Skip to main content
International Journal of Pediatrics logoLink to International Journal of Pediatrics
. 2017 Oct 18;2017:3169098. doi: 10.1155/2017/3169098

Implementing an Oxygen Supplementation and Monitoring Protocol on Inpatient Pediatric Bronchiolitis: An Exercise in Deimplementation

Brian LeCleir 1, Leslie Jurecko 2, Alan T Davis 3,4, Nicholas J Andersen 5, Dominic Sanfilippo 6,7, Surender Rajasekaran 6,7,, Anthony Olivero 6,7
PMCID: PMC5664324  PMID: 29181038

Abstract

Aim

Our goal in this study is to evaluate the effectiveness of our oxygen (O2) protocol to reduce length of stay (LOS) for children hospitalized with bronchiolitis.

Methods

In this retrospective cohort study, the outcomes of children ≤ 24 months old that were admitted with bronchiolitis and placed on the O2 protocol were compared to historical controls. The primary outcome was hospital length of stay. Secondary outcomes were duration of O2 supplementation, rates of pediatric intensive care unit transfer, and readmission.

Results

Groups were not significantly different in age, gender, and rates of respiratory distress score assessment. Significantly more severely ill patients were in the O2 protocol group. There were no significant differences between control and O2 protocol groups with regard to mean LOS, rates of pediatric intensive care unit transfer, or seven-day readmission rates. By multiple regression analysis, the use of the O2 protocol was associated with a nearly 20% significant decrease in the length of hospitalization (p = 0.030).

Conclusion

Use of O2 supplementation protocol increased LOS in the more ill patients with bronchiolitis but decreased overall LOS by having a profound effect on patients with mild bronchiolitis.

1. Introduction

Lower respiratory tract infections such as bronchiolitis and viral pneumonia place tremendous strain on the health of young children and the healthcare system. The propensity of these viral infections to affect the most vulnerable of pediatric populations along with their highly variable clinical course leads to frequent hospital admissions that often occur regardless of severity [1]. The respiratory syncytial virus (RSV) alone affects roughly 800,000 children in the United States leading to approximately 20% of the annual birth cohort requiring medical attention yearly [2]. This results in $500 million of direct hospital costs in the United States alone [3].

Hypoxemia requiring supplemental oxygen (O2) is a key determinant in the decision to hospitalize infants with bronchiolitis and contributes to increased length of stay (LOS) [4]. Updated clinical practice guidelines released by the American Academy of Pediatrics (AAP) in 2014 identify O2 supplementation and hydration as the mainstay of treatment for bronchiolitis [5]. They establish a blood O2 saturation (spO2) of <90%, measured by pulse oximetry as a threshold for initiating O2 therapy and encourage discontinuing O2 supplementation and spO2 monitoring after improvement [6]. However, the integration of those guidelines can be quite challenging as they require ongoing “deimplementation,” a term describing the practice of discouraging care not supported by evidence-based research [7, 8]. These practices are difficult to discourage and often need a concerted effort to eliminate, even in the face of well-executed collaboration [9]. While there are numerous studies evaluating the impact of deimplementing interventions such as chest X-rays, antibiotics, and corticosteroids [1016], few studies specifically evaluate the impact of a protocol based O2 supplementation practice [1719]. Our institution developed and implemented an inpatient pediatric O2 supplementation and pulse oximetry protocol based on AAP guidelines [5] that aligns with the realities of our clinical practice. We hypothesize that the implementation of this protocol and deimplementation of certain practices lead to a significant decrease in hospital LOS for children admitted with bronchiolitis.

2. Methods

2.1. Intervention

A multidisciplinary team of clinicians at Helen DeVos Children's Hospital, a tertiary care pediatric hospital, designed and implemented a standardized O2 supplementation and continuous pulse oximetry protocol (Figure 1) in February 2013. Significant changes to prior medical practice included lowering the threshold for O2 supplementation from 94% to 90% and clearly defining both the steps and duration over which O2 supplementation would be titrated and discontinued. This protocol created a formal algorithm that was in clear contrast to a previously highly variable system that was driven by individual care providers. We performed education in the form of online modules, didactics, and formalized multidisciplinary rounds with respiratory therapists, nurses, and providers at the hospital. We also used education to stress and deemphasize some of the practices that were not supported by clinical evidence (Table 1).

Figure 1.

Figure 1

Standardized O2 supplementation and continuous pulse oximetry protocol.

