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    Bronchiolitis v.6.0: HFNC (ED)

    For questions concerning this pathway,

    contact: [email protected] 2015 Seattle Childrens Hospital, all rights reserved, Medical Disclaimer

    Prior to HFNC initiation:

    Call respiratory therapist

    Respiratory score, suction, score

    MD to order:

    Place PIV (consider normal saline bolus)

    Obtain blood gas (may start HFNC prior to result)

    NPO

    Continuous CR and O2 sat monitoring

    Admit to general medicine (Medical Hospitalist to be called for all

    pathway eligible patients, participate in 90 minute huddle)

    Consider PICU consult/admission if clinical concerns remain or RS

    remains >8 (even if improving)

    While awaiting transfer:

    Score, Suction, Score and VS Q1 hour

    RN/RT may adjust FiO2 to maintain saturations >90% awake, 88%

    asleep

    Note: For patients with initial PCO2 >55 who improve

    with HFNC, a CBG may be rechecked after the huddle. If

    PCO2 then falls to 55, patient may still be eligible for

    general medicine admission.

    Initiate HFNC, 50% FiO2:

    4 lpm for 30-90 days

    6 lpm for 91 days to 2 years

    RS, RR, SpO2 and HR Q 30 minutes

    Notify Medical Hospitalist (76058)

    Huddle 90 minutes

    post HFNC initiation

    (RN, RT, ED providers, admitting

    resident, Medical Hospitalist,+/- PICU provider)

    Arrange for ICU transfer

    May exceed maximum flow

    rates / increase FiO2 while

    waiting for transfer

    Failing (Clinically unchanged or worsening) Clinically improving

    Sign of clinical improvement:

    Improving respiratory score

    Lower RR (not inappropriately lower than normal for age)

    Lower HR

    Improved CBG (if repeated; not necessary for all patients)

    Off

    Pathway

    Patients require ICU transfer for any of the

    following:

    Failure to improve on HFNC trial (or does notmeet inclusion criteria for inpatient part of HFNC

    pathway after 90-minute huddle)

    CO2 > 55 or pH < 7.30

    Any apnea > 20 seconds requiring intervention

    Desaturations below 90% despite 50% FiO2 Altered mental status (irritability, lethargy), poor

    perfusion (cool extremities, capillary refill >3

    seconds)

    Go To HFNC Inpatient Phase

    Last Updated: January 201

    Valid Until: December 2016

    HFNC Inclusion Criteria Previously healthy children with bronchiolitis

    Age 44 weeks CGA to 2 years

    ONE of the following:

    1) Severe respiratory distress, or

    2) Significant Hypoxia, (see chart) or

    3) Respiratory score persistently 8-12 with

    significantly increased WOB

    HFNC Exclusion Criteria ANYpre-existing medical condition

    Born prematurely at less than 34 weeks

    History of intubation for respiratory failure

    Concern for respiratory failure:

    Apnea requiring intervention

    PCO2 > 55, pH

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    For questions concerning this pathway,

    contact: [email protected] 2011, Seattle Childrens Hospital, all rights reserved, Medical Disclaimer

    Bronchiolitis v.6.0: HFNC (Inpatient)

    For questions concerning this pathway,

    contact: [email protected] 2015, Seattle Childrens Hospital, all rights reserved, Medical Disclaimer

    Prior to HFNC initiation: Score, suction, score

    Consider albuterol trial ONCE if not already done

    Call RRT; resident to notify attending MD

    Notify Medical Hospitalist (76058, charge RN to notify)

    MD to order (using HFNC orderset): Place PIV (consider normal saline bolus)

    Obtain CBG (may start HFNC prior to result)

    NPO

    NG/OG if anticipated NPO > 2 days

    Wean flow rates as tolerated

    May orally feed only if patient has weaned at least 2 lpm from

    maximum flow rate

    Initiate HFNC, 50% FiO2:

    4 lpm for 30-90 days

    6 lpm for 91 days2 y

    RS, RR, SpO2 and HR Q 30

    minutes

    Score, suction, score Q 1 h for 4

    hours post initiation

    Huddle 90 minutes

    post HFNC initiation

    (Bedside RN, RISK RN,

    RT, senior, intern,

    Medical Hospitalist)

    Arrange for ICU transfer

    May exceed maximum flow

    rates / increase FiO2 while

    waiting for transfer,

    with ICU guidance

    Weaning HFNC:

    FiO2 may be weaned by RN/RT after 90 minute huddle to maintain

    saturations >90% awake and >88% asleep.

