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Lower percentages of CD4+ T lymphocytes are associated with adverse clinical outcomes among children and adolescents infected with human immunodeficiency virus (HIV). CD4+ lymphocyte percentage generally increases with receipt of highly active antiretroviral therapy (HAART), but long-term follow-up is required to assess whether these increases in CD4+ cell percentage are maintained and whether they lead to normal CD4+ cell percentages in children with severe immunosuppression.
The study population included 1236 children and adolescents perinatally infected with HIV who were enrolled in a US-based multicenter prospective cohort study (Pediatric AIDS Clinical Trials Group 219/219C) and who were not receiving HAART at study initiation. We estimated the effects of HAART, HAART with protease inhibitors, and HAART with nonnucleoside reverse-transcriptase inhibitors on CD4+ cell percentage, using marginal structural models to account for confounding by severity.
Initiation of any type of HAART increased CD4+ cell percentage by 2.34% (95% confidence interval, 1.35%–3.33%) in the first year, relative to noninitiation of HAART. The substantial increases in CD4+ cell percentage observed after the first year of experience with these combination therapies were followed by relatively smaller increases that continued for 5 years after initiation. Although larger increases in CD4+ cell percentage were observed among children with a greater degree of immunosuppression at baseline, the mean CD4+ cell percentage after 5 years of HAART did not reach normal levels.
Our study supports the initiation of HAART in children before severe immunosuppression occurs for long-term maintenance of normal CD4+ cell percentages. This beneficial result must be weighed against the evidence of potential adverse events associated with the prolonged use of such therapy.
Among children and adolescents infected with HIV, low CD4+ T lymphocyte counts have been associated with weight growth failure  and mortality [1–5]. CD4+ cells serve as important immunologic markers of HIV disease progression that facilitate both clinical decision-making about when to initiate antiretroviral therapy and clinical monitoring of treatment effectiveness and drug resistance. Use of HAART has been associated with improved clinical outcomes, such as growth [6, 7] and survival of HIV-infected children [8, 9]. These associations are likely to be partly mediated through the effect of HAART on CD4+ cell counts. Numerous studies have found an association between combination antiretroviral therapy and increases in CD4+ cell count in children [10–24]. However, the majority of these studies included only small numbers of children and/or had follow-up periods of <1 year [10–21]. Of the studies evaluating the association between HAART and CD4+ cells, 2 recent studies observed >200 children for >1 year [22, 23]. These studies compared CD4+ cell percentage before initiation with CD4+ cell percentage after initiation and found substantial improvements in CD4+ cell percentage after the first year of therapy, followed by relatively smaller increases in the subsequent years. These immediate and prolonged effects were particularly observed among younger children (<5 years of age) and those children who initiated HAART with low CD4+ cell percentages (<15%).
Our study aimed to evaluate whether the CD4+ cell percentage increases associated with HAART were sustained for >5 years after HAART initiation and whether these increases resulted in a CD4+ cell percentage >25%, a level considered to be the lower limit of normal for children >1 year of age . We further aimed to evaluate separately HAART including a protease inhibitor (PI) and HAART including a nonnucleoside reverse-transcriptase inhibitor (NNRTI). Either PIs or NNRTIs are strongly recommended for inclusion in initial regimens for HIV-infected children  and are a basis for the definition of HAART. We investigated the mean change in CD4+ cell percentage after HAART exposure, because CD4+ cell percentage is a more stable measure of CD4+ lymphocytes in children than is absolute CD4+ cell count .
The study population included participants from Pediatric AIDS Clinical Trials Group (PACTG) Protocols 219 and 219C, both of which are longitudinal prospective studies designed to evaluate the long-term effects of HIV infection and in utero and postnatal exposure to antiretroviral therapy. Beginning in April 1993, infected and uninfected children from >80 study sites in the United States were eligible for enrollment in PACTG 219 and for subsequent enrollment in 219C if they were born to HIV-infected mothers and were younger than 21 years of age at study entry. These studies were approved by the human subjects review boards at each participating institution, and written informed consent was obtained from each child’s parent or legal guardian. The population eligible for this study included 1236 perinatally infected children enrolled in PACTG 219 or 219C from 1 January 1996 through 30 June 2006 who were HAART naive at their baseline visit and had complete data on covariates of interest at some point before HAART initiation. This period includes the introduction of PIs into clinical practice and captures data on those children who initiated HAART.
