates were retrieved for study patients and compared with A. baumannii isolates from environmental sources from the Kandahar military hospital using pulsed-field gel electrophoresis (PFGE).
During the study period, six Canadian Forces (CF) soldiers were injured in Afghanistan, required mechanical ventilation and were repatriated to Canadian hospitals. Four of these patients developed A. baumannii VAP. A. baumannii was also isolated from one environmental source in Kandahar – a ventilator air intake filter. Patient isolates were genetically indistinguishable from each other and from the isolates cultured from the ventilator filter. These isolates were resistant to numerous classes of antimicrobials including the carbapenems.
These results suggest that the source of A. baumannii infection for these four patients was an environmental source in the military field hospital in Kandahar. A causal linkage, however, was not established with the ventilator. This study suggests that infection control efforts and further research should be focused on the military field hospital environment to prevent further multi-drug resistant A. baumannii infections in injured soldiers.
Acinetobacter baumannii is a gram-negative bacterium that can cause infectious outbreaks in critically-ill patients, often with limited treatment options due to antibiotic resistance [1–3]. In November, 2004, the Centers for Disease Control and Prevention (CDC) reported an increasing number of multi-drug resistant (MDR) A. baumannii bloodstream infections in United States military personnel returning from service in Iraq and Afghanistan . The source of these infections is unknown. We report the results of an infection control investigation of four Canadian Forces members who developed ventilator associated pneumonia (VAP) from MDR A. baumannii after injury in Afghanistan.
In November 2005, Canadian Forces (CF) members deployed to Kandahar, Afghanistan. Surgical support was provided by the 248th Combat Support Hospital, a US medical unit. However, a Canadian-led medical unit (Role Three Multinational Medical Unit (R3MMU)) assumed command of the facility on February 7, 2006. Two of the authors (HCT and AB) were part of the first Canadian medical contingent to arrive at this facility in Kandahar. Three mechanical ventilators (iVent201, Versamed Inc, Pearl River, NY) were purchased from the departing US organization, and were left in the facility for use by the R3MMU. At the time of the hand-over, this facility had 11 beds in a small, common room. The intensive care unit consisted of three of these beds which were equipped with the iVent ventilators. The R3MMU has basic laboratory support, but does not have any microbiological testing capability.
While working at this hospital, the authors (HT and AB) treated a Canadian soldier (patient one) who suffered a severe head injury and required mechanical ventilation. After this patient was evacuated back to Canada, they were informed that he developed MDR A. baumannii VAP. As a result, they took environmental samples from inside and around the hospital. These included numerous soil samples from around the operating room, ICU and resuscitation bay. Because the hospital did not have microbiological testing capabilities, they collected all samples using sterile forceps or sterile basins, and placed them into sterile specimen containers. Also, they dismantled the patient's (patient one) mechanical ventilator, and collected samples (including the air intake filter) from it using sterile forceps and specimen containers. These were all couriered to microbiology laboratories in Canadian hospitals for testing. The samples arrived in Canada approximately 72 hours after collection.
Several months after returning to Canada, the authors(HCT & AB) then identified all CF members who were injured in Kandahar and who required mechanical ventilation using aeromedical evacuation records (obtained through the Canadian Forces Health Services) from 1 January 2006 to 1 September 2007. In general, injured CF members are evacuated by US Air Force medical teams to a US army hospital in Germany (Landstuhl Regional Medical Center or LRMC). Canadian medical teams then bring casualties from LRMC to civilian Canadian hospitals. During the study period time, CF members were repatriated to five different civilian tertiary care centers in Canada.
We reviewed the medical records of these patients from Kandahar, LRMC and their respective Canadian hospitals, if available. We also contacted the attending physicians responsible for each patient in Canada to discuss each patient's clinical course in hospital. We also contacted the microbiology department of LRMC and all involved Canadian hospitals to obtain the microbiological record for each patient. Our primary outcome of interest was the development of A. baumannii ventilator associated pneumonia, as defined by the CDC's National Nosocomial Infection Surveillance system . A. baumannii respiratory isolates were then retrieved, if available, for all patients who developed A. baumannii VAP. Patient isolates were then compared to each other, and to any positive environmental isolates from the hospital in Kandahar.
