Effect of Biofield Treatment on Antimicrobials Susceptibility Pattern of Acinetobacter baumannii – An Experimental Study
Global emergence of Acinetobacter baumannii (A. baumannii) displays a mechanism of resistance to all existing antimicrobials. Objective of this study was to investigate the effect of biofield treatment on antimicrobial sensitivity pattern, minimum inhibitory concentration (MIC), biochemical reactions and biotype number of A. baumannii. A. baumannii cells were procured from MicroBioLogics in sealed packs bearing the American Type Culture Collection (ATCC 19606) number and stored according to the recommended storage protocols until needed for experiments. Two sets of ATCC samples were taken in this experiment and denoted as A and B. ATCC-A sample was revived and divided into two parts i.e. Gr.I (control) and Gr.II (revived) analyzed on day 5 and 10, respectively; likewise, ATCC-B was labeled as Gr.III (lyophilized) and was assessed on day 10. Gr.II and III were treated with Mr. Trivedi’s biofield and were analyzed for its antimicrobial sensitivity, MIC value, biochemical reactions and biotype number with respect to control. Experimental results showed the impact of biofield treatment directly onto the revived and lyophilized form of A. baumannii and found alteration both in qualitative and quantitative aspect as compared with untreated groups. These results showed altered sensitivity pattern of antimicrobials in biofield treated group as compared to control. Apart from altered MIC values, changes were also observed in biotype number of revived treated group as compared to control. These findings suggest that biofield treatment can prevent the emergence of absolute resistance of existing antimicrobials to A. baumannii.
Acinetobacter baumannii is a typically short, almost round, rod-shaped (coccobacillus) Gram-negative bacterium. It can be an opportunistic pathogen in humans, affecting people with compromised immune systems, and is becoming increasingly important as a hospital-derived (nosocomial) infection. It has also been isolated from environmental soil and water samples. Bacteria of this genus lack flagella, whip-like structures many bacteria use for locomotion, but exhibit twitching or swarming motility. This may be due to the activity of type IV pili, pole-like structures that can be extended and retracted. Motility in A. baumannii may also be due to the excretion of exopolysaccharide, creating a film of high-molecular-weight sugar chains behind the bacterium to move forward. Clinical microbiologists typically differentiate members of the Acinetobacter genus from other Moraxellaceae by performing an oxidase test, as Acinetobacter spp. are the only members of the Moraxellaceae to lack cytochrome c oxidases. A. baumannii is part of the ACB complex (A. baumannii, A. calcoaceticus, and Acinetobacter genomic species 13TU). Members of the ACB complex are difficult to determine the specific species, and comprise the most clinically relevant members of the genus. A. baumannii has also been identified as an ESKAPE pathogen (Enterococcus faecalis, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, and Enterobacter species), a group of pathogens with a high rate of antibiotic resistance that are responsible for the a majority of nosocomial infections. Colloquially, A. baumannii is referred to as 'Iraqibacter' due to its seemingly sudden emergence in military treatment facilities during the Iraq War. It has continued to be an issue for veterans and soldiers who served in Iraq and Afghanistan. Multidrug-resistant A. baumannii has spread to civilian hospitals in part due to the transport of infected soldiers through multiple medical facilities.
Virulence factors and determinants
Many microbes, including A. baumannii, have several properties that allow them to be more successful as pathogens. These properties may be virulence factors such as toxins or toxin delivery systems which directly affect the host cell. They may also be virulence determinants, which are qualities contributing to a microbe's fitness and allow it to survive the host environment, but that do not affect the host directly. These characteristics are just some of the known factors which make A. baumannii effective as a pathogen:
AbaR resistance islands
Pathogenicity islands, relatively common genetic structures in bacterial pathogens, are composed of two or more adjacent genes that increase a pathogen's virulence. They may contain genes that encode toxins, coagulate blood, or, as in this case, allow the bacteria to resist antibiotics. AbaR-type resistance islands are typical of drug-resistant A. baumannii, and different variations may be present in a given strain. Each consists of a transposon backbone of about 16.3 Kb that facilitates horizontal gene transfer. Transposons allow portions of genetic material to be excised from one spot in the genome and integrate into another. This makes horizontal gene transfer of this and similar pathogenicity islands more likely because, when genetic material is taken up by a new bacterium, the transposons allow the pathogenicity island to integrate into the new microorganism's genome. In this case, it would grant the new microorganism the potential to resist certain antibiotics. AbaRs contain several genes for antibiotic resistance, all flanked by insertion sequences. These genes provide resistance to aminoglycosides, aminocyclitols, tetracycline, and chloramphenicol.
