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Emerg Infect Dis. Jun 2005; 11(6): 943–946.
PMCID: PMC3367611

Hospitalization and Antimicrobial Resistance in Salmonella Outbreaks, 1984–2002

Abstract

Few studies have evaluated the health consequences of antimicrobial-resistant Salmonella strains associated with outbreaks. Among 32 outbreaks occurring in the United States from 1984 to 2002, 22% of 13,286 persons in 10 Salmonella-resistant outbreaks were hospitalized, compared with 8% of 2,194 persons in 22 outbreaks caused by pansusceptible Salmonella strains (p<0.01).

Keywords: Keywords: Salmonella, Outbreaks, Hospitalization, Antibiotic resistance

Nontyphoidal Salmonella strains are a frequent cause of foodborne disease outbreaks in the United States; they account for ≈13% of outbreaks reported to the Centers for Disease Control and Prevention (CDC) from 1993 to 1997 (1). Antimicrobial resistance is common among salmonellae and has been increasing, particularly in Salmonella enterica serotype Typhimurium, the most common Salmonella serotype (2,3). In the 1990s, a strain of S. Typhimurium resistant to ampicillin, chloramphenicol, streptomycin, sulfonamides, and tetracycline (R-type ACSSuT) emerged in the United States and Europe; most of these isolates were phage definitive type 104 (DT104) (2).

Antimicrobial therapy is not required for most Salmonella infections, but it may be lifesaving in patients with or at risk for extraintestinal infection (4). Increasing levels of antimicrobial resistance are concerning because treatment may fail if the infecting strain of Salmonella is resistant to the prescribed agent (5). Also, when the proportion of Salmonella strains that are resistant increases, the total prevalence of human Salmonella infections increases (6). Resistant salmonellae preferentially cause illness in persons who take antimicrobial drugs for medical conditions unrelated to Salmonella infection (79).

One previous study has formally evaluated the human health consequences of antimicrobial-resistant Salmonella strains associated with outbreaks. In 1984, Holmberg et al. reviewed CDC investigations conducted from 1973 to 1983 to determine the rate of hospitalization and death in outbreaks caused by antimicrobial-resistant salmonellae compared with outbreaks caused by pansusceptible salmonellae (10). Because the epidemiology of both Salmonella infections and antimicrobial resistance has changed in the past 20 years, we repeated this analysis for outbreaks investigated from 1984 to 2002.

The Study

We reviewed final reports of nontyphoidal Salmonella outbreaks investigated by CDC from 1984 to 2002. We excluded outbreaks that occurred in a healthcare setting or outside the United States, including on cruise ships. When antimicrobial susceptibility was not recorded in the final report, we searched CDC microbiology records for susceptibility test results on isolates collected as part of the outbreak. Outbreaks were only included if susceptibility data were available for >1 isolate. Because different laboratories performed susceptibility testing, the antimicrobial agents tested and the methods used varied between outbreaks. We classified outbreaks as resistant when the outbreak strain was resistant to ≥1 antimicrobial agent; other outbreaks were considered pansusceptible. Outbreaks caused by resistant strains were additionally classified as R-type AC/KSSuT when the outbreak strain was at least resistant to ampicillin, chloramphenicol or kanamycin, streptomycin, sulfamethoxazole, and tetracycline. Outbreaks were additionally classified as resistant to a clinically important agent when the outbreak strain was at least resistant to ampicillin, trimethoprim-sulfamethoxazole, aminoglycosides, fluoroquinolones, or a third-generation cephalosporin.

Data from the final investigative reports were used for the analysis. When analyzing data according to outbreaks, we calculated the medians for percentage hospitalized and percentage who died and compared medians with the Wilcoxon rank-sum test. When analyzing data according to ill persons, we pooled data from the reports, calculated proportions, and compared proportions with chi-square or, when appropriate, Fisher exact test. The denominators for percentage hospitalized and died varied depending on the number of persons in whom outcome data were ascertained. All p values were 2-tailed. Data were analyzed by using SAS v.9 (SAS Institute, Cary, NC, USA).

From 1984 to 2002, CDC investigated 48 community outbreaks of nontyphoidal Salmonella strains in the United States. Of these, 47 (98%) had a final report available for review (Table A1). We restricted our analyses to the 39 (83%) outbreaks in which data about antimicrobial susceptibility were available. These 39 outbreaks affected 23,206 persons. The largest outbreak occurred in 1985, in which culture-confirmed S. Typhimurium infection associated with milk consumption developed in 16,659 persons (11).

