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The risks to healthcare workers are very low
Although Neisseria meningitidis is a
relatively uncommon cause of overt infection (2580 notifications in
1998),1 the horrors of its clinical presentation have
stimulated intense media interest, particularly after outbreaks. With
the disappearance of many infectious competitors in the latter half of
this century, meningococcal disease has become the leading infectious
cause of death in childhood and is now the third most common cause of
death in children outside infancy (after accidents and
malignancy).2 The introduction in October 1999 of a
serogroup C protein-polysaccharide conjugate vaccine for children and
young adults has the potential to reduce significantly the incidence of
disease.3 Nevertheless, most cases are caused by serogroup
B meningococci, for which no vaccine is available, and the disease will
remain prevalent in the United Kingdom. As a result of the dramatic
presentation of cases and the high fatality rate the perceived risk of
meningococcal disease is high among those who have had contact with a case.
Close contact with nasopharyngeal secretions from a case is necessary
for transmission. Therefore secondary attack rates (increased risk
relative to the general population) are as high as 1200 in household
contacts, 160 in secondary schools, 60 in primary schools, and 1.8 in
universities in the days after presentation of the index
case.4 Despite the perceived risk, however, only a few cases arise from contact with a case and only 0.5% of all cases are
associated with family contacts.5
A few healthcare workers have very close contact with a patient
suffering from meningococcal disease during assessment, resuscitation, and stabilisation. The nasopharynx of patients with meningococcal disease often contains viable organisms at presentation, even after
antibiotic therapy in the community with penicillin.6 Although the fears of healthcare workers might seem justified, few
published reports exist of healthcare workers
7 8
or
laboratory staff
9 10
developing invasive meningococcal
disease. However, a recent report from France again highlights this
issue: a paediatrician developed meningococcaemia a week after she
intubated a comatose child with meningococcal disease.11
Doctors, nurses, and paramedics who are directly exposed to
nasopharyngeal secretions or pulmonary oedema from such patients, mainly during airway management (mouth to mouth resuscitation, intubation, and airway toilet), may therefore be at some increased risk
of meningococcal disease. Current guidelines in the United Kingdom
advise offering antibiotic chemoprophylaxis only to those undertaking
mouth to mouth resuscitation.12 In the United States chemoprophylaxis is recommended for healthcare workers who have had
"intensive unprotected contact (without wearing a mask) with infected
patients (eg intubating, resuscitating, or closely examining the
oropharynx of patients)."13
The risk of transmission and disease for healthcare workers with
close contact to airway secretions has not been quantified but is
probably very low, and this risk should be further reduced after
antibiotic chemoprophylaxis. Other healthcare workers who are not
directly exposed to nasopharyngeal secretions but otherwise care
for the patient are at negligible risk. However, these individuals may
be highly concerned, particularly after presentation of a fulminant
case. Local consultants in communicable disease provide a valuable role
in assessing and explaining the relative risks and the place of
antibiotic chemoprophylaxis in this situation.
In the United Kingdom chemoprophylaxis with rifampicin, ciprofloxacin,
or ceftriaxone is currently offered for household and kissing contacts
of patients with meningococcal infection and for healthcare workers
undertaking mouth to mouth resuscitation12 and is
effective in reducing carriage.14 The offer of antibiotic chemoprophylaxis should be extended to all healthcare workers in the
United Kingdom who have direct exposure to nasopharyngeal secretions
from a patient with meningococcal infection. The aim of such
chemoprophylaxis is to prevent colonisation in recently exposed
healthcare workers and thereby reduce the risk of disease, both in the
recipients of chemoprophylaxis and in their close contacts.
Chemoprophylaxis is not completely effective in preventing disease,15 so individuals with significant exposure should
be advised of the symptoms of the disease.
