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International Nosocomial Infection
Control Consortium (INICC) report,
data summary for 2003-2008, issued
June 2009
Victor D. Rosenthal, MD,a Dennis G Maki, MD,b Silom Jamulitrat, MD,c Eduardo A. Medeiros, MD,d Subhash Kumar Todi, MD,e
David Yepes Gomez, MD,f Hakan Leblebicioglu, MD,g Ilham Abu Khader, MD,h Marıa Guadalupe Miranda Novales, MD,i
                                                                                  ´
Regina Berba, MD,j Fernando Martın Ramırez Wong, MD,k Amina Barkat, MD,l Osiel Requejo Pino, MD,m Lourdes Duenas, MD,n
                                  ´      ´                                                                          ˜
Zan Mitrev, MD,o Hu Bijie, MD,p Vaidotas Gurskis, MD,q S. S. Kanj, MD,r Trudell Mapp, RN,s Rosalıa Fernandez Hidalgo, RN,t
                                                                                                ´      ´
Nejla Ben Jaballah, MD,u Lul Raka, MD,v Achilleas Gikas, MD,w Altaf Ahmed, MD,x Le Thi Anh Thu, MD,y
Marıa Eugenia Guzman Siritt, MD,z and INICC Members
    ´                ´
     Buenos Aires, Argentina; Madison, Wisconsin; Songkla, Thailand; Sao Paulo, Brazil; Kolkata, India; Medellın,    ´
     Colombia; Samsun, Turkey; Amman, Jordan; Mexico City, Mexico; Manila, Philippines; Lima, Peru; Rabat, Morocco;
     Havana, Cuba; San Salvador, El Salvador; Skopje, Macedonia; Shanghai, China; Kaunas, Lithuania; Beirut, Lebanon;
                                    ´
     Panama City, Panama; San Jose, Costa Rica; Tunis, Tunisia; Prishtina, Kosova; Heraklion, Greece; Karachi, Pakistan;
     Ho Chi Minh City, Vietnam; and Caracas, Venezuela


     We report the results of the International Infection Control Consortium (INICC) surveillance study from January 2003 through
     December 2008 in 173 intensive care units (ICUs) in Latin America, Asia, Africa, and Europe. During the 6-year study, using Centers
     for Disease Control and Prevention (CDC) US National Healthcare Safety Network (NHSN; formerly the National Nosocomial Infec-
     tion Surveillance system [NNIS]) definitions for device-associated health care-associated infection, we collected prospective data
     from 155,358 patients hospitalized in the consortium’s hospital ICUs for an aggregate of 923,624 days. Although device utilization
     in the developing countries’ ICUs was remarkably similar to that reported from US ICUs in the CDC’s NHSN, rates of device-asso-
     ciated nosocomial infection were markedly higher in the ICUs of the INICC hospitals: the pooled rate of central venous catheter
     (CVC)-associated bloodstream infections (BSI) in the INICC ICUs, 7.6 per 1000 CVC-days, is nearly 3-fold higher than the 2.0 per
     1000 CVC-days reported from comparable US ICUs, and the overall rate of ventilator-associated pneumonia (VAP) was also far
     higher, 13.6 versus 3.3 per 1000 ventilator-days, respectively, as was the rate of catheter-associated urinary tract infection (CAUTI),
     6.3 versus 3.3 per 1000 catheter-days, respectively. Most strikingly, the frequencies of resistance of Staphylococcus aureus isolates
     to methicillin (MRSA) (84.1% vs 56.8%, respectively), Klebsiella pneumoniae to ceftazidime or ceftriaxone (76.1% vs 27.1%, respec-
     tively), Acinetobacter baumannii to imipenem (46.3% vs 29.2%, respectively), and Pseudomonas aeruginosa to piperacillin (78.0%
     vs 20.2%, respectively) were also far higher in the consortium’s ICUs, and the crude unadjusted excess mortalities of device-related
     infections ranged from 23.6% (CVC-associated bloodstream infections) to 29.3% (VAP).
