Skip directly to site content Skip directly to page options Skip directly to A-Z link Skip directly to A-Z link Skip directly to A-Z link
Volume 10, Number 10—October 2004
Research

Epidemiology and Cost of Nosocomial Gastroenteritis, Avon, England, 2002–2003

Article Metrics
193
citations of this article
EID Journal Metrics on Scopus
Author affiliations: *Health Protection Agency, London, UK; †Health Protection Agency, Bristol, UK; ‡United Bristol Healthcare Trust, Bristol, UK; §North Bristol NHS Trust, Bristol, UK; ¶Royal United Hospital Bath NHS Trust, Bath, UK

Cite This Article

Abstract

Healthcare-associated outbreaks of gastroenteritis are an increasingly recognized problem, but detailed knowledge of the epidemiology of these events is lacking. We actively monitored three hospital systems in England for outbreaks of gastroenteritis in 2002 to 2003. A total of 2,154 patients (2.21 cases/1,000-hospital-days) and 1,360 healthcare staff (0.47 cases/1,000-hospital-days) were affected in 227 unit outbreaks (1.33 outbreaks/unit-year). Norovirus, detected in 63% of outbreaks, was the predominant etiologic agent. Restricting new admissions to affected units resulted in 5,443 lost bed-days. The cost of bed-days lost plus staff absence was calculated to be £635,000 (U.S.$ 1.01 million) per 1,000 beds. By our extrapolation, gastroenteritis outbreaks likely cost the English National Health Service £115 (U.S.$ 184) million in 2002 to 2003. Outbreaks were contained faster (7.9 vs. 15.4 days, p = 0.0023) when units were rapidly closed to new admissions (<4 days). Implementing control measures rapidly may be effective in controlling outbreaks.

Nosocomial gastroenteritis outbreaks, particularly those caused by noroviruses, have become increasingly important in Europe (1) and North America and have attracted media interest (24). However, unlike bloodstream, surgical-site, respiratory, skin, and urinary tract infections, tools for detecting and measuring hospital-associated gastroenteritis outbreaks have not been well developed, thus precluding accurate measurement of incidence and cost of these infections (58).

In England and Wales, the Health Protection Agency Communicable Disease Surveillance Centre has operated a passive surveillance system for gastroenteritis outbreaks. From 1992 to 2000, information was collected on >5,000 outbreaks, 27% of which occurred in hospitals and 28% in residential facilities, primarily nursing homes (1,3). Of these outbreaks, >50% were caused by norovirus and 25% were presumed viral on the basis of clinical signs and symptoms and outbreak characteristics, including high frequency of vomiting, short duration of illness, and short incubation period (1). Particular patterns of transmission have been observed in the outbreaks in healthcare facilities, in which economic effects are likely to be considerable (3).

Because noroviruses are the most common cause of gastroenteritis in the community (9), keeping the virus from being introduced into healthcare settings is difficult, particularly in winter months. For this reason, control measures focus on minimizing the spread of virus within and between hospital units (10). Closing a unit to new patient admissions, excluding affected staff from work for 48 hours postrecovery, and rigorous disinfection are the key features of current control guidelines.

Studies have reported that annually 20%–25% of the population has gastroenteritis (11); however, these surveys excluded persons in healthcare facilities (9). Although many hospital outbreaks of gastroenteritis have been described (1214), information from systematic, population-based surveillance of gastroenteritis in healthcare settings is lacking (10).

We performed active surveillance of hospital outbreaks of gastroenteritis to determine incidence, microbiologic cause, economic cost, and effectiveness of control measures in the county of Avon, England, an area likely to be broadly representative of England as a whole.

Methods

Surveillance System
Clinical Definitions

Figure 1

Thumbnail of Definition of an outbreak of gastroenteritis in healthcare settings.

Figure 1. Definition of an outbreak of gastroenteritis in healthcare settings.

Since this surveillance system is designed for detecting outbreaks of gastroenteritis, a two-tiered definition (of cases and outbreaks) was required (Figure 1). These definitions, which draw on Kaplan’s criteria of an outbreak of viral gastroenteritis (15), were developed in consultation with public health professionals at all levels of infection control. Ethical approval for this work was obtained from the South West Multi-centre Research Ethics Committee.