A. baumannii has been shown to produce at least one beta-lactamase, which is an enzyme responsible for cleaving the four-atom lactam ring typical of beta-lactam antibiotics. Beta-lactam antibiotics are structurally related to penicillin, which inhibits synthesis of the bacterial cell wall. The cleaving of the lactam ring renders these antibiotics harmless to the bacteria. The beta-lactamase OXA-23 was found to be flanked by insertion sequences, suggesting it was acquired by horizontal gene transfer.
A. baumannii has been noted for its apparent ability to survive on artificial surfaces for an extended period of time, therefore allowing it to persist in the hospital environment. This is thought to be due to its ability to form biofilms. For many biofilm-forming bacteria, the process is mediated by flagella. However, for A. baumannii, this process seems to be mediated by pili. Further, disruption of the putative pili chaperone and usher genes csuC and csuE were shown to inhibit biofilm formation. The formation of biofilms has been shown to alter the metabolism of microorganisms within the biofilm, consequently reducing their sensitivity to antibiotics. This may be because less nutrients are available deeper within the biofilm. A slower metabolism can prevent the bacteria from taking up an antibiotic or performing a vital function fast enough for particular antibiotics to have an effect. They also provide a physical barrier against larger molecules and may prevent desiccation of the bacteria.
Many virulent bacteria possess the ability to generate a protective capsule around each individual cell. This capsule, made of long chains of sugars, provides an extra physical barrier between antibiotics, antibodies, and complement. The association of increased virulence with presence of a capsule was classically demonstrated in Griffith's experiment. A gene cluster responsible for secretion of the polysaccharide capsule has been identified and shown to inhibit the antibiotic effect of complement when grown on ascites fluid. A decrease in killing associated with loss of capsule production was then demonstrated using a rat virulence model.
Efflux pumps are protein machines that use energy to pump antibiotics and other small molecules that get into the bacterial cytoplasm and the periplasmic space out of the cell. By constantly pumping antibiotics out of the cell, bacteria can increase the concentration of a given antibiotic required to kill them or inhibit their growth when the target of the antibiotic is inside the bacterium. A. baumannii is known to have two major efflux pumps which decrease its susceptibility to antimicrobials. The first, AdeB, has been shown to be responsible for aminoglycoside resistance. The second, AdeDE, is responsible for efflux of a wide range of substrates, including tetracycline, chloramphenicol, and various carbapenems.
Adhesion can be a critical determinant of virulence for bacteria. The ability to attach to host cells allows bacteria to interact with them in various ways, whether by type III secretion system or simply by holding on against the prevailing movement of fluids. Outer membrane protein A has been shown to be involved in the adherence of A. baumannii to epithelial cells. This allows the bacteria to invade the cells through the zipper mechanism. The protein was also shown to localize to the mitochondria of epithelial cells and cause necrosis by stimulating the production of ROS.
Course of treatment for infection
Because most infections are now resistant to multiple drugs, it is necessary to determine what susceptibilities the particular strain has for treatment to be successful. Traditionally, infections were treated with imipenem or meropenem, but a steady rise in carbapenem-resistant A. baumannii has been noted. Consequently, treatment methods often fall back on polymyxins, particularly colistin. Colistin is considered a drug of last resort because it often causes kidney damage among other side effects. Prevention methods in hospitals focus on increased hand-washing and more diligent sterilization procedures.
