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The 2009 pandemic influenza A (H1N1) (pH1N1) virus continues to circulate worldwide. Determining the roles of chronic conditions and bacterial coinfection in mortality is difficult because of the limited data for children with pH1N1-related critical illness.
We identified children (<21 years old) with confirmed or probable pH1N1 admitted to 35 US PICUs from April 15, 2009, through April 15, 2010. We collected data on demographics, baseline health, laboratory results, treatments, and outcomes.
Of 838 children with pH1N1 admitted to a PICU, the median age was 6 years, 58% were male, 70% had ≥1 chronic health condition, and 88.2% received oseltamivir (5.8% started before PICU admission). Most patients had respiratory failure with 564 (67.3%) receiving mechanical ventilation; 162 (19.3%) received vasopressors, and 75 (8.9%) died. Overall, 71 (8.5%) of the patients had a presumed diagnosis of early (within 72 hours after PICU admission) Staphylococcus aureus coinfection of the lung with 48% methicillin-resistant S aureus (MRSA). In multivariable analyses, preexisting neurologic conditions or immunosuppression, encephalitis (1.7% of cases), myocarditis (1.4% of cases), early presumed MRSA lung coinfection, and female gender were mortality risk factors. Among 251 previously healthy children, only early presumed MRSA coinfection of the lung (relative risk: 8 [95% confidence interval: 3.1–20.6]; P < .0001) remained a mortality risk factor.
Children with preexisting neurologic conditions and immune compromise were at increased risk of pH1N1-associated death after PICU admission. Secondary complications of pH1N1, including myocarditis, encephalitis, and clinical diagnosis of early presumed MRSA coinfection of the lung, were mortality risk factors.
The 2009 pandemic influenza A (H1N1) virus was associated with high rates of hospitalization and death in children worldwide. Limited data for children with pH1N1-related critical illness make it difficult to determine the role of chronic conditions and bacterial coinfection in mortality.
Children with neurologic conditions and compromised immune function had an increased risk of mortality from 2009 pandemic H1N1. Coinfection with methicillin-resistant Staphylococcus aureus was a strong risk factor for mortality, increasing the risk of death in previously healthy children eightfold.
Although it is regarded as a mild-to-moderate pandemic,1 2009 pandemic influenza A (H1N1) [pH1N1] has been associated with school outbreaks,2–4 high incidence5 and illness complication rates,6 hospitalizations,7–11 and critical illness and death12 in pediatric populations worldwide. To date, clinical data are available for only limited numbers of critically ill children with pH1N1 virus infection-related complications13–16 or fatalities.17,18 Results have varied across studies: pH1N1-related PICU mortality rates ranged from 7% in 57 Canadian14 and 107 Australian-New Zealand19 children to 39% in 147 children in Argentina.13 Independent risk factors associated with fatal outcomes have not been well established because of limited sample sizes.
To assess critical illness among children during the 2009 influenza A (H1N1) pandemic, we established a large multicenter registry of patients admitted to PICUs in major US pediatric hospitals. In this report we describe the detailed clinical characteristics and hospital course of this large cohort of critically ill children with pH1N1 virus infection and discuss the role of chronic medical conditions and bacterial coinfections in mortality.
This 1-year multicenter retrospective and prospective observational cohort study identified patients with influenza virus infection admitted to 35 Pediatric Acute Lung Injury and Sepsis Investigators' (PALISI) network hospital PICUs (see Fig 1 for site locations) from April 15, 2009, through April 15, 2010. The study was initiated as a collaborative effort among the US National Institutes of Health, Centers for Disease Control and Prevention, the Assistant Secretary for Preparedness and Response, US Department of Health and Human Services, the National Heart, Lung, and Blood Institute's ARDSNet, and the PALISI network to track pH1N1-associated critical illness in adults (ARDSNet sites) and children (PALISI sites). The ARDSNet clinical coordinating center coordinated data management. After institutional review board approval, sites identified patients with any positive influenza A test result from April 15 through August 31, 2009, and any positive influenza test result or suspected case of influenza from September 1, 2009, through April 15, 2010. The first institutional review board approval was received November 15, 2009. Decisions regarding diagnostic testing were determined solely by clinicians. We excluded patients without laboratory confirmation of influenza and those with evidence of seasonal influenza A (H1N1 or H3N2) or B virus infections.