Study Population

Gastroenteritis, particularly of viral etiology, is inconsistently reported (16). The county of Avon, England, was selected to focus efforts on collecting complete, high-quality data. The all-cause, age-standardized death rate, and deprivation measures and age distribution indicate that the population of Avon is very similar to that of the whole of England and Wales (http://www.avon.nhs.uk).

Three National Health Service administrations (known as NHS Trusts), comprising four major acute hospitals (similar to secondary/tertiary hospitals in the United States) and 11 smaller community hospitals (similar to primary-level hospitals in the United States) that operate in the sentinel area, were monitored under the surveillance network. Combined, these hospitals have 2,900 inpatient beds, which, on average, maintain 95.6% occupancy of their acute-care beds. In total, 171 “functional care units” were monitored; these units were defined as a room area or ward regarded as a self-contained area that monitored 171 inpatients. The median number of beds on an inpatient unit was 20 (range 1–38), which reflects the large size of units in NHS hospitals compared to those in many other European or North American designs.

Nursing, medical, and other staff members were included in the population at risk. Time-at-risk for staff members was collected from whole-time equivalent staffing levels supplied by human resources departments. Time-at-risk for patients was calculated by using bed occupancy data from the administration system.

Surveillance and Outbreak Investigation

Each NHS Trust has an infection control team that includes a medically trained microbiologist, a senior infection control nurse, and a team of dedicated infection control nurses. A total of 11 infection control nurses worked at the three trusts. Infection control nurses were responsible for monitoring the populations in their hospitals. Infection control nurses became aware of outbreaks during ward rounds or were alerted to incidents by nurses working on wards. When an event occurred that met the definition of an outbreak (Figure 1), institutions were requested to contact the study coordinator at the Health Protection Agency in Colindale, London. The study coordinator was responsible for ensuring completeness of reports, overseeing data entry, and performing analyses. The study coordinator also solicited monthly null reports in months that no outbreaks were reported in order to confirm that no outbreaks occurred.

Sampling and Diagnostics

Staff members who managed outbreaks were asked to take specimens from the first 10 patients in an outbreak for virologic analysis and from the first 3 patients for bacterial analysis. Such a large number was suggested because of the low sensitivity of viral diagnostics (17). Fecal specimens were preferred, but vomit samples were also accepted for virologic testing. Explicit instructions, based on the Health Protection Agency standard operating procedure (18,19), about taking and sending the samples, were provided. Specimens were tested for viral pathogens at the regional public health laboratory. Specimens were first screened with an in-house enzyme-linked immunosorbent assay (ELISA), followed by reverse transcription-polymerase chain reaction (RT-PCR) for detection of norovirus (20,21).

Outbreak Data

Case forms and an outbreak summary form were completed by infection control nurses as an outbreak progressed. Forms were returned by mail shortly after an outbreak ended. The duration of an outbreak was calculated as the number of days from the onset of the first case to the onset of the last case.

Statistical Analysis

Data were entered and stored in an Access (Microsoft, Redmond, WA) database. Analyses were performed on Microsoft Excel and Stata 8.0 (22). The t-test was used to compare means; the χ2 test was used to compare proportions. Continuous data were analyzed with linear regression. Spearman rank test was used to assess correlation of seasonal patterns.

Economic Analysis

The National Health Service of England is a socialized healthcare system. Funding originates from taxpayer money and is distributed by the Department of Health. Resources are allocated to Primary Care Trusts, which commission hospital services from NHS Hospital Trusts (23). Allocations are based on the age distribution of the population served by the hospitals, with adjustments made for maternal needs, mental health, and ambulatory needs of the population (24). Thus, funding is not directly based on the services provided. If healthcare provision is disrupted by an avoidable event, such as hospital-acquired infection, the allocated resources are not used optimally. In other words, opportunity costs (the difference between actual performance of an investment and the optimum expected outcome) are incurred.