Table 1.

Clinical practices discouraged on initiation of protocol.

Discouraged Encouraged
Chest radiography Weaning O2 flow and FIO2
Viral panel testing Accepting saturation of >90% if child does not appear distressed
Blood draws for laboratory testing Discontinuing supplemental gas flow when patient is on room air
β-Agonist therapy Calling the physician for any perception of deterioration
Steroids Spot checks in pulse oximetry
Antibiotic therapy

2.2. Study Sample

In order to assess this quality initiative, we performed a retrospective review of the medical charts of infants and children (≤24 months of age) hospitalized with bronchiolitis during the preintervention study period of November 1, 2011, through April 30, 2012 (control group), and during the postintervention study period of November 1, 2013, through April 30, 2014 (O2 protocol group). Exclusion criteria included hospital admission directly to the pediatric intensive care unit (PICU), home O2 used immediately before or after hospitalization, presence of a tracheostomy tube, congenital heart disease, sickle cell disease, severe anemia, hypotonia, cystic fibrosis, and age > 24 months.

2.3. IRB Statement

Spectrum Health Institutional Review Board reviewed the study as a quality improvement (QI) project and thus was exempted from full review.

2.4. Data Sources

The medical records of patients who met the entry criteria with discharge diagnoses of “acute bronchiolitis” were reviewed. Patients were identified using electronic medical record search queries for International Classification of Diseases, Ninth Revision (ICD-9), primary or secondary diagnosis codes 466.1 (acute bronchiolitis), 466.11 (acute bronchiolitis due to respiratory syncytial virus), and 466.19 (acute bronchiolitis due to other infectious organisms).

2.5. Study Variables

Patient age at admission, gender, respiratory distress score (RDS), duration of supplemental O2, LOS, seven-day readmission rate, rate of PICU transfer, and coexisting medical problems were collected. LOS, as noted in hours, was determined as the period from the time of admission to the inpatient unit until the time of discharge. We evaluated bronchiolitis illness severity at the time of the first respiratory therapist evaluation by using a modified RDS tool, an evaluation tool based on respiratory rate, accessory muscle use, wheezing, O2 requirement, and inspiratory to expiratory ratio (Table 2) [20]. RDS values ≥3 were considered to be indicative of moderate to severe bronchiolitis.

Table 2.

Respiratory distress score (RDS) calculation.

Respiratory distress score
Respiratory rate
 □ 0 Normal (respiratory rate (rr) up to 40 breathes/minute)
 □ 1 Elevated (RR 40–60 breaths/minute)
 □ 2 Tachypnea (RR greater than 60 breaths/minute)
Accessory muscle use
 □ 0 Normal
 □ 1 Retractions (substernal, subcostal, intercostal)
 □ 2 Neck or abdominal muscle use
Wheezing
 □ 0 None or scattered end expiratory wheezes
 □ 1 Wheezes throughout expiration
 □ 2 Entire inspiration and expiration wheezes
Oxygen requirement
 □ 0 Maintains SpO2 above 90% on room air
 □ 1 Maintains SpO2 above 90% on less than 1 Lpm oxygen
 □ 2 Requires 1 Lpm oxygen or more to maintain SpO2 above 90%
Inspiratory to expiratory ratio
 □ 0 I : E ratio less than 1 : 2
 □ 1 I : E ratio 1 : 2 to 1 : 3
 □ 2 I : E ratio greater than 1 : 3

2.6. Statistical Methods

The data was analyzed using IBM Statistics SPSS v. 21 (Armonk, New York). Quantitative data was compared using a t-test and was reported as the mean ± SD. Nominal data was compared using the χ2 test and Fisher's exact test (when appropriate) and was reported as percentages. Due to the nonnormal distribution of LOS and duration of O2 supplementation, both of these variables were transformed prior to analysis, while the summary statistics shown are for the untransformed data. The LOS was transformed using the natural log, while the duration of O2 supplementation was transformed using the inverse hyperbolic sine. In addition, a multiple regression analysis was performed, using the log transformed LOS as the dependent variable, with patient age, O2 protocol group versus control group, PICU transfer, and RDS score as the independent variables. Significance was assessed at p < 0.05.

3. Results

From the collective study periods, a total of 263 children met the study criteria: 141 children in the control group and 122 children in the O2 protocol group. Table 3 shows the patient's demographics and characteristics. There were no significant differences based on age, gender, and PICU transfer rates between control and O2 protocol groups (Table 3). Only three children were readmitted within seven days, one in the control group and two in the O2 protocol group.