Strains from 11 (28%) outbreaks were resistant, and 28 (72%) were pansusceptible. The 11 outbreaks caused by resistant strains involved 18,698 persons. Of these 11 outbreaks, 7 (64%), involving 17,182 persons, had strains that were at least R-type AC/KSSuT, and 9 (82%), involving 17,919 persons, had strains that were resistant to a clinically important agent.

Hospitalization data were available for 32 outbreaks involving 21,702 ill persons. The hospitalization rates were higher for each type of outbreak caused by resistant salmonellae compared with outbreaks caused by susceptible salmonellae (p<0.01 for each comparison) (Table). To account for differences in the size of outbreaks, we compared the median proportion of persons hospitalized and compared hospitalization rates after excluding a large Salmonella outbreak that occurred in 1985. The median proportion hospitalized for each type of outbreak caused by resistant strains (26%) was >2.5 times higher than the median proportion hospitalized for outbreaks caused by pansusceptible strains (10%, p<0.05 for all resistance patterns). The difference in hospitalization rates between outbreaks caused by resistant and susceptible strains was similar after we excluded the large 1985 outbreak of resistant S. Typhimurium, in which the percentage hospitalized was 22%. The results also remained similar after excluding S. Enteritidis outbreaks, in which rates of hospitalization and isolate resistance were low.

Table
Hospitalization and death rates among nontyphoidal Salmonella outbreaks by resistance pattern, 1984–2002*

Mortality data were available for 24 outbreaks involving 21,927 persons. A greater proportion of persons died in resistant outbreaks than in pansusceptible outbreaks, but the difference was not significant (0.1% in outbreaks caused by resistant strains vs. 0.06% in outbreaks caused by pansusceptible strains, p = 0.57) (Table).

The 8 outbreaks in which no susceptibility data were available involved 1,914 ill persons. Three (38%) outbreaks were due to S. Enteritidis and 2 (25%) to S. Typhimurium. In the 6 outbreaks for which hospitalization data were available, 70 (20%) of 353 persons were hospitalized. In the 4 outbreaks for which mortality data were available, 7 (0.4%) of 1,708 persons died.

Conclusions

Outbreaks caused by antimicrobial-resistant, nontyphoidal salmonellae were associated with an increased rate of hospitalization compared with outbreaks caused by pansusceptible salmonellae. The results were similar regardless of the definition of resistance used. This association has been found previously in studies of sporadic illness (12,13).

Several possible mechanisms may explain the higher hospitalization rate. Persons who take antimicrobial drugs for reasons unrelated to gastroenteritis have an increased risk of developing antimicrobial-resistant Salmonella infections; such patients may be taking antimicrobial drugs because they have medical conditions that increase their risk for hospitalization (79). We doubt that this explains the differential hospitalization rate observed in our study, because the outbreaks we studied occurred in diverse community settings. A second explanation for the higher hospitalization rate is that persons with resistant Salmonella infections may fail empiric antimicrobial treatment, and their physicians subsequently hospitalize them for inpatient therapy. A third explanation is that resistant salmonellae may be more virulent because of some unknown factor. In the United States, resistant salmonellae are more often associated with hospitalization and bloodstream infection compared to pansusceptible salmonellae (13). In Canada and Denmark, studies have also found excess death rates associated with resistant Salmonella infection (14,15). In England and Wales, a study found no association between resistance and bloodstream infection, but that study had substantial limitations, including the failure to use pansusceptible salmonellae as a referent group and the failure to adjust for confounders, such as age (16).

Since the review of Salmonella outbreaks published in 1984, several changes have occurred in the epidemiology of antimicrobial-resistant salmonellae. First, S. Typhimurium DT104 has emerged as a cause of antimicrobial-resistant Salmonella infections. Five outbreaks in this study were caused by S. Typhimurium with R-type AC/KSSuT; isolates with this resistance pattern are often DT104 (2,17). The hospitalization rate was higher in these 5 outbreaks (median proportion hospitalized: 17%) than in 3 outbreaks caused by pansusceptible S. Typhimurium, which suggests that resistance or related factors, rather than just serotype, contribute to the differential rates of hospitalization. Second, a strain of S. Newport resistant to at least 9 agents and with diminished susceptibility to ceftriaxone recently emerged in the United States; 1 outbreak in this review was caused by this strain and had a hospitalization rate greater than that seen in most other resistant outbreaks (18). Third, S. Enteritidis has emerged as a frequent cause of foodborne outbreaks (19). S. Enteritidis strains are infrequently resistant to antimicrobial agents, and in this review, S. Enteritidis outbreaks were associated with low hospitalization rates. Excluding S. Enteritidis outbreaks did not change the results of our analysis.