We analyzed the opportunity costs of nosocomial gastroenteritis outbreaks to the healthcare service and lost productivity of patients (and the families of pediatric patients). Bed-day loss from new admission restriction for affected units and staff absence from illness were estimated as the two main costs related to gastroenteritis outbreaks in hospitals. Other possible economic effects may include cancelled operations, overuse of beds caused by delayed discharge, additional cleaning procedures, and increased drug prescribing. However, these costs are probably limited, since the illness is relatively short-lived, cleaning is a relatively minor expense, and no treatment is available for viral gastroenteritis except rehydration. We also estimated the societal cost of lost productivity from missed days of work. Intangible costs, such as pain and psychological distress from delayed or cancelled operations and admissions, which are difficult to quantify (25), were not calculated.

Figures from the Unit Costs of Health and Social Care 2002 report were used to estimate the economic loss from empty beds and staff absence (26). Average wage estimates for England were obtained from the Office of National Statistics (27). All costs are in Great British pounds (2002) and converted to U.S. dollars at the rate of £1: $1.6, based on the 5-year average 1999–2003 (http://www.forexdirectory.net/home.html).

For economic estimates, the following assumptions were made. Staff members were, on average, grade E nurses, the mid-range of NHS nursing staff. This figure is probably an underestimate of cost since medical staff, who have higher wages, were also affected in outbreaks. A lost bed-day is a real economic loss in terms of opportunity cost. Since these trusts operate at >95% occupancy of inpatient beds, the result is bed-days lost because the bed would likely have been used. These expenditures cannot be reallocated since infection control guidelines stipulate that staff members from affected units are not to work on unaffected units, and patients from affected units are not to be transferred to unaffected units (10).

Patients of working age (18–64 for men and 18–59 for women) and one family member of each pediatric patient (<18 years) were assumed to be economically active. We assumed that 5 of 7 days of work were missed for each day of illness in these categories. This figure is an overestimate since many days of hospital-acquired gastroenteritis illness would have been spent in the hospital whether the person acquired gastroenteritis or not. Individual length-of-stay data were not available. Hospital staff absence was considered a cost to the healthcare sector, rather than society.

Results

Outbreaks, Cases, and Incidence

Figure 2

Thumbnail of Monthly outbreaks of gastroenteritis in hospitals: Avon, England, April 2002–March 2003 (n = 227).

Figure 2. Monthly outbreaks of gastroenteritis in hospitals: Avon, England, April 2002–March 2003 (n = 227).

Figure 3

Thumbnail of Monthly distribution of outbreaks with diagnostic results (n = 122). Negative outbreaks followed a similar seasonal pattern to norovirus outbreaks. u, unconfirmed (only one positive specimen).

Figure 3. Monthly distribution of outbreaks with diagnostic results (n = 122). Negative outbreaks followed a similar seasonal pattern to norovirus outbreaks. u, unconfirmed (only one positive specimen).

In the 171 inpatient units followed, a total of 227 outbreaks occurred; the outbreak incidence was 1.33 outbreaks per unit-year of risk (95% confidence interval [CI] 1.16–1.51) (Figures 2 and 3). All enrolled hospital trusts were affected by outbreaks. Hospital outbreaks peaked in November, with 46 affected units. A smaller peak occurred July, with 22 outbreaks.

Within the 227 outbreaks, 2,154 hospital patients and 1,360 hospital staff met the case definition. The incidence among patients was 2.21 cases per 1,000 hospital-days at risk (95% CI 2.16–2.25) and among staff was 0.47 cases per 1,000 hospital-days at risk (95% CI 0.45–0.50). Units with outbreaks were significantly larger than those that did not have an outbreak in the study period (21.4 vs. 12.6, p value < 0.0001, t-test).

Diagnostic Results

Specimens were taken for diagnostic analyses in 122 (51%) of the 227 hospital unit outbreaks (Table 1). Norovirus was the confirmed etiologic agent in 61 outbreaks (50%) and was detected in a single specimen in 16 outbreaks (13%). The second most prevalent organism was Clostridium difficile, which was confirmed in nine outbreaks (7%) and detected in a single sample in eight outbreaks (6.5%). Six outbreaks (4.9%) occurred in which both norovirus and C. difficile were detected. Rotavirus and Campylobacter outbreaks were also detected. Outbreaks from which all specimens were negative for rotavirus and Campylobacter (n = 31, 25%) had a similar seasonal pattern to norovirus outbreaks (p = 0.13, Spearman rank test) (Figure 3). The monthly distribution of outbreaks in which no specimens were taken correlated with the monthly distribution of norovirus-confirmed outbreaks.