     Key Words: Hospital infection; nosocomial infection; health care-associated infection; INICC; International Nosocomial Infection
     Consortium; device-associated infection; antibiotic resistance; ventilator-associated pneumonia; catheter-associated urinary tract
     infection; central line-associated bloodstream infections; bloodstream infection; urinary tract infection; developing countries;
     limited resources countries; low income countries; network.
     Copyright ª 2010 by the Association for Professionals in Infection Control and Epidemiology, Inc. Published by Elsevier Inc. All rights
     reserved. (Am J Infect Control 2010;38:95-106.)

From the International Nosocomial Infection Control Consortium, Bue-          Liaquat National Hospital, Karachi, Pakistanx; Cho Ray Hospital, Ho Chi
nos Aires, Argentinaa; University of Wisconsin Medical School, Madison,       Minh City, Vietnamy; Hospital Militar Dr. Carlos Arvelo, Caracas,
WIb; Songklanagarind Hospital, Songkla, Thailandc; Hospital Sao Paulo,        Venezuela.z
Sao Paulo, Brazild; AMRI Hospitals, Kolkata, Indiae; Clınica CES, Medellın,
                                                       ´                ´
                                                                              Address correspondence to Victor D. Rosenthal, MD, MSc, CIC,
Colombiaf; Ondokuz Mayis University Medical School, Samsun, Turkeyg;
                                                                              International Nosocomial Infection Control Consortium (INICC),
Jordan University Hospital, Amman, Jordanh; Hospital de Pediatrıa        ´
                                                                              Corrientes Ave # 4580, Floor 11, Apt A, ZIP C1195AAR, Buenos Aires.
CMN Siglo XXI, IMSS, Mexico City, Mexicoi; Philippine General Hospital,
                                                                              Argentina. E-mail: victor_rosenthal@inicc.org.
Manila, Philippinesj; Hospital Marıa Auxiliadora, Lima, Peruk; Children
                                   ´
Hospital of Rabat, Rabat, Moroccol; Hospital Universitario Gral. Calixto,
  ˆ                                                                           For a list of members of the International Nosocomial Infection Control
Garcıa Havana, Cubam; Hospital Nacional de Ninos Benjamin Bloom, San
     ´                                           ˜                            Consortium, see Appendix 1 available online at www.ajicjournal.org.
Salvador, El Salvadorn; Filip II Special Cardiosurgery Hospital, Skopje,      Conflicts of interest: None to report.
Macedoniao; Zhongshan Hospital, Shanghai, Chinap; Kaunas University
of Medicine, Children Clinic, Kaunas, Lithuaniaq; American University of      0196-6553/$36.00
Beirut Medical Center, Beirut, Lebanonr ; Clınica Hospital San Fernando
                                             ´
                                                                              Copyright ª 2010 by the Association for Professionals in Infection
Panama, Panama City, Panamas; Hospital Clınica Bıblica, San Jose, Costa
                                            ´       ´             ´
                                                                              Control and Epidemiology, Inc. Published by Elsevier Inc. All rights
Ricat; Hopital d’Enfants, Tunis, Tunisiau; National Institute for Public
         ˆ
                                                                              reserved.
Health of Kosova and Medical School, Prishtina University, Prishtina,
Kosovav; University Hospital of Heraklion, Heraklion, Greecew;                doi:10.1016/j.ajic.2009.12.004



                                                                                                                                                   95
96   Rosenthal et al.                                                                  American Journal of Infection Control
                                                                                                                March 2010


   This report is a summary of data on device-associ-           Infection control professionals (ICPs) collect data on
ated infections (DAI) within intensive care units (ICUs)     central line-associated primary bloodstream infections
collected by hospitals participating in the International    (CLABs), catheter-associated urinary tract infections
Nosocomial Infection Control Consortium (INICC)1-13          (CAUTIs), and ventilator-associated pneumonias (VAPs)
between January 2003 and December 2008.                      occurring in patients hospitalized in a specific patient
   The INICC is an international nonprofit, open, multi-      care location, in nearly all hospitals. ICUs are stratified
center, collaborative health care-associated infection       according to the patient population: adult, pediatric,
control program with a surveillance system based on          or neonatal units (NICUs).
