Volume 7, Number 2—April 2001
4th Decennial International Conference on Nosocomial and Healthcare-Associated Infections
Prevention is Primary
"Cloud" Health-Care Workers
Certain bacteria dispersed by health-care workers can cause hospital infections. Asymptomatic health-care workers colonized rectally, vaginally, or on the skin with group A streptococci have caused outbreaks of surgical site infection by airborne dispersal. Outbreaks have been associated with skin colonization or viral upper respiratory tract infection in a phenomenon of airborne dispersal of Staphylococcus aureus called the "cloud" phenomenon. This review summarizes the data supporting the existence of cloud health-care workers.
variety of infectious agents can be transmitted from health-care workers to patients (1,2). Certain of these agents are transmissible through the air, which means that transmission from health-care workers can occur in spite of standard infection control measures such as handwashing. Thus, airborne transmission increases the likelihood that an outbreak can occur. While it is well known that health-care workers can transmit infections such as tuberculosis, varicella, and influenza by the airborne route, it is less well appreciated that they can also transmit certain bacterial pathogens through the air.
Bacteria transmissible through the air for which no data support transmission by health-care workers include Clostridium diphtheriae, Haemophilus influenzae, Neisseria meningiditis, Streptococcus pneumoniae, and Yersinia pestis. For all these agents except S. pneumoniae, the epidemiologic data supporting airborne transmission are strong enough that the Centers for Disease Control and Prevention recommends that infected patients be placed on droplet precautions (3). However, for all five agents, no episodes are well documented of health-care workers transmitting such infections to other patients by the airborne route, perhaps because workers with such infections may be too sick to work. For three other bacteria, Bordetella pertussis, Streptococcus pyogenes, and Staphylococcus aureus, strong data support airborne transmission from health-care workers to patients.
Although most children are vaccinated against B. pertussis and the vaccine is quite effective up to age 12, approximately 50% of adults are nonimmune (4). Thus, in a vaccinated population, transmission of pertussis is primarily from adults to either nonimmune children (<1 year of age) or to adults whose immunity has waned. Several well-described hospital outbreaks of pertussis have occurred in which B. pertussis was thought to be transmitted to or from health-care workers in a manner suggesting airborne transmission (Table 1) (5–9). Most hospital outbreaks have involved pediatric patients (5,6,8,9), but at least one outbreak has occurred in a nursing home (7). No prolonged carrier state has been identified (10,11), and transmission is most likely associated with active symptoms, particularly coughing (12). The use of air samplers and polymerase chain reaction analysis has shown that B. pertussis DNA can be found in the air surrounding patients with B. pertussis infection, providing further evidence of airborne spread (13). Terminating B. pertussis hospital outbreaks involves removing symptomatic health-care workers from clinical care, isolating symptomatic or exposed patients, and treating symptomatic and exposed health-care workers and patients with antibiotics.
Health-care worker-associated GAS outbreaks attributed to airborne spread are uncommon, associated only with asymptomatic health-care workers, and involving only surgical site infections (14–18). The health-care workers carrying GAS may be present during surgery (e.g., anesthesiologist, operating room nurse) (16,17) or not present at all (e.g., medical attendant, operating room technician) (14,15,18). In five GAS outbreaks associated with health-care workers (Table 2), volumetric or settle plate air cultures showed that the health-care workers dispersed GAS into the air. Sites of GAS colonization identified on the health-care workers include the rectum, vagina, and skin. The mechanism by which GAS becomes airborne is not entirely clear and could include increased activity (14), friction with clothing, or, in the case of an anesthesiologist who was a rectal carrier, flatulence. Such outbreaks may cause substantial illness and even death. Termination of GAS health-care worker-associated outbreaks requires eradicating the carrier state with antibiotics. In some cases eradication has been difficult because the health-care workers' family was also colonized with GAS, which may have led to initial treatment failure.