Attack Rates within Outbreaks

In hospital outbreaks, attack rates among staff members (staff affected/staff working on unit: 19.6%, 95% CI 16.6%–22.7%) were significantly lower than those of patients (patients affected/unit beds: 46.8%, 95% CI 40.9%–52.8%) (p < 0.001, t-test). In outbreaks in which norovirus was the confirmed etiologic agent, attack rates were somewhat higher than all outbreaks at 24.5% for staff (95% CI 17.8%–31.2%) and 53.2% for patients (95% CI 41.5%–65.0%), although not significantly so. Attack rates among staff were not higher in the first outbreak (20.6%; 95% CI 16.4%–25.0%) compared to subsequent outbreaks that occurred in the same unit (21.5%; 95% CI 17.2–25.9) (p = 0.8; t-test).

Closing Units to New Admissions and Bed-Day Loss

One hundred and fifty-eight (69.6%) of the 227 hospital unit outbreaks resulted in the affected unit’s being closed to new admissions (Table 2). Outbreaks in which norovirus was detected did not result in unit closure to new admissions more frequently than outbreaks in which diagnostic results were negative (71.3% compared to 70.6%, respectively) (p = 0.9, χ2 test).

Units were closed for a mean of 9.65 (95% CI 8.5–10.8) days, but in the most extreme example, a unit was closed to new admissions for 48 days because of a single outbreak. On average, 3.57 (95% CI 1.86–5.2) bed-days were lost for every day of unit closure to new admissions, which resulted in an estimated 5,443 bed-days lost from gastroenteritis outbreaks.

Economic Loss

Unit closures to new admissions were distributed among unit type specialties (Table 3). The cost of empty beds to the three hospitals was £1.49 million (U.S.$ 2.24 million) or approximately £480,000 (U.S.$ 768,000) per 1,000 beds.

Costs associated with staff absence were calculated as shown in Table 4. A total of 1,360 infections were in staff members; mean duration of illness was 2.4 days. Hospital staff members were advised not to work for 2 days after recovering from gastrointestinal illness (10). If the staff members work 5 days a week, an estimated 3.14 days of work were missed because of illness [(2.4 days ill + 2 days absence postrecovery) x (5 working days/7 days)]. The cost of one day absence was £113 (U.S.$ 181); therefore, outbreaks cost £482,000 (U.S.$ 771) or £156,000 (U.S.$ 249,000) per 1,000 beds. Total cost of bed-day loss and staff absence was £1.97 million (U.S.$ 3.15 million), or £635,000 million (U.S.$ 1.01 million) per 1,000 beds.

A total of 971 days of illness occurred among working age men (433 days), working age women (241 days), and children <18 years of age (297 days). Therefore, 139 (971/5 x 5/7) 5-day work weeks were potentially lost. At £476 (U.S.$ 761) per week, total productivity loss is estimated to be £66,000 (U.S.$ 106,000) or £22,700 (U.S.$ 36,400) per 1,000 beds.

Restricting New Admissions

Information about unit closure was available for 52 (85%) of the 61 norovirus-confirmed outbreaks. Forty-nine (94%) of these outbreaks resulted in the unit’s being closed to new admissions, but only 7 (13.7%) were closed within 3 days of the date of onset of the primary case. Outbreaks in which the affected unit was closed within the first 3 days were contained in a mean 7.9 days (95% CI 4.3–11.5); outbreaks in units that were not closed or were closed >3 days after the first case lasted for a mean of 15.4 days (95% CI: 13.6–17.3) (p value = 0.002, t-test). Although not reaching levels of statistical significance, the attack rates for patients (0.52 compared to 0.68, p = 0.38), staff members (0.14 compared to 0.27, p = 0.21), and all cases (16.3 compared to 23.7, p = 0.065) all increased if the unit was not shut within 3 days. Units closed within 3 days of outbreak were not different from other units in terms of size, according to linear regression models. Unit size and specialty did not affect the estimated cost of closing the unit to new admissions.