Occurrence in veterans injured in Iraq and Afghanistan
Soldiers in Iraq and Afghanistan are at risk for traumatic injury due to gunfire and improvised explosive devices. Previously, infection was thought to occur due to contamination with A. baumannii at the time of injury. Subsequent studies have shown, although A. baumannii may be infrequently isolated from the natural environment, the infection is more likely nosocomially acquired, likely due to the ability of A. baumannii to persist on artificial surfaces for extended periods, and the several facilities to which injured soldiers are exposed during the casualty-evacuation process. Injured soldiers are first taken to level-I facilities, where they are stabilized. Depending on the severity of the injury, the soldiers may then be transferred to a level-II facility, which consists of a forward surgical team, for additional stabilization. Depending on the logistics of the locality, the injured soldiers may transfer between these facilities several times before finally being taken to a major hospital within the combat zone (level III). Generally after 1–3 days, when the patients are stabilized, they are transferred by air to a regional facility (level IV) for additional treatment. For soldiers serving in Iraq or Afghanistan, this is typically Landstuhl Regional Medical Center in Germany. Finally, the injured soldiers are transferred to hospitals in their home country for rehabilitation and additional treatment. This repeated exposure to many different medical environments seems to be the reason A. baumannii infections have become increasingly common. Multidrug-resistant A. baumannii is a major factor in complicating the treatment and rehabilitation of injured soldiers, and has led to additional deaths.
Incidence of A. baumannii in hospitals
The importation of A. baumannii and subsequent presence in hospitals has been well documented. A. baumannii is usually introduced into a hospital by a colonized patient. Due to its ability to survive on artificial surfaces and resist desiccation, it can remain and possibly infect new patients for some time. A baumannii growth is suspected to be favored in hospital settings due to the constant use of antibiotics by patients in the hospital. In a study of European intensive care units in 2009, A. baumannii was found to be responsible for 19.1% of ventilator-associated pneumonia (VAP) cases.
- Yeom, J; Shin, JH; Yang, JY; Kim, J; Hwang, GS (2013). "(1)H NMR-Based Metabolite Profiling of Planktonic and Biofilm Cells in Acinetobacter baumannii 1656-2.". PLoS ONE 8 (3): e57730. doi:10.1371/journal.pone.0057730. PMID 23483923.
- McQueary, CN; Kirkup, BC; Si, Y; Barlow, M; Actis, LA; Craft, DW; Zurawski, DV (June 2012). "Extracellular stress and lipopolysaccharide modulate Acinetobacter baumannii surface-associated motility.". Journal of microbiology (Seoul, Korea) 50 (3): 434–43. doi:10.1007/s12275-012-1555-1. PMID 22752907.
- Garrity, edited by G. (2000). Bergey's Manual of Systematic Bacteriology Vol. 2, Pts. A & B: The Proteobacteria. (2nd ed., rev. ed.). New York: Springer. p. 454. ISBN 0-387-95040-0.
- O'Shea, MK (May 2012). "Acinetobacter in modern warfare.". International journal of antimicrobial agents 39 (5): 363–75. doi:10.1016/j.ijantimicag.2012.01.018. PMID 22459899.
- Gerner-Smidt, P (October 1992). "Ribotyping of the Acinetobacter calcoaceticus-Acinetobacter baumannii complex.". Journal of clinical microbiology 30 (10): 2680–5. PMID 1383266.
- Rice, LB (Apr 15, 2008). "Federal funding for the study of antimicrobial resistance in nosocomial pathogens: no ESKAPE.". The Journal of infectious diseases 197 (8): 1079–81. doi:10.1086/533452. PMID 18419525.
- Drummond, Katie. "Pentagon to Troop-Killing Superbugs: Resistance Is Futile". Wired.com. Condé Nast. Retrieved 8 April 2013.
- Seputiene, V.; Povilonis, J.; Suziedeliene, E. (30 January 2012). "Novel Variants of AbaR Resistance Islands with a Common Backbone in Acinetobacter baumannii Isolates of European Clone II". Antimicrobial Agents and Chemotherapy 56 (4): 1969–1973. doi:10.1128/AAC.05678-11. PMC 3318354. PMID 22290980.