that of the US National Healthcare Safety Network               All NICUs are level III or level II/III units, and ICPs
(NHSN; formerly the National Nosocomial Infection            collect data on CLABs and umbilical catheter-associ-
Surveillance system [NNIS]).3 Founded in Argentina in        ated primary BSIs or VAPs for each of 5 birth-weight
1998, the INICC is the first multinational research net-      categories (,750 g, 750-1000 g, 1001-1500 g, 1501-
work established to control and reduce DAI through the       2500 g, .2500 g). Corresponding denominator data,
analysis of data collected on a voluntary basis by a pool    patient-days, and specific device-days are also
of hospitals worldwide. The INICC has the following          collected.
goals: Create a dynamic global network of hospitals             Small proportion of hospitals, with previous long-
in the developing world that conducts surveillance of        lasting experience conducting surveillance of DAIs,
health care-associated infections (HAIs) using stan-         sent aggregated data to the INICC. Original and aggre-
dardized definitions and established methodologies,           gated data were collected to calculate DAI rates. Only
promote implementation of evidence-based infection           original data were collected to calculate mortality and
control practices, and carry out applied infection con-      lengh of stay.
trol research; provide training and surveillance tools          The Process Surveillance Component includes the
to individual hospitals that can allow them to conduct       following modules: hand hygiene compliance monitor-
outcome and process surveillance of HAIs, measure            ing in ICUs; central and peripheral vascular catheter
their consequences, and assess the impact of infection       care compliance monitoring; urinary catheter care
control practices; to improve the safety and quality of      compliance monitoring; monitoring of compliance
health care worldwide through implementation of sys-         with measures to prevent VAP; and performance feed-
tematized programs to reduce rates of HAI, associated        back. Data from the Process Surveillance Module on
mortality, excess lengths of stay, excess costs, and bac-    hand hygiene compliance are included in this report.
terial resistance.                                           The identity of all INICC hospitals, cities, and countries
                                                             is confidential, in accordance with the INICC charter.
METHODS
                                                             RESULTS
   The INICC at this time has focused on surveillance and
prevention of DAI in adult and pediatric ICUs and high-         Characteristics of 173 ICUs from 25 countries in
risk nurseries.3 The data are collected using standardized   Latin America, Asia, Africa, and Europe currently par-
CDC NNIS/NHSN protocols and definitions.14-16                 ticipating in the INICC that contributed data for this re-
   The INICC has both outcome surveillance and pro-          port are shown in Table 1. The participation of
cess surveillance components. The modules of the             hospitals on the INICC Program is as follows: mean
components may be used singly or simultaneously,             length of participation 6 SD, 22.9 6 21.6 months,
but, once selected, they must be used for a minimum          range 1 to 72 months. One hundred thirty-nine out
of 1 calendar month.                                         of 173 (81%) of ICUs collected and sent original data
   All DAIs of the Outcome Surveillance Component,           to INICC headquarters, and 34 out of 173 (19%) of
are categorized using standard CDC NNIS definitions           ICUs collected and sent aggregated data to INICC head-
that include laboratory and clinical criteria. Both labo-    quarters. Original and aggregated data were used to
ratory-confirmed bloodstream infections (BSIs) and            calculate DAI rates. Only original data were used to
clinical sepsis without microbiologic confirmation of         calculate mortality and lengh of stay.
BSI are recorded and reported.15                                For the Outcome Surveillance Component, DAI
   Within the Outcome Surveillance Component, data           rates, device utilization (DU) ratios, crude excess mor-
are classified into specific module protocols addressing       tality by specific type of DAI, antimicrobial utilization,
the following: DAI rates: excess length of stay, evalua-     and bacterial resistance for January 2003 through
tion of HAI costs, crude excess mortality, microbiologic     December 2008 are summarized (Tables 2-17).
profile, bacterial resistance, and antimicrobial-use data.       Tables 2-7 show DAI rates and DU ratios by infection
In addition, INICC methodology includes a process for        type (CLAB, CAUTI, VAP) in adult and pediatric ICUs. The
adjudication of and validation of reported HAIs.3            data were not stratified by type or size of hospital.