Discussion

In our study, the first published systematic assessment of healthcare-associated gastroenteritis outbreaks (primarily caused by noroviruses), we have demonstrated the cost of such outbreaks. On average, each hospital unit (or ward) had 1.33 outbreaks in the 1-year follow-up period. To control the spread of disease as recommended in national guidelines (10), 158 of the 227 outbreaks resulted in closing the unit to new admissions. This closure resulted in 5,443 lost bed-days, ≈0.5% of all available acute bed-days. This bed loss, combined with staff absence, cost an estimated £635,000 (U.S.$ 1.01 million) per 1,000 beds. The measures taken to control the outbreak are costly, but these data indicate that they may be effective in controlling the duration of an outbreak. Units closed within the first 3 days of an outbreak are contained faster than those not closed or closed after day 4 (7.9 vs. 15.4 days; p = 0.002).

The incidence rates in hospital patients and hospital staff were determined to be 2.21 and 0.47 cases per 1,000 hospital-days of risk, respectively. In other words, a patient who spent a year in the hospital would have an 80% chance of having a case of gastroenteritis during an outbreak. This estimate translates to a 1.5% chance for the average inpatient length of stay (≈7 days). Full-time hospital staff members had a 17% chance of being affected during the year of follow-up. Norovirus was the predominant etiologic agent detected in 63% of hospital unit outbreaks.

The strength of this study and the high quality of data collected were due to the active and systematic approach. The definitions were designed to ascertain outbreaks by using a clear designation of the spatial boundaries. Thus, if infection spread from one unit to another, the events were counted as two separate outbreaks. However, the role of sporadic gastroenteritis in healthcare settings was not assessed in this study. The study team applied standard case and outbreak definitions. Null reporting was used on a monthly basis to confirm that an outbreak had not occurred when none was reported. The full range of modern diagnostics for viral gastroenteritis, including ELISA and RT-PCR assays, was used. However, even using these tests, viral pathogens are not always identified (17). The seasonal pattern of outbreaks in which all specimens were negative in this study suggests that many may also have been caused by noroviruses.

In 2002, norovirus epidemics occurred in the United States, England, Wales, and the rest of Europe (28,29), raising the question: Are the figures reported here representative or the product of an anomalous year? For this reason, this surveillance will continue in forthcoming years to determine whether the cost of the 2002–2003 season is characteristic or not.

Noroviruses are the predominant agent for outbreaks of gastroenteritis in healthcare settings, a finding that is consistent with previous studies from the United States (4), Sweden (30), and historical surveillance data from England and Wales (1,3). However, our study extends these etiologic studies by determining the economic cost of gastroenteritis outbreaks and incidence rates in a defined population. The rates of infection were highest in children and the elderly (31). We could not assess whether length of stay was directly affected by hospital-acquired gastroenteritis or whether death rates increased, since these data were not available.

At U.S.$ 1 million per 1,000 beds, the direct costs to the health sector are substantial and outweigh the indirect cost of lost productivity (overestimated to be U.S.$ 36,400 per 1,000 beds.) This proportional cost to health service is largely because of the age distribution of hospital populations that were affected: <20% of patients were pediatric patients or economically active. Other healthcare sector costs, such as cancelled operations, bed blocking from delayed discharge, additional cleaning procedures, and increased drug prescribing, could be estimated in future studies. However, these costs are probably limited since the illness is relatively short-lived, cleaning is a relatively minor expense, and viral gastroenteritis has no treatment except rehydration. For these reasons, the indirect cost of nosocomial gastroenteritis outbreaks in the community at large are probably small compared to the indirect cost of other hospital-acquired infections that can require postdischarge treatment. However, these results demonstrate the direct effect of nosocomial gastroenteritis outbreaks on healthcare.

“Cost per bed-day” is a broad measure derived from the total net revenue expenditure divided by the total number of inpatient days (26). Thus, cost per bed-day includes overhead expenses, medical and nursing staff payroll, and equipment and treatment costs. U.K. guidelines stipulate that staff members or patients (ill or well) from affected units are to be excluded from unaffected units (10). In other words, as a measure to control further spread, reallocation of resources is prohibited by the guidelines. This restriction can be seen in terms of opportunity cost or a reduction from maximum efficiency. For example, although staff members who are not ill remain at work, they cannot be assigned to other units. Thus, when beds become empty, new admissions are restricted, and nursing services will not be used at maximum efficiency. The quantity of care will decrease, and the resources allocated towards such care will not decline.

