sickle cell pain management in the emergency department

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  • 8/13/2019 Sickle Cell Pain Management in the Emergency Department

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    Sickle Cell Pain Management

    in the Emergency Department

    B. Probst, MD; J. Williams, RN;

    D. Speed, RN, MSN; M. Cichon, DO;C. Jackson, MD; M. Pearlman, MS4

    Loyola University Chicago

    LOYOLA

    UNIVERSITY

    HEALTH SYSTEM

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    Sickle cell patients in the ED:small volume, LARGE PROBLEMSOpportunity to

    Improve:

    Pain assessment Treatment of pain

    Disposition

    Desired Outcome:

    Consistent pain

    assessment &

    documentation

    Standardize

    treatment

    Expedite timely

    disposition to

    home or admission

    to hospital

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    Opportunity Knocks

    Subjective nature of pain

    Opioid-tolerant patients

    Little use of adjunctive

    agents

    Timeliness of

    assessment andtreatment

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    Solutions Implemented Convened a multi-disciplinary team

    General Medicine, Anesthesia Pain Service,Social Work, ED Physicians & Nurses

    Developed and implemented a focusedguideline

    Educated ED caregivers & patients

    Collaborated with General Medicineinitiative for inpatient sickle cellmanagement

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    Progress to Date

    Guideline implemented July, 2002

    Minor adjustments made to guideline after

    feedback from Caregivers Identified and collected data measures:

    Documentation of VAS

    Analgesic usage

    Adjunct usage

    Time-to-treatment

    Length-of-stay

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    Pain Assessment

    VASdocumentationimproved at all

    time intervals Reassessment of

    pain aftermedicationadministration is

    an area that offersan opportunity forimprovement

    Documentation of VAS

    70% 70%

    60%

    100%

    100% 89%

    100%

    75%

    63%

    100%

    82% 81%

    94%

    83%87%

    0%

    10%

    20%

    30%

    40%

    50%

    60%

    70%80%

    90%

    100%

    Triage After 1st Med After 2nd Med

    Time Intervals

    P

    ercentDocumented

    Baseline Jul-02 Aug-02 Sep-02 Jan-03

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    Pain Medications

    Use of Dilaudid has

    increased since

    guidelineimplementation

    Demerol utilization

    has decreased

    Pain Medication Usage

    3.7%

    14.6%

    97%

    6.7%

    84%

    0%

    16%

    90.2%

    3.7%

    76.7%

    8.5%

    0% 0%

    86.3%

    7.0%

    0%

    20%

    40%

    60%

    80%

    100%

    Dilaudid Morphine Demerol

    PercentUsage

    Baseline Jul-02 Aug-02 Sep-02 Jan

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    Time to Treatment & LOS

    Time to treatment

    decreased from 80

    to 57 minutes

    ED length of stay

    has decreased

    from 271 minutes

    to 232 minutes

    Time-To-Treatment

    and

    ED Length of Stay

    80

    61

    212

    102

    58

    207

    57

    232271 267

    0

    50

    100

    150

    200

    250

    300

    Time to Rx LOS

    Minutes

    Baseline Jul-02 Aug-02 Sep-02 Jan

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    Adjunctive Effect of Toradol

    Patients that

    received Toradol, in

    addition to opioidanalgesics, were

    more likely to be

    discharged home

    from the ED, than

    admitted to thehospital

    Toradol Effects on Disposition

    31%

    66% 63%

    33%

    0%

    20%

    40%

    60%

    80%

    100%

    Discharge to Home Hospital Admission

    Disposition

    Percentage

    w-Toradol (N=20) w/o-Toradol (N=48)

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    Conclusions

    Focused guideline usage has improvedcare for sickle cell patients in the ED: Improved pain assessment

    Decreased time to treatment & length-of-stay

    Decreased demerol usage

    Increased discharge to home with toradoladjunct

    Sickle Cell Guideline has proven to be auseful resource for physicians managingpain in patients with Sickle Cell disease.

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    Next Steps

    Continue utilization of guideline

    Further education of staff onreassessment after pain medications and

    treatment of pain Increase utilization of toradol

    Refine guideline based on feedback

    Ongoing review of compliance toguideline