Factors affecting the airborne dispersal of S. aureus have been studied more intensively than those of any other organism. In the general population, airborne dispersal of S. aureus is uncommon and appears to be quantitatively related to the number of S. aureus colonizing the anterior nares (19). Up to 10% of healthy S. aureus nasal carriers disperse the organism into the air (20), and females are much less likely to disperse the organism than males (21,22). Such airborne dispersers typically were surrounded by 0.01 to 0.1 CFU/m3 of S. aureus and, rarely, as high as 2.6 CFU/m3 (21,22). Hare and Thomas demonstrated that when agar plates were held directly under the noses of nasal carriers of S. aureus, airborne dispersal was insignificant with nasal breathing, counting, coughing 6 times, or sneezing once (23). Only with snorting did substantial dispersal occur. In contrast, when the same volunteers were moving, large numbers of S. aureus were dispersed into the air. This dispersal was attributed to S. aureus on the skin and clothing, thought to be liberated into the air by friction and movement. Coughing increases airborne dispersal of organisms other than S. aureus, and lack of airborne dispersal of S. aureus through coughing is thought to be due to its rare presence in the oropharyngeal cavity. In other studies, talking increased dispersal of organisms other than S. aureus, and sneezing dramatically increased the number of bacteria dispersed into the air, including S. aureus (24,25). Ehrenkranz demonstrated that oral tetracycline caused the number of S. aureus in the nose of a nasal carrier of tetracycline-resistant S. aureus to increase by tenfold and concommitantly increased the number of S. aureus dispersed into the air (26).
In detailed studies of S. aureus transmission in a newborn nursery setting (27,28), Rammelkamp et al. found that newborn infants exposed to nurses who handled colonized infants acquired S. aureus 14% of the time if good handwashing was performed and 43% of the time in the absence of good handwashing (presumed direct contact transmission). Infants acquired S. aureus 10% of the time when they were exposed to nurses who were not colonized with S. aureus and who did not handle infants colonized with S. aureus (presumed airborne transmission). Under these controlled circumstances, airborne transmission was about two thirds as likely as contact transmission. The infants infected by presumed airborne transmission were four times more likely to acquire the organism first in their noses than were the infants infected by direct contact (4/16 vs. 3/49; p=0.056). During a 3-year period, Nobel demonstrated that a few patients (8/3,675) were associated with airborne dispersal of S. aureus (29). One of eight dispersers identified was associated with an outbreak. While inactive, such patients were associated with air counts of up to 0.3 CFU/m3 air. The highest number of S. aureus in the air was found in association with bedmaking of colonized patients (up to 4.9 CFU/m3). Elevated airborne dispersal has also been associated with individual patients (30,31). Hare and Cooke found that airborne dispersal was facilitated by eczema, mycosis fungoids, or perineal carriage (31). In a few published outbreaks, health-care workers have been identified who clearly dispersed S. aureus into the air (32,33); in one case, dispersal was thought to be due to heavy skin colonization with S. aureus (15). In other outbreaks where airborne transmission has been suspected, no air cultures were performed, so the contribution of airborne transmission was not determined (34,35). Thus, although airborne dispersal from both patients and health-care workers occurs, under the circumstances previously studied, it is relatively uncommon.
However, outbreaks associated with such airborne dispersers are frequent (>10%) (29,32). Clearly, if some factor augments the ability of S. aureus carriers to produce airborne dispersal, the potential for S. aureus outbreaks to occur might be greatly increased. In 1960, the American Journal of Diseases of Children preceded an article with a brief editorial entitled "The Preposterous Cloud Baby" (36). The first sentence of the introduction stated "Once in a blue moon a journal is privileged to publish an article which introduces an important revolutionary concept." In the report that followed, Eichenwald et al. described a group of S. aureus-colonized, virally infected newborn infants who had the ability to disperse S. aureus from their noses into the air--so-called "cloud babies" (36). These researchers demonstrated by culture and epidemiologic study that a viral upper respiratory infection (e.g., with adenovirus or echo virus) was the essential "cloud factor." Up to 75% of newborn infants who carried S. aureus nasally became cloud babies once they acquired a viral upper respiratory infection. Most importantly, these cloud babies were also capable of causing S. aureus outbreaks (36). Although these infants had no greater risk for staphylococcal infection, the families of cloud babies had a fourfold higher risk for infection than the families of infants colonized with S. aureus that were not cloud babies. In spite of what was believed to be a revolutionary concept, no further observations about cloud babies have been published since Eichenwald's study in 1960.
