Clostridium difficile Surveillance Report 2016

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Clostridium difficile Surveillance Report 2016 EMERGING INFECTIONS PROGRAM

Clostridium difficile Surveillance Report 2016 Minnesota Department of Health Emerging Infections Program PO Box 64882, St. Paul, MN 55164-0882 651-201-5414 or 1-877-676-5414 www.health.state.mn Upon request, this material will be made available in an alternative format such as large print, Braille or audio recording. 2

In 2009 the Minnesota Commissioner of Health designated sentinel surveillance for Clostridium difficile in Benton, Morrison, Stearns, and Todd Counties under the authority of the Communicable Disease Rule, Chapter 4605. In 2012, surveillance was expanded to include Olmsted County. This population-based active laboratory surveillance for Clostridium difficile infection (CDI) is conducted by the Minnesota Department of Health (MDH) Emerging Infections Program (EIP) in collaboration with the Centers for Disease Control and Prevention (CDC). The surveillance includes all patients at least 1 year of age, with a positive C. difficile test, residing in Benton, Morrison, Stearns, Todd, or Olmsted Counties. Patients are categorized into three epidemiologic classifications depending on the location and timing of the C. difficile positive sample in relation to their healthcare exposure. The definitions are as follows. Epidemiologic classifications: Community-Associated (CA): a patient who developed CDI while in the community and had no overnight stay in a healthcare facility in the prior 12 weeks; or developed CDI within the first 3 days of admission to a healthcare facility. Community-Onset, Healthcare Facility Associated (CO-HCFA): a patient who developed CDI while in the community and had an overnight stay in a healthcare facility in the prior 12 weeks. Healthcare Facility-Onset (HCFO): a patient who developed CDI while in a healthcare facility and had a C. difficile specimen collected 4 days after admission to a healthcare facility. A healthcare facility is defined as an acute care hospital, long-term acute care hospital, or long-term care facility. Specimen classification definitions: Duplicate: a positive C. difficile test collected less than 2 weeks after a previous positive C. difficile test. Recurrent: a positive C. difficile test collected between 2 and 8 weeks after a previous positive C. difficile test. Incident: a positive C. difficile test collected greater than 8 weeks after any previous positive C. difficile test. This document summarizes the surveillance data collected during 2016. 3

In 2016, 1152 case reports from residents within the catchment area who were at least 1 year of age were submitted to MDH; Figure 1 below shows the proportion of incident, recurrent, and duplicate specimens. Figure 1 Classification of Clostridium difficile Reports Submitted to MDH, 2016 (n=1152) Incident 903 (78%) Recurrent 225 (20%) Duplicate 24 (2%) Of the 903 incident reports with medical records available, 526 (58%) were classified as community-associated. Figure 2 below shows the proportion of the epidemiologic classifications. Figure 2 Minnesota Clostridium difficile Incident Cases by Epidemiologic Classification, 2016 (n=903) HCFO 150 (17%) CO-HCFA 227 (25%) CA 526 (58%) 4

Of the 150 HCFO cases, 83 (55%) cases were likely acquired in a hospital setting and 67 (45%) were likely acquired in a long-term care facility. Figure 3 Minnesota Clostridium difficile HCFO Cases by Facility Type, 2016 (n=150) Long-term care facility 67 (45%) Hospital 83 (55%) Of the 227 CO-HCFA cases, 197 (87%) had a prior overnight hospital stay, 24 (11%) had both an overnight hospital and long-term care facility stay, 6 (3%) had only a prior long-term care facility stay, and no cases had a prior hospital, long-term acute care hospital, and long-term care facility stay. Figure 4 Minnesota Clostridium difficile CO-HCFA Cases by Associated Facility Type, 2016 (n=227) Hospital and LTCF 24 (11%) Hospital 197 (87%) Long-term Care Facility 6 (3%) 5

Figure 5 Number of Incident Cases 400 350 300 250 200 150 100 50 0 Surveillance County Distribution of Incident Clostridium difficile Cases in Minnesota, 2016 (n=903) Benton Morrison Olmsted Stearns Todd Number of Incident Cases Minnesota Surveillance County 300 250 200 150 100 50 Incidence Rate Per 100,000 Population 0 Incidence Rate per 100,000 Population *Rates are based upon estimated 2015 population (ages 1 yr.) data for Benton, Morrison, Olmsted, Stearns, and Todd Counties Table 1: Number of Cases and Rates of Incident Clostridium difficile by Gender and Age Group in Minnesota, 2016 Gender Incident Cases n (%) Incidence Rate per 100,000 population* Male 389 (43) 196 Female 514 (57) 258 Age 1-17 years 63 (7) 70 18-44 years 218 (24) 151 45-64 years 256 (28) 247 65+ years 366 (41) 617 Totals 903 227 *Rates are based upon estimated 2015 population (ages 1 yr.) data for Benton, Morrison, Olmsted, Stearns, and Todd Counties 6