At each study visit, data on sociodemographic characteristics, clinical diagnoses, antiretroviral therapies received, and laboratory measurements of CD4+ cell percentage, total lymphocyte count, WBC count, hematocrit, and albumin level were collected. These laboratory measures have been previously identified as possible predictors of clinical progression in pediatric HIV infection [27, 28] and were, therefore, considered to be potential confounders of the effect of HAART on CD4+ cell percentage. Clinical diagnoses were reviewed by a study physician and classified as category C or N/A/B on the basis of the Centers for Disease Control and Prevention (CDC) criteria for classification of HIV disease in children <13 years of age and 13 years of age [29, 30]. HIV RNA measurements were not routinely collected before 2000, because they were not available when PACTG 219 was designed and were not standardized for pediatrics until the late 1990s .
HAART exposure was defined as the concomitant use of 3 drugs from 2 classes of HIV therapy. HIV drugs are classified into 3 main categories: nucleoside and/or nucleotide reverse-transcriptase inhibitors (NRTIs), NNRTIs, and PIs. HAART with PI was defined as a HAART regimen containing a PI, and HAART with NNRTI was defined as a HAART regimen containing an NNRTI (the 2 categories were not mutually exclusive). To evaluate the effects of treatment over time, patients in the HAART, HAART with PI, and HAART with NNRTI groups were classified into categories of years since the initiation of first HAART treatment. Once a participant initiated HAART, he or she was considered to be receiving therapy for the length of the follow-up period. In PACTG 219, actual dates of initiation of medication or dates of changes in the use of medications were not available. In accordance with a previous PACTG 219 study , we assumed that the midpoint between the first visit date at which the use of a new medication was recorded and the date of the prior visit was the date of initiation of that medication. We also conducted analyses in which the date of initiation was randomly assigned (unconditionally or conditionally on the basis of CD4+ cell percentage) during the interval between the 2 visits. These analyses resulted in similar estimates of the effect of HAART on CD4+ cell percentage.
Each child was able to contribute a maximum of 10 person-visits of follow-up beginning with his or her baseline visit and ending with (1) the patient’s final follow-up visit, (2) the first visit with missing CD4+ cell percentage data, or (3) 30 June 2006 (i.e., completion of study), whichever came first. In analyses of HAART with PI and HAART with NNRTI, children were censored on the last visit before switching to HAART regimens that did not include a PI and that did not include an NNRTI, respectively. For those children who enrolled in PACTG 219 before the start of the study period (1 January 1996), the first study visit after this date was set as the baseline visit. For children who enrolled after 1 January 1996 in either PACTG 219 or 219C, the first study visit was set as the baseline visit. For participants who were missing baseline data for any time-varying covariate, baseline was redefined as the first visit with complete data. Children with previous or current use of HAART at the baseline visit were excluded.
To estimate the effect of HAART on mean change in CD4+ cell percentage, we fit a repeated-measures linear regression model with CD4+ cell percentage at year t as the outcome and with the following covariates: an indicator for ever having received HAART by year t−1, age, sex, race or ethnicity, week of follow-up, calendar year, baseline CDC clinical category, baseline CD4+ cell percentage, baseline total lymphocyte count, baseline WBC count, baseline hematocrit, and baseline albumin level. To account for within-subject correlation caused by repeated measures, we fit this model using generalized estimating equations. To appropriately control for time-varying confounders, we weighted each child at each year by the inverse of the probability that they received their actual treatment history, given their measured time-varying covariates. Under the assumption of no unmeasured confounders, this model, which has parameters that are those of a marginal structural model [32, 33], estimates the difference in mean CD4+ cell percentage for those patients who initiated HAART, compared with those who did not initiate HAART. We used similar models to estimate the effect of HAART with PI and HAART with NNRTI on the mean CD4+ cell percentage.