Data were recorded in a REDCap20 Web-based electronic case-report form and transmitted to the clinical coordinating center. PICU day 0 was the PICU admission day. Baseline values were the first recorded values in the PICU and, if unavailable, the values closest to admission (from transport, the emergency department, or referral hospital). Data on days 3, 7, and 14 were collected as close to 8:00 am as possible; unavailable data were considered missing. Final outcome (survival/death) was tracked to initial PICU discharge date for all patients and up to hospital day 90 for patients transferred to the ward. Cause of death was classified as primary respiratory, cardiovascular, multiorgan failure, severe brain injury and/or brain death, or other.
Those who were considered to be previously healthy patients were healthy before the index illness, had no underlying medical conditions, and did not depend on medications or medical devices. The Pediatric Risk of Mortality III (PRISM III) acute physiology score21 was used to measure severity of illness within the first 24 hours of admission in children younger than 18 years, and the Acute Physiology and Chronic Health Evaluation II (APACHE II) score22 was used in those aged 18 to 20 years.
Noninvasive ventilation was defined as delivery of continuous or bilevel positive airway pressure from a mechanical ventilator via a mask. Shock requiring vasopressors was defined as receiving a dopamine infusion of >5 μg/kg per minute or any epinephrine, norepinephrine, or phenylephrine infusion to maintain blood pressure. Diagnosis of encephalitis was based on MRI findings, high cerebrospinal fluid protein level, and/or neurology consultation. Myocarditis was defined as the major clinical diagnosis underlying the reason for PICU admission. Mortality was defined as death that occurred anytime during the PICU stay and up to hospital day 90 for patients transferred to the ward. A confirmed case of pH1N1 was defined as that of a PICU patient with a respiratory specimen that tested positive for pH1N1 virus infection by real-time reverse transcription polymerase chain reaction assay using primers specific for pH1N1 virus or viral culture. A probable case of pH1N1 was defined as that of a PICU patient with a respiratory specimen that tested positive for influenza A virus infection by any influenza testing without further identification of subtype. Patients with early presumed bacterial coinfection of the lung had (1) a clinical diagnosis of bacterial pneumonia, (2) evidence of bacterial superinfection within 72 hours of the initial PICU admission, and (3) a bacterial pathogen identified in their respiratory secretions.
With univariate analyses we examined the association between multiple factors and mortality by using χ2 and Fisher's exact tests. Unadjusted relationships between continuous variables were evaluated by using simple linear regression. Factors examined for their association with mortality were demographics; PICU admission clinical conditions including comorbidities and coinfections; treatments; and secondary influenza-related complications (eg, encephalitis, myocarditis). Factors possibly associated with mortality (P ≤ .10) were considered for inclusion in the multivariable model containing all independent predictors of mortality (P < .05). Missing data were not imputed. All analyses were completed by using SAS 9.2 (SAS Institute, Inc, Cary, NC). SAS's PROC GENMOD procedure produced adjusted relative risks (RRs) by using a generalized linear model. Adjusted risk estimates are reported with 95% confidence intervals (CIs).
We enrolled 940 PICU patients and excluded 102 (14 aged ≥21 years, 9 with seasonal influenza A, 6 with influenza B, and 73 with no positive influenza test result [some met >1 criterion]). Of the 838 patients included, 545 (65%) had pH1N1 confirmed by real-time reverse transcription polymerase chain reaction or viral culture, and 293 (35%) were classified as having probable pH1N1 on the basis of a positive direct fluorescent antibody or rapid influenza diagnostic test result for influenza A without additional subtyping. Most children (553 [66%]) were prospectively identified; 62% were admitted to the PICU during September through November 2009, during the reported peak of influenza-related hospital admissions for the 2009–2010 season.