Figure 6 Number of Incident Cases of Clostridium difficile by Month and Epidemiologic Class in Minnesota, 2016 Number of Incident Cases 100 90 80 70 60 50 40 30 20 10 0 CA CO-HCFA HCFO TOTAL Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Month of Specimen Collection Figure 7 Incidence Rate Per 100,000 Population* 250 200 150 100 50 0 Incidence Rates* of Clostridium difficile Infections in Minnesota by Year and Epidemiologic Classification CA HCFO CO-HCFA Total 2009 2010 2011 2012 2013 2014 2015 2016 Surveillance Year** *Rates are based upon estimated 2015 population (ages 1 yr.) data for Benton, Morrison, Olmsted, Stearns, and Todd Counties ** One major clinical laboratory switched laboratory testing methods from EIA to PCR in 2010 7

Table 2 Percent of Cases Prescribed Antibiotics in Previous 12 weeks, According to Medical Record, 2016 (n=903) Total 62% CA 52% CO-HCFA 75% HCFO 77% Attempts to contact all CA cases were made to administer a health interview inquiring about risk factors in the previous 12 weeks, including antibiotic use. In 2016, 342 health interviews were completed, 186 (54%) cases reported taking antibiotics in the 12 weeks prior to symptom onset or stool collection. Figure 8 Of the 342 interviewed CA cases, 60 (18%) had no outpatient healthcare and no antibiotic exposure documented in their medical record or reported on interview. Percent of Patients Taking Any Antibiotic 60 50 40 30 20 10 0 Reported Indications for Antimicrobial Prescription by C. difficile cases in Minnesota, 2016 (n=275) Ear / Sinus / URI Urinary Tract Infection Dental Work Surgery Skin Infection Bronchitis/ Pneumonia Problem for Which Antibiotic Was Taken 8

Discussion CLOSTRIDIUM DIFFICILE SURVEILLANCE REPORT Clostridium difficile infections are an important public health concern in Minnesota; the incidence is highest in people age 65 years and older, and women are more often affected than men. A majority of Minnesota s CDI cases have no inpatient or overnight healthcare exposure, and at least 18% of interviewed CA patients had no documented healthcare or antibiotic exposure, the main modifiable risk factors for C. difficile infection. This signifies further investigation of community-associated CDI is needed to identify risk factors for acquiring C. difficile. Antibiotic use is a known risk factor for CDI; overall, 62% of Minnesota cases in 2016 were prescribed an antibiotic prior to their C. difficile infection. Attention to appropriate antibiotic prescribing practices, especially in the case of asymptomatic bacteriuria, upper respiratory illnesses, and dental treatment and prophylaxis, could be an important avenue for CDI prevention. 9

Publications Utilizing Minnesota Clostridium difficile Surveillance Data 1. DEATH DUE TO COMMUNITY-ASSOCIATED CLOSTRIDIUM DIFFICILE IN A WOMAN RECEIVING PROLONGED ANTIBIOTIC THERAPY FOR SUSPECTED LYME DISEASE Holzbauer S, Kemperman M, Lynfield R. Death due to community-associated Clostridium difficile in a woman receiving prolonged antibiotic therapy for suspected Lyme disease. Clin Infect Dis. August 1, 2010;51(1):369-70. Available at: http://cid.oxfordjournals.org/content/51/3/369.long 2. EPIDEMIOLOGY OF COMMUNITY-ASSOCIATED CLOSTRIDIUM DIFFICILE INFECTION, 2009 THROUGH 2011 Chitnis AS, Holzbauer SM, Belflower RM, Winston LG, Bamberg WM, Lyons C, Farley MM, Dumyati GK, Wilson LE, Beldavs ZG, Dunn JR, Gould LH, Maccannell DR, Gerding DN, McDonald LC, Lessa FC. Epidemiology of community-associated Clostridium difficile infection, 2009 through 2011. JAMA Intern Med. 2013 Jul; 173(14): 1359-67. Available at: http://archinte.jamanetwork.com/article.aspx?articleid=1697791 3. EFFECT OF NUCLEIC ACID AMPLIFICATION TESTING ON POPULATION-BASED INCIDENCE RATES OF CLOSTRIDIUM DIFFICILE INFECTION Gould CV, Edwards JR, Cohen J, Bamberg WM, Blark LA, Farley MM, Johnsonton H, Nadle J, WIndston L, Gerding DN, McDonald LC, Lessa FC. Effect of nucleic acid amplicfication testing on population-based incidence rates of Clostridium difficile infection. Clin Infect Dis. 2013 November; 57(9):1304-1307. Available at: http://cid.oxfordjournals.org/content/57/9/1304.long 4. IMPACT OF CHANGES IN CLOSTRIDIUM DIFFICILE TESTING PRACTICES ON STOOL REJECTION POLICIES AND C. DIFFICILE POSITIVITY RATES ACROSS MULTIPLE LABORATORIES IN THE UNITED STATES Cohen J, Limbago B, Dumyati G, Holzbauer S, Johnston H, Perlmutter R, Dunn J, Nadle J, Lyons C, Phipps E, Beldays Z, Clark LA, Lessa FC and Investigators CDC s Clostridium difficile Infection Surveillance. Impact of changes in Clostridium difficile testing practices on stool rejection policies and C. difficile positivity rates across multiple laboratories in the United States. J Clin Microbiol. 2014 Feb; 52(2): 632-4. Available at: http://jcm.asm.org/content/52/2/632.short 5. CLOSTRIDIUM DIFFICILE INFECTION AMONG CHILDREN ACROSS DIVERSE U.S. GEOGRAPHIC LOCATIONS Wendt JM, Cohen JA, Mu Y, Dumyati GK, Dunn JR, Holzbauer SM, Winston LG, Johnston HL, Mek JI, Farley MM, Wilson LE, Phipps EC, Beldavs ZG, Gerding DN, McDonald LC, Gould CV, Lessa FC. Clostridium difficile infection among children across diverse U.S. geographic locations. 10