We estimated stabilized inverse probability weights for initiating HAART and for censoring at the time of each visit [32–34]. For each child and each visit, the denominator of the weight is informally the probability that they received their actual treatment history and remained uncensored up to that time, conditional on their past covariate history. These weights create a statistical population in which the probabilities of treatment and censoring are unrelated to the time-varying confounders included in the models used to estimate weights . Unlike conventional unweighted models, inverse probability weighted models may appropriately adjust for time-varying confounders that are affected by prior HAART use or are on the causal pathway between HAART and changes in CD4+ cell percentage [32, 33, 35]. We estimated the weights by fitting pooled logistic regression models for the probability of HAART initiation and censoring at each visit, given baseline and past time-varying covariates [32, 33]. The covariates included in these models were age, sex, race or ethnicity, year of follow-up, and calendar year at baseline, together with baseline and time-varying values for CDC clinical category, CD4+ cell percentage, total lymphocyte count, WBC count, hematocrit, and albumin level. Year of follow-up and time-varying CD4+ cell percentage were modeled using flexible cubic splines with knots at the fifth, 25th, 50th, 75th, and 95th percentiles of the year of follow-up and CD4+ cell percentage, respectively. Data were structured for analysis purposes into 1-year intervals, and covariate information was carried forward from the most recently observed value when data were missing. For model comparison purposes, an unweighted generalized estimating equation model including only baseline covariates and a standard unweighted generalized estimating equation model including both baseline and time-varying covariates were used to estimate the effect of HAART, HAART with PI, and HAART with NNRTI on CD4+ cell percentage.
Characteristics of the 1236 participants at baseline are presented in table 1. At baseline, 29% of participants were <5 years of age, 51% were female, 56% were black, 20% had a CD4+ cell percentage <15%, and 28% had CDC clinical category C disease. In the analysis of the overall effects of HAART on CD4+ cell percentage, the median length of follow-up for the entire cohort was 3 years (interquartile range, 1–7 years). A total of 330 participants (27%) remained in follow-up through 30 June 2006; the remaining 906 (73%) were censored at the first visit with missing CD4+ cell percentage data. There were 3043 HAART-free person-years of follow-up, and 610 participants (49%) initiated HAART; these participants had a total of 3109 person-years of follow-up while receiving HAART. Among the HAART initiators, the median cumulative exposure was 3 years (interquartile range, 1–7 years). The corresponding follow-up characteristics for the HAART with PI and HAART with NNRTI analyses are presented in table 2.
Of the 610 initial HAART regimens, 387 (63%) included only PIs in combination with NRTIs, of which nelfinavir (177 regimens; 46%) and ritonavir (174 regimens; 45%) were the most common. Sixty-seven (11%) of the initial HAART regimens included only NNRTIs in combination with NRTIs; efavirenz was used in 34 (51%) of these regimens, and nevirapine was used in 33 (49%). Of the initial HAART regimens, 156 included both PIs and NNRTIs with NRTIs; nevirapine was the most common NNRTI used, in combination with ritonavir in 61 (39%) of the regimens and nelfinavir in 46 (29%). Most HAART regimens included 2 NRTIs, the most common combinations being lamivudine with either stavudine (107 [33%] of 329) or zidovudine (92 [28%] of 329).