The characteristics of patients with confirmed or probable pH1N1 are listed in Table 1 and Supplemental Table 5. Most (60%) asthmatics were on weekly asthma-control medications. Reported influenza-related signs and symptoms in patients included fever (79%), cough (73%), shortness of breath (54%), vomiting (30%), diarrhea (12%), and seizures (10%) (Supplemental Table 5) (mean onset: 4 days [SD: 6.3]; median: 3 days [interquartile range (IQR): 1–5]; n = 694) before PICU admission. The majority of patients (579 [69.1%]) were transferred to the PICU from an emergency department, but 239 patients (28.5%) had been an inpatient at the same or another hospital, including 31 (3.7%) in another hospital's ICU, for a median of 1 day (IQR: 0.5–3.0) before PICU admission.
The median Pediatric Risk of Mortality III score was 5 (IQR: 2–10) for the patients younger than 18 years, and the median Acute Physiology and Chronic Health Evaluation II score was 14.5 (IQR: 8–20) for those aged 18 years or older. At presentation, 90 patients (10.7%) received vasopressors for shock, 11 (1.3%) were in cardiac arrest, and 29 (3.5%) had suspected central nervous system complications. Most patients (536 [64%]) presented with evidence of acute lower respiratory disease; 57.5% received assisted breathing on the day of PICU admission (excluding 27 patients on chronic mechanical ventilation). Chest radiographs were performed on 92.5% of the patients at or around PICU admission, and 51.4% had infiltrates in at least 2 of 4 quadrants. Selected laboratory testing parameters closest to admission are listed in Table 2.
Viral coinfections were reported in 4.8% (40) of the patients, including respiratory syncytial virus (14) and adenovirus (4). Thirty-three percent (274 of 838) of the patients had a clinical diagnosis of bacterial pneumonia or other evidence of bacterial infection present within ≤72 hours of PICU admission. Pathogens identified in respiratory secretions included S aureus in 26% (71 of 274; 48% [34 of 71] were methicillin-resistant Staphylococcus aureus [MRSA]), Pseudomonas (all species) in 11% (30 of 274), Streptococcus pneumoniae in 5.5% (15 of 274), Haemophilus influenzae in 5% (13 of 274), Streptococcus pyogenes in 3% (7 of 274), and other bacteria in 20% (54 of 274) (Supplemental Table 6). No pathogens were identified in 33% (91 of 274) of the patients. Most of the patients presumed to be coinfected with Pseudomonas (87% [26 of 30]) had chronic lung disease (17 of 26 had tracheostomies). Empyema (with thoracostomy) was diagnosed in 3.5% (29 of 838) of the patients. Nearly 5% of the patients had bacteremia within 72 hours of PICU admission, and S aureus was the most common bacteria identified (11 of 38, 7 of which were MRSA and 4 of 7 also had MRSA in respiratory specimens ≤72 hours of admission).
The majority of patients (67.3% [564 of 838]) received mechanical ventilator support (median duration: 5 days [IQR: 2–13]). The median PICU stay was 4 days (IQR: 2–9). Of the 75 (8.9%) children who died, death occurred in 31% on PICU days 0 to 2 and 35% on PICU days 3 to 14. All PICU deaths occurred within 90 days of admission except for 1 previously healthy teenager who died on PICU day 124 after lung transplant for pulmonary necrosis, presumably from MRSA coinfection. The primary cause of death reported was inability to ventilate or oxygenate the patient (46.7%), multiorgan failure (25.3%), brain death or severe brain injury (14.7%), refractory cardiovascular collapse (2.7%), and other causes (10.7%). Adjunctive treatments administered to patients are listed in Table 3. Extracorporeal membrane oxygenation (ECMO) was used in 33 patients (3.9%; median age: 8 years [IQR: 5–14]; n = 18 [54.5%] on day 0), for a mean of 18.9 days (SD: 21.4; range: 1–123) with 39% survival. A tracheostomy was performed on 3.1% (26) of the patients. The majority of the 763 survivors (745 [97.6%]) were discharged, but 18 (2.4%) remained hospitalized 90 days after PICU admission (7 were still in a PICU); 22 (2.9%) were transferred to a rehabilitation facility.