    Please call provider to wean patients flow rate Q4 hours as indicated

    if patient meets all of below criteria:

    Clinically improving

    RS < 8 after suctioning

    FiO2 < 30%

    Flow rate may be weaned by provider in 1 lpm increments.

    When HFNC is stable at 2 lpm for 4 hours, next step is to trial patientdirectly to room air or to low flow NC O2 (start at lpm and titrate to

    keep sats >90% awake, 88% asleep).

    If patient worsens after a wean, contact

    provider to evaluate and increase flow

    rate to previous levels. If patient

    must increase beyond previous

    level, or is at pathway maximum,

    call RRT.

    !

    Do not exceed

    flow rates of:

    4 lpm for 30-90 days old

    6 lpm for 91 days to 2

    years on the floor.

    Failing (Clinically unchanged or worsening) Clinically improving

    ign of clinical improvement:

    Improving RS

    Lower RR (not inappropriately lower than normal for age)

    Lower HR

    Improved CBG (if repeated; not necessary for all

    patients)

    Off

    Pathway

    Criteria for transfer to the ICU:

    Failure to improve on HFNC trial

    CO2 > 55 or pH < 7.30

    Any apnea > 20 seconds requiring intervention

    Desaturations below 90% despite 50% FiO2

    Altered mental status (irritability, lethargy), poorperfusion (cool extremities, capillary refill >3

    seconds)

    Criteria for transfer from the ICU to floor:

    Stable on flow rate at or below the floor

    maximum for >12 hours

    Have a respiratory score

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    Self-Assessment

    Completion qualifies you for 1 hour of Category II CME credit. If you are taking this self-assessment as a

    part of required departmental training at Seattle Childrens Hospital , you MUST logon to Learning Center.

    http://learningcenter/TPOnline/TPOnline.dll/Homehttp://learningcenter/TPOnline/TPOnline.dll/Homehttp://learningcenter/TPOnline/TPOnline.dll/Homehttp://learningcenter/TPOnline/TPOnline.dll/Homehttp://learningcenter/TPOnline/TPOnline.dll/Homehttp://learningcenter/TPOnline/TPOnline.dll/Homehttp://learningcenter/TPOnline/TPOnline.dll/Home
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    HFNC Answer Key

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    Executive Summary

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    Executive Summary

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    Executive Summary

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    Executive Summary

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    Bronchiolitis and HFNC Citation

    Title: Bronchiolitis and HFNC Pathway

    Authors:

    Seattle Childrens Hospital

    Lauren Wilson

    Anne Slater

    Elaine Beardsley

    Dave Crotwell

    Jason Debley

    Jeff Foti

    Michael Leu

    Jennifer Magin

    Coral Ringer

    Joan Roberts

    Date: December 10, 2013

    Retrieval Website:http://www.seattlechildrens.org/pdf/bronchiolitis-pathway.pdf

    http://www.seattlechildrens.org/pdf/HFNC-pathway.pdf

    Example:

    Seattle Childrens Hospital, Wilson L, Slater A, Beardsley E, Crotwell D, Debley J, Foti J, Michael

    Leu, Magin J, Ringer C, Roberts J.2013 December. Bronchiolitis and HFNC Pathway. Available

    from: http://www.seattlechildrens.org/pdf/bronchiolitis-pathway.pdf

    http://www.seattlechildrens.org/pdf/HFNC-pathway.pdf

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    Evidence Ratings

    To Bibliography

    This pathway was developed through local consensus based on published evidence and expert

    opinion as part of Clinical Standard Work at Seattle Childrens. Pathway teams include

    representatives from Medical, Subspecialty, and/or Surgical Services, Nursing, Pharmacy, Clinical

    Effectiveness, and other services as appropriate.

    When possible, we used the GRADE method of rating evidence quality. Evidence is first assessedas to whether it is from randomized trial or cohort studies. The rating is then adjusted in the

    following manner (from: Guyatt G et al. J Clin Epidemiol. 2011;4:383-94.):

    Quality ratings are downgradedif studies:

    Have serious limitations

    Have inconsistent results

    If evidence does not directly address clinical questions

    If estimates are imprecise OR

    If it is felt that there is substantial publication bias

    Quality ratings are upgradedif it is felt that: The effect size is large

    If studies are designed in a way that confounding would likely underreport the magnitude

    of the effect OR

    If a dose-response gradient is evident

    GuidelineRecommendation is from a published guideline that used methodology deemed

    acceptable by the team.

