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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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Going Beyond the Simple Fix
PA PSRS Patient Saf Advis 2007 Jun;4(2):63. 
 

Here is an example of one Pennsylvania facility’s in-depth efforts to resolve a patient safety problem. Butler Health System submitted the following report to PA-PSRS: 

An experienced laboratory technician interpreted a control slide as a patient slide. She reported that a patient’s synovial fluid contained gram-positive organisms, but the correct result was no organisms. The laboratory technician then recognized the error and contacted the nurse and orthopedic surgeon. The patient was in the operating room under anesthesia. Fortunately, the correct result was reported before the surgical procedure  was started. 

The facility’s investigation revealed that both the control slides and patient slides were identical in design — plain, clear, non-distinct glass. While the technicians initialed and dated control slides, it was not their practice to document on the slide its control status. Moreover, at the time of this occurrence, no procedure existed to differentiate between control slides and patient slides. Although there was a procedure to monitor for misreads, this monitoring ordinarily occurred the following day. 

As a result of this occurrence, the facility purchased a new type of control slide that was frosted at one end. This slide is used solely for gram stain controls. In addition, the facility implemented a new procedure requiring staff to write “GS” on the slide to indicate that it is a gram stain control. 

While, on the surface, these changes might appear to fix the problem, the facility dug deeper to uncover underlying issues that contributed to this occurrence. One system breakdown identified was distraction in the workplace. The facility implemented a process in which technicians place an orange caution sign at their work stations to prevent others from interrupting them while they are performing readings. The employees were educated about the new slides and processes. 

The technician involved in this occurrence was distraught about the event. The facility offered support and counseling, and reinforced the fact that her timely reporting of this error prevented unnecessary surgery and further patient harm. 

Finally, the facility revised its misreads protocol to heighten awareness to all laboratory staff involved. All laboratory employees receive the following information: misreads divided by the total number of reads per employee (deidentified). Moreover, the manager provides each individual with his/her rate of misreads on an ongoing basis. This information is used as a springboard for the healthcare team to identify, together, further systems or process breakdowns and oppor-tunities for patient safety improvement.  For more information about how Butler Health System  responded to this issue, contact 724-284-4862.

 
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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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