Only 5.8% (49 of 838) of the patients had documentation of receiving influenza antiviral medications before PICU admission (initiation dates were unavailable). Most of the patients (88.2%) received enteral oseltamivir in a PICU for a median of 4 days (IQR: 2–5). Reported use of other influenza antiviral agents is indicated in Table 3.
Nonsurvivors had higher Pediatric Risk of Mortality III scores (median: 17 [IQR: 9–29]) at PICU admission than survivors (median: 4 [IQR: 0–9]; P < .0001). Of the selected laboratory parameters documented close to PICU admission in patients who were tested, leukocytopenia, neutropenia, thrombocytopenia, elevated creatinine level, and severe hypoxia were associated with mortality (Table 2). Patients who received adjunctive therapies (eg, ECMO, dialysis) had a higher risk of death (see Table 3).
The associations of mortality with patient-related factors present before PICU admission (demographics, underlying health conditions, bacterial coinfections) and influenza-related clinical syndromes are listed in Table 4. The mortality was higher in patients transferred from another ICU (RR: 3.1 [95% CI: 1.6–5.9]; P = .0008). No females were pregnant. Height data were not routinely collected to determine the association of BMI with mortality. Encephalitis (14 [1.7%]) and myocarditis (12 [1.4%]) were uncommon but associated with mortality (see patient details in Supplemental Table 7 and Supplemental Table 8). Viral coinfection was not associated with mortality. MRSA was the only organism cultured from respiratory secretions within ≤72 hours of admission and presumed to be causing pneumonia or a bacterial infection that was associated with mortality (Table 4 and Supplemental Table 9). In a multivariable analysis of factors present at admission, female gender, having a preexisting neurologic condition or previous immune compromise, early presumed MRSA coinfection of the lung, encephalitis, and myocarditis remained significant independent predictors of mortality (Table 4).
When the analysis was restricted to the 251 previously healthy patients, there were 26 (10.4%) with early presumed S aureus coinfection of the lung (Supplemental Table 10), and this infection was present in 8 of 18 (44%) of the previously healthy children who died. S aureus was cultured from endotracheal tube specimens of 25 of 26 and from empyema fluid of 1 of 26. Early presumed MRSA coinfection of the lung was the only previously identified factor that remained associated with mortality (RR: 8 [95% CI: 3.1–20.6]; P < .0001) (Supplemental Table 9). Of the 6 previously healthy children with MRSA coinfection of the lung who died, 5 were treated before or within 2 hours of PICU admission with intravenous vancomycin (Supplemental Table 10).
To our knowledge, this is the largest study to date of critically ill children with pH1N1 virus infection, which included 838 patients hospitalized at 35 US PICUs. Disease progression was rapid and often fulminant; 69% were admitted to a PICU from an emergency department, 58% received assisted ventilation at PICU admission, and 8.9% died. Sixty-two percent had critical illness from pH1N1 virus infection with no suspicion or evidence of secondary bacterial pneumonia or other bacterial infection at PICU admission. Independent risk factors for mortality were female gender, presence of a chronic neurologic condition or immune compromise, diagnosis of acute myocarditis or encephalitis, and early presumed MRSA coinfection of the lung. For the 30% of children who were previously healthy, only early presumed MRSA coinfection of the lung, which increased the RR of death eightfold, was strongly associated with mortality.