Hospital-acquired infections have been estimated to cost the NHS £930 million (U.S. $1,488 million) annually (32). If these costs are distributed evenly across the NHS, hospital-acquired infections would cost the three NHS Trusts (1.7% of all beds in the United Kingdom) in this study £16 million (U.S.$ 25.6 million). Our study suggests that gastroenteritis outbreaks account for 12.5% of that cost, and similar to urinary tract infections, are the most costly healthcare-acquired infection to NHS (32), costing £115 million (U.S.$ 184 million) or ≈1% of the total inpatient services budget. Attributing costs to healthcare-acquired infections is complex, particularly in the case of gastroenteritis outbreaks, because little of the added expense will go directly toward the affected patient.

Not admitting susceptible patients is an effective means of containing nosocomial norovirus outbreaks. Recognizing outbreaks of viral gastroenteritis in hospitals can be difficult because of the high frequency of incontinence and other causes of gastroenteritis, such as antimicrobial-associated diarrhea. ELISA diagnostic kits facilitate rapid diagnosis of norovirus infections (17). Hospital infection control teams should be encouraged to take fecal samples from patients with suspected cases of viral gastroenteritis and to seek diagnoses. A positive confirmation of norovirus should result in immediate restriction of new admissions to the affected unit. Our data suggest that this restriction can be achieved within 3 days of diagnosis of the first case, approximately 1 week of the outbreak’s duration can be prevented.

High levels of bed occupancy, the large size of care units, and lack of isolation units in NHS hospitals may make them particularly vulnerable to norovirus outbreaks. Cohorting affected patients is difficult in English hospitals. Units are large (median 20 beds, in this study) and occupancy is very high (>95%), so patients are not easily maneuvered. Policies, procedures, and building design may have major effects on transmission of these infections and should be explored by epidemic modeling, institutional clinical trials, and international studies that analyze the effect of the environment. Thus, our cost estimates are specific to the context of the English NHS. A hospital system that operated at a lower bed-occupancy level or those with smaller numbers of beds per unit may be able to provide nursing care to affected patients, with minimal effect on occupancy or other hospital processes. Economic analyses should be specifically tailored to the healthcare system that is being assessed.

Previous studies on the cost of hospital-acquired infections may have underestimated the effect of gastrointestinal infections because surveillance methods for such outbreaks have historically been lacking. This analysis of an active, enhanced surveillance scheme of three major hospital administrations in a defined geographic area quantifies the cost of gastroenteritis outbreaks to the health service, the important etiologic role of noroviruses, and the positive effect of control efforts.

Mr. Lopman is an epidemiologist at the Imperial College of London. At the Health Protection Agency Communicable Disease Surveillance Centre in London, his research focuses on viral gastroenteritis, healthcare-associated infection, and molecular epidemiology of foodborne viruses in Europe.

Top

Acknowledgments

We thank members of the Enhanced Surveillance for Gastroenteritis Outbreaks study team, including Helen Tucker, Lauren Tew, Maja Rollings, Samantha Matthews, Liz Bowden, Joanna Davies, Stephanie Carroll, Denise Myers, Erwin Brown, John Leeming, Eleri Davies, Kim Jacobsen, Nicky Lambourne, Dianne Lloyd, Dave Thomas, James Barrow, Marc Hollier, John Jefferies, John Buckingham, Andrew Tanner, and the nursing home staff; Richard Slack, Keith Neal, David Carrington, and Owen Caul for the helpful discussions; and Celia Penman, Kirsty Alexander, Maggie Roebuck, Katie Christou, and Meera Sirvanesan for their support.

Funding was provided by the Health Protection Agency.