Table 3.

Demographic and clinical variables.

Variable Control group (n = 141) O2 protocol group (n = 122) p value
Age (months) 6.2 ± 5.5 7.0 ± 6.3 0.31
Gender: male/female 77 (54.6%)/64 (45.4%) 70 (57.4%)/52 (42.6%) 0.65
RDS assessed 125/141 (88.7%) 110/122 (90.2%) 0.69
RDS 2.0 ± 1.5 2.7 ± 1.6 <0.001
LOS (h)a 69.6 ± 67.5 72.5 ± 77.4 0.374
 LOS: RDS < 3a,b 70.6 ± 60.3 51.6 ± 42.6 0.005
 LOS: RDS ≥ 3a,c 74.0 ± 53.4 95.2 ± 95.7 0.535
Duration of O2 supplementation (h)a 38.3 ± 58.4 40.9 ± 62.9 0.638
Number requiring supplemental O2 134/141 (95.0%) 113/122 (92.6%) 0.414
PICU transfer 10/141 (6.7%) 13/122 (9.7%) 0.310
7-day readmission 1/141 (0.7%) 2/122 (1.6%) 0.598

Data are presented as the mean ± SD or as percentages; O2, oxygen; LOS, length of stay; RDS, respiratory distress score; PICU, pediatric intensive care unit. aData were analyzed using log transformed data, values shown are untransformed data. bControl group n = 87; oxygen protocol group n = 49. cControl group n = 38; oxygen protocol group n = 61.

Contrary to our hypothesis, there was not a statistically significant difference in LOS between the control and O2 protocol groups. However, the O2 protocol group had a significantly higher severity of illness at admission based on their initial RDS independent of assessment rates.

Next, we assessed the relationship between LOS and bronchiolitis severity, as defined by the RDS. Patients in the O2 protocol group with mild bronchiolitis (RDS < 3) had a statistically significant shorter LOS compared to control (RDS ≥ 3) (p = 0.005). Interestingly, O2 protocol group subjects with moderate to severe bronchiolitis (RDS ≥ 3) had a 29% increase in LOS, although this was not statistically significant (p = 0.535). Furthermore, O2 protocol group subjects with mild disease had a significantly shorter LOS compared with the O2 protocol patients with moderate to severe bronchiolitis (Table 4). This data suggests that LOS may be dependent on disease severity. O2 protocol group subjects with mild bronchiolitis disproportionately improve compared with moderate to severe disease. Furthermore, the O2 protocol may have a negative affect when bronchiolitis is more severe. However, no direct conclusive relationship between LOS and the protocol could be inferred for moderate to severe disease due to the disproportionately higher RDS patients in the O2 protocol.

Table 4.

Study group LOSa and PICU transfer compared by RDS.

Outcome measure RDS < 3 (n = 136) RDS ≥ 3 (n = 99) p value
Control group LOS (h)b 70.6 ± 60.3 74.0 ± 53.4 0.697
O2 protocol group LOS (h)c 51.3 ± 41.4 92.4 ± 94.3 0.005
PICU transfer 9/136 (6.6%) 12/99 (12.1%) 0.144

Data are presented as the mean ± SD or as percentages; O2, oxygen; LOS, length of stay; RDS, respiratory distress score; PICU, pediatric intensive care unit. aData analyzed using log transformed data, values shown are untransformed data. bRDS < 3 group n = 87; RDS ≥ 3 group n = 38; cRDS < 3 group n = 49; RDS ≥ 3 group n = 61.

We performed a multiple regression analysis to independently assess each subject group and variables affecting the LOS (Table 5). We found age, RDS, and PICU transfer all had a significant correlation with LOS. A one-month increase in age significantly decreased LOS. RDS significantly impacted LOS, whereas a one-unit increase in RDS significantly increased LOS by 11.3% and a two-unit increase in RDS increased LOS by 23.9%. Transfer to the PICU significantly increased LOS by 2.9 fold. The O2 protocol had a significant inverse association with LOS compared to the control group; patients in the O2 protocol group had a 19.7%, decrease in LOS (Table 4).

Table 5.

Multiple regression analysis, with log transformed length of stay (LOS) as the dependent variable.