Organisms were identified using standard laboratory methods, including Gram stain appearance, colonial morphology, negative oxidase reaction, and the VITEK-2 ID-GNB card (bioMérieux, Hazelwood, MO). Antibiotic susceptibility testing was done using the VITEK-2 AST-N019 card according to the manufacturer's instructions (bioMérieux). Genomic DNA from all A. baumannii isolates was digested with ApaI for molecular typing by PFGE . Interpretation of DNA profiles generated by PFGE was done visually. Isolates were considered to be genetically related if their PFGE patterns differed by three of fewer bands .
Institutional review ethics approval was obtained to conduct this study. However, individual consent was not obtained from each patient as some had been already discharged from hospital. As the number of critically wounded CF casualties was small during the study period, we only present aggregate demographic data (means ± standard deviation), as individual information may identify specific patients. Statistical analysis was performed using SAS version 8.02 (SAS Institute, Carey, NC).
During the study period, six CF members required mechanical ventilation and were evacuated through LRMC to five different Canadian hospitals. Four of these patients developed multi-drug resistant A. baumannii VAP. Their mean age was 26.5 years (± 8.5). Three sustained multiple injuries from improvised explosive devices; one received a severe head injury. On average, they required 68 days of mechanical ventilation (± 70 days).
During this same period of time, a total of 42 injured CF members were evacuated from Kandahar to Canadian hospitals, through Landstuhl Regional Medical Centre. On review of the A. baumannii screening results from LRMC (which was performed shortly after admission), there were skin culture reports found for 25 of these patients; reports were not found for 17. Only two patients had positive screening tests that were positive for A. baumannii (preliminary, non-published results). One of the positive screening tests was from one of the four study patients (patient one). Unfortunately, the isolate was not available for testing by PFGE.
Antibiogram of MDR A. baumanni isolates
Sensitivity (MIC) MDR A. baumanniiisolates
R (≥ 32)
R (≥ 16)
R (≥ 16)
R (≥ 64)
R (≥ 4)
R (≥ 64)
R (≥ 32/16)
S (≤ 2)
R (≥ 64)
R (≥ 64)
R (≥ 16)
R (≥ 128)
R (≥ 128)
R (≥ 16)
S (≤ 1)
R (≥ 64)
R (≥ 8)
We report four cases of multi-drug resistant A. baumannii infections in CF members injured in Afghanistan. MDR A. baumannii VAP was first diagnosed in three of these four patients at the US army hospital in Landstuhl, Germany and continued to be an issue for them in Canada. Patient four developed A. baumannii VAP while hospitalized in Canada. Originally, we suspected that the source of these infections was LRMC, as all four patients had molecularly identical strains of MDR A. baumannii VAP, and all four had been treated at LRMC where MDR A. baumannii infections are prevalent. However, the filter isolate was also identical to the MDR A. baumannii isolated from these four patients, suggesting that the field hospital was the original source of infection.
We were only able to demonstrate A. baumannii in one environmental sample – the ventilator filter isolate. If the field hospital were contaminated, we would expect fairly widespread contamination and therefore, would have expected multiple environmental samples to have been positive for A. baumannii. However, as mentioned previously, the R3MMU field hospital does not have microbiological testing capability; therefore, all samples were couriered to Canada for culture. This resulted in a delay of at least 72 hours prior to processing; this delay may be responsible for the low yield of positive cultures in our environmental samples.