Although in previous decades invasive bacterial coinfection with MRSA was not identified as a major organism associated with pediatric influenza-related mortality, reports from 2003 onward suggest that its role in severe and fatal seasonal influenza complications among US children and adults might have increased.23–30 Although guidelines for empiric antimicrobial treatment of hospitalized adults with community-acquired pneumonia, including for suspected MRSA, exist,31 no guidance existed for hospitalized children with community-acquired pneumonia during the study period. Although our data support empiric antibiotic treatment of MRSA,32 in addition to treatment for other common coinfections (eg, S pneumoniae, S pyogenes), in the initial management of children with suspected or confirmed influenza and severe lower respiratory tract disease, there are not clear criteria for prospective identification of patients with bacterial coinfection.
The median age of children in our study was 6 years, similar to that reported for Canada14,33 and South Korea34 but higher than that for Argentina, where more than half of the children were infants.13 The proportion of children with chronic medical conditions and the overall mortality were similar to those reported for Canada.14 Our mortality and proportion of invasive mechanical ventilation were lower than those reported in 1 Argentina study.13 Although more male than female children were admitted to our PICUs with pH1N1-associated complications, female patients were at a significantly higher risk of death. This risk was not caused by pregnancy, which is a known risk factor.35 There were no gender differences in mortality rate among previously healthy children.
Neurologic and neuromuscular disorders have previously been identified as risk factors for influenza-related complications and hospitalization in children,36 and they were present in 31% of our patients. The rate of neurologic disorders is reportedly high in children who die from pH1N1-related complications17; ours is the first study to identify that presence of an underlying neurologic condition was an independent risk factor for death. Acute neurologic manifestations associated with pH1N1 also occurred; seizures occurred in 10% of the patients before admission, suspected central nervous system complications occurred in 3.5%, and acute encephalitis was diagnosed in 1.7%. Although there have been case reports of severe encephalopathy or encephalitis in patients with pH1N1,37–40 the size of our study allowed us to identify acute encephalitis with pH1N1 virus infection as an independent risk factor for mortality.
Confirming a previous report on Korean children,34 we found pH1N1-related acute myocarditis to be an independent risk factor for death. Seasonal influenza virus infection of the respiratory tract is associated with acute myocarditis,41 and myocarditis cases related to pH1N1 have been described.34,42–44 Current management of influenza-associated myocarditis is supportive care.
In a previous population-based report,45 11.6% of primarily adult patients with pH1N1 admitted to the ICU received ECMO in Australia and New Zealand compared with 3.9% of the patients in our study. We report 39% survival for pediatric patients with pH1N1 who received ECMO, which is much lower than the 71% survival previously reported for mostly adults.46 Other rescue therapies were also associated with high mortality. ECMO support was used in 7 of 10 of the patients who died; 4 had early presumed S aureus lung coinfection.
Most patients received oseltamivir treatment; antiviral medication use at any time during the PICU course was not associated with lower mortality. The authors of 1 study of PICU patients in Argentina reported that initiation of oseltamivir treatment within ≤24 hours of admission was associated with lower mortality.13 Authors of a study of adult ICU patients in Mexico also reported a survival benefit of neuraminidase inhibitor treatment.47 Others have reported the effectiveness of early antiviral treatment with oseltamivir to prevent progression of pH1N1 virus infection to severe and fatal illness.8,35,48 Data on the timing of oseltamivir initiation was not collected in our study. The vast majority of patients began receiving it after PICU admission; we cannot assess if earlier treatment could have improved outcome.
This study is subject to several limitations. First, although pH1N1 was confirmed in 65% of the cases, we believe that classifying 35% of the patients who tested positive for influenza A as having probable pH1N1 was valid, because US influenza surveillance identified 99% of influenza A viruses tested during the study period as pH1N1 viruses.49 It is likely that some patients with pH1N1 at participating PICUs were missed because of the use of less sensitive influenza tests.50 Although most clinical data were collected retrospectively, most data elements were easily captured from the patients' charts. It is unfortunate that bacterial isolates were not available for strain typing or identification of virulence factors such as Panton-Valentine leukocidin. A majority of presumed bacterial lung coinfections were detected by culture of endotracheal aspirate specimens; the sensitivity and specificity of such lower respiratory tract sampling is currently unknown. In addition, testing for other respiratory viruses or bacterial infections was performed as clinically indicated and was not done on a systematic basis or with more sensitive diagnostics, and administration of broad-spectrum antibiotics might have produced negative culture results for some bacterial pathogens. This might have underestimated certain coinfections that have been identified with greater frequency in other studies.51,52 We included children admitted to large PICUs in regional referral pediatric centers. Therefore, we could not determine pH1N1-associated risk factors for more severe illness. Children admitted to smaller PICUs were not represented.