In 1986 we reported that an S. aureus nasal carrier, a nurse, caused outbreaks in two newborn nurseries at different hospitals in association with upper respiratory infections (34). The nurse's strain of S. aureus and the outbreak strains were identical by phage typing. Infants' risk for acquiring staphylococcal skin disease was fivefold greater when the nurse had a upper respiratory infection. She was treated with topical bacitracin ointment and hexachlorophene baths to eradicate her S. aureus carrier state, and no further outbreaks of staphylococcal skin disease occurred. We postulated then that the probable source of the outbreak might be a cloud adult (4).
In 1996, an outbreak of methicillin-resistant S. aureus (MRSA) pneumonia occurred in an intensive care unit (33). Multivariant analysis demonstrated that the only independent risk factors for MRSA pneumonia were intubation and exposure to a single physician, who was nasally colonized with the outbreak strain of MRSA as shown by molecular typing. During the outbreak period, this physician had a prolonged upper respiratory infection, and an experimental rhinovirus upper respiratory infection caused him to increase airborne dispersal of S. aureus 40-fold and become a cloud adult. The use of a mask during this experimental rhinovirus infection caused a 75% reduction in the airborne dispersal of S. aureus.
To a hospital epidemiologist, the identification of two cloud adults as the cause of the only two tightly clustered S. aureus outbreaks investigated during his career is either a striking coincidence or an indication that the frequency with which airborne transmission plays a role in S. aureus outbreaks has been underestimated. Many hospital outbreaks of S. aureus infections have been reported that were thought to be due to a single health-care worker (32–35,37–52). A few of these were probably related to heavy skin colonization (32) or sinusitis (35), but in most cases no other risk factor was apparent that could account for these persons' being capable of causing an outbreak. The role of airborne transmission was investigated in only two studies (32,33). In the group without identifiable risk factors, virtually all the health-care workers were nasally colonized with S. aureus. Indeed, S. aureus nasal colonization in health-care workers is quite common (20% to 90%) (53–56). However, if S. aureus nasal colonization was the only factor necessary to cause an outbreak, the high frequency of S. aureus nasal colonization in health-care workers should be associated with a high frequency of S. aureus outbreaks. Since this is not the case, some other factor(s) must modify the S. aureus nasal carrier state to facilitate the outbreak. One such factor is likely a viral upper respiratory infection. Since adults have an average of two viral upper respiratory infection each year (57), cloud adults may be working around patients all year.
We recently investigated the generalizability of the cloud adult phenomenon by giving six persistent nasal carriers of S. aureus a rhinovirus infection (58). One of the six volunteers became an unequivocal cloud adult, with a 40-fold increase in S. aureus airborne dispersal that could be blocked by a mask. Another volunteer had a similar increase in airborne dispersal, but it could not be prevented by a mask. The six volunteers came from a group of 18 persistent nasal carriers of S. aureus identified from 95 volunteers screened for S. aureus nasal carriage. These findings suggest that the ability to become a cloud adult could occur with a frequency of up to 6% or more in the general population.
Viral upper respiratory infections facilitate the transmission of other bacterial infections, including the following pathogens that colonize the nose: S. pneumoniae, S. pyogenes, H. influenzae, and N. meningitidis (59–62). Thus, cloud adults have the potential to play a role in the transmission of other organisms and might be involved with some of the explosive outbreaks of infection occasionally seen in day-care centers, homeless shelters, the military, and hospitals. Further work is necessary to understand the importance of cloud adults in the transmission of hospital infections.