- Post, V; White, PA; Hall, RM (June 2010). "Evolution of AbaR-type genomic resistance islands in multiply antibiotic-resistant Acinetobacter baumannii.". The Journal of antimicrobial chemotherapy 65 (6): 1162–70. doi:10.1093/jac/dkq095. PMID 20375036.
- Higgins, PG; Pérez-Llarena, FJ; Zander, E; Fernández, A; Bou, G; Seifert, H (Feb 25, 2013). "OXA-235, a novel Class D Beta-Lactamase Involved in Resistance to Carbapenems in Acinetobacter baumannii.". Antimicrobial agents and chemotherapy 57 (5): 2121–6. doi:10.1128/AAC.02413-12. PMID 23439638.
- Espinal, P; Martí, S; Vila, J (January 2012). "Effect of biofilm formation on the survival of Acinetobacter baumannii on dry surfaces.". The Journal of hospital infection 80 (1): 56–60. doi:10.1016/j.jhin.2011.08.013. PMID 21975219.
- Tomaras, AP; Dorsey, CW; Edelmann, RE; Actis, LA (December 2003). "Attachment to and biofilm formation on abiotic surfaces by Acinetobacter baumannii: involvement of a novel chaperone-usher pili assembly system.". Microbiology (Reading, England) 149 (Pt 12): 3473–84. doi:10.1099/mic.0.26541-0. PMID 14663080.
- Worthington, RJ; Richards, JJ; Melander, C (Oct 7, 2012). "Small molecule control of bacterial biofilms.". Organic & biomolecular chemistry 10 (37): 7457–74. doi:10.1039/c2ob25835h. PMID 22733439.
- Kleinman, HK; McGarvey, ML; Hassell, JR; Star, VL; Cannon, FB; Laurie, GW; Martin, GR (Jan 28, 1986). "Basement membrane complexes with biological activity.". Biochemistry 25 (2): 312–8. doi:10.1021/bi00350a005. PMID 2937447.
- Luke, NR; Sauberan, SL; Russo, TA; Beanan, JM; Olson, R; Loehfelm, TW; Cox, AD; St Michael, F; Vinogradov, EV; Campagnari, AA (May 2010). "Identification and characterization of a glycosyltransferase involved in Acinetobacter baumannii lipopolysaccharide core biosynthesis.". Infection and immunity 78 (5): 2017–23. doi:10.1128/iai.00016-10. PMID 20194587.
- Magnet, S; Courvalin, P; Lambert, T (December 2001). "Resistance-nodulation-cell division-type efflux pump involved in aminoglycoside resistance in Acinetobacter baumannii strain BM4454.". Antimicrobial agents and chemotherapy 45 (12): 3375–80. doi:10.1128/aac.45.12.3375-3380.2001. PMID 11709311.
- Chau, SL; Chu, YW; Houang, ET (October 2004). "Novel resistance-nodulation-cell division efflux system AdeDE in Acinetobacter genomic DNA group 3.". Antimicrobial agents and chemotherapy 48 (10): 4054–5. doi:10.1128/aac.48.10.4054-4055.2004. PMID 15388479.
- Choi, CH; Lee, JS; Lee, YC; Park, TI; Lee, JC (Dec 10, 2008). "Acinetobacter baumannii invades epithelial cells and outer membrane protein A mediates interactions with epithelial cells.". BMC microbiology 8: 216. doi:10.1186/1471-2180-8-216. PMID 19068136.
- Lee, JS; Choi, CH; Kim, JW; Lee, JC (June 2010). "Acinetobacter baumannii outer membrane protein A induces dendritic cell death through mitochondrial targeting.". Journal of microbiology (Seoul, Korea) 48 (3): 387–92. doi:10.1007/s12275-010-0155-1. PMID 20571958.
- Su, CH; Wang, JT; Hsiung, CA; Chien, LJ et al. (2012). "Increase of carbapenem-resistant Acinetobacter baumannii infection in acute care hospitals in Taiwan: Association with hospital antimicrobial usage". PLOS ONE 7 (5): e37788. Bibcode:2012PLoSO...737788S. doi:10.1371/journal.pone.0037788. PMID 22629456.