Pediatrics. 2014 April; 133(4): 1-8. Available at: http://pediatrics.aappublications.org/content/early/2014/02/25/peds.2013-3049 6. NAP1 STRAIN TYPE PREDICTS OUTCOMES FROM CLOSTRIDIUM DIFFICILE INFECTION See I, Mu Y, Cohen J, Beldav ZG, Winston LG, Dumyati G, Holzbauer S, Dunn J, Farley MM, Lyons C, Johnston H, Phipps E, Perlmutter R, Anderson L, Gerding DN, Lessa FC. NAP1 strain type predicts outcomes from Clostridium difficile infection. Clin Infect Dis. 2014 May 15; 58(10): 1394-1400. Available at: http://cid.oxfordjournals.org/content/58/10/1394.long 7. DETERMINANTS OF CLOSTRIDIUM DIFFICILE INFECTIONS ACROSS DIVERSE U.S. GEOGRAPHIC LOCATIONS Lessa FC, Mu Y, Winston LG, Dumyati GK, Farley MM, Beldavs ZG, Kast K, Holzbauer SM, Meek JI, Cohen J, McDonald LC, Fridkin SK. Determinants of Clostridium difficile infections across diverse U.S. geographic locations. Open Forum Infect Dis (Summer 2014) 1 (2): doi:10.1093/ofid/ofu047. Available at: http://ofid.oxfordjournals.org/content/1/2/ofu048.full 8. BURDEN OF CLOSTRIDIUM DIFFICILE INFECTION IN THE UNITED STATES Lessa FC, Mu Y, Bamberg WM, Beldavs ZG, Dumyati GK, Dunn JR, Farley MM, Holzbauer SM, Meek JI, Phipps EC, Wilson LE, Winston LG, Cohen JA, Limbago BM, Firdkin SK, Gerding DN, McDonald LC. Burden of Clostridium difficile infections in the United States. N Engl J Med. 2015 Feb 26; 372(9): 825-834. Available at: http://www.nejm.org/doi/full/10.1056/nejmoa1408913 9. ASSOCIATION BETWEEN OUTPATIENT ANTIBIOTIC PRESCRIBING PRACTICES AND COMMUNITY-ASSOCIATED CLOSTRIDIUM DIFFICILE INFECTION. Dantes R, Mu Y, Hicks LA, Cohen J, Bamberg W, Beldavs ZG, Dumyati G, Farley MM, Holzbauer S, Meek J, Phipps E, Wilson L, Winston LG, McDonald LC, Lessa FC. Open Forum Infect Dis. 2015 Aug 11;2(3):ofv113. doi: 10.1093/ofid/ofv113. Available at: http://www.ncbi.nlm.nih.gov/pmc/articles/pmc4551478/ 10. BURDEN OF NURSING HOME ONSET CDI IN THE UNITED STATES Hunter JC, Mu Y, Dumyati GK, et al. Burden of Nursing Home-Onset Clostridium difficile Infection in the United States: Estimates of Incidence and Patient Outcomes. Open Forum Infect Dis. 2016 Jan 18; 3(1): 1-8. Available at: http://www.ncbi.nlm.nih.gov/pmc/articles/pmc4719744/ 11