Table 3 presents estimates of the effects of HAART on mean CD4+ cell percentage by years since HAART initiation. All 3 HAART exposures resulted in a >2% increase in CD4+ cell percentage after 1 year of therapy, compared with no HAART exposure. A small increase in CD4+ cell percentage was observed each year after the large increase in the first year after initiation. This steady trend extended at least 5 years after combination therapy initiation. Similar to previous analyses, the largest increases in CD4+ cell percentage during the years since combination therapy initiation were observed in those children with the lowest baseline CD4+ cell percentage. After 1 year of HAART, children with a CD4+ cell percentage <15% at baseline experienced a 4.44% increase (95% CI, 2.27%–6.62%) in CD4+ cell percentage, compared with a 2.78% increase (95% CI, 1.52%–4.03%) among children with a CD4+ cell percentage of 15%–24% at baseline and a 1.19% increase (95% CI, 0.01%–2.38%) among children with a CD4+ cell percentage 25% at baseline. Despite the greater increase in CD4+ cell percentage, however, the mean CD4+ cell percentage of children with a CD4+ cell percentage <15% at baseline did not recover to a level >25%, even 5 years after HAART initiation (figure 1). Age at baseline did not modify these effects further. The effect of years since initiation of HAART with PI and years since initiation of HAART with NNRTI showed the same pattern of change by CD4+ cell percentage and age at baseline.
As expected, conventional unweighted regression models yielded attenuated estimates. The estimated difference in mean CD4+ cell percentage after 1 year of HAART use versus no HAART was 1.76% (95% CI, 0.83%–2.70%) in an unweighted repeated-measures model with baseline covariates only and was 0.76% (95% CI, 0.18%–1.35%) when the time-varying covariates were added to the model.
Our findings suggest that the initial increases in CD4+ cell percentage observed in the first year after HAART initiation are sustained for at least 5 years after HAART initiation among children and adolescents infected with HIV and that greater increases occur among those with the greatest degree of immunosuppression. Our findings also suggest that PI-based and NNRTI-based HAART regimens cause similar increases in mean CD4+ cell percentage. Although age at baseline did not significantly modify these findings, larger improvements in CD4+ cell percentage attributable to HAART initiation were observed among younger children (<5 years of age), compared with older children (5 years of age). This is consistent with previous studies evaluating CD4+ cell response to HAART and may support the hypothesis of greater thymic activity among young children [14, 22, 23]. However, the differences between the age groups could be attributable to alternative explanations, such as adherence issues among adolescents  or a survivor effect.
Although the ideal goal of long-term therapy is to recover CD4+ cell percentage to normal levels, only 36% of children with CD4+ cell percentage <15% and 59% of children with CD4+ cell percentages of 15%–24% at baseline achieved CD4+ cell percentages 25% at 5 years after HAART initiation. Given these descriptive findings, we evaluated whether HAART initiation was associated with normal CD4+ cell percentage values after adjustment for time-dependent confounding and found that HAART initiation was associated with 2-fold greater odds of normal CD4+ cell percentage, compared with noninitiation of HAART (OR, 2.26; 95% CI, 1.65–3.10). Similarly, initiation of HAART with PI and initiation of HAART with NNRTI were associated with normal CD4+ cell percentage values, compared with noninitiation (OR for HAART with PI, 2.63 [95% CI, 1.87–3.68]; OR for HAART with NNRTI, 4.69 [95% CI, 2.63– 8.34]).
Our results were consistent with the previous PACTG 219 study investigating the effect of PI-based HAART on CD4+ cell percentage . Although that study used different approaches to examine this association, both studies found HAART with PI to be associated with significant increases in CD4+ cell percentage that were maintained over time. The previous PACTG 219 study estimated the mean changes in CD4+ cell percentage from baseline to 3 years after initiation of HAART with PI. Our approach aimed to estimate the effect of initiating HAART on CD4+ cell percentage, compared with not initiating HAART. This approach used a non-HAART comparison group to account for changes in CD4+ cell percentage over time that were unrelated to HAART initiation, such as age-related changes in CD4+ cell percentage .
Our results are not directly comparable to those of Walker et al. , because those authors compared HAART use with no use of any antiretroviral therapy. We were unable to compare the effect of HAART on CD4+ cell percentage with the effect of no treatment, because only 20 children in our cohort had no experience with antiretroviral therapy. These treatment-naive children were more likely to have enrolled in the later years of the study than in the earlier years.
