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N W Preston

Publications and source records attributed to N W Preston.

At least 19 recordsLinked to original sources

Current pharmacotherapy of pertussis.

Human infection with Bordetella pertussis and Bordetella parapertussis causes significant morbidity and mortality. While universal immunisation represents the mainstay of prevention, the purpose of this review is to summarise the current options for antimicrobial chemotherapy of pertussis. Several chemotherapeutic approaches have an important place in therapy and in infection control. Supportive treatment including nasopharyngeal suction, oxygen and parenteral fluids, is essential for infants < 1 year who are at greatest risk of complications and permanent sequelae. Steroids and beta2-agonists are also used in the management of severe neonatal pertussis. Several antibiotics have been shown to reduce the level of bacterial colonisation of the respiratory tract, however, erythromycin is accepted to be the treatment of choice. Erythromycin reduces severity and duration of disease, even if started during the paroxysmal phase. A 14 day course is recommended although side effects may limit compliance; a recent study indicates that a 7 day course may have similar efficacy in terms of eradication and prevention of relapse. Alternatives to erythromycin are clarithromycin, azithromycin and trimethoprim-sulfamethoxazole. Fluoroquinolones have good in vitro activity against both B. pertussis and B. parapertussis and may be useful in the treatment of adult patients with pertussis, although there are no supporting clinical data at present. Erythromycin prophylaxis is also recommended for close household contacts of patients with pertussis.

Animals↗

Application of pulsed field gel electrophoresis to the 1993 epidemic of whooping cough in the UK.

The purpose of this study was to DNA fingerprint the majority (64%) of isolates received at the Pertussis Reference Laboratory during the 1993 whooping cough epidemic by pulsed field gel electrophoresis of Xba I-generated restriction digests. Two DNA restriction patterns, types 1 and 3, predominated (40% and 23%, respectively, of 180 isolates) but type 2, identified in a previous study was notably absent. Twenty-one new DNA types occurred (24% of isolates), some being atypical as bands 155-230 kb were no longer conserved, but there was no statistically significant difference in their incidence in the upswing (June-September) compared to the downswing (October-December) phase of the epidemic. There was a relatively high proportion of new types, compared to type 1, at the peak (September). About 50% of isolates received were from the North Western Region, where 44% of isolates were DNA type 1. Whereas only 1 out of 10 isolates from Scotland were of this type, suggesting some geographic variation. Statistically significant findings included a higher proportion of isolates from female patients (P < 0.01), most marked in the 12-24 months age group (P < 0.05); a higher proportion of infants under 12 months requiring hospital admission compared to older children (P < 0.05); and a greater number of isolates from unvaccinated children (P < 0.01). Analysis of serotype according to four age groups (under 3 months, 3-12 months, 12-24 months and above 2 years) showed statistically significant differences (P < 0.05) with a noticeably lower proportion (38%) of serotype 1,3 in 3-12 months age group and higher prevalence (74%) of serotype 1,3 in the 12-24 months age group. There was no correlation between DNA type and serotype.

Age Factors↗

Cholera treatment.

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Administration, Oral↗