International Nosocomial Infection Control Consortium 2010
International Nosocomial Infection Control Consortium 2010
International Nosocomial Infection Control Consortium 2010
International Nosocomial Infection Control Consortium 2010
International Nosocomial Infection Control Consortium 2010
International Nosocomial Infection Control Consortium 2010
International Nosocomial Infection Control Consortium 2010
International Nosocomial Infection Control Consortium 2010
International Nosocomial Infection Control Consortium 2010
International Nosocomial Infection Control Consortium 2010

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International Nosocomial Infection Control Consortium 2010

  • 1. International Nosocomial Infection Control Consortium (INICC) report, data summary for 2003-2008, issued June 2009 Victor D. Rosenthal, MD,a Dennis G Maki, MD,b Silom Jamulitrat, MD,c Eduardo A. Medeiros, MD,d Subhash Kumar Todi, MD,e David Yepes Gomez, MD,f Hakan Leblebicioglu, MD,g Ilham Abu Khader, MD,h Marıa Guadalupe Miranda Novales, MD,i ´ Regina Berba, MD,j Fernando Martın Ramırez Wong, MD,k Amina Barkat, MD,l Osiel Requejo Pino, MD,m Lourdes Duenas, MD,n ´ ´ ˜ Zan Mitrev, MD,o Hu Bijie, MD,p Vaidotas Gurskis, MD,q S. S. Kanj, MD,r Trudell Mapp, RN,s Rosalıa Fernandez Hidalgo, RN,t ´ ´ Nejla Ben Jaballah, MD,u Lul Raka, MD,v Achilleas Gikas, MD,w Altaf Ahmed, MD,x Le Thi Anh Thu, MD,y Marıa Eugenia Guzman Siritt, MD,z and INICC Members ´ ´ Buenos Aires, Argentina; Madison, Wisconsin; Songkla, Thailand; Sao Paulo, Brazil; Kolkata, India; Medellın, ´ Colombia; Samsun, Turkey; Amman, Jordan; Mexico City, Mexico; Manila, Philippines; Lima, Peru; Rabat, Morocco; Havana, Cuba; San Salvador, El Salvador; Skopje, Macedonia; Shanghai, China; Kaunas, Lithuania; Beirut, Lebanon; ´ Panama City, Panama; San Jose, Costa Rica; Tunis, Tunisia; Prishtina, Kosova; Heraklion, Greece; Karachi, Pakistan; Ho Chi Minh City, Vietnam; and Caracas, Venezuela We report the results of the International Infection Control Consortium (INICC) surveillance study from January 2003 through December 2008 in 173 intensive care units (ICUs) in Latin America, Asia, Africa, and Europe. During the 6-year study, using Centers for Disease Control and Prevention (CDC) US National Healthcare Safety Network (NHSN; formerly the National Nosocomial Infec- tion Surveillance system [NNIS]) definitions for device-associated health care-associated infection, we collected prospective data from 155,358 patients hospitalized in the consortium’s hospital ICUs for an aggregate of 923,624 days. Although device utilization in the developing countries’ ICUs was remarkably similar to that reported from US ICUs in the CDC’s NHSN, rates of device-asso- ciated nosocomial infection were markedly higher in the ICUs of the INICC hospitals: the pooled rate of central venous catheter (CVC)-associated bloodstream infections (BSI) in the INICC ICUs, 7.6 per 1000 CVC-days, is nearly 3-fold higher than the 2.0 per 1000 CVC-days reported from comparable US ICUs, and the overall rate of ventilator-associated pneumonia (VAP) was also far higher, 13.6 versus 3.3 per 1000 ventilator-days, respectively, as was the rate of catheter-associated urinary tract infection (CAUTI), 6.3 versus 3.3 per 1000 catheter-days, respectively. Most strikingly, the frequencies of resistance of Staphylococcus aureus isolates to methicillin (MRSA) (84.1% vs 56.8%, respectively), Klebsiella pneumoniae to ceftazidime or ceftriaxone (76.1% vs 27.1%, respec- tively), Acinetobacter baumannii to imipenem (46.3% vs 29.2%, respectively), and Pseudomonas aeruginosa to piperacillin (78.0% vs 20.2%, respectively) were also far higher in the consortium’s ICUs, and the crude unadjusted excess mortalities of device-related infections ranged from 23.6% (CVC-associated bloodstream infections) to 29.3% (VAP). Key Words: Hospital infection; nosocomial infection; health care-associated infection; INICC; International Nosocomial