To obtain a completely unbiased estimate of the effect of HAART on CD4+ cell percentage, information on all potential confounders of the association is a necessity. Although we were able to control for some important confounders, such as age and CDC clinical category, we were unable to adjust for potential confounding by plasma HIV RNA level (i.e., viral load), because this information was not routinely collected or available until 2000. If clinicians were using viral load information to make treatment initiation decisions during our study period, then the HAART-associated increases in CD4+ cell percentage reported in our study may be underestimated.
In this study, children were required to be naive to HAART at study entry; therefore, a large percentage (56%) of subjects in PACTG 219/219C were ineligible for our study because of previous HAART exposure. This was especially true for subjects who enrolled after 2000. This exclusion allowed for the observation of treatment history prior to HAART initiation and the identification of predictors of HAART initiation. We therefore needed to make the “no confounding” assumption for therapy initiation but not for therapy continuation.
Also, we assumed that children continued to receive HAART after initiation. This assumption was correct for 87% of 3109 person-years after HAART initiation. However, because 13% of the visits occurred among persons who had stopped using HAART, our analysis did not attempt to estimate the effect of continuous HAART versus no HAART, but the effect of HAART initiation (the “intention-to-treat effect”) versus no HAART in a hypothetical randomized clinical trial in which (1) participants were randomly assigned to begin continuous HAART at different visits, (2) all participants initially complied and began HAART at their assigned visit, and (3) 13% later discontinued HAART. Because many of the study participants who discontinued HAART did so because of toxicity (rather than for nonmedical reasons), it is this intention-to-treat effect, not the effect of continuous HAART use, that would be a parameter of public health interest. This is because, had we estimated the effect of continuous HAART, we would have been estimating the effect of forcing people to continue therapy even in the presence of toxicity (something that did not occur in reality).
In conclusion, this study assessed the long-term effect of HAART initiation on CD4+ cell percentage among children and adolescents infected with HIV. Overall, HAART initiation was associated with a significant increase in CD4+ cell percentage. The substantial increases in CD4+ cell percentage observed after the first year of HAART were followed by relatively smaller increases continuing for at least 5 years after initiation. Although larger increases in CD4+ cell percentage were observed among children with a greater degree of immunosuppression at baseline, their mean CD4+ cell percentage after 5 years of HAART treatment did not approach normal levels. This study adds to previous studies that have addressed the debate about when to initiate HAART in children. Although our study supports the initiation of HAART in children before severe immunosuppression occurs to maintain normal CD4+ cell percentages, this beneficial result must be weighed against evidence of potential adverse events associated with the prolonged use of such therapy [22, 36–40]. Continued follow-up is therefore required, not only to observe long-term events, but also to determine if the effects of HAART on CD4+ cell percentage are maintained beyond the 5-year period documented in this study and whether children who initiate HAART at low CD4+ cell percentages eventually rebound to normal levels.
We thank the children and families, for their participation in PACTG 219/219C, the individuals and institutions involved in the conduct of PACTG 219/219C, and Dr. Roger Logan, for his technical assistance.
Financial support. National Institute of Allergy and Infectious Diseases (NIAID), the National Institute of Child Health and Human Development, the Statistical and Data Analysis Center at the Harvard School of Public Health (NIAID cooperative agreement #5 U01 AI41110 with the Pediatric AIDS Clinical Trials Group and cooperative agreement #1 U01 AI068616 with the International Maternal Pediatric Adolescent AIDS Clinical Trials Group), and National Institutes of Health-NIAID Biostatistics/Epidemiology Training Grant in AIDS (T-32 AI07358 to K.P.).
