eMedicine Specialties > Pediatrics: General Medicine > Infectious Disease

Hospital-Acquired Infections: Treatment & Medication

Author: Quoc V Nguyen, MD, Assistant Professor, Department of Pediatrics, New York State Health Department
Contributor Information and Disclosures

Updated: Jan 14, 2009

Treatment

Medical Care

Symptomatic treatment of shock, hypoventilation, and other complications should be provided, along with the administration of empiric broad-spectrum antimicrobials, antifungals, and antivirals.

Infections caused by methicillin-resistant Staphylococcus aureus (MRSA) are not worse than those caused by susceptible S aureus. MRSA requires treatment with different families of antibiotics. Although the pathogenicity does not generally differ from that of susceptible strains of S aureus, MRSA strains that carry the loci for Panton-Valentine leukocidin can be hypervirulent and can cause lymphopenia, rapid tissue necrosis, and severe sepsis.

  • Bloodstream infections
    • Line removal should be considered if the line is suspected in the cause of sepsis.
    • Broad-spectrum antibiotics should be selected according to the local epidemiologic patterns of microbial susceptibility.
    • Antifungals (eg, fluconazole, caspofungin, voriconazole, amphotericin B) are added to empiric antibiotics in some cases.
    • Antivirals (eg, ganciclovir, acyclovir) could be used in the treatment of suspected disseminated viral infections.
  • Pneumonia
    • Change nasotracheal tubes to orotracheal tubes, if feasible.
    • Broad-spectrum antibiotics are administered with guidance from the results of rapid examination of the sputum, endotracheal suction material, and bronchial lavage wash.
    • Macrolide antibiotics are indicated in legionellosis.
    • Antivirals (neuraminidase inhibitors for both influenza A and influenza B) are used if viral pneumonia is suspected. Since the 2005-2006 influenza season, the CDC has not recommended amantadine and rimantadine because of resistance. Laboratory testing by the CDC on the predominant strain of influenza (H3N2) currently circulating in the United States shows that it is resistant to these drug.
    • Indications for the use of neuraminidase inhibitors in children have been defined for oseltamivir phosphate (approved for treatment and prophylaxis in children >1 y) and zanamivir (approved for treatment in children ≥7 y and for prophylaxis in children ≥5 y).
    • Anti-influenza therapy has been used to treat symptomatic patients and patients with immunodeficiency or chronic lung diseases to limit morbidity and mortality.
    • Oseltamivir (Tamiflu) resistance has emerged in the United States during the 2008-2009 influenza season.
      • The CDC has issued revised interim recommendations for antiviral treatment and prophylaxis of influenza. Preliminary data from a limited number of states indicate a high prevalence of influenza A (H1N1) virus strains resistant to oseltamivir (Tamiflu). Because of this, zanamivir (Relenza) is recommended as the initial choice for antiviral prophylaxis or treatment when influenza A infection or exposure is suspected. A second-line alternative is a combination of oseltamivir plus rimantadine, rather than oseltamivir alone. Local influenza surveillance data and laboratory testing can assist the physician regarding antiviral agent choice.
      • Influenza A viruses, including 2 subtypes (H1N1 and H3N2), and influenza B viruses currently circulate worldwide; the prevalence of each can vary among communities and within a single community over the course of an influenza season. In the United States, 4 prescription antiviral medications (oseltamivir, zanamivir, amantadine, rimantadine) are approved for treatment and chemoprophylaxis of influenza. Since January 2006, the neuraminidase inhibitors (oseltamivir, zanamivir) have been the only recommended influenza antiviral drugs because of widespread resistance to the adamantanes (amantadine, rimantadine) among influenza A (H3N2) virus strains. The neuraminidase inhibitors have activity against influenza A and B viruses, whereas the adamantanes have activity against only influenza A viruses.
      • In 2007-2008, a significant increase in the prevalence of oseltamivir resistance was reported among influenza A (H1N1) viruses worldwide. During the 2007-2008 influenza season, 10.9% of H1N1 viruses tested in the United States were resistant to oseltamivir. Complete recommendations are available from the CDC.
    • Overall, the most cost-effective prevention measure is seasonal vaccination against influenza A and B. The 2007-2008 vaccine strains consist of A/Solomon Island/3/2006 (H1N1)–like, A/Wisconsin/67/2005 (H3N2)–like, and B/Malaysia/2506/2004–like antigens.
  • Urinary tract infection
    • Indwelling catheters should be removed, if feasible.
    • Empiric antibiotic and antifungal therapy is based on the preliminary results of urinalysis and urine Gram staining.
  • Surgical-site infections: These should be managed with a combination of surgical care and aggressive antibiotic therapy guided by the results of deep-tissue Gram staining and culturing. Fasciitis is of special concern because it is associated with mucoid group A streptococci and high morbidity and mortality rates.
  • C difficile colitis: Management of C difficile colitis includes the discontinuation of the offending antibiotics and the use of oral metronidazole or vancomycin. Macrobiotics may be beneficial.