Infection Consortium; device-associated infection; antibiotic resistance; ventilator-associated pneumonia; catheter-associated urinary tract infection; central line-associated bloodstream infections; bloodstream infection; urinary tract infection; developing countries; limited resources countries; low income countries; network. Copyright ª 2010 by the Association for Professionals in Infection Control and Epidemiology, Inc. Published by Elsevier Inc. All rights reserved. (Am J Infect Control 2010;38:95-106.) From the International Nosocomial Infection Control Consortium, Bue- Liaquat National Hospital, Karachi, Pakistanx; Cho Ray Hospital, Ho Chi nos Aires, Argentinaa; University of Wisconsin Medical School, Madison, Minh City, Vietnamy; Hospital Militar Dr. Carlos Arvelo, Caracas, WIb; Songklanagarind Hospital, Songkla, Thailandc; Hospital Sao Paulo, Venezuela.z Sao Paulo, Brazild; AMRI Hospitals, Kolkata, Indiae; Clınica CES, Medellın, ´ ´ Address correspondence to Victor D. Rosenthal, MD, MSc, CIC, Colombiaf; Ondokuz Mayis University Medical School, Samsun, Turkeyg; International Nosocomial Infection Control Consortium (INICC), Jordan University Hospital, Amman, Jordanh; Hospital de Pediatrıa ´ Corrientes Ave # 4580, Floor 11, Apt A, ZIP C1195AAR, Buenos Aires. CMN Siglo XXI, IMSS, Mexico City, Mexicoi; Philippine General Hospital, Argentina. E-mail: victor_rosenthal@inicc.org. Manila, Philippinesj; Hospital Marıa Auxiliadora, Lima, Peruk; Children ´ Hospital of Rabat, Rabat, Moroccol; Hospital Universitario Gral. Calixto, ˆ For a list of members of the International Nosocomial Infection Control Garcıa Havana, Cubam; Hospital Nacional de Ninos Benjamin Bloom, San ´ ˜ Consortium, see Appendix 1 available online at www.ajicjournal.org. Salvador, El Salvadorn; Filip II Special Cardiosurgery Hospital, Skopje, Conflicts of interest: None to report. Macedoniao; Zhongshan Hospital, Shanghai, Chinap; Kaunas University of Medicine, Children Clinic, Kaunas, Lithuaniaq; American University of 0196-6553/$36.00 Beirut Medical Center, Beirut, Lebanonr ; Clınica Hospital San Fernando ´ Copyright ª 2010 by the Association for Professionals in Infection Panama, Panama City, Panamas; Hospital Clınica Bıblica, San Jose, Costa ´ ´ ´ Control and Epidemiology, Inc. Published by Elsevier Inc. All rights Ricat; Hopital d’Enfants, Tunis, Tunisiau; National Institute for Public ˆ reserved. Health of Kosova and Medical School, Prishtina University, Prishtina, Kosovav; University Hospital of Heraklion, Heraklion, Greecew; doi:10.1016/j.ajic.2009.12.004 95
  • 2. 96 Rosenthal et al. American Journal of Infection Control March 2010 This report is a summary of data on device-associ- Infection control professionals (ICPs) collect data on ated infections (DAI) within intensive care units (ICUs) central line-associated primary bloodstream infections collected by hospitals participating in the International (CLABs), catheter-associated urinary tract infections Nosocomial Infection Control Consortium (INICC)1-13 (CAUTIs), and ventilator-associated pneumonias (VAPs) between January 2003 and December 2008. occurring in patients hospitalized in a specific patient The INICC is an international nonprofit, open, multi- care location, in nearly all hospitals. ICUs are stratified center, collaborative health care-associated infection according to the patient population: adult, pediatric, control program with a surveillance system based on or neonatal units (NICUs). that of the US National Healthcare Safety Network All NICUs are level III or level II/III units, and ICPs (NHSN; formerly the National Nosocomial Infection collect data on CLABs and umbilical catheter-associ- Surveillance system [NNIS]).3 Founded in Argentina in ated primary BSIs or VAPs for each of 5 birth-weight 1998, the INICC is the first multinational research net- categories (,750 g, 750-1000 g, 1001-1500 g, 1501- work established to control and reduce DAI through the 2500 g, .2500 