SGMI Sierre - PowerPoint PPT Presentation

1 / 20
About This Presentation
Title:

SGMI Sierre

Description:

Adverse Drug Event Rates Involving Nephrotoxic and Renally Excreted Drugs In ... Results VI: Culprit Drugs. ADEs prev n (%) non-prev. Antibiotics 100 (37.0) 6 (42.9) ... – PowerPoint PPT presentation

Number of Views:38
Avg rating:3.0/5.0
Slides: 21
Provided by: loca220
Category:
Tags: sgmi | culprit | sierre

less

Transcript and Presenter's Notes

Title: SGMI Sierre


1
  • Adverse Drug Event Rates Involving Nephrotoxic
    and Renally Excreted Drugs In Community Hospitals
  • Balthasar L. Hug, MD, MBA
  • Division of General Internal Medicine,
  • Brigham and Womens Hospital, Boston, MA
  • Division of Internal Medicine,
  • Basel University Hospital

2
  • Background I Incidence
  • Adverse Drug Events (ADEs) are common
  • 19.4 of in-hospital harm is medication related
    (Harvard Medical Practice Study, Brennan TA, NEJM
    1991324370)
  • Large academic hospitals 6.5 ADEs/100 admissions
    (Bates DW, JAMA 19982801311)

3
  • Background II Incidence Renal Failure
  • 1 on hospital admission
  • 2-5 during hospitalization
  • 4-15 in patients with certain surgical
    procedures such as cardiopulmonary bypass surgery
    (Thadhani R et al, NEJM 1996334(22)1448)

4
  • Background III Definitions
  • Medication Error (ME) Error anywhere in the
    process of drug ordering, delivering or
    application regardless of whether or not it
    harmed the patient. (Bates DW J Gen Intern Med
    199510199)
  • Adverse Drug Event (ADE) Injury resulting from
    a medical intervention related to a drug (Bates
    DW, JAMA 199527429)
  • Near Miss (potential ADE) ME with potential for
    harm. Intercepted Harm did not reach patient,
    non-intercepted error did no harm.

5
  • Background IV Politics
  • Massachusetts Hospital CPOE Initiative 2006 CPOE
    in all acute care hospitals by 2010
    (www.mtpc.org)
  • CPOEComputerized Physician Order Entry

6
  • Specific Aim
  • To assess the incidence and severity of adverse
    drug events (ADEs) in patients with renal failure
    in six community hospitals.

7
  • Methods
  • Design Multicenter, retrospective cohort study
  • Study sites 6 community hospitals 150-300 beds
    in MA
  • Study Duration 20 months (1/05-8/06)
  • Randomly selected 150 patient charts/hospital in
    patients with creatinin gt 1.5 mg/dL (114.4µmol/L)
  • 2 independent reviewers

8
  • Results I Demographics
  • All patients n109,641
  • Age mean 63.2 y (range 18-107)
  • 18-44 23,599 (21.5)
  • 45-54 12,344 (11.3)
  • 55-64 14,809 (13.5)
  • 65-74 18,095 (16.5)
  • 75-84 25,413 (23.2)
  • 85 and gt 15,380 (14.0)
  • Gender Female 58.1
  • Race Caucasian 89.9

9
  • Results II Demographics Unique patients with
    ADE (n89)
  • Age mean 70.3 y (SD 15.2) plt0.001 (vs.
    all patients, T-test)
  • 18-44 6 (6.7)
  • 45-54 7 (7.9)
  • 55-64 16 (18.0)
  • 65-74 19 (21.4)
  • 75-84 23 (25.8)
  • 85 and gt 18 (20.2)
  • Gender Female 37 (41.6) p0.002
    (Fishers exact test)
  • Race Caucasian 82 (96.5)
    p0.88 (Fishers exact test)
  • 1 patient with two ADEs, others with 1
    ADE/patient

10
  • Results III Incidents by severity (all sites)
  • ADEs n () R/100 adm (95 CI)
  • Significant 40 (44.4) 4.4 (3.2,6.0)
  • Serious 46 (51.1) 5.1 (3.8,6.7)
  • Life-threat. 4 (4.5) 0.44 (0.14,1.0)
  • Total 90 (100) 10.0 (8.1, 12.2)
  • Near Misses
  • Significant 219 (44.0) 24.4 (21.4,27.8)
  • Serious 271 (54.4) 30.1 (26.7,33.8)
  • Life-threat. 8 (1.6) 0.9 (0.41,1.7)
  • Total 489 (100) 55.3 (50.6,60.3)