Dr. Sherertz is chief of infectious diseases at Wake Forest University School of Medicine and associate hospital epidemiologist. His research interests include the pathogenesis and prevention of vascular catheterinfections, as well as mechanisms of transmission of nosocomial infections, particularly S. aureus.
This report was supported in part by RO1 AI-46558.
- Sherertz RJ, Marosok RD, Streed SA. Infection control aspects of hospital employee health. In: RP Wenzel, editor. Prevention and Control of Nosocomial Infections. Baltimore: Williams & Wilkins; 1987. p. 295-332.
- Decker MD, Schaffner W. Nosocomial diseases in healthcare workers spread by the airborne or contact routes (other than tuberculosis). In: Mayhall CG, editor. Hospital epidemiology and infection control. Baltimore: Williams & Wilkins; 1996. p. 859-82.
- Garner JS; Hospital Infection Control Practices Advisory Committee. Guideline for isolation precautions in hospitals. CDC Hospital Infections Program Guidelines and Recommendations. 1997 Feb 18. Available from: URL:www.cdc.gov/ncidod/hip/ISOLAT/isolat.htm.
- Lambert HJ. Epidemiology of a small pertussis outbreak in Kent County, Michigan. Public Health Rep. 1965;80:365–9. DOIPubMedGoogle Scholar
- Kurt TL, Yeager AS, Guenette S, Dunlop S. Spread of pertussis by hospital staff. JAMA. 1972;221:264–7. DOIPubMedGoogle Scholar
- Linneman CC Jr, Ramundo N, Perlstein PH, Minton SD, Englender GS. Use of pertussis vaccine in an epidemic involving hospital staff. Lancet. 1975;2:540–3. DOIPubMedGoogle Scholar
- Addis DG, Davis JP, Meade BD, Burstyn DG, Meissner M, Zastrow JA, A pertussis outbreak in a Wisconsin nursing home. J Infect Dis. 1991;164:704–10. DOIPubMedGoogle Scholar
- Christie CD, Gover AM, Wilke MJ, Marx ML, Reising SF, Hutchinson NM. Containment of pertussis in the regional pediatric hospital during the Greater Cincinnati epidemic of 1993. Infect Control Hosp Epidemiol. 1995;16:556–63. DOIPubMedGoogle Scholar
- Nouvellon M, Gehanno J, Pestel-Caron M, Weber C, Lemeland J, Guiso N. Usefulness of pulse-field gel electropheresis in assessing nosocomial transmission of pertussis. Infect Control Hosp Epidemiol. 1999;20:758–60. DOIPubMedGoogle Scholar
- Jenkinson D, Pepper JD. A search for subclinical infection during a small oubreak of whooping cough: implications for clinical diagnosis. J R Coll Gen Pract. 1986;36:547–8.PubMedGoogle Scholar
- Krantz I, Alestig K, Trollfors B, Zackrisson G. The carrier state in pertussis. Scand J Infect Dis. 1986;18:121–3. DOIPubMedGoogle Scholar
- Hewlett EL. Bordetella species. In: Mandell GL, Bennett JE, Dolin R, editors. Principles and practice of infectious diseases. Philadelphia: Churchill Livingstone: 2000. p. 2414-21.