Variable β-Coefficient 95% CI p value
O2 protocol group −0.22
−0.42–−0.02
0.030
Age −0.02 −0.04–−0.01 0.008
RDS 0.11 0.04–0.17 0.001
PICU Transfer 1.06 0.72–1.41 <0.001

CI, confidence interval; O2, oxygen; RDS, respiratory distress score; PICU, pediatric intensive care unit. Control group (reference group) versus the O2 protocol group.

4. Discussion

High variability in clinical care often contributes to higher healthcare costs and poor adherence to evidence-based practices [21]. For this reason, health care professionals have developed protocols to drive therapies and reduce the lack of concordance. Studies have shown clinical outcomes from nonphysician directed protocols compare favorably with physician driven interventions in multiple settings [2224]. Such protocols used in the PICU have the potential to save money and reduce resource allocation when used in the non-ICU setting. Our study suggests that this is potentially true. We reduced LOS for patients with mild bronchiolitis (initial RDS < 3) after the implementation of the O2 protocol and deimplementation of unnecessary practices. However, LOS appeared to increase for patients with higher RDS following protocol implementation. The actual impact of RDS on LOS is somewhat confounded by the fact that RDS was higher in the postimplementation years even though the rates of assessment were similar in both groups. When we controlled for the RDS effect by using multivariate regression analysis there was a demonstrable aggregate benefit that was more than compensated for the increased LOS in sicker patients.

Deimplementation and deinnovation are quality improvement (QI) terms that emphasize the abandonment of unnecessary care that is not supported by evidence-based research [7, 8]. These terms focus on the ideal of discouraging use rather than discouraging underuse and have been used in the context of eliminating nonevidenced-based practices in bronchiolitis [9]. We paired the initiation of O2 use protocol along with deimplementation of unnecessary practices and hypothesized that a collective approach would have specific value in reducing unnecessary care. This provided a mechanism to overcome the inertia of so-called “established” clinical practice and increase the provider's sense of efficacy.

The AAP prioritizes the prevention of unnecessary care [5, 6], and a recent study showed benefit to eliminating practices such as X-rays and alpha-agonist therapy in community hospital settings [9]. The deimplementation of such practices requires constant education. It was our experience that the respiratory therapists were the strongest advocates for avoiding such unnecessary therapy. Applications of nebulized β-agonist therapy and/or hypertonic saline were rarely tried, and when attempted, they were discontinued once lack of efficacy was established. Such an approach has benefit in saving money, eliminating unnecessary interventions, and focusing care on the sickest during the time of the year that hospitals are busiest [25].

There is wide variation in the clinical course of bronchiolitis and thus it is difficult to distinguish which patients will require only titration of O2 therapy from those who will require a more involved escalation of care [26, 27]. For example, there have been efforts in the past to define clinical criteria that could predict inpatient LOS for children with bronchiolitis that have shown that initial spO2 values do not predict LOS in children with bronchiolitis [26]. Our protocol attempts to surmount some of that dilemma by predicating appropriate care and letting the clinical course dictate the level of care the patient receives.

This study does have limitations in that the single center retrospective design with historical controls limits our ability to conclusively state that there is benefit to the O2 supplementation protocol. This study design by nature is an observational study. It is possible that natural cycle of viral virulence, unknown changes to childhood immunity, and other unknown variations may affect this study. In addition, other interventions independent of this oxygen protocol may have played a role in these outcomes, in particular LOS. One criticism for our study might be that the RDS score we used is more of an amalgam of other scores available in the literature rather than a validated score. However, the score was uniformly applied to all patients, and clearly an increase in the score was associated with an increase in respiratory distress. Also, the RDS scores were notably higher on average in the O2 protocol group. It is possible this is due to a true difference in illness severity between the seasons evaluated, or the increased frequency of respiratory therapist monitoring mandated by the O2 protocol resulted in increased provider confidence in keeping patients with higher illness severity on general inpatient floors. Regardless, we presented data that the weaning protocol might have benefit in a selected group of milder bronchiolitis cases.

5. Conclusion

This study is unique in that it highlights both the benefit and the unforeseen effect of applying protocols to patient care. Our application of the AAP guidelines in a collaborative manner saw a decrease in LOS of children with milder bronchiolitis while LOS for the sicker patients increased. However, the overall effect was one of the benefits with potential to exert an impact on appropriate hospital triage and cost. This translates into a benefit for both patients and their families.

Acknowledgments

The authors thank Matthew Pridgeon, MD, who helped to conceive and implement the oxygen supplementation protocol, and Stephanie Raymundo, MD, who aided in data acquisition and in conceptualizing this study.