g). Corresponding denominator data, analysis of data collected on a voluntary basis by a pool patient-days, and specific device-days are also of hospitals worldwide. The INICC has the following collected. goals: Create a dynamic global network of hospitals Small proportion of hospitals, with previous long- in the developing world that conducts surveillance of lasting experience conducting surveillance of DAIs, health care-associated infections (HAIs) using stan- sent aggregated data to the INICC. Original and aggre- dardized definitions and established methodologies, gated data were collected to calculate DAI rates. Only promote implementation of evidence-based infection original data were collected to calculate mortality and control practices, and carry out applied infection con- lengh of stay. trol research; provide training and surveillance tools The Process Surveillance Component includes the to individual hospitals that can allow them to conduct following modules: hand hygiene compliance monitor- outcome and process surveillance of HAIs, measure ing in ICUs; central and peripheral vascular catheter their consequences, and assess the impact of infection care compliance monitoring; urinary catheter care control practices; to improve the safety and quality of compliance monitoring; monitoring of compliance health care worldwide through implementation of sys- with measures to prevent VAP; and performance feed- tematized programs to reduce rates of HAI, associated back. Data from the Process Surveillance Module on mortality, excess lengths of stay, excess costs, and bac- hand hygiene compliance are included in this report. terial resistance. The identity of all INICC hospitals, cities, and countries is confidential, in accordance with the INICC charter. METHODS RESULTS The INICC at this time has focused on surveillance and prevention of DAI in adult and pediatric ICUs and high- Characteristics of 173 ICUs from 25 countries in risk nurseries.3 The data are collected using standardized Latin America, Asia, Africa, and Europe currently par- CDC NNIS/NHSN protocols and definitions.14-16 ticipating in the INICC that contributed data for this re- The INICC has both outcome surveillance and pro- port are shown in Table 1. The participation of cess surveillance components. The modules of the hospitals on the INICC Program is as follows: mean components may be used singly or simultaneously, length of participation 6 SD, 22.9 6 21.6 months, but, once selected, they must be used for a minimum range 1 to 72 months. One hundred thirty-nine out of 1 calendar month. of 173 (81%) of ICUs collected and sent original data All DAIs of the Outcome Surveillance Component, to INICC headquarters, and 34 out of 173 (19%) of are categorized using standard CDC NNIS definitions ICUs collected and sent aggregated data to INICC head- that include laboratory and clinical criteria. Both labo- quarters. Original and aggregated data were used to ratory-confirmed bloodstream infections (BSIs) and calculate DAI rates. Only original data were used to clinical sepsis without microbiologic confirmation of calculate mortality and lengh of stay. BSI are recorded and reported.15 For the Outcome Surveillance Component, DAI Within the Outcome Surveillance Component, data rates, device utilization (DU) ratios, crude excess mor- are classified into specific module protocols addressing tality by specific type of DAI, antimicrobial utilization, the following: DAI rates: excess length of stay, evalua- and bacterial resistance for January 2003 through tion of HAI costs, crude excess mortality, microbiologic December 2008 are summarized (Tables 2-17). profile, bacterial resistance, and antimicrobial-use data. Tables 2-7 show DAI rates and DU ratios by infection In addition, INICC methodology includes a process for type (CLAB, CAUTI, VAP) in adult and pediatric ICUs. The adjudication of and validation of reported HAIs.3 data were not stratified by type or size of hospital.