- Aintablian N, Walpita P, Sawyer MH. Detection of Bordetella pertussis and respiratory syncytial virus in air samples from hospital rooms. Infect Control Hosp Epidemiol. 1998;19:918–23. DOIPubMedGoogle Scholar
- McKee WM, di Caprio JM, Roberts CE Jr, Sherris JC. Anal carriage as the probable source of a streptococcal epidemic. Lancet. 1966;2:1007–9. DOIPubMedGoogle Scholar
- McIntyre DM. Epidemic of Streptococcus pyogenes puerperal and postoperative sepsis with unusual carrier site - anus. Am J Obstet Gynecol. 1968;101:308–14.PubMedGoogle Scholar
- Schaffner W, Lefkowitz LB, Goodman JS, Koenig MG. Hospital outbreak of infection with group A streptococci traced to an asymptomatic anal carrier. N Engl J Med. 1969;280:1224–5. DOIPubMedGoogle Scholar
- Berkelman RL, Martin D, Graham DR, Mowry J, Freisem R, Weber JA, Streptococcal wound infections caused by a vaginal carrier. JAMA. 1982;247:2680–2. DOIPubMedGoogle Scholar
- Mastro TD, Farley TA, Elliott JA, Facklam RR, Perks JR, Hadler JL, An outbreak of surgical wound infections due to group A streptococcus carried on the scalp. N Engl J Med. 1990;323:968–72. DOIPubMedGoogle Scholar
- White A. Relation between quantitative nasal cultures and dissemination of staphylococci. J Lab Clin Med. 1961;58:273–7.PubMedGoogle Scholar
- Huijsmans-Evers AG. Results of routine tests for the detection of dispersers of Staphylococcus aureus. Archivum Chirurgicum Neerlandia. 1978;30:141–50.PubMedGoogle Scholar
- Bethune DW, Blowers R, Parker M, Pask EA. Dispersal of Staphylococcus aureus by patients and surgical staff. Lancet. 1965;1:480–3. DOIPubMedGoogle Scholar
- Hill J, Howell A, Blowers R. Effect of clothing on dispersal of Staphylococcus aureus by males and females. Lancet. 1974;2:1131–3. DOIPubMedGoogle Scholar
- Hare R, Thomas CGA. The transmission of Staphylococcus aureus. BMJ. 1956;2:840–4. DOIPubMedGoogle Scholar
- Hare R, Mackenzie DM. The source and transmission of nasopharyngeal infections due to certain bacteria and viruses. BMJ. 1946;1:865–70. DOIPubMedGoogle Scholar
- Duguid JP, Wallace AT. Air infection with dust liberated from clothing. Lancet. 1948;2:845–9. DOIPubMedGoogle Scholar
- Ehrenkranz NJ. Person-to-person transmission of Staphylococcus aureus. Quantitative characterization of nasal carriers spreading infection. N Engl J Med. 1964;271:225–30. DOIPubMedGoogle Scholar
- Rammelkamp CH Jr, Mortimer EA Jr, Wolinsky E. Transmission of streptococcal and staphylococcal infections. Ann Intern Med. 1964;60:753–8.PubMedGoogle Scholar
- Mortimer EA, Wolinsky E, Gonzaga AJ, Rammelkamp CH. Role of airborne transmission in staphylococcal infections. BMJ. 1966;1:319–22. DOIPubMedGoogle Scholar
- Nobel WC. The dispersal of staphylococci in hospital wards. J Clin Pathol. 1962;15:552–8. DOIPubMedGoogle Scholar
- Shooter RA, Smith MA, Griffiths JD, Brown MEA, Williams REO, Rippon JE, Spread of staphylococci in a surgical ward. BMJ. 1958;1:607–13. DOIPubMedGoogle Scholar
- Hare R, Cooke EM. Self-contamination of patients with staphylococcal infections. BMJ. 1961;2:333–6. DOIPubMedGoogle Scholar
- Tanner EI, Bullin J, Bullin CH, Gamble DR. An outbreak of post-operative sepsis due to a staphylococcal disperser. J Hyg (Lond). 1980;85:219–25. DOIPubMedGoogle Scholar
- Sherertz RJ, Reagan DR, Hampton KD, Robertson KL, Streed SA, Hoen HM, A cloud adult: the Staphylococcus aureus-virus interaction revisited. Ann Intern Med. 1996;124:539–47.PubMedGoogle Scholar