The previous analysis by Holmberg et al. found that the rate of death was significantly greater in outbreaks caused by resistant strains (4%) compared with outbreaks caused by pansusceptible strains (0.2%) (10). Rates of death in our study were lower. Because this study covered a more recent period, improvements in medical care may explain the overall lower death rates. Studies with larger sample sizes are needed to determine whether antimicrobial resistance is associated with increased fatality rates.

Our study has some limitations, the most important of which is selection bias. State health departments investigate hundreds of Salmonella outbreaks annually. Occasionally, state health departments request assistance from CDC in investigating these outbreaks. The reasons for such requests vary but may be related to size, severity, setting, or other features of the outbreak. While concern about a high hospitalization rate might encourage a state health department to request assistance from CDC in a Salmonella outbreak, susceptibility results are usually not known initially and are unlikely by themselves to influence the request for assistance.

Another limitation is that our study was based on final reports, not raw data. As a result, we were unable to adjust for the different patient populations affected, including age, medical condition, and other factors that could affect hospitalization. Excluding outbreaks that occurred in healthcare settings may have reduced some of this bias. Adjustment for serotype, which could also affect hospitalization rates, was also not possible because of the small sample size.

Despite these limitations, we believe this study adds to the weight of evidence about the health effects of antimicrobial-resistant salmonellae. The evidence now includes data from outbreaks and sporadic illness in the United States from 1970 to 2002. Data from sporadic illness and 1 outbreak is also available from Denmark (14,20). Across these diverse studies, higher hospitalization rates are consistently found in patients infected with resistant salmonellae. Such data about the adverse human health effects of resistant salmonellae should be incorporated into programs that promote appropriate antimicrobial use in humans and animals.

Biography

• 

Dr. Varma is an internist and epidemiologist with CDC. He currently serves as chief of the Tuberculosis Prevention and Control Section for the Thailand MOPH–CDC collaboration in Bangkok, Thailand. His areas of interest include infectious disease epidemiology, international health, and public health surveillance.

Table A1

Domestic, community, nontyphoidal Salmonella outbreaks investigated by the Centers for Disease Control and Prevention, 1984–2002
YearStateSerotypeResistance pattern*Implicated vehicleNo. hospitalized/total (%)†No. died/total (%)‡
1984OregonTyphimuriumTSSalad bar45/388 (12)0/715 (0)
1984PennsylvaniaInfantisPansusceptibleTurkey/beef sandwich1/203 (0)0/203 (0)
1985CaliforniaNewportACKSSuTGround beef22/45 (49)2/298 (1)
1985MissouriThompsonNAPorkNANA
1985IllinoisTyphimuriumAKSSuTMilk2777/12624 (22)18/16659 (0)
1986GeorgiaTyphimuriumPansusceptibleTurkey4/719 (1)0/719
1986Multiple§Enteritidis, HeidelbergPansusceptibleEggs (in frozen pasta)13/166 (8)1/166 (1)
1987GeorgiaHavanaTChicken36/73 (49)1/73 (1)
1987HawaiiAgonaPansusceptibleChickenNA0/202 (0)
1989MaineHeidelbergPansusceptibleUnknownNANA
1989MinnesotaJavianaPansusceptibleCheeseNANA
1989Multiple§ChesterPansusceptibleCantaloupeNANA
1989NevadaTyphimuriumPansusceptibleDeli platterNANA
1990PennsylvaniaEnteritidisPansusceptibleEggs5/26 (19)0/94 (0)
1990South CarolinaAgonaNATurkeyNA0/850 (0)
1992GeorgiaInfantisPansusceptibleEggs (in rice pudding)0/113 (0)0/113 (0)
1992New YorkEnteritidisNAEggs (in mayonnaise)8/98 (8)0/98 (0)
1993MissouriTyphimuriumNAWater13/27 (48)7/650 (1)
1993Multiple§MontevideoPansusceptibleRaw tomatoes, lettuce15/62 (24)0/84 (0)
1993TexasEnteritidisNAEgg rolls2/19 (11)NA
1994GeorgiaEnteritidisPansusceptibleEggs (in ice cream)0/129 (0)NA
1995ArizonaStanleyKTBAlfalfa sprouts5/19 (26)NA
1995FloridaHartfordPansusceptibleOrange juice7/32 (22)NA
1995UtahEnteritidisPansusceptibleEggs5/43 (12)NA
1996ColoradoEnteritidisPansusceptibleKomodo dragon8/37 (22)NA
1996South DakotaThompsonPansusceptibleRoast beef0/43 (0)0/52 (0)
1996HawaiiEnteritidisPansusceptibleUnknownNANA
1997WashingtonTyphimuriumACSSuTCheese (queso fresco)5/54 (9)0/54 (0)
1997VermontTyphimuriumACSSuTMilk (raw)1/9 (11)NA
1997MarylandHeidelbergKSTHam (stuffed)NA2/706 (0)
1997Kansas, MissouriInfantis, AnatumPansusceptibleSprouts18/67 (27)0/114 (0)
1997South CarolinaEnteritidisPansusceptibleEggs4/192 (2)0/192 (0)
1997NevadaEnteritidisPansusceptibleEggs (in hollandaise sauce)15/63 (24)0/91 (0)
1998OhioTyphimuriumAKSSuTFarm exposure5/19 (26)NA
1998Multiple§AgonaPansusceptibleOat cereal33/88 (38)1/409 (0)
1998MassachusettsTyphimuriumPansusceptibleMilk (raw)2/47 (4)NA
1999ColoradoTyphimuriumPansusceptibleClover sprouts3/20 (15)0/81 (0)
1999MassachusettsNewportMDR-AmpCFarm exposure11/32 (34)0/46 (0)
1999MissouriTyphimuriumNAWater17/110 (15)0/110 (0)
2000Multiple§BareillyNAWater19/46 (41)NA
2000Multiple§EnteritidisPansusceptibleOrange juice13/88 (15)NA
2000North CarolinaEnteritidisNAEggs11/53 (21)NA
2000Pennsylvania, New JerseyTyphimuriumAKSSuTMilk6/23 (26)0/93 (0)
2001MississippiJavianaPansusceptibleAmphibian exposure9/57 (16)0/73 (0)
2002FloridaJavianaPansusceptibleTomatoes3/82 (4)NA
2002TexasEnteritidisPansusceptibleUnknown3/41 (7)0/650 (0)
2002Washington, DCMuenchenPansusceptiblePasta salad3/40 (8)0/40 (0)