Surgical Care

  • Surgical debridement is an integral part of management of surgical-site infections or superinfected decubitus ulcers. Tissue sample should be processed using appropriate stains and cultures to identify the pathogen and its susceptibility.

Consultations

  • Many patients with nosocomial infections require expert care from an ICU team.
  • Infectious disease specialists, burn care specialists, and surgical teams are usually involved in the care of these complicated cases.

Medication

Pharmacologic treatment depends on the underlying etiology.

More on Hospital-Acquired Infections

Overview: Hospital-Acquired Infections
Differential Diagnoses & Workup: Hospital-Acquired Infections
Treatment & Medication: Hospital-Acquired Infections
Follow-up: Hospital-Acquired Infections
References

References

  1. National Nosocomial Infections Surveillance (NNIS) System. National Nosocomial Infections Surveillance (NNIS) System report, data summary from October 1986-April 1998, issued June 1998. Am J Infect Control. Oct 1998;26(5):522-33. [Medline].

  2. Wenzel R, Edmond MD. The impact of Hospital Acquired Blood Stream Infections. Emerg Inf Dis. Mar-Apr 2001;7(174).

  3. Richards MJ, Edwards JR, Culver DH, Gaynes RP. Nosocomial infections in pediatric intensive care units in the United States. National Nosocomial Infections Surveillance System. Pediatrics. Apr 1999;103(4):e39. [Medline].

  4. Dancer SJ. Mopping up hospital infection. J Hosp Infect. Oct 1999;43(2):85-100. [Medline].

  5. Davey P, Brown E, Fenelon L, et al. Interventions to improve antibiotic prescribing practices for hospital inpatients. In: Cochrane Database of Systematic Reviews. John Wiley & Sons, Ltd; 2005.

  6. Deville JG, Adler S, Azimi PH, et al. Linezolid versus vancomycin in the treatment of known or suspected resistant gram-positive infections in neonates. Pediatr Infect Dis J. Sep 2003;22(9 Suppl):S158-63. [Medline].

  7. Garner JS. Guideline for isolation precautions in hospitals. The Hospital Infection Control Practices Advisory Committee [published erratum appears in Infect Control Hosp Epidemiol 1996 Apr;17(4):214]. Infect Control Hosp Epidemiol. Jan 1996;17(1):53-80. [Medline].

  8. McKibben L, Horan T, Tokars JI, et al. Guidance on public reporting of healthcare-associated infections: recommendations of the Healthcare Infection Control Practices Advisory Committee. Am J Infect Control. May 2005;33(4):217-26. [Medline].

  9. Moellering RC Jr. Vancomycin-resistant enterococci. Clin Infect Dis. May 1998;26(5):1196-9. [Medline].

  10. Rice LB, Shlaes DM. Vancomycin resistance in the enterococcus. Relevance in pediatrics. Pediatr Clin North Am. Jun 1995;42(3):601-18. [Medline].

  11. Scott PT, Petersen K, Fishbain J. Acinetobacter baumannii Infections Among Patients at Military Medical Facilities Treating Injured US Service Members, 2002-2004. MMWR. 2004;53:1063-1066.

  12. Siegel JD, Rhinehart E, Jackson M, Chiarello L. Management of Multidrug-Resistant Organisms in Health Care Settings, 2006. Atlanta, GA: Healthcare Infection Control Practices Advisory Committee; 2006. 1-74.

  13. Standfast SJ, Michelsen PB, Baltch AL. A prevalence survey of infections in a combined acute and long-term care hospital. Infect Control. Apr 1984;5(4):177-84. [Medline].