The pH1N1 virus continues to circulate worldwide. In addition to influenza antiviral treatment, early empiric antimicrobial treatment of critically ill children with suspected or confirmed influenza and lower respiratory tract disease, shock, or sepsis should cover MRSA and other bacterial pathogens associated with influenza. It is important to note that most of the children coinfected with MRSA who died in our study received vancomycin promptly at or before PICU admission, which indicates that prevention and control strategies for increasing influenza-related immunity and optimizing antiviral treatment of influenza, new therapies for treating severe influenza, and new treatment strategies for MRSA pneumonia complicating influenza are urgently needed for children.
This work was supported by National Institutes of Health, National Heart, Lung, and Blood Institute, Department of Health and Human Services (contract N01 HR 56179).
The PALISI network participants include the following: Arkansas Children's Hospital (Little Rock, AR): Ronald C. Sanders, MD, and Glenda Hefley, MNsc, RN; Phoenix Children's Hospital (Phoenix, AZ): David W. Tellez, MD, and Velva Woodward, RN; Miller Children's Hospital Long Beach (Long Beach, CA): Christopher Babbitt, MD, and Rosalynn Gurrola, RN; Children's Hospital of Los Angeles (Los Angeles, CA): Barry Markovitz, MD, Jeff Terry, MBA, and Karen Waters, RN; Children's Hospital of Central California (Madera, CA): Ana Lia Graciano, MD, Melita Baldwin, CHCC, and Aurelia Ayala, RN; Children's Hospital and Research Center (Oakland, CA): Heidi Flori, MD, and Julie Simon, RN; Children's Hospital of Orange County (Orange, CA): Nick Anas, MD, and Stephanie Osborne, RN; UCSF Children's Medical Center (San Francisco, CA): Anil Sapru, MD, and Maureen Convery, RN; Yale-New Haven Children's Hospital (New Haven, CT): John S. Giuliano Jr, MD, and Kellie Martino; The Children's Hospital (Aurora, CO): Angela Czaja, MD, Peter Mourani, MD, and Susanna Burr; Connecticut Children's Medical Center (Hartford, CT): Christopher L. Carroll, MD, and Indira Sadhu, RN; Holtz Children's Hospital (Miami, FL): Gwenn McLaughlin, MD, and Yenis Mijares; Children's Healthcare of Atlanta at Egleston (Atlanta, GA): Matthew Paden, MD, and Rich Toney, RN; Kapi'olani Center for Women and Children (Honolulu, HI): Rupert Cheng, MD, Len Tanaka, MD, and Sara Murakami; Kosair Children's Hospital (Louisville, KY): Vicki Montgomery, MD, and Kara Richardson, RN; Children's Hospital Boston (Boston, MA): Adrienne Randolph, MD, MSc, Grace Yoon, RN, NNP, Ryan Sullivan RN, and Anna Agan, BA; Johns Hopkins Children's Center (Baltimore, MD): Melania Bembea, MD, MPH, and Beth White, RN; St Louis Children's Hospital (St Louis, MO): Allan Doctor, MD, Bertram Hicks, RN, and Regina Yu; Helen DeVos Children's Hospital (Grand Rapids, MI): Raja Surender, MD, and Jeni Wincek, RN, MSN; Duke Children's Hospital and Health Center (Durham, NC): David A. Turner, MD, and Samantha Tate; Children's Hospital of Nebraska (Omaha, NE): Edward Truemper, MD, and Machelle Zink, BSN, MEd; Children's Hospital at Dartmouth (Lebanon, NH): Daniel L. Levin, MD, and J. Dean Jarvis, RN; Golisano Children's Hospital (Rochester, NY): Kate Ackerman, MD, Jill Cholette, MD, and Eileen Tallie; Nationwide Children's Hospital (Columbus, OH): Mark W. Hall, MD, and Kristin Greathouse, BSN, MS; Children's Hospital at St Francis (Tulsa, OK): R. Philip Barton, MD, Kellie Brown, RN, and