    Expert OpinionOur expert opinion is based on available evidence that does not meet GRADE

    criteria (for example, case-control studies).

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    Summary of Version Changes

    Version 1 (10/10/2011):Go live

    Version 1.1 and 1.2 (07/20/2012):Copyrighted photos and diagrams removed

    Version 2.0 (10/22/2012):Updated to SpO2 monitoring recommendations

    Version 3.0 (12/10/2013):Go live of Bronchiolitis HFNC Pathway

    Version 3.1 (12/13/2013): Changes made to add contact hospitalist; correction to oral feeds to

    match training slide; wording change in trial of albuterol to match the orders

    Version 3.2 (01/15/2014): Changes to inclusion and exclusion criteria; changes to reflectmedical hospitalist at ED 90 minute huddle; admit to medical hospitalist

    Version 4.0 (02/5/2014): Pathway document was divided into two documents and posted as

    Bronchiolitis Pathway and HFNC Pathway

    Version 5.0 (10/01/2014):Removal of daily CBG while on HFNC; highlighting of ability to

    recheck PC02 after HFNC started for improved patients to meet floor admit criteria; PCO2

    removed from inclusion criteria; composition of members of ED huddle; ability to admit to general

    medicine service; abilityto trial patient on RA or low flow NC O2 after stable on HFNC at 2 lpm

    for 4 hours

    Version 6.0 (01/30/2015):Update to the pathway inclusion criteria to include severe respiratory

    distress; added ICU to floor transfer criteria and link to education slide in transfer criteria box

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    Medical Disclaimer

    Medicine is an ever-changing science. As new research and clinical experience broaden our

    knowledge, changes in treatment and drug therapy are required.

    The authors have checked with sources believed to be reliable in their efforts to provide

    information that is complete and generally in accord with the standards accepted at the time of

    publication.

    However, in view of the possibility of human error or changes in medical sciences, neither the

    authors nor Seattle Childrens Healthcare System nor any other party who has been involved in

    the preparation or publication of this work warrants that the information contained herein is in

    every respect accurate or complete, and they are not responsible for any errors or omissions or

    for the results obtained from the use of such information.

    Readers should confirm the information contained herein with other sources and are

    encouraged to consult with their health care provider before making any health care decision.

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    Bibliography

    Identification HFNC

    Screening

    Eligibility

    Included

    Flow diagram adapted from Moher D et al. BMJ 2009;339:bmj.b2535

    Studies were identified by searching electronic databases using search strategies developed and

    executed by a medical librarian, Susan Klawansky. Searches were performed in May 2013. The

    following databases were searchedon the Ovid platform: Medline (2002 to date), Cochrane

    Database of Systematic Reviews (2005 to date), Cochrane Central Register of Controlled Trials

    (2002 to date); elsewhereEmbase (2002 to date), CINAHL (2002 to date), National Guideline

    Clearinghouse and TRIP (2002 to date). Retrieval was limited to humans 0-18 and English,French or German languages. As none of the searched databases provided index terminology

    for the concept of high flow nasal cannula, all searching was conducted using textwords/

    synonyms in various combinations. All retrieval was further limited to certain evidence

    categories, such as relevant publication types, Clinical Queries, index terms for study types and

    other similar limits. Additional articles were identified by team members and added to results.

    Susan Klawansky, MLS, AHIP

    December 3, 2013

    Identification

    70 records identified through

    database searching

    1 additional records identified

    through other sources

    71 records after duplicates removed

    71 records screened 45 records excluded

    10 full-text articles excluded26 full-text articles assessed for eligibility

    16 studies included in pathway

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    BibliographyBronchiolitis HFNC

    Return to Home

    Abboud, P. A., Roth, P. J., Skiles, C. L., Stolfi, A., & Rowin, M. E. (2012). Predictors of failure in infant

    with viral bronchiolitis treated with high-flow, high-humidity nasal cannula therapy*.Pediatric Critic

    Care Medicine, 13(6), e343-9. doi:http://dx.doi.org/10.1097/PCC.0b013e31825b546f

    Arora, B., Mahajan, P., Zidan, M. A., & Sethuraman, U. (2012). Nasopharyngeal airway pressures in

    bronchiolitis patients treated with high-flow nasal cannula oxygen therapy.Pediatric EmergencyCare, 28(11), 1179-1184. doi:http://dx.doi.org/10.1097/

    de Klerk, A. (2008). Beyond the basics. humidified high-flow nasal cannula: Is it the new and improved