  14. Steed CJ. Common infections acquired in the hospital: the nurse's role in prevention. Nurs Clin North Am. Jun 1999;34(2):443-61. [Medline].

  15. Tablan OC, Anderson LJ, Besser R, Bridges C, Hajjeh R. MMWR Recommendations and Reports: Guidelines for Preventing Health Care-Associated Pneumonia. Atlanta, GA: CDC; March 26, 2004. 1-36.

  16. Weinstein JW, Mazon D, Pantelick E. A decade of prevalence surveys in a tertiary-care center: trends in nosocomial infection rates, device utilization, and patient acuity. Infect Control Hosp Epidemiol. Aug 1999;20(8):543-8. [Medline].

  17. Witte W, Braulke C, Cuny C, et al. Emergence of methicillin-resistant Staphylococcus aureus with Panton-Valentine leukocidin genes in central Europe. Eur J Clin Microbiol Infect Dis. Jan 2005;24(1):1-5. [Medline].

Further Reading

Keywords

hospital-acquired infections, health care–acquired infections, nosocomial infection, vancomycin-resistant enterococcus, VRE, methicillin-resistant Staphylococcus aureus, MRSA, Pseudomonas, candidiasis, Legionella, respiratory syncytial virus, thrush, Clostridium difficile, viral respiratory infections, influenza, parainfluenza, sinusitis, otitis, tracheitis, phlebitis, line infection, bloodstream infection, ventilator-associated pneumonia, urinary tract infection, UTI, surgical-site infection, coagulase-negative staphylococci, enterococci, fungi, , pseudomonads,

Contributor Information and Disclosures

Author

Quoc V Nguyen, MD, Assistant Professor, Department of Pediatrics, New York State Health Department
Disclosure: Nothing to disclose.

Medical Editor

David Jaimovich, MD, Chief Medical Officer, Joint Commission International and Joint Commission Resources
David Jaimovich, MD is a member of the following medical societies: American Academy of Pediatrics
Disclosure: Nothing to disclose.

Pharmacy Editor

Mary L Windle, PharmD, Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy, Pharmacy Editor, eMedicine
Disclosure: Pfizer Inc Stock Investment from financial planner; Avanir Pharma Stock Investment from financial planner ; WebMD Salary and stock Employment and investment from financial planner

Managing Editor

Joseph Domachowske, MD, Professor of Pediatrics, Microbiology and Immunology, Department of Pediatrics, Division of Infectious Diseases, State University of New York-Upstate Medical University
Joseph Domachowske, MD is a member of the following medical societies: Alpha Omega Alpha, American Academy of Pediatrics, American Society for Microbiology, Infectious Diseases Society of America, Pediatric Infectious Diseases Society, and Phi Beta Kappa
Disclosure: Nothing to disclose.

CME Editor

Robert W Tolan Jr, MD, Chief, Division of Allergy, Immunology and Infectious Diseases, The Children's Hospital at Saint Peter's University Hospital; Clinical Associate Professor of Pediatrics, Drexel University College of Medicine
Robert W Tolan Jr, MD is a member of the following medical societies: American Academy of Pediatrics, American Medical Association, American Society for Microbiology, American Society of Tropical Medicine and Hygiene, Infectious Diseases Society of America, Pediatric Infectious Diseases Society, Phi Beta Kappa, and Physicians for Social Responsibility
Disclosure: GlaxoSmithKline Honoraria Speaking and teaching; MedImmune Honoraria Consulting; MedImmune Honoraria Speaking and teaching; Merck Honoraria Speaking and teaching; Novartis Honoraria Speaking and teaching; sanofi pasteur Grant/research funds Unrestricted research grant; sanofi pasteur  Consulting; sanofi pasteur Honoraria Speaking and teaching; Tap Honoraria Speaking and teaching; Baxter Healthcare Honoraria Speaking and teaching

Chief Editor

Russell W Steele, MD, Head, Division of Pediatric Infectious Diseases, Ochsner Children's Health Center; Clinical Professor, Department of Pediatrics, Tulane University School of Medicine
Russell W Steele, MD is a member of the following medical societies: American Academy of Pediatrics, American Association of Immunologists, American Pediatric Society, American Society for Microbiology, Infectious Diseases Society of America, Louisiana State Medical Society, Pediatric Infectious Diseases Society, Society for Pediatric Research, and Southern Medical Association
Disclosure: None None None

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