- Abbo, A; Navon-Venezia, S; Hammer-Muntz, O; Krichali, T et al. (January 2005). "Multidrug-resistant Acinetobacter baumannii". Emerging Infectious Diseases 11 (1): 22–9. doi:10.3201/eid1101.040001. PMID 15705318.
- Spapen, H; Jacobs, R; Van Gorp, V; Troubleyn, J et al. (May 25, 2011). "Renal and neurological side effects of colistin in critically ill patients". Annals of Intensive Care 1 (1): 14. doi:10.1186/2110-5820-1-14. PMID 21906345.
- "Acinetobacter in Healthcare Settings". CDC. Retrieved April 8, 2013.
- "Army Medical Logistics". FM 4-02.1. United States. Retrieved April 8, 2013.
- Meghoo, CA; Dennis, JW; Tuman, C; Fang, R (May 2012). "Diagnosis and management of evacuated casualties with cervical vascular injuries resulting from combat-related explosive blasts.". Journal of vascular surgery 55 (5): 1329–36; discussion 1336–7. doi:10.1016/j.jvs.2011.11.125. PMID 22325667.
- Murray, CK (March 2008). "Epidemiology of infections associated with combat-related injuries in Iraq and Afghanistan.". The Journal of trauma 64 (3 Suppl): S232–8. doi:10.1097/ta.0b013e318163c3f5. PMID 18316967.
- Jones, A; Morgan, D; Walsh, A; Turton, J; Livermore, D; Pitt, T; Green, A; Gill, M; Mortiboy, D (June 2006). "Importation of multidrug-resistant Acinetobacter spp infections with casualties from Iraq". The Lancet infectious diseases 6 (6): 317–8. doi:10.1016/S1473-3099(06)70471-6. PMID 16728314.
- Dijkshoorn, L; Nemec, A; Seifert, H (December 2007). "An increasing threat in hospitals: multidrug-resistant Acinetobacter baumannii.". Nature Reviews Microbiology 5 (12): 939–51. doi:10.1038/nrmicro1789. PMID 18007677.
- Koulenti, D; Lisboa, T; Brun-Buisson, C; Krueger, W; Macor, A; Sole-Violan, J; Diaz, E; Topeli, A; DeWaele, J; Carneiro, A; Martin-Loeches, I; Armaganidis, A; Rello, J; EU-VAP/CAP Study, Group (August 2009). "Spectrum of practice in the diagnosis of nosocomial pneumonia in patients requiring mechanical ventilation in European intensive care units.". Critical Care Medicine 37 (8): 2360–8. doi:10.1097/ccm.0b013e3181a037ac. PMID 19531951.
- Ng, J; Gosbell, IB; Kelly, JA; Boyle, MJ; Ferguson, JK (November 2006). "Cure of multiresistant Acinetobacter baumannii central nervous system infections with intraventricular or intrathecal colistin: case series and literature review.". The Journal of antimicrobial chemotherapy 58 (5): 1078–81. doi:10.1093/jac/dkl347. PMID 16916866.
- Farrugia, DN; Elbourne, LD; Hassan, KA; Eijkelkamp, BA; Tetu, SG; Brown, MH; Shah, BS; Peleg, AY; Mabbutt, BC; Paulsen, IT (2013). "The Complete Genome and Phenome of a Community-Acquired Acinetobacter baumannii". PLoS ONE 8 (3): e58628. Bibcode:2013PLoSO...858628F. doi:10.1371/journal.pone.0058628. PMID 23527001.
- Werneck, JS; Picão, RC; Carvalhaes, CG; Cardoso, JP; Gales, AC (February 2011). "OXA-72-producing Acinetobacter baumannii in Brazil: a case report.". The Journal of antimicrobial chemotherapy 66 (2): 452–4. doi:10.1093/jac/dkq462. PMID 21131320.
- Martins, N; Martins, IS; de Freitas, WV; de Matos, JA; Magalhães, AC; Girão, VB; Dias, RC; de Souza, TC; Pellegrino, FL; Costa, LD; Boasquevisque, CH; Nouér, SA; Riley, LW; Santoro-Lopes, G; Moreira, BM (June 2012). "Severe infection in a lung transplant recipient caused by donor-transmitted carbapenem-resistant Acinetobacter baumannii.". Transplant infectious disease : an official journal of the Transplantation Society 14 (3): 316–20. doi:10.1111/j.1399-3062.2011.00701.x. PMID 22168176.