Christy Dallis, RN; Doernbecher Children's Hospital (Portland, OR): Aileen Kirby, MD; Penn State Hershey Children's Hospital (Hershey, PA): Neal Thomas, MD, Jill Raymond, RN, MSN, and Debra Spear, RN; Children's Hospital of Philadelphia (Philadelphia, PA): Mark Helfaer, MD, Mary Ann Diliberto, RN, and Ashleigh Clair, MS; Monroe Carell Jr Children's Hospital at Vanderbilt (Nashville, TN): Rick Barr, MD, MSc, and Pamela Berry, RN, CCRP; Dell Children's Medical Center of Central Texas (Austin, TX): Renee Higgerson, MD, LeeAnn Christie, RN, and Tamika Rhodes; University of Texas Southwestern Children's Medical Center at Dallas (Dallas, TX): Cindy Darnell, MD, and Julie Long, PhD; Texas Children's Hospital (Houston, TX): Laura L. Loftis, MD, Yvonne Kay Henry, BS, Nancy Jaimon, RN, Ursula Kyle, MS, RD/LD; University of Virginia Children's Medical Center (Charlottesville, VA): Douglas F. Willson, MD, and Christine Traul, MD; Seattle Children's Hospital (Seattle, WA): Jerry Zimmerman, MD, and Ruth Barker, RRT, NPS, CCRC; and Children's Hospital of Wisconsin (Milwaukee, WI): Rainer Gedeit, MD, Kathy Murkowski, RRT, and Kate Luther.
We thank Elizabeth Higgs, MD, and Andrea Harabin, PhD, for helpful comments on the manuscript. Anna Agan and Cathryn Oldmixon, RN, provided administrative coordination, and David Schoenfeld, PhD, provided statistical and data-management oversight. In addition, we thank all of the PALISI network participants.
Dr Randolph (principal investigator) conceived and designed the study, recruited the enrolling sites, designed the case-report forms, oversaw data acquisition and analysis, interpreted the data, drafted the manuscript, made multiple revisions, and approved the final version for submission for publication; Drs Uyeki, Rubinson, Thompson, and Rice made substantial contributions to the study conception and design, provided important input on data interpretation, revised the manuscript for important intellectual content, and approved the final version to be submitted for publication; Dr Vaughn (statistician) performed the main data analysis and interpretation, revised the manuscript for important intellectual content, and approved the final version to be submitted for publication; Mr Sullivan and Ms Yoon (study coordinators) made substantial contributions to the acquisition, analysis, and interpretation of the data, revised the manuscript for important intellectual content, and approved the final version to be submitted for publication; Ms Smoot (statistician) assisted with data acquisition and analysis, revised the manuscript for important intellectual content, and approved the final manuscript to be submitted for publication; and Drs Loftis, Helfaer, Doctor, Paden, Flori, Babbitt, Graciano, Gedeit, Sanders, Giuliano, and Zimmerman (site principal investigators) provided input on the design of the study, collected data at their sites, revised the manuscript critically for important intellectual content, and approved the final version of the manuscript before submission for publication.
The findings and conclusions in this article are those of the authors and do not necessarily represent the official position of the Centers for Disease Control and Prevention or the US Department of Health and Human Services.
FINANCIAL DISCLOSURE: The authors have indicated they have no financial relationships relevant to this article to disclose.
Funded by the National Institutes of Health (NIH).