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Patient Safety Authority
333 Market Street
Lobby Level
Harrisburg, PA 17120


Phone: 717-346-0469
Fax: 717-346-1090


 
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Brevity is the Soul of Wit, but Not of Safety
PA PSRS Patient Saf Advis 2005 Dec;2(4):10.   
 

PA-PSRS received a report of an overdose of morphine via PCA. The complete narrative read “PCA pump set incorrectly. Pt. required CPR and intubation.” The cause of the problem, inferred from the narrative, was incorrect programming of the PCA pump. Information in the patient’s record and the inci­dent report provides a more complete account.

The patient was transferred from another facility to repair a complex fracture, arriving in the middle of the night. In the morning, the patient’s request for medication to control the pain, exacerbated by the transfer, brought to light the ab­sence of a pain medication order. 

The patent was ordered an injectable synthetic narcotic, every 6 hours as needed. This proved inadequate. Three hours later a second dose was given , and a 75 microgram fentanyl patch was added. This combination proved inade­quate. Seen hours after that, a morphine PCA was added just before change of shift with 1 mg/hr base rate and 1 mg on patient demand with 8-minute lockout. The patient com­plained of itching and was given benadryl. 

An hour later, after change of shift, the new evening nurse observed that the patient was hard to arouse. The nurse stopped the base rate infusion, leaving the patient on demand only mode. Five hours later, the patient was observed to be more arousable, but three hours later was unresponsive. When seen by the same nurse an hour after that, the patient was both unresponsive and briefly without a pulse. CPR was initiated, and the patient was intubated. The pupils were pinpoint and Narcan was given. The patient responded to the treatment.

The physician on the scene told the covering attending that the fentenyl patch was no longer present, but inspection showed the patch in place. It was removed. Inspection also showed large areas of urticaria. In trying to determine how much morphine the patient had received, the pump’s memory revealed that no doses had been given on demand, that 14 mg of morphine had infused total and that the pump had been programmed to stop the base rate infusion at the AM hour, not the PM hour that the nurse wrote in the notes.  

The complete narrative makes it obvious that more problems were present:

  • The patient’s pain was poorly managed by the physi­cians.
  • A likely allergy to morphine was not managed appropriately.
  • The patient's overdose was not identified in a timely fashion.
  • The assessment of the patient by the physician dur­ing the resuscitation was incomplete.
  • The specific programming problem was the same as many experience with their alarm clocks, setting for PM when they intend AM or vise-versa.

An understanding of the event produces more useful informa­tion than a classification of the event – an understanding that may prevent many more problems in the future – an under­standing that can be conveyed in a narrative description.

 
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THE PENNSYLVANIA PATIENT SAFETY AUTHORITY AND ITS CONTRACTORS  
PSA LOGO The Pennsylvania Patient Safety Authority is an independent state agency created by Act 13 of 2002, the Medical Care Availability and Reduction of Error (“Mcare”) Act. Consistent with Act 13, ECRI Institute, as contractor for the Authority, is issuing this publication to advise medical facilities of immediate changes that can be instituted to reduce Serious Events and Incidents. For more information about the Pennsylvania Patient Safety Authority, see the Authority’s Web site at www.patientsafetyauthority.org .      
ECRI LOGO ECRI Institute, a nonprofit organization, dedicates itself to bringing the discipline of applied scientific research in healthcare to uncover the best approaches to improving patient care. As pioneers in this science for more than 40 years, ECRI Institute marries experience and independence with the objectivity of evidence-based research. More than 5,000 healthcare organizations worldwide rely on ECRI Institute’s expertise in patient safety improvement, risk and quality management, and healthcare processes, devices, procedures and drug technology.      

ISMP Logo The Institute for Safe Medication Practices (ISMP) is an independent, nonprofit organization dedicated solely to medication error prevention and safe medication use. ISMP provides recommendations for the safe use of medications to the healthcare community including healthcare professionals, government agencies, accrediting organizations, and consumers. ISMP’s efforts are built on a nonpunitive approach and systems-based solutions.      
 
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