- Superti, SV; Martins Dde, S; Caierão, J; Soares Fda, S; Prochnow, T; Zavascki, AP (Mar–Apr 2009). "Indications of carbapenem resistance evolution through heteroresistance as an intermediate stage in Acinetobacter baumannii after carbapenem administration.". Revista do Instituto de Medicina Tropical de Sao Paulo 51 (2): 111–3. doi:10.1590/s0036-46652009000200010. PMID 19390741.
- Gionco, B; Pelayo, JS; Venancio, EJ; Cayô, R; Gales, AC; Carrara-Marroni, FE (October 2012). "Detection of OXA-231, a new variant of blaOXA-143, in Acinetobacter baumannii from Brazil: a case report.". The Journal of antimicrobial chemotherapy 67 (10): 2531–2. doi:10.1093/jac/dks223. PMID 22736746.
- Zhao, WS; Liu, GY; Mi, ZH; Zhang, F (March 2011). "Coexistence of blaOXA-23 with armA and novel gyrA mutation in a pandrug-resistant Acinetobacter baumannii isolate from the blood of a patient with haematological disease in China.". The Journal of hospital infection 77 (3): 278–9. doi:10.1016/j.jhin.2010.11.006. PMID 21281989.
- Xiao, SC; Zhu, SH; Xia, ZF; Ma, B; Cheng, DS (November 2009). "Successful treatment of a critical burn patient with obstinate hyperglycemia and septic shock from pan-drug-resistant strains.". Medical science monitor : international medical journal of experimental and clinical research 15 (11): CS163–5. PMID 19865060.
- Wu, YC; Hsieh, TC; Sun, SS; Wang, CH; Yen, KY; Lin, YY; Kao, CH (November 2009). "Unexpected cloud-like lesion on gallium-67 scintigraphy: detection of subcutaneous abscess underneath the skin with normal appearance in a comatose patient in an intensive care setting.". The American journal of the medical sciences 338 (5): 388. doi:10.1097/maj.0b013e3181a6dd36. PMID 19770790.
- Duan, X; Yang, L; Xia, P (March 2010). "Septic arthritis of the knee caused by antibiotic-resistant Acinetobacter baumannii in a gout patient: a rare case report.". Archives of orthopaedic and trauma surgery 130 (3): 381–4. doi:10.1007/s00402-009-0958-x. PMID 19707778.
- Wagner, JA; Nenoff, P; Handrick, W; Renner, R; Simon, J; Treudler, R (February 2011). "[Necrotizing fasciitis caused by Acinetobacter baumannii : A case report].". Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete 62 (2): 128–30. doi:10.1007/s00105-010-1962-3. PMID 20835812.
- Aivazova, V; Kainer, F; Friese, K; Mylonas, I (January 2010). "Acinetobacter baumannii infection during pregnancy and puerperium.". Archives of gynecology and obstetrics 281 (1): 171–4. doi:10.1007/s00404-009-1107-z. PMID 19462176.
- Schulte, B; Goerke, C; Weyrich, P; Gröbner, S; Bahrs, C; Wolz, C; Autenrieth, IB; Borgmann, S (December 2005). "Clonal spread of meropenem-resistant Acinetobacter baumannii strains in hospitals in the Mediterranean region and transmission to South-west Germany.". The Journal of hospital infection 61 (4): 356–7. doi:10.1016/j.jhin.2005.05.009. PMID 16213625.
- Piparsania, S; Rajput, N; Bhatambare, G (Sep–Oct 2012). "Intraventricular polymyxin B for the treatment of neonatal meningo-ventriculitis caused by multi-resistant Acinetobacter baumannii--case report and review of literature.". The Turkish Journal of Pediatrics 54 (5): 548–54. PMID 23427525.
