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Mark H Reacher a Public
Health Laboratory Service Communicable Disease Surveillance Centre,
London NW9 5EQ, b Antibiotic Resistance Monitoring and Reference Laboratory,
PHLS Central Public Health Laboratory, London NW9 5HT, c Respiratory and Systemic
Infection Laboratory, PHLS Central Public Health Laboratory, d PHLS Antimicrobial
Susceptibility Surveillance Unit, Queen's Medical Centre, Nottingham
NG7 2UH, e PHLS Statistics Unit, London NW9 5EQ, f PHLS Headquarters, London NW9 5DF, g International Medical
Department, SmithKline Beecham, SB House, Brentford, Middlesex TW8 9BD
Correspondence to: M Reacher mreacher{at}phls.nhs.uk
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Abstract |
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Objectives:
Determination of causes, trends, and
antibiotic resistance in reports of bacterial pathogens isolated from
blood in England and Wales from 1990 to 1998.
Culture of blood is a fundamental investigation in infection.
Illness associated with bacteraemia ranges from self limiting infection
to life threatening sepsis that requires rapid and aggressive antimicrobial treatment,1 which is complicated by
increasing antibiotic resistance
worldwide.2-5 Information on trends and antibiotic
resistance in bacteraemia is needed to inform prescribing and infection
control policy and to guide development of new antibiotics and
vaccines.
1 3-7
Since 1989 blood isolates judged to be clinically significant by
microbiologists working in laboratories in England and Wales have been
reported to the Public Health Laboratory Service
Communicable Disease Surveillance Centre; this moved from paper to
electronic transmission with EpiBase8 then
CoSurv.9 Trends in resistance to key antibiotics have been
published for Staphylococcus aureus,
10 11
Streptococcus pneumoniae,12 and
Escherichia coli.13 Here we present the
first overall description of the system and causative organisms with
further information on antibiotic resistance.
Blood isolates reported to the surveillance centre from 1990 to
1998 were entered on a computer database (LabBase).8
Replicate reports were identified by matching on date of birth, sex,
specimen date, organism, antibiotic susceptibility, and source
laboratory and merged if the specimen dates were less than eight days
apart. This was undertaken manually from 1990 to 1994 and then by
computer program.
We identified laboratories in England and Wales that reported
blood isolates to the surveillance centre in 1998 from the Directory of
the Association of Medical Microbiologists.14 Annual total bacteraemias and annual counts for each of 34 "categories" of bacteraemia defined by causative organism15 were analysed
by Poisson regression analysis.16 Categories showing a
year on year proportional increase were further analysed within age
groups. The causes of bacteraemia between age groups were examined.
Trends in the proportion resistant were determined for the subset of reports with a completed antibiotic susceptibility field. Intermediate resistance was recorded in less than 0.7% of reports and was counted as resistance.
Of 229 laboratories identified in England and Wales in the
directory,14 208 (91%) reported blood isolates to the
surveillance centre in 1998. Reports increased from
31 763 in 1990 to 51 232 in 1998 (P<0.05) (fig 1). E coli, Staph
aureus, coagulase negative staphylococci, Strep
pneumoniae, and either Enterococcus species (including E faecium, E faecalis, and
group D streptococci) or Klebsiella
species (fig 1) accounted for 60% of all reports each year. A further
20% comprised either Klebsiella species or
Enterococcus species,
Design:
Description of bacterial isolates from blood, judged to be clinically significant by microbiology staff, reported to
the Communicable Disease Surveillance Centre.
Setting:
Microbiology laboratories in England and Wales.
Subjects:
Patients yielding clinically significant
isolates from blood.
Main outcome measures:
Frequency and Poisson
regression analyses for trend of reported causes of bacteraemia and
proportions of antibiotic resistant isolates.
Results:
There was an upward trend in total numbers of
reports of bacteraemia. The five most cited organisms accounted for
over 60% of reports each year. There was a substantial increase in the
proportion of reports of Staphylococcus aureus resistant to methicillin, Streptococcus pneumoniae resistance to
penicillin and erythromycin, and Enterococcus faecalis
and Enterococcus faecium resistance to vancomycin. No
increase was seen in resistance of Escherichia coli to gentamicin.
Conclusions:
Reports from laboratories provide
valuable information on trends and antibiotic resistance in bacteraemia and show a worrying increase in resistance to important antibiotics.
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Introduction
Top
Abstract
Introduction
Methods
Results
Discussion
References
![]()
Methods
Top
Abstract
Introduction
Methods
Results
Discussion
References
![]()
Results
Top
Abstract
Introduction
Methods
Results
Discussion
References
and non-haemolytic
streptococci (other than pneumococci), and Proteus
species, Enterobacter species, and Pseudomonas
aeruginosa.

View larger version (34K):
[in a new window]
Fig 1.
Incidence of commonly reported causes of
bacteraemia in England and Wales, 1990 to 1998
Poisson regression showed a year on year proportional increase for seven categories (table 1) that was also present within each age group. Haemophilus influenzae declined steeply from 1992. Most reports were from adults but the reporting rate was high in infants: 1149 reports for infants aged 0-28 days and 1169 for infants aged 29 to 365 days in 1998 (table 2).