Abbreviations

RSV:

Respiratory syncytial virus

O2:

Oxygen

LOS:

Length of stay

AAP:

American Academy of Pediatrics

spO2:

Blood oxygen saturation

PICU:

Pediatric intensive care unit

QI:

Quality improvement

ICD-9:

International Classification of Diseases, Ninth Revision

RDS:

Respiratory distress score.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

References

  • 1.Norwood A., Mansbach J. M., Clark S., Waseem M., Camargo C. A., Jr. Prospective multicenter study of bronchiolitis: Predictors of an unscheduled visit after discharge from the emergency department. Academic Emergency Medicine. 2010;17(4):376–382. doi: 10.1111/j.1553-2712.2010.00699.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Hall C. B., Weinberg G. A., Iwane M. K., et al. The Burden of respiratory syncytial virus infection in young children. The New England Journal of Medicine. 2009;360(6):588–598. doi: 10.1056/NEJMoa0804877. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Hasegawa K., Tsugawa Y., Brown D. F. M., Mansbach J. M., Camargo C. A., Jr. Trends in bronchiolitis hospitalizations in the United States, 2000-2009. Pediatrics. 2013;132(1):28–36. doi: 10.1542/peds.2012-3877. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Schroeder A. R., Marmor A. K., Pantell R. H., Newman T. B. Impact of pulse oximetry and oxygen therapy on length of stay in bronchiolitis hospitalizations. Archives of Pediatrics & Adolescent Medicine. 2004;158(6):527–530. doi: 10.1001/archpedi.158.6.527. [DOI] [PubMed] [Google Scholar]
  • 5.Ralston S., Lieberthal A., Meissner H., et al. Clinical practice guideline: the diagnosis, management, and prevention of bronchiolitis. Pediatrics. 2014;134(5):e1474–e1502. doi: 10.1542/peds.2014-2742. [DOI] [PubMed] [Google Scholar]
  • 6.Quinonez R. A., Schroeder A. R. Safely doing less and the new AAP bronchiolitis guideline. Pediatrics. 2015;135(5):793–795. doi: 10.1542/peds.2014-3703. [DOI] [PubMed] [Google Scholar]
  • 7.Prasad V., Ioannidis J. P. A. Evidence-based de-implementation for contradicted, unproven, and aspiring healthcare practices. Implementation Science. 2014;9(1, article no. 1) doi: 10.1186/1748-5908-9-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Ubel P. A., Asch D. A. Creating value in health by understanding and overcoming resistance to de-innovation. Health Affairs. 2015;34(2):239–244. doi: 10.1377/hlthaff.2014.0983. [DOI] [PubMed] [Google Scholar]
  • 9.Ralston S. L., Garber M. D., Rice-Conboy E., et al. A multicenter collaborative to reduce unnecessary care in inpatient bronchiolitis. Pediatrics. 2016;137(1) doi: 10.1542/peds.2015-0851.e20150851 [DOI] [PubMed] [Google Scholar]
  • 10.Schuh S., Lalani A., Allen U., et al. Evaluation of the utility of radiography in acute bronchiolitis. Journal of Pediatrics. 2007;150(4):429–433. doi: 10.1016/j.jpeds.2007.01.005. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Purcell K., Fergie J. Lack of usefulness of an abnormal white blood cell count for predicting a concurrent serious bacterial infection in infants and young children hospitalized with respiratory syncytial virus lower respiratory tract infection. The Pediatric Infectious Disease Journal. 2007;26(4):311–315. doi: 10.1097/01.inf.0000258627.23337.00. [DOI] [PubMed] [Google Scholar]
  • 12.Kellner J. D., Ohlsson A., Gadomski A. M., Wang E. E. L. Efficacy of bronchodilator therapy in bronchiolitis: a meta-analysis. Archives of Pediatrics & Adolescent Medicine. 1996;150(11):1166–1172. doi: 10.1001/archpedi.1996.02170360056009. [DOI] [PubMed] [Google Scholar]
  • 13.Gadomski A. M., Scribani M. B. Bronchodilators for bronchiolitis. Cochrane Database of Systematic Reviews. 2014;6:1–74. doi: 10.1002/14651858.CD001266.pub4.CD001266 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Hartling L., Wiebe N., Russell K., Patel H., Klassen T. P. A meta-analysis of randomized controlled trials evaluating the efficacy of epinephrine for the treatment of acute viral bronchiolitis. Archives of Pediatrics & Adolescent Medicine. 2003;157(10):957–964. doi: 10.1001/archpedi.157.10.957. [DOI] [PubMed] [Google Scholar]