The following institutions and individuals participated in PACTG Protocol 219C, by order of enrollment. Baylor Texas Children’s Hospital: Mary E. Paul, Chivon D. Jackson, Faith Minglana, and Heidi Schwarzwald; University of Florida, Jacksonville: Mobeen H. Rathore, Ayesha Mirza, Kristy Champion, and Almer Mendoza; Chicago Children’s Memorial Hospital: R. Yogev and E. Chadwick; University of Puerto Rico, University Children’s Hospital AIDS Program: Irma L. Febo, Licette Lugo, Ruth Santos, and Ibet Heyer; Bronx Lebanon Hospital Center: M. Purswani, S. Baksi, E. Stuard, and M. Dummit; San Juan Hospital: M. Acevedo, M. Gonzalez, L. Fabregas, and M. E. Texidor; University of Miami: Gwendolyn B. Scott, Charles D. Mitchell, Claudia Florez, and Joan Gamber; University of Medicine & Dentistry of New Jersey: Arlene Bardeguez, Arry Dieudonne, Linda Bettica, and Juliette Johnson; Charity Hospital of New Orleans & Earl K. Long Early Intervention Clinic: M. Silio, T. Alchediak, C. Boe, M. Cowie, and R. Van Dyke; University of California at San Diego Mother, Child & Adolescent HIV Program: Stephen A. Spector, Rolando M. Viani, Mary Caffery, and Kimberly Norris; Howard University: Sohail Rana, Helga Finke, Patricia Yu, and Jhoanna Roa; Jacobi Medical Center: M. Donovan, R. Serrano, M. Burey, and R. Auguste; St. Christopher’s Hospital for Children, Philadelphia: J. Chen and J. Foster; Baystate Medical Center Children’s Hospital: B. W. Stechenberg, D. J. Fisher, A. M. Johnston, and M. Toye; Los Angeles County Medical Center/University of Southern California: J. Homans, M. Neely, L. S. Spencer, and A. Kovacs; Children’s Hospital Boston: S. Burchett and N. Karthas; Children’s Hospital of Michigan: E. Moore and C. Cromer; St. Jude Children’s Research Hospital, Memphis: Aditya Gaur, Katherine Knapp, Nehali Patel, and Marion Donohoe; New York University School of Medicine/Bellevue Hospital: Maryam Minter, Thomas Hastings, Seham Akleh, and William Borkowsky; The Children’s Hospital at Downstate: E. Handelsman, H. J. Moallem, D. M. Swindell, and J. M. Kaye; The Columbia Presbyterian Medical Center & Cornell University New York Presbyterian Hospital: A. Higgins, M. Foca, P. LaRussa, and A. Gershon; The Children’s Hospital of Philadelphia: Steven D. Douglas, Richard M. Rutstein, Carol A. Vincent, and Patricia C. Coburn; Children’s Hospital of Oakland: Ann Petru, Teresa Courville, Katherine Eng, and Karen Gold; University of California, San Francisco, Moffitt Hospital: Diane W. Wara, Nicole Tilton, and Mica Muscat; Children’s Hospital, University of Colorado, Denver: E. McFarland and C. Salbenblatt; Johns Hopkins University Department of Pediatrics: N. Hutton, B. Griffith, M. Joyner, and C. Kiefner; Children’s Hospital and Regional Medical Center, University of Washington: Michele Acker, Ann J. Melvin, Kathleen M. Mohan, and Suzanne Phelps; Metropolitan Hospital Center: Mahrukh Bamji, Indu Pathak, Savita Manwani, and Ekta Patel; Children’s National Medical Center: Diana Dobbins, Deidre Wimbley, Tracy Perron, and Hans Spiegel; University of Massachusetts Medical School: K. Luzuriaga and R. Moriarty; University of Alabama at Birmingham: R. Pass and M. Crain; University of Maryland School of Medicine: D. Watson, J. Farley, K. Klipner, and C. Hilyard; Schneider Children’s Hospital: V. R. Bonagura, S. J. Schuval, C. Colter, and L. Campbell; Boston Medical Center: Stephen I. Pelton, E. R. Cooper, Lauren Kay, and Ann Marie Regan; University of Illinois: K. C. Rich, K. Hayani, M. Bicchinella, and J. Camacho; State University of New York, Stony Brook: Sharon Nachman, Denise Ferraro, Jane