Ideally, healthcare and laboratory workers who are at occupational risk
of exposure to N meningitidis would be offered vaccination, although the number of cases prevented by such a strategy would be very
small. The risk of disease in healthcare workers will be reduced even
further as the vaccines now available in the United Kingdom reduce
hospital admissions for serogroup C disease. Vaccines for large scale
prevention of the more prevalent serogroup B strains are not yet
available, although early trials in laboratory workers have
demonstrated immunogenicity.16
Until the arrival of new vaccines offers the hope of real protection,
antibiotics should be offered to healthcare workers with direct
exposure to potentially infected secretions. Those who are afraid
of contracting the disease but are not at risk can be reassured.
Division of Infectious Diseases and Immunology, British
Columbia's Children's Hospital and British Columbia Research
Institute for Children's and Women's Health, Vancouver, BC V5Z 4H4,
Canada (ajpollard{at}compuserve.com) PHLS Communicable Disease Surveillance Centre, London NW9
5EQ
Norman Begg
| 1. | Notifications of Infectious Diseases. Comm Dis Rep 1999; 9: 21. |
| 2. | 1995 Communicable disease statistics. London: Office of National Statistics, 1997. |
| 3. | Donaldson L, Moores Y, Howe J. Introduction of immunisation against group C meningococcal infection. London: Department of Health, 1999:1-6. |
| 4. | Hastings L, Stuart J, Andrews N, Begg N. A retrospective survey of clusters of meningococcal disease in England and Wales, 1993 to 1995: estimated risks of further cases in household and educational settings. Commun Dis Rep CDR Rev 1997; 7: R195-R200[Medline]. |
| 5. | Cooke RP, Riordan T, Jones DM, Painter MJ. Secondary cases of meningococcal infection among close family and household contacts in England and Wales, 1984-7. BMJ 1989; 298: 555-558. |
| 6. | Cartwright K, Reilly S, White D, Stuart J. Early treatment with parenteral penicillin in meningococcal disease. BMJ 1992; 305: 143-147. |
| 7. | Feldman HA. Some recollections of the meningococcal diseases. JAMA 1972; 220: 1107-1112[Medline]. |
| 8. |
Nosocomial meningococcemia Wisconsin.
MMWR
1978;
27:
358-363.
|
| 9. |
Guibourdenche M, Darchis JP, Boisivon A, Collatz E, Riou JY.
Enzyme electrophoresis, sero- and subtyping, and outer membrane protein characterization of two Neisseria meningitidis strains involved in laboratory-acquired infections.
J Clin Microbiol
1994;
32:
701-704 |
| 10. |
Paradis JF, Grimard D.
Laboratory-acquired invasive meningococcus Quebec.
Can Commun Dis Rep
1994;
20:
12-14[Medline].
|
| 11. | Gehanno J-F, Kohen-Couderc L, Lemeland J-F, Leroy J. Nosocomial meningococcemia in a physician. Infect Control Hosp Epidemiol 1999; 20: 564-565[Medline]. |
| 12. | Control of meningococcal disease: guidance for consultants in communicable disease control. PHLS Meningococcal Infections Working Group and Public Health Medicine Environmental Group. Commun Dis Rep CDR Rev 1995; 5: R189-R195[Medline]. |
| 13. | Immunization of healthcare workers: recommendations of the advisory committee on immunization practices (ACIP) and the hospital infection control practices advisory committee (HICPAC). MMWR 1997; 46: 1-42[Medline]. |
| 14. | Cartwright KA, Stuart JM, Robinson PM. Meningococcal carriage in close contacts of cases. Epidemiol Infect 1991; 106: 133-141[Medline]. |
| 15. | Cartwright KA, Hunt D, Fox A. Chemoprophylaxis fails to prevent a second case of meningococcal disease in a day nursery. Commun Dis Rep CDR Rev 1995; 5: R199[Medline]. |
| 16. | Fischer M, Carlone GM, Holst J, Williams D, Stephens DS, Perkins BA. Neisseria meningitidis serogroup B outer membrane vesicle vaccine in adults with occupational risk for meningococcal disease. Vaccine 1999; 17: 2377-2383[Medline]. |
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