- Belani A, Sherertz RJ, Sullivan ML, Russell BA, Reumen PD. Outbreak of staphylococcal infection in two hospital nurseries traced to a single nasal carrier. Infect Control. 1986;7:487–90.PubMedGoogle Scholar
- Boyce JM, Opal SM, Potter-Bynoe G, Medeiros AA. Spread of methicillin-resistant Staphylococcus aureus in a hospital after exposure to a health care worker with chronic sinusitis. Ann Intern Med. 1993;17:496–504.PubMedGoogle Scholar
- Eichenwald H, Kotsevalov O, Fasso LA. The "cloud baby": an example of bacterial-viral interaction. Am J Dis Child. 1960;100:161–73.PubMedGoogle Scholar
- Dunkle LM, Naqvi SH, McCallum R, Lofgren JP. Eradication of epidemic methicillin-gentamicin-resistant Staphylococcus aureus in an intensive care nursery. Am J Med. 1981;70:455–8. DOIPubMedGoogle Scholar
- Hedberg K, Ristinen TL, Soler JT, White KE, Hedberg CW, Osterholm MT, Outbreak of erythromycin-resistant staphylococcal conjunctivitis in a newborn nursery. Pediatr J Infect Dis. 1990;9:268–73. DOIPubMedGoogle Scholar
- Coovadia YM, Bhana RH, Johnson AP, Haffejee I, Marples RR. A laboratory-confirmed outbreak of rifampin-methicillin resistant Staphylococcus aureus (MRSA) in a newborn nursery. J Hosp Infect. 1989;14:303–12. DOIPubMedGoogle Scholar
- Dancer SJ, Poston SM, East J, Simmons NA, Noble WC. An outbreak of pemphigus neonatorum. J Infect. 1990;20:73–82. DOIPubMedGoogle Scholar
- Gaynes R, Marosok R, Mowry-Hanley J, Laughlin C, Foley K, Friedman C, Mediastinitis following coronary artery bypass surgery: a 3-year review. J Infect Dis. 1991;163:117–21. DOIPubMedGoogle Scholar
- Simon PA, Chen RT, Elliott JA, Schwartz B. Outbreak of pyogenic abscesses after diphtheria and tetanus toxoids and pertussis vaccination. Pediatr J Infect Dis. 1993;12:368–71. DOIPubMedGoogle Scholar
- Nakashima AK, Allen JR, Martone WJ, Plikaytis BD, Stover B, Cook LN, Epidemic bullous impetigo in a nursery due to a nasal carrier of Staphylococcus aureus: role of epidemiology and control measures. Infect Control. 1984;5:326–31.PubMedGoogle Scholar
- Hoeger PH, Elsner P. Staphylococcal scaled skin syndrome: transmission of exfoliatin-producing Staphylococcus aureus by an asymptomatic carrier. Pediatr Infect Dis J. 1988;7:340–2. DOIPubMedGoogle Scholar
- Richardson JF, Quoraishi AH, Francis BJ, Marples RR. Beta-lactamase-negative, methicillin-resistant Staphylococcus aureus in a newborn nursery: report of an outbreak and laboratory investigations. J Hosp Infect. 1990;16:109–21. DOIPubMedGoogle Scholar
- Back NA, Linnemann CC Jr, Pfaller MA, Staneck JL, Morthland V. Recurrent epidemics caused by a single strain of erythromycin-resistant Staphylococcus aureus. The importance of molecular epidemiology. JAMA. 1993;270:1363–4. DOIPubMedGoogle Scholar
- Chowdhury MN, Kambal AM. An outbreak of infection due to Staphylococcus aureus phage type 52 in a neonatal intensive care unit. J Hosp Infect. 1992;22:299–305. DOIPubMedGoogle Scholar
- Walter CW, Kundsin RB, Brubaker MM. The incidence of airborne wound infection during operation. JAMA. 1963; 908–13.PubMedGoogle Scholar
- Venezia RA, Harris V, Miller C, Peck H. san Antanio M. Investigation of an outbreak of methicillin-resistant Staphylococcus aureus in patients with skin disease using DNA restriction patterns. Infect Control Hosp Epidemiol. 1992;13:472–6. DOIPubMedGoogle Scholar