*A, ampicillin; C, chloramphenicol; K, kanamycin; S, streptomycin; Su, sulfamethoxazole; T, tetracycline; B, trimethoprim-sulfamethoxazole; MDR-AMPC, ACSSuT + amoxicillin/clavulanic acid, cephalothin, cefoxitin, ceftiofur, ceftriaxone (reduced susceptibility); NA, not available.
†Denominator includes those for whom hospitalization status was ascertained. In many outbreaks, hospitalization was only ascertained for patients enrolled in an analytic study.
‡Denominator includes those for whom mortality was assessed. If this number was not available, the total number of ill persons in the outbreak was included as the denominator.
§Outbreak involving ≥3 states.

Footnotes

Suggested citation for this article: Varma JK, Greene KD, Ovitt J, Barrett TJ, Medalla F, Angulo FJ. Hospitalization and antimicrobial resistance in Salmonella outbreaks, United States, 1984–2002. Emerg Infect Dis [serial on the Internet]. 2005 Jun [date cited]. http://dx.doi.org/10.3201/eid1106.041231

References

1. Olsen SJ, MacKinnon LC, Goulding JS, Bean NH, Slutsker L Surveillance for foodborne disease outbreaks. MMWR Surveill Summ. 2000;49:1–62 [PubMed]
2. Glynn MK, Bopp C, Dewitt W, Dabney P, Mokhtar M, Angulo F Emergence of multidrug-resistant Salmonella enterica serotype Typhimurium DT104 infections in the United States. N Engl J Med. 1998;338:1333–8 10.1056/NEJM199805073381901 [PubMed] [Cross Ref]
3. Centers for Disease Control and Prevention National Antimicrobial Resistance Monitoring System for Enteric Bacteria: annual report, 2002. Atlanta: The Centers; 2004
4. Guerrant RL, Van Gilder T, Steiner TS, Thielman NM, Slutsker L, Tauxe RV, et al. Practice guidelines for the management of infectious diarrhea. Clin Infect Dis. 2001;32:331–50 10.1086/318514 [PubMed] [Cross Ref]
5. Bryan JP, Rocha H, Scheld WM Problems in salmonellosis: rationale for clinical trials with newer β-lactam agents and quinolones. Rev Infect Dis. 1986;8:189–207 10.1093/clinids/8.2.189 [PubMed] [Cross Ref]
6. Barza M Potential mechanisms of increased disease in humans from antimicrobial resistance in food animals. Clin Infect Dis. 2002;34:S123–5 10.1086/340249 [PubMed] [Cross Ref]
7. Holmberg SD, Osterholm MT, Senger KA, Cohen ML Drug-resistant Salmonella from animals fed antimicrobials. N Engl J Med. 1984;311:617 10.1056/NEJM198409063111001 [PubMed] [Cross Ref]
8. Tacket CO, Dominguez LB, Fisher HJ, Cohen ML An outbreak of multiple-drug-resistant Salmonella enteritis from raw milk. JAMA. 1985;253:2058 10.1001/jama.1985.03350380074024 [PubMed] [Cross Ref]
9. Riley LW, Cohen ML, Seals JE, Blaser MJ, Birkness KA, Hargrett NT, et al. Importance of host factors in human salmonellosis caused by multiresistant strains of Salmonella. J Infect Dis. 1984;149:878–83 10.1093/infdis/149.6.878 [PubMed] [Cross Ref]