    CPAP?Advances in Neonatal Care (Elsevier Science), 8(2), 98-106. Retrieved from http://

    search.ebscohost.com/login.aspx?direct=true&db=cin20&AN=2009897598&site=ehost-live

    Hasan, R. A., & Habib, R. H. (2011). Effects of flow rate and airleak at the nares and mouth opening o

    positive distending pressure delivery using commercially available high-flow nasal cannula system

    A lung model study.Pediatric Critical Care Medicine, 12(1), e29-33. doi:http://dx.doi.org/10.1097/

    PCC.0b013e3181d9076d

    Hegde, S., & Prodhan, P. (2013). Serious air leak syndrome complicating high-flow nasal cannulatherapy: A report of 3 cases.Pediatrics, 131(3), e939-44. doi:http://dx.doi.org/10.1542/peds.2011-

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    Kelly GS, Simon HK, Sturm JJ. (2013) High Flow Nasal Cannula Use in Children With Respiratory

    Distress in the Emergency Department: Predicting the Need for Subsequent Intubation. Pediatr

    Emer Care.;29: 888-92

    Lee, J. H., Rehder, K. J., Williford, L., Cheifetz, I. M., & Turner, D. A. (2013). Use of high flow nasal

    cannula in critically ill infants, children, and adults: A critical review of the literature.Intensive Care

    Medicine, 39(2), 247-257.

    Matecki, S., Milesie, C., Baleine, J., Jacquot, A., & Cambonie, G. (2013). Effect of high-flow nasal

    cannula nasal on nasopharyngeal airway pressure and respiratory muscles loading in young infanwith severe acute viral bronchiolitis.Fundamental and Clinical Pharmacology, 27, 89.

    Mayfield, S., Hough, J., Pham, T., & Schibler, A. (2011). High flow nasal prong oxygen reduces the

    need for mechanical ventilation in bronchiolitic infants.Pediatric Critical Care Medicine, 12(3),

    A118.

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    McKiernan, C., Chua, L. C., Visintainer, P. F., & Allen, H. (2010). High flow nasal cannulae therapy in

    infants with bronchiolitis.Journal of Pediatrics, 156(4), 634-638. doi:http://dx.doi.org/10.1016/

    j.jpeds.2009.10.039

    Milesi, C., Baleine, J., Matecki, S., Durand, S., Combes, C., Rideau Batista Novais, A., & Combonie,

    G. (2013). Is treatment with a high flow nasal cannula effective in acute viral bronchiolitis? A

    physiologic study.Intensive Care Medicine, 39(6), 1088-1094. doi:http://dx.doi.org/10.1007/

    s00134-013-2879-y

    Schibler, A., Pham, T. M., Dunster, K. R., Foster, K., Barlow, A., Gibbons, K., & Hough, J. L. (2011).

    Reduced intubation rates for infants after introduction of high-flow nasal prong oxygen delivery.

    Intensive Care Medicine, 37(5), 847-852. doi:http://dx.doi.org/10.1007/s00134-011-2177-5

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    Sood, R., Stolfi, A., & Rowin, M. (2012). Use of high flow high humidity nasal cannula therapy for

    infants with bronchiolitis.Journal of Investigative Medicine, 60(1), 453.

    Spentzas, T., Minarik, M., Patters, A. B., Vinson, B., & Stidham, G. (2009). Children with respiratory

    distress treated with high-flow nasal cannula.Journal of Intensive Care Medicine, 24(5), 323-328.

    doi:http://dx.doi.org/10.1177/0885066609340622

    Thorburn, K., & Ritson, P. (2012). Heated, humidified high-flow nasal cannula therapy in viral

    bronchiolitis--panacea, passing phase, or progress?*.Pediatric Critical Care Medicine, 13(6),

    700-701. doi:http://dx.doi.org/10.1097/PCC.0b013e3182677456

    Wing, R., James, C., Maranda, L. S., & Armsby, C. C. (2012). Use of high-flow nasal cannula support

    in the emergency department reduces the need for intubation in pediatric acute respiratory

    insufficiency.Pediatric Emergency Care, 28(11), 1117-1123. doi:http://dx.doi.org/10.1097/

    PEC.0b013e31827122a9

    BibliographyBronchiolitis HFNC

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