- John, TM; Jacob, CN; Ittycheria, CC; George, AM; Jacob, AG; Subramaniyam, S; Puthiyaveettil, J; Jayaprakash, R (March 2012). "Macrophage activation syndrome following Acinetobacter baumannii sepsis.". International Journal of Infectious Diseases 16 (3): e223–4. doi:10.1016/j.ijid.2011.12.002. PMID 22285540.
- Sharma, A; Shariff, M; Thukral, SS; Shah, A (October 2005). "Chronic community-acquired Acinetobacter pneumonia that responded slowly to rifampicin in the anti-tuberculous regime.". The Journal of infection 51 (3): e149–52. doi:10.1016/j.jinf.2004.12.003. PMID 16230195.
- Jeong, HL; Yeom, JS; Park, JS; Seo, JH; Park, ES; Lim, JY; Park, CH; Woo, HO; Youn, HS (Jul–Aug 2011). "Acinetobacter baumannii isolation in cerebrospinal fluid in a febrile neonate". The Turkish journal of pediatrics 53 (4): 445–7. PMID 21980849.
- Hong, KB; Oh, HS; Song, JS; Lim, JH; Kang, DK; Son, IS; Park, JD; Kim, EC; Lee, HJ; Choi, EH (July 2012). "Investigation and control of an outbreak of imipenem-resistant Acinetobacter baumannii Infection in a Pediatric Intensive Care Unit.". The Pediatric Infectious Disease Journal 31 (7): 685–90. doi:10.1097/inf.0b013e318256f3e6. PMID 22466324.
- Lee, YK; Kim, JK; Oh, SE; Lee, J; Noh, JW (December 2009). "Successful antibiotic lock therapy in patients with refractory peritonitis.". Clinical nephrology 72 (6): 488–91. doi:10.5414/cnp72488. PMID 19954727.
- Lee, SY; Lee, JW; Jeong, DC; Chung, SY; Chung, DS; Kang, JH (August 2008). "Multidrug-resistant Acinetobacter meningitis in a 3-year-old boy treated with i.v. colistin.". Pediatrics international : official journal of the Japan Pediatric Society 50 (4): 584–5. doi:10.1111/j.1442-200x.2008.02677.x. PMID 18937759.
- Adams, D; Yee, L; Rimmer, JA; Williams, R; Martin, H; Ovington, C (Feb 10–23, 2011). "Investigation and management of an A. Baumannii outbreak in ICU.". British journal of nursing (Mark Allen Publishing) 20 (3): 140, 142, 144–7. PMID 21378633.
- Pencavel, TD; Singh-Ranger, G; Crinnion, JN (May 2006). "Conservative treatment of an early aortic graft infection due to Acinetobacter baumanii.". Annals of vascular surgery 20 (3): 415–7. doi:10.1007/s10016-006-9030-2. PMID 16602028.
- Gusten, WM; Hansen, EA; Cunha, BA (Jan–Feb 2002). "Acinetobacter baumannii pseudomeningitis.". Heart & lung : the journal of critical care 31 (1): 76–8. doi:10.1067/mhl.2002.120258. PMID 11805753.
- Fitzpatrick, MA; Esterly, JS; Postelnick, MJ; Sutton, SH (Jul–Aug 2012). "Successful treatment of extensively drug-resistant Acinetobacter baumannii peritoneal dialysis peritonitis with intraperitoneal polymyxin B and ampicillin-sulbactam". Annals of Pharmacotherapy 46 (7–8): e17. doi:10.1345/aph.1r086. PMID 22811349.
- Patel, JA; Pacheco, SM; Postelnick, M; Sutton, S (Aug 15, 2011). "Prolonged triple therapy for persistent multidrug-resistant Acinetobacter baumannii ventriculitis.". American journal of health-system pharmacy : AJHP : official journal of the American Society of Health-System Pharmacists 68 (16): 1527–31. doi:10.2146/ajhp100234. PMID 21817084.
- Sullivan, DR; Shields, J; Netzer, G (June 2010). "Fatal case of multi-drug resistant Acinetobacter baumannii necrotizing fasciitis.". The American surgeon 76 (6): 651–3. PMID 20583528.
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