Perillo, and Michele Kelly; North Broward Hospital District: Ana M. Puga, Guillermo Talero, James Blood, and Stefanie Juliano; Duke University: Carole Mathison, Kareema Whitfield, Felicia Wiley, and Margaret Donnelly; Harlem Hospital: S. Champion, M. Frere, M. DiGrado, and E. J. Abrams; Cook County Hospital: James B. McAuley, Kenneth M. Boyer, Maureen Haak, and Jamie Martinez; University of South Alabama: Mary Mancao and Benjamin Estrada; Connecticut Children’s Medical Center: Juan C. Salazar and Gail Karas; University of North Carolina at Chapel Hill: Tom Belhorn, Jean Eddleman, and Betsy Pitkin; Ruiz Arnau University Hospital: W. Figueroa and E. Reyes; State University of New York Upstate Medical University: L. B. Weiner, K. A. Contello, W. A. Holz, and M. J. Famiglietti; Children’s Medical Center Dallas, University of Texas Southwestern: O. Ramilo; University of Florida at Gainesville: R. Lawrence, J. Lew, C. Delany, and C. Duff; Children’s Hospital at Albany Medical Center: A. D. Fernandez, P. A. Hughes, N. Wade, and M. E. Adams; Lincoln Medical & Mental Health Center; Phoenix Children’s Hospital: J. P. Piatt, J. Foti, and L. Clarke-Steffen; Public Health Unit of Palm Beach County: J. Sleasman and C. Delaney; Medical College of Georgia: Stuart Foshee, Chitra S. Mani, Dennis L. Murray, and Christopher White; Yale University School of Medicine: Warren A. Andiman, Leslie Hurst, Janette de Jesus, and Donna Schroeder; Vanderbilt University Medical Center: G. Wilson; University of Rochester Medical Center: Geoffrey A. Weinberg, Francis Gigliotti, Barbra Murante, and Susan Laverty; St. Josephs Hospital and Medical Center, New Jersey: N. Hutchcon and A. Townley; Emory University Hospital: S. Nesheim and R. Dennis; University of South Florida: P. Emmanuel, J. Lujan-Zilberman, C. Graisberry, and S. Moore; Children’s Hospital of the King’s Daughters: R. G. Fisher, K. M. Cunnion, T. T. Rubio, and D. Sandifer; Medical University of South Carolina: G. M. Johnson; University of Mississippi Medical Center: H. Gay and S. Sadler; Harbor-UCLA Medical Center: Margaret A. Keller, Nasser Redjal, Spring Wettgen, and Sheryl Sullivan; Mount Sinai Medical Center: D. Johnson; Children’s Hospital of Los Angeles: J. Church, T. Dunaway, and C. Salata; Long Beach Memorial: Susan Marks, Karen Elkins, Jagmohan Batra, and Audra Deveikis; Robert Wood Johnson Medical School: S. Gaur, P. Whitley-Williams, A. Malhotra, and L. Cerracchio; Sinai Children’s Hospital: M. Dolan, J. D’Agostino, and R. Posada; The Medical Center, Pediatric Columbus, Georgia: C. Mani and S. Cobb; Medical College of Virginia: S. R. Lavoie and T. Y. Smith; Cooper Hospital-University Medical Center: A. Feingold and S. Burrows-Clark; University of Cincinnati: J. Mrus and R. Beiting; Columbus Children’s Hospital: M. Brady, J. Hunkler, and K. Koranyi; Sacred Heart Children’s Medical Center of Florida: W. Albritton; St. Luke’s/Roosevelt Hospital Center: R. Warford and S. Arpadi; Incarnation Children’s Center, New York: A. Gershon and P. Miller; Montefiore Medical–Albert Einstein College of Medicine: A. Rubinstein and G. Krienik; Children’s Hospital of Los Angeles: A. Kovacs and E. Operskalski; San Francisco General Hospital: D. Wara, A. Kamrin, S. Farrales, N. Tilton, and M. Muscat; Cornell University New York Presbyterian: R. Johan-Liang and K. O’Keefe; St. Louis Children’s Hospital: K. A. McGann, L. Pickering, and G. A. Storch; North Shore University Hospital: S. Pahwa and L. Rodriquez; and Oregon Health and Science University: P. Lewis and R. Croteau.
Potential conflicts of interest. All authors: no conflicts.