- Trilla A, Nettleman MD, Hollis RJ, Fredrickson M, Wenzel RP, Pfaller MA. Restriction endonuclease analysis of plasmid DNA from methicillin-resistant Staphylococcus aureus: clinical application over a three-year period. Infect Control Hosp Epidemiol. 1993;14:29–35. DOIPubMedGoogle Scholar
- Payne RW. Severe outbreak of surgical sepsis due to Staphylococcus aureus of unusual type and origin. BMJ. 1967;4:17–20. DOIPubMedGoogle Scholar
- Allen KD, Anson JJ, Parsons LA, Frost NG. Staff carriage of methicillin-resistant Staphylococcus aureus (EMRSA 15) and the home environment: a case report. J Hosp Infect. 1997;37:74–5.PubMedGoogle Scholar
- Williams REO. Healthy carriage of Staphylococcus aureus: its prevalence and importance. Bacteriol Rev. 1963;27:56–71.PubMedGoogle Scholar
- Haley RW, Bregman DA. The role of understaffing and overcrowding in recurrent outbreaks of staphylococcal infection in a neonatal special-care unit. J Infect Dis. 1982;145:875–85. DOIPubMedGoogle Scholar
- Reagan DR, Doebbeling BN, Pfaller MA, Sheetz CT, Houston AK, Hollis RJ, Elimination of coincident S. aureus nasal and hand carriage with intranasal application of mupirocin calcium ointment. Ann Intern Med. 1991;114:101–6.PubMedGoogle Scholar
- Waldvogel FA. Staphylococcus aureus (including toxic shock syndrome). In: Mandell GL, Bennett JE, Dolin R, editors. Principles and practice of infectious diseases. New York: Churchill Livingston; 1995. p. 1754-77.
- Hamre D, Connelly AP Jr, Procknow JJ. Virologic studies of acute respiratory disease in young adults. Am J Epidemiol. 1966;83:238–49.PubMedGoogle Scholar
- Bassetti S, Bassetti-Wyss B, D'Agostino R, Gwaltney JM, Pfaller MA, Sherertz RJ. "Cloud adults" exist: airborne dispersal of Staphylococcus aureus associated with a rhinovirus infection [Abstract #115]. 38th Annual Meeting of the Infectious Diseases Society of America; Sept 7-10 2000; New Orleans, Louisiana.
- Nichol KP, Cherry JD. Bacterial-viral interrelations in respiratory infections of children. N Engl J Med. 1967;277:667–72. DOIPubMedGoogle Scholar
- Gwaltney JM, Sande MA, Austrian R, Hendley JO. Spread of Streptococcus pneumoniae in families. Relation of transfer of S. pneumoniae to incidence of colds and serum antibody. J Infect Dis. 1975;132:62–8. DOIPubMedGoogle Scholar
- Harrison LH, Armstrong CW, Jenkins SR, Harmon MW, Ajello GW, Miller GB Jr, A cluster of meningococcal disease on a school bus following epidemic influenza. Arch Intern Med. 1991;151:1005–9. DOIPubMedGoogle Scholar
- Gwaltney JM, Hayden FG. The nose and infection. Ed. by. In: Proctor DF, Andersen I, editors. The nose: upper airway physiology and the atomspheric environment. Amsterdam: Elsevier Biomedical Press; 1982. p.399-422.
TablesCite This Article
Table of Contents – Volume 7, Number 2—April 2001
|EID Search Options|
|Advanced Article Search – Search articles by author and/or keyword.|
|Articles by Country Search – Search articles by the topic country.|
|Article Type Search – Search articles by article type and issue.|
Please use the form below to submit correspondence to the authors or contact them at the following address:
Robert J. Sherertz, Department of Internal Medicine, Wake Forest University School of Medicine, Medical Center Boulevard, Winston-Salem, NC 27157-1042; fax: 336-716-3825