The origin of the A. baumannii infections in soldiers injured in Afghanistan and Iraq is still unknown. These infections may have been acquired from environmental sources in the field, during treatment at military field hospitals, during evacuation from the theatre of operations, or during treatment at hospitals outside of the conflict area. During the Vietnam War, A. baumannii was recovered from traumatic injuries to extremities . More recent reports have also identified A. baumannii infections in patients who suffered traumatic injuries, suggesting environmental contamination of wounds as a potential source . Our report also suggests that these MDR A. baumannii organisms originated from an environmental source in the theatre of operations. All MDR A. baumannii isolates from these four patients were molecularly identical to the ventilator filter isolate from Kandahar.
A. baumannii has often been linked to infectious outbreaks involving the mechanical ventilation circuit [10–12]. However, this study does not definitively establish a causal link between the contaminated ventilator in Kandahar and the subsequent four cases of MDR A. baumannii VAP. A. baumannii is a ubiquitous micro-organism that colonizes inanimate surfaces and medical equipment. Our patients may have just as easily acquired the MDR A. baumannii through lack of hand hygiene in health workers, microaspiration or even hematogenous spread from an infected IV site. Once acquired, the ventilator may have been secondarily contaminated.
Unfortunately, because of limitations of the field environment, we were unable to trace contact exposures of infected patients back to specific health care workers. Because of limitations in personnel, patients were not assigned to specific health care workers; instead, two to three nurses were on duty for each shift, and collectively cared for all patients in the facility. As a result, all patients were exposed to all health care workers because of the small numbers of hospital staff. Likewise, we were unable to screen the hands of hospital health care workers, as the facility did not have microbiological testing capability.
Even so, the results of this report suggest that the field hospital environment is the source of MDR A. baumannii infections and that increased infection control measures are required at the field hospital level in military theatre of operations. For example, regular ventilator cleaning and maintenance is difficult in the field setting, and outgoing staff from the 248th CSH reported that air-intake filters and antibacterial circuit filters were difficult to obtain. As a result, antibacterial circuit filters were not routinely used, and the air-intake filters were not routinely changed. Based on our findings, the ventilators are now regularly maintained, and air-intake filters are changed as recommended by the manufacturer. Anti-bacterial circuit filters are also now used (Intersurgical Filta-Therm Filter, Intersurgical Ltd, Wokingham Berkshire UK). As well, hospital cleaners have been hired and hand-washing stations have been established in patient care areas.
Our findings are likely applicable to US and British military field hospitals as well. Our ventilators were previously used by the 248th CSH. As well, the environmental and logistical problems that faced both the 248th CSH and the R3MMU are common across field hospitals in Afghanistan and Iraq [13, 14]. Other contributory factors may have included non-restrictive antibiotic use at the field hospitals to compensate for poor environmental conditions .
Identifying the etiology of multi-drug resistant Acinetobacter infection in returning soldiers is important for preventing nosocomial transmission to other vulnerable patients. Zapor reported 53 cases of nosocomial transmission of MDR Acinetobacter that have directly resulted in four fatalities in US military hospitals . Jones has also reported on one British service member who may have imported an MDR A. baumannii strain from Iraq that caused a large outbreak in National Health Service hospitals in the UK .
Ongoing surveillance remains critical for monitoring the efficacy of infection control measures. In Canada, critically injured service members are cared for in the civilian health care system. As a result, the Canadian Forces Health Services is collaborating with the Public Health Agency of Canada (PHAC) to implement a national surveillance strategy for MDR Acinetobacter infections in injured soldiers. The multinational nature of military coalitions and medical care, however, highlight the need for health care providers to also communicate across national borders.
We conclude that the military field hospital was the source of multi-drug resistant A. baumannii that later lead to the development of ventilator associated pneumonia in four CF members who were injured in Kandahar, Afghanistan. Further research and infection control efforts should be focused on the field hospital environment to prevent future A. baumannii infections.
This study was funded by the Canadian Forces Health Services.