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Staph aureus was among the top five causes of
bacteraemia in every age group, whereas E
coli, coagulase negative staphylococci, Strep
pneumoniae, and Enterococcus species ranked
lower at certain ages (fig 2).
and non-haemolytic streptococci
(excluding pneumococci) accounted for 5-7% of bacteraemias
in children of all ages and for 2-4% aged over 14 years. Group
B streptococci comprised 22% of reports in infants aged 0 to 28 days,
5% in infants aged 29 days to 1 year, were rare in children aged
between 1 and 14 years (three reports in
1998), but contributed 1-2% in the adult age groups. Neisseria
meningitidis accounted for 11-17% of reports in
age groups from birth to 14 years, 2% from 15 to 44 years, and less than 1% in older age groups. The proportion of reports contributed by each age group to each category of bacteraemia was
similar in every year.
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The subset of reports with completion of the antibiotic
susceptibility field generally declined in 1996 and 1997 and recovered in 1998 (fig 3). Methicillin resistance in Staph aureus
increased from 1.7% to 3.8% from 1990 to 1993, rose steeply
to 32% in 1997 and to 34% in 1998 (fig 3). Gentamicin resistance in
E coli increased from 1.7% in 1990 to 3% in 1997 declining to 2.2% in 1998. Vancomycin resistance in Ent faecium
reached 6.3% in 1993, 20% in 1995, and 24% in 1998. Vancomycin resistance in Ent faecalis was under 3% from
1990 to 1996, increasing to 5% in 1998. Ampicillin resistance, however, was recorded in 15% of Ent faecalis and
ampicillin sensitivity in 17% of Ent faecium reports in
1998, suggesting frequent mis-speciation. Penicillin resistance in
Strep pneumoniae was under 1% in 1990 and 1991, increasing to 3.7% in 1996, to 7.4% in 1997, and 3.6% in 1998. Erythromycin resistance in Strep pneumoniae increased from 5% in 1990 to stabilise at about 11% from 1994 onwards.
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Discussion |
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The number of reports increased yearly; a steep increase between 1996 and 1998 (fig 1) coincided with efforts to encourage reporting, including "free" installation of CoSurv9 into laboratories, but the number bearing data on antimicrobial susceptibility did not increase except for methicillin against Staph aureus (fig 3). This was probably due to problems in the introduction of CoSurv and different degrees of effort in chasing up missing results for each antimicrobial susceptibility. Increased reporting may also have reflected rising incidence due to improved survival of severely ill patients. 17 18
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What is already known on this subject
Bacteraemia series from laboratories and programmes of nosocomial infection surveillance are generally derived from individual or small numbers of institutions The collated data may be unrepresentative of the general population and inferences may lack precision because of the small number of reports The need for representative and precise information on the causes and trends in antibiotic resistance in blood stream infections at national level made an overview of the system desirable at this time What this paper addsOver 90% of laboratories in England and Wales reported clinically significant blood isolates to the communicable disease surveillance centre in 1998, with total reports ranging from about 30 000 in 1990 to 50 000 in 1998 This reporting system probably captures information on a sizeable proportion of episodes of bacteraemia at national level The value of this system for national level monitoring of antibiotic resistance and trends in the causes of bacteraemia has been demonstrated; regional analyses with multivariable methods may prove useful in the future |
The causes of bacteraemia were similar to those seen in other large series.17-19 Categories with a marked upward trend (table 1) are a priority for further research. The trend for Corynebacterium species and diphtheroids may reflect a change from regarding these organisms as skin contaminants to being clinically significant, as occurred for coagulase negative staphylococci.20 Marked increases in Acinetobacter species, Serratia species, Citrobacter species, and Enterobacter species may reflect their facility to develop mutational resistance to cephalosporin antibiotics, which were used increasingly during the survey period. We found no shift to Gram positive organisms as reported elsewhere. 1 17-20 This may have occurred before the study period or be specific to certain patient groups, such as patients with neutropaenia. The fall in H influenzae followed introduction of Hib immunisation in 1992.21
The rise in antibiotic resistance in blood isolates emphasises the
importance of sound hospital infection control,
6 7
rational prescribing policies, and the need for new antimicrobial drugs
and vaccines.3-5 Validation of reported data on
resistance has been undertaken by comparison with centralised testing
of nationally representative sample
strains.13 Regional analyses have been developed for
methicillin against Staph
aureus22 (http://www.phls.co.uk/facts/bact.htm). Further analysis of these data could include the determination of the
independent effect on antibiotic resistance of region, year, age, and
sex by using multivariable methods.16 This national reporting system should complement local surveillance of bacteraemia in
which extensive data on risk factors may be
collected.
23 24
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Acknowledgments |
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We thank the microbiology laboratory staff in England and Wales for reporting isolates to the surveillance centre.
Contributors: MHR designed and coordinated the study, supervised the downloading and analysis of data, and wrote the paper. AS retrieved and processed data. DML advised on the design of the study and reviewed and contributed to writing the paper. MCJW advised on the design of the study and reviewed the paper. CG undertook the statistical analyses. APJ contributed to the design of the project and reviewed the paper. HH advised and assisted in the retrieval of data and reviewed the paper. MAM and KFB developed the routine bacteraemia reporting system, which provided the framework for this paper, and each reviewed the paper. DJ monitored the completeness of antibiotic susceptibility reporting and chased up missing data. RCG advised on design of the project and reviewed the paper. MHR, DML, and HH are guarantors for the paper.
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Footnotes |
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Funding: Public Health Laboratory Service.
Competing interests: None declared.
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References |
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(Accepted 5 November 1999)
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