Continuous Narcotic Infusion with Patient-Controlled Analgesia for Chronic Cancer Pain in Outpatients

  1. IAN G. KERR, M.D.;
  2. MARCIA SONE, R.N.;
  3. CARLO DeANGELIS, PHARM.D.;
  4. NEILL ISCOE, M.D.;
  5. ROBERT MacKENZIE, M.D.; and
  6. TRUDI SCHUELLER, B.Sc., PHARM.D.
  1. TORONTO, ONTARIO
    CANADA

    Abstract

    Study Objective: To determine the feasibility and safety of outpatient continuous narcotic infusions with additional bolus capabilities (patient-controlled analgesia) in patients with cancer pain.

    Design: A single arm (non-randomized) series.

    Setting: Outpatient with contact by telephone and through outpatient clinic.

    Patients: Consecutive series of 18 patients with poorly controlled cancer pain or significant side effects from regular administration of various narcotics.

    Interventions: Patients taught and supervised to use portable pump capable of delivering a continuous narcotic infusion with bolus capabilities.

    Measurements and Main Results: All patients had improvement in pain control as judged by the use of a linear analogue scale. Side effects and safety profile were highly acceptable. Narcotics used and maximum doses were meperidine, 50 mg/h; morphine, 80 mg/hr; and hydromorphone, 60 mg/hr. Infusion duration ranged from 7 to 225 days (mean, 54 days).

    Conclusions: Continuous narcotic infusions using a programmable portable pump with bolus capabilities is a safe and reliable method of delivering narcotics to outpatients.

    Article and Author Information

    • ▸From the Toronto-Bayview Regional Cancer Centre, Sunnybrook Medical Centre, and University of Toronto; Toronto, Ontario, Canada.

    • ▸Requests for reprints should be addressed to Ian G. Kerr, M.D.; Toronto-Bayview Cancer Centre, 2075 Bay view Avenue; Toronto, Ontario, Canada M4N 3M5.

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