Top

References

  1. Meakins  SM, Adak  GK, Lopman  BA, O’Brien  SJ. General outbreaks of infectious intestinal disease (IID) in hospitals, England and Wales, 1992–2000. J Hosp Infect. 2003;53:15. DOIPubMedGoogle Scholar
  2. Gotz  H, Ekdahl  K, Lindback  J, de Jong  B, Hedlund  KO, Giesecke  J. Clinical spectrum and transmission characteristics of infection with Norwalk-like virus: findings from a large community outbreak in Sweden. Clin Infect Dis. 2001;33:6228. DOIPubMedGoogle Scholar
  3. Lopman  BA, Adak  GK, Reacher  MH, Brown  DW. Two epidemiologic patterns of norovirus outbreaks: surveillance in England and Wales, 1992–2000. Emerg Infect Dis. 2003;9:717.PubMedGoogle Scholar
  4. Green  KY, Belliot  G, Taylor  JL, Valdesuso  J, Lew  JF, Kapikian  AZ, A predominant role for Norwalk-like viruses as agents of epidemic gastroenteritis in Maryland nursing homes for the elderly. J Infect Dis. 2002;185:13346. DOIPubMedGoogle Scholar
  5. National Nosocomial Infections Surveillance (NNIS) System Report, Data Summary from January 1992–June 2001, issued August 2001. Am J Infect Control. 2001;29:40421. DOIPubMedGoogle Scholar
  6. Gaynes  RP, Horan  TC. Surveillance of nosocomial infections. In: Mayhall CG, editor. Hospital epidemiology and infection control. Philadelphia: Lippincott Williams & Wilkins; 1999. p. 1285–318.
  7. National Audit Office. The management and control of hospital acquired infection in acute NHS trusts in England. London: The Stationary Office; 2000
  8. Haley  RW, Morgan  WM, Culver  DH, White  JW, Emori  TG, Mosser  J, Update from the SENIC project. Hospital infection control: recent progress and opportunities under prospective payment. Am J Infect Control. 1985;13:97108. DOIPubMedGoogle Scholar
  9. Wheeler  JG, Sethi  D, Cowden  JM, Wall  PG, Rodrigues  LC, Tompkins  DS, Study of infectious intestinal disease in England: rates in the community, presenting to general practice, and reported to national surveillance. The Infectious Intestinal Disease Study Executive. BMJ. 1999;318:104650.PubMedGoogle Scholar
  10. Chadwick  PR, Beards  G, Brown  D, Caul  EO, Cheesbrough  J, Clarke  I, Management of hospital outbreaks of gastroenteritis due to small round structured viruses. J Hosp Infect. 2000;45:110. DOIPubMedGoogle Scholar
  11. de Wit  MA, Koopmans  MP, Kortbeek  LM, Wannet  WJ, Vinje  J, van Leusden  F, Sensor, a population-based cohort study on gastroenteritis in the Netherlands: incidence and etiology. Am J Epidemiol. 2001;154:66674. DOIPubMedGoogle Scholar
  12. Russo  PL, Spelman  DW, Harrington  GA, Jenney  AW, Gunesekere  IC, Wright  PJ, Hospital outbreak of Norwalk-like virus. Infect Control Hosp Epidemiol. 1997;18:5769. DOIPubMedGoogle Scholar
  13. Lo  SV, Connolly  AM, Palmer  SR, Wright  D, Thomas  PD, Joynson  D. The role of the pre-symptomatic food handler in a common source outbreak of food-borne SRSV gastroenteritis in a group of hospitals. Epidemiol Infect. 1994;113:51321. DOIPubMedGoogle Scholar
  14. Fone  DL, Lane  W, Salmon  RL. Investigation of an outbreak of gastroenteritis at a hospital for patients with learning difficulties. Commun Dis Public Health. 1999;2:358.PubMedGoogle Scholar
  15. Kaplan  JE, Feldman  R, Campbell  DS, Lookabaugh  C, Gary  GW. The frequency of a Norwalk-like pattern of illness in outbreaks of acute gastroenteritis. Am J Public Health. 1982;72:132932. DOIPubMedGoogle Scholar
  16. Sethi  D, Wheeler  J, Rodrigues  LC, Fox  S, Roderick  P. Investigation of under-ascertainment in epidemiological studies based in general practice. Int J Epidemiol. 1999;28:10612. DOIPubMedGoogle Scholar
  17. Richards  AF, Lopman  B, Gunn  A, Curry  A, Ellis  D, Cotterill  H, Evaluation of a commercial ELISA for detecting Norwalk-like virus antigen in faeces. J Clin Virol. 2003;26:10915. DOIPubMedGoogle Scholar
