Design

To assess the effectiveness of the program, we

Design.

To assess the effectiveness of the program, we performed a before-after trial comparing patient’s self-reported pain management and experience before and after program implementation. We included all adult patients hospitalized for more than 24 hours and discharged either to their home

or to a nursing facility, between March 1, 2001 and March 31, 2001 (before program implementation) and between September 15, 2005 and October 15, 2005 (after program implementation).

Setting.

A teaching hospital of 2,096 beds in Geneva, Switzerland.

Patients.

All adult TH-302 nmr patients hospitalized for more than 24 hours and discharged between 1 to 31 March 2001 (before program) and 15 September to 15 October 2005 (after program implementation).

Interventions.

Implementation 3-deazaneplanocin A mouse of a collaborative quality improvement program using multifaceted interventions (staff education, opinion leaders, patient education, audit, and feedback) to

improve pain management at hospital level.

Outcome Measures.

Patient-reported pain experience, pain management, and overall hospital experience based on the Picker Patient Experience questionnaire, perceived health (SF-36 Health survey).

Results.

After implementation of the program only 2.3% of the patients reported having no pain relief during their hospital stay (vs 4.5% in 2001, P = 0.05). Among nonsurgical patients, improvements were observed for pain assessment (42.3% vs 27.9% of the patients had pain intensity measured with a visual analog scale, P = 0.012), pain management (staff did everything they could to help in GDC-0994 supplier 78.9% vs 67.9% of cases P = 0.003), and pain relief (70.4% vs 57.3% of patients reported full pain relief P = 0.008). In surgical patients, pain assessment also improved (53.7.3% vs 37.6%) as well as pain treatment. More patients received treatments to relieve pain regularly or intermittently after program implementation (95.1% vs 91.9% P = 0.046).

Conclusion.

Implementation of a collaborative quality improvement program at hospital level improved

both pain management and pain relief in patients. Further studies are needed to determine the overall cost-effectiveness of such programs.”
“Study Design.

Case report.

Objective.

To report an unusual case of refractory positional vertigo without headache that developed after the placement of an epidural catheter for postoperative pain and that was treated with an epidural blood patch.

Summary of the Background Data.

Although it is common practice to use epidural blood patch (EBP) to treat positional headache from postdural puncture (PDP), the literature is limited to one letter to the editor describing PDP positional vertigo treated with EBP.

Methods.

Description of a clinical case.

Results.

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