- Urban C, Segal-Maurer S, Rahal J: Considerations in control and treatment of nosocomial infections due to multidrug-resistant Acinetobacter baumannii. Clin Infect Dis. 2003, 36: 1268-1274. 10.1086/374847.View ArticlePubMedGoogle Scholar
- Simor AE, Lee M, Vearncombe M, Jones-Paul L, Barry C, Gomez M, Fish JS, Cartotto RC, Palmer R, Louie M: An outbreak due to multi-resistant Acinetobacter baumannii in a burn unit: risk factors form acquisition and management. Infect Control Hosp Epidemiol. 2002, 23: 261-7. 10.1086/502046.View ArticlePubMedGoogle Scholar
- Fournier PE, Richet H: The epidemiology and control of Acinetobacter baumannii in health care facilities. Clin Infect Dis. 2006, 42: 692-9. 10.1086/500202.View ArticlePubMedGoogle Scholar
- Centers for Disease Control: Acinetobacter Baumannii infections among patients at military medical facilities treating injured U.S. service members, 2002–2004. MMWR Morb Mortal Wkly Rep. 2004, 53: 1063-1066.Google Scholar
- Horan TC, Gaynes RP: Surveillance of nosocomial infections. Hospital epidemiology and infection control. Edited by: Mayhall CG. 2004, Philadelphia, Lippincott Williams & Wilkins, 1659-702. 3Google Scholar
- Seifert H, Gerner-Smidt P: Comparison of ribotyping and pulsed-field gel electrophoresis for molecular typing of Acinetobacter isolates. J Clin Microbiol. 1995, 33: 1402-7.PubMedPubMed CentralGoogle Scholar
- Tenover FC, Arbeit RD, Goering RV, Mickelsen PA, Murray BE, Persing DH, Swaminathan B: Interpreting chromosomal DNA restriction patterns produced by pulsed-field gel electrophoresis: criteria for bacterial strain typing. J Clin Microbiol. 1995, 33: 2233-9.PubMedPubMed CentralGoogle Scholar
- Tong MJ: Septic complications of war wounds. JAMA. 1972, 219: 1044-7. 10.1001/jama.219.8.1044.View ArticlePubMedGoogle Scholar
- Heath CH, Orrell CT, Lee RC, Pearman JW, McCullough C, Christiansen KJ: A review of the Royal Perth Hospital Bali experience: an infection control perspective. Australian Infection Control. 2003, 2: 43-54.View ArticleGoogle Scholar
- Cox TR, Roland WE, Dolan ME: Ventilator-related Acinetobacter outbreak in an intensive care unit. Mil Med. 1998, 163 (6): 389-91.PubMedGoogle Scholar
- Dealer S: Nosocomial outbreak of multi-resistant Acinetobacter sp. on an intensive care unit: possible association with ventilation equipment. J Hosp Infect. 1998, 38: 147-48. 10.1016/S0195-6701(98)90068-8.View ArticleGoogle Scholar
- Cefai C, Richards J, Gould FK, McPeake P: An outbreak of Acinetobacter respiratory tract infection resulting from incomplete disinfection of respiratory equipment. J Hosp Infect. 1993, 25: 15-32. 10.1016/0195-6701(93)90005-K.View ArticleGoogle Scholar
- Gawande A: Casualties of War – Military Care for the Wounded from Iraq and Afghanistan. N Engl J Med. 2004, 351: 2471-2475. 10.1056/NEJMp048317.View ArticlePubMedGoogle Scholar
- Jones A, Morgan D, Walsh A, Turton J, Livermore D, Pitt T, Green A, Gill M, Mortiboy D: Importation of multidrug-resistant Acinetobacter spp infections with casualties from Iraq. Lancet Infect Dis. 2006, 6 (6): 317-318. 10.1016/S1473-3099(06)70471-6.View ArticlePubMedGoogle Scholar
- Zapor M, Moran KA: Infectious diseases during wartime. Curr Opin Infect Dis. 2005, 18 (5): 395-399. 10.1097/01.qco.0000182102.50430.2c.View ArticlePubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2334/7/95/prepub
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.