  18. Standard Operating Procedure  PHLS. Investigation of faecal specimens for bacterial pathogens. 2003 [cited 2004 Jul 21]. Available from http://www.hpa.org.uk/srmd/div_esl_su/sops_docs/bsops/bsop30i4.pdf
  19. Minimum Testing Algorithm  PHLS. Gastroenteritis outbreaks. 2003. [cited 2004 Jul 21]. Available from http://www.hpa.org.uk/srmd/div_esl_su/sops_docs/vsops/vsop3i4.pdf
  20. Green  SM, Lambden  PR, Deng  Y, Lowes  JA, Lineham  S, Bushell  J, Polymerase chain reaction detection of small round-structured viruses from two related hospital outbreaks of gastroenteritis using inosine-containing primers. J Med Virol. 1995;45:197202. DOIPubMedGoogle Scholar
  21. Vipond  IB, Pelosi  E, Williams  J, Ashley  CR, Lambden  PR, Clarke  IN, A diagnostic EIA for detection of the prevalent SRSV strain in United Kingdom outbreaks of gastroenteritis. J Med Virol. 2000;61:1327. DOIPubMedGoogle Scholar
  22. STATA 8.0. College Station (TX): STATA Corporation; 2002.
  23. Ham  C. Health policy in Britain: The politics and organization of the National Health Service. New York: Palgrave;1992.
  24. Department of Health. Resource allocation: weighted capitation formula; 2003. [cited 2003 Dec 16]. Available from www.doh.gov.uk
  25. Drummond  MF, O’Brien  B, Stoddart  GL, Torrance  GW. Basic types of economic evaluation. Methods for the economic evaluation of healthcare programmes. Oxford: Oxford University Press; 2000. p. 6–26
  26. Netten  A, Curtis  L. Unit costs of health and social care 2002. Canterbury, UK: University of Kent at Canterbury; 2002.
  27. Office of National Statistics. New Earnings Survey. 2003. [cited 2004 Feb 18]. Available from http://www.statistics.gov.uk/downloads/theme_labour/LMT_NES2003ARTICLE_FINAL.pdf
  28. Centers for Disease Control and Prevention. Norovirus activity—United States, 2002. MMWR Morb Mortal Wkly Rep. 2003;52:415.PubMedGoogle Scholar
  29. Lopman  BA, Reacher  M, Gallimore  C, Adak  GK, Gray  JJ, Brown  DW. A summer time peak of “winter vomiting disease”: surveillance of noroviruses in England and Wales, 1995 to 2002. BMC Public Health. 2003;3:13. DOIPubMedGoogle Scholar
  30. Billgren  M, Christenson  B, Hedlund  KO, Vinje  J. Epidemiology of Norwalk-like human caliciviruses in hospital outbreaks of acute gastroenteritis in the Stockholm area in 1996. J Infect. 2002;44:2632. DOIPubMedGoogle Scholar
  31. Lopman  BA, Reacher  MH, Vipond  IB, Sarangi  J, Brown  DW. Clinical manifestation of norovirus gastroenteritis in healthcare settings. Clin Infect Dis. 2004;29:31824. DOIGoogle Scholar
  32. Plowman  R, Graves  N, Griffin  MA, Roberts  JA, Swan  AV, Cookson  B, The rate and cost of hospital-acquired infections occurring in patients admitted to selected specialties of a district general hospital in England and the national burden imposed. J Hosp Infect. 2001;47:198209. DOIPubMedGoogle Scholar

Top

Figures
Tables

Top

Cite This Article

DOI: 10.3201/eid1010.030941

Table of Contents – Volume 10, Number 10—October 2004

EID Search Options
presentation_01 Advanced Article Search – Search articles by author and/or keyword.
presentation_01 Articles by Country Search – Search articles by the topic country.
presentation_01 Article Type Search – Search articles by article type and issue.

Top

Comments

Please use the form below to submit correspondence to the authors or contact them at the following address:

Ben Lopman, Department of Infectious Disease Epidemiology, Imperial College London, St Mary’s Campus, Norfolk Place, London W2 1PG; fax: 020-7594-3282,

Send To

10000 character(s) remaining.

Top

Page created: March 30, 2011
Page updated: March 30, 2011
Page reviewed: March 30, 2011
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.
file_external