11
  • Results IV Incident rates and preventability
    (all sites)
  • n () Rate/100 admissions (95 CI)
  • ADEs 90 (15.2) 10.0 (8.1, 12.2)
    p0.04
  • Preventable 82 (91.1) 9.1 (7.3, 11.2)
    p0.02
  • Non-prev. 8 (8.9) 0.9 (0.41, 1.65)
    N/A
  • Near Misses 498 (84.1) 55.3 (50.6, 60.3)
    p0.0006
  • Non-interc. 481 (96.6) 53.4 (48.8, 58.4)
    p0.002
  • Intercepted 17 (3.4) 1.9 (1.1, 2.9)
    p0.44
  • MEs 4 (0.7) 0.4 (0.14, 1.0)
    N/A
  • Total 592 (100) 68.5 (60.6, 71.2)
  • Chi-squared test for equal rates across sites
  • N/A not applicable

12
  • Results V Incident rates and preventability (all
    sites)
  • 82/82 preventable ADEs preventable by renal dose
    checking.
  • Of near misses, nearly all (99.8 497/498)
    preventable by CPOE systems with decision
    support
  • 495 (99.4) by renal dose checking,
  • 1 (0.2) by drug dose suggestion,
  • 1 (0.2) by cumulative dose check
  • 1 near miss (0.2) was not preventable by CPOE.

13
  • Potential ADE reduction by CPOE
  • Prevention Strategy Preventable ADEs
    Preventable Near Misses
  • n () n ()
  • Drug Laboratory Check 37 (27.4) 26 (4.7)
  • Renal Function Check 26 (19.3) 74 (13.4)
  • Drug Dose Suggestion 12 (8.9) 95 (17.2)
  • Drug Cum. Dose Check - 106 (19.2)
  • Drug Age Check 12 (8.9) 4 (0.7)
  • Drug-specific Guidelines 9 (6.7) 19 (3.4)
  • Drug Allergy Check 5 (3.7) 12 (2.2)
  • Drug Frequency Check 4 (3.0) 38 (6.9)
  • Drug Drug Interaction Check 3 (2.2) 17 (3.1)
  • Duplicate Drug Check 1 (0.7) 23 (4.2)
  • Basic CPOE Legibility - 19 (3.4)
  • Drug route suggestion - 11 (2.0)
  • Patient Characteristic 1 (0.7) 9 (1.6)
  • Drug Duration Check - 4 (0.7)
  • Not preventable by CPOE 25 (18.5) 95 (17.2)
  • Total 135 (100) 552 (100)

14
  • Results VI Culprit Drugs
  • ADEs prev n () non-prev
  • Antibiotics 100 (37.0) 6 (42.9)
  • Analgesics 85 (31.5) 3 (21.4)
  • Cardiovascular 44 (16.3) 4 (28.6)
  • Oral Antidiabetics 12 (4.4) -
  • Antifungal Agents 11 (4.1) -
  • Neurotropic Drugs 2 (0.7) -
  • Others 16 (5.9) 1 (7.1)
  • Total 270 (100) 14 (100)

15
  • Conclusions
  • ADEs in patients with renal failure are common in
    community hospitals (10.0/100 admissions).
  • Virtually all of ADEs and near misses in these
    patients are potentially averted by CPOE with
    decision support.
  • Antibiotics, analgesics and CV drugs most
    prevalent in ADEs.

16
  • Daniel J. Witkowski, M.D., M.S.
  • Colin M. Sox, M.D.
  • Carol A. Keohane, B.S.N., R.N.
  • Diane L. Seger, R.Ph.
  • Catherine Yoon, M.S.
  • Michael E. Matheny, M.D., M.S., M.P.H.
  • Judith A. Melin, M.D.
  • David W. Bates, M.D., M.Sc.

17
Thank you
bhug_at_uhbs.ch
18
  • IHI Trigger Tool
  • Triggers for potential ADEs (T1-T19)
  • Examples
  • Diphenhydramine anti-allergic
  • Vitamine K (warfarine)
  • INR gt6
  • Anti-emetics (droperidol, metoclopramine etc.)
  • Naloxone (opiates)
  • Kayexalate (hyperkalemia)
  • (www.ihi.org)

19
  • ADR Definition WHO
  • noxious and unintended, and which occurs at
    doses used in man for prophylaxis, diagnosis and
    therapy.

20
  • Challenge Switzerland
  • Swiss Technology Collaborative?
  • Teamwork, Stakeholders
  • Academia
  • Industry
  • Insurance companies
  • Politics
Write a Comment
User Comments (0)
About PowerShow.com