  • 15.Fernandes R. M., Bialy L. M., Vandermeer B., et al. Glucocorticoids for acute viral bronchiolitis in infants and young children. Cochrane Database of Systematic Reviews. 2013;(6) doi: 10.1002/14651858.CD004878.pub4.CD004878 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Farley R., Spurling G. K. P., Eriksson L., Del Mar C. B. Antibiotics for bronchiolitis in children under two years of age. Cochrane Database of Systematic Reviews. 2014;10 doi: 10.1002/14651858.CD005189.pub4.CD005189 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Cheney J., Barber S., Altamirano L., et al. A clinical pathway for bronchiolitis is effective in reducing readmission rates. Journal of Pediatrics. 2005;147(5):622–626. doi: 10.1016/j.jpeds.2005.06.040. [DOI] [PubMed] [Google Scholar]
  • 18.Cunningham S., Rodriguez A., Adams T., et al. Oxygen saturation targets in infants with bronchiolitis (BIDS): A double-blind, randomised, equivalence trial. The Lancet. 2015;386(9998):1041–1048. doi: 10.1016/S0140-6736(15)00163-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Cunningham S., McMurray A. Observational study of two oxygen saturation targets for discharge in bronchiolitis. Archives of Disease in Childhood. 2012;97(4):361–363. doi: 10.1136/adc.2010.205211. [DOI] [PubMed] [Google Scholar]
  • 20.Downes J. J., Vidyasagar D., Morrow G. M., Boggs T. R. Respiratory distress syndrome of newborn infants: I. New clinical scoring system (RDS score) with acid-base and blood- gas correlations. Clinical Pediatrics. 1970;9(6):325–331. doi: 10.1177/000992287000900607. [DOI] [PubMed] [Google Scholar]
  • 21.Willson D. F., Horn S. D., Hendley J. O., Smout R., Gassaway J. Effect of practice variation on resource utilization in infants hospitalized for viral lower respiratory illness. Pediatrics. 2001;108(4):851–855. doi: 10.1542/peds.108.4.851. [DOI] [PubMed] [Google Scholar]
  • 22.Martin S., Martin J., Seigler T. Evidence-based protocols to guide pulse oximetry and oxygen weaning in inpatient children with asthma and bronchiolitis: a pilot project. Journal of Pediatric Nursing. 2015;30(6):888–895. doi: 10.1016/j.pedn.2015.02.003. [DOI] [PubMed] [Google Scholar]
  • 23.Werre N. D., Boucher E. L., Beachey W. D. Comparison of therapist-directed and physician-directed respiratory care in COPD subjects with acute pneumonia. Respiratory Care. 2015;60(2):151–154. doi: 10.4187/respcare.03208. [DOI] [PubMed] [Google Scholar]
  • 24.Hermeto F., Bottino M. N., Vaillancourt K., Sant'Anna G. M. Implementation of a respiratory therapist-driven protocol for neonatal ventilation: Impact on the premature population. Pediatrics. 2009;123(5):e907–e916. doi: 10.1542/peds.2008-1647. [DOI] [PubMed] [Google Scholar]
  • 25.Ralston S. L., Atwood E. C., Garber M. D., Holmes A. V. What works to reduce unnecessary care for bronchiolitis? A qualitative analysis of a national collaborative. Academic Pediatrics. 2017;17(2):198–204. doi: 10.1016/j.acap.2016.07.001. [DOI] [PubMed] [Google Scholar]
  • 26.Roback M. G., Baskin M. N. Failure of oxygen saturation and clinical assessment to predict which patients with bronchiolitis discharged from the emergency department will return requiring admission. Pediatric Emergency Care. 1997;13(1):9–11. doi: 10.1097/00006565-199702000-00003. [DOI] [PubMed] [Google Scholar]
  • 27.Brown L., Reiley D. G., Jeng A., Green S. M. Bronchiolitis: can objective criteria predict eligibility for brief hospitalization? Canadian Journal of Emergency Medicine. 2003;5(04):239–244. doi: 10.1017/S1481803500008423. [DOI] [PubMed] [Google Scholar]

Articles from International Journal of Pediatrics are provided here courtesy of Wiley

RESOURCES