10. Holmberg SD, Wells JG, Cohen ML Animal-to-man transmission of antimicrobial-resistant Salmonella: investigations of U.S. outbreaks, 1971–1983. Science. 1984;225:833–4 10.1126/science.6382605 [PubMed] [Cross Ref]
11. Ryan CA, Nickels MK, Hargrett-Bean NT, Potter ME, Endo T, Mayer L, et al. Massive outbreak of antimicrobial-resistant salmonellosis traced to pasteurized milk. JAMA. 1987;258:3269–74 10.1001/jama.1987.03400220069039 [PubMed] [Cross Ref]
12. Lee LA, Puhr ND, Maloney EK, Bean NH, Tauxe RV Increase in anti-microbial resistant Salmonella infections in the United States, 1989–1990. J Infect Dis. 1994;170:128–34 10.1093/infdis/170.1.128 [PubMed] [Cross Ref]
13. Varma JK, Mølbak K, Barrett TJ, Beebe JL, Jones TF, Rabatsky-Ehr T, et al. Antimicrobial-resistant nontyphoidal Salmonella is associated with excess bloodstream infections and hospitalizations. J Infect Dis. 2005;191:554–61 10.1086/427263 [PubMed] [Cross Ref]
14. Helms M, Vastrup P, Gerner-Smidt P, Mølbak K Excess mortality associated with antimicrobial drug-resistant Salmonella Typhimurium. Emerg Infect Dis. 2002;8:490–5 [PMC free article] [PubMed]
15. Martin LJ, Fyfe M, Dore K, Buxton JA, Pollari F, Henry B, et al. Increased burden of illness associated with antimicrobial-resistant Salmonella enterica serotype Typhimurium infections. J Infect Dis. 2004;189:377–84 10.1086/381270 [PubMed] [Cross Ref]
16. Threlfall EJ, Ward LR, Rowe B Multiresistant Salmonella typhimurium DT104 and salmonella bacteraemia. Lancet. 1998;352:287–8 10.1016/S0140-6736(05)60261-9 [PubMed] [Cross Ref]
17. Rabatsky-Ehr T, Whichard J, Rossiter S, Holland B, Stamey K, Headrick ML, et al. Multidrug-resistant strains of Salmonella enterica Typhimurium, United States, 1997–1998. Emerg Infect Dis. 2004;10:795–801 [PMC free article] [PubMed]
18. Gupta A, Fontana J, Crowe C, Bolstorff B, Stout A, Van Duyne S, et al. Emergence of multidrug-resistant Salmonella enterica serotype Newport infections resistant to expanded-spectrum cephalosporins in the United States. J Infect Dis. 2003;188:1707–16 10.1086/379668 [PubMed] [Cross Ref]
19. Patrick ME, Adcock PM, Gomez TM, Altekruse SF, Holland BH, Tauxe RV, et al. Salmonella Enteritidis infections, United States, 1985–1999. Emerg Infect Dis. 2004;10:1–7 [PMC free article] [PubMed]
20. Mølbak K, Baggesen DL, Aarestrup FM, Ebbesen JM, Engberg J, Frydendahl K, et al. An outbreak of multidrug resistant Salmonella enterica serotype Typhimurium DT104. N Engl J Med. 1999;341:1420–5 10.1056/NEJM199911043411902 [PubMed] [Cross Ref]

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