![Infectious Diseases News Brief](/web/20061210212101im_/http://www.phac-aspc.gc.ca/bid-bmi/dsd-dsm/nb-ab/gfx/idnb_e.gif)
First Recurrence of Clostridium difficile-Associated Disease (CDAD):
Quebec (2003-2004)
During an epidemic of CDAD caused by a strain that is a hyper-producer
of toxins A and B, the frequency of a first recurrence after metronidazole
treatment of the initial episode doubled in 2003-2004, compared with 1991-2002.
To examine whether administration of metronidazole as treatment for a
first recurrence of CDAD remained appropriate, data for patients with
CDAD diagnosed in a hospital in Quebec, during 1991-2005, who experienced
a first recurrence was reviewed. A total of 463 patients had a first recurrence
of CDAD, of whom 154 (33.3%) experienced a second recurrence. Independent
predictors of a second recurrence were age and duration of hospitalization
after the first recurrence; this latter finding suggested that many such
episodes were reinfections rather than relapses. Neither choice of treatment
drug (metronidazole or vancomycin) nor use of the same drug for treatment
of first recurrence, as had been used during the initial episode, was
associated with increased risk of a second recurrence. However, 51 patients
(11.0%) developed at least 1 complication during the first recurrence.
Older age, a high leukocyte count, and renal failure at first recurrence
were strongly associated with a complicated CDAD. Metronidazole is not
inferior to vancomycin for treatment of patients with a first recurrence
of CDAD, but the risk of complications with any treatment of CDAD may
be higher than has previously been documented.
Source: Clinical Infectious Diseases, Volume 42, Number 6, 15 March 2006
Pertussis Vaccine: Quebec
The goal of pertussis control in Canada is to reduce the morbidity and
mortality of pertussis across the entire lifespan. In 2003, the National
Advisory Committee on Immunization (NACI) recommended administering
a single dose of the adolescent/adult formulation of acellular pertussis
vaccine to preadolescents and adolescents who have not received a dose
of acellular vaccine. In 2004, the Quebec Department of Health and Social
Services introduced the combined diphtheria-tetanus-acellular pertussis
(dTap) vaccine to replace the diphtheria-tetanus vaccine ( d2T5) given
as a booster to adolescents. The Canadian Immunization Guide recommends
that d2T5 not be administered < 5 years after the last dose of the
same vaccine, because the occurrence of adverse events is higher when
repeated doses are given at close intervals. There was reason to anticipate
the same phenomenon when dTap was administered < 5 years after a
previous vaccinations with d2T5. When cases of pertussis occurred in
Montreal high schools, it was decided that the benefit of protection
against pertussis was greater than the risk of adverse events following
the second vaccination. The dTap vaccine was offered to 1,367 high school
students, whether they had previously received d2T5 or not. School nurses
vaccinated 839 students, or 61% of the total. Follow-up to these vaccinations
made it possible to compare the occurrence of vaccine adverse events
in relation to the time that had elapsed since the last dose of d2T5
vaccine. These data on a total of 465 individuals suggest that previous
vaccination with d2T5 does not increase the risk of local reaction at
the injection site following vaccination with dTap. These results are
consistent with recent results from the Yukon and Prince Edward Island.
The reported adverse events and their severity are consistent with those
described as common in the Protocole d'immunisation du Québec
in cases where the vaccine is administered after an interval of > 5
years. In conlusion, the data in this study do not suggest any increase
in vaccine adverse events when dTap is administered to an adolescent
who has recently been vaccinated with d2T5.
Source: Canada Communicable Disease Report, Volume 32, Number 3, 3 February
2006
Pneumoccocal Vaccine: United Kingdom
The Department of Health has introduced pneumococcal vaccine to its childhood
immunization schedule. The vaccine is being added to the schedule at
2, 4, and 13 months. There are around 5000 cases of invasive pneumococcal
disease in England and Wales each year, around 530 of these in children < 2
years of age. Since the introduction of a similar programme in the United
States, cases in young children caused by the strains in the vaccine
have fallen by 94%, and cases in the over 65s have dropped by two thirds.
Source: Communicable Disease Weekly, Volume 16, Number 6, 9 February 2006
The details given are for information only and may be very provisional. Where incidents are considered of national importance and are ongoing, the initial report will be updated as new information becomes available.
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