Medication Safety Component — Annual Hospital Survey |
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Instructions for this form are available at: |
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*required for saving |
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Tracking #: |
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Facility ID: |
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*Survey Year: |
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Section 1. Facility Characteristics |
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□ For profit |
□ Not for profit, including church |
□ Government |
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□ Military |
□ Veterans Affairs |
□ Physician owned |
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If facility is a Hospital: |
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For any Hospital: |
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4. . *Is your hospital a teaching hospital for physicians and/or physicians-in-training or nursing students? |
□ Yes |
□ No |
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If Yes, what type: |
□ Major |
□ Graduate |
□ Undergraduate |
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5. *Number of beds set up and staffed in the following location types (as defined by NHSN): |
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a. ICU (including adult, pediatric, and neonatal levels II/III and III): |
__________________________ |
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b. All other inpatient locations: |
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□ Glycemic Control Module |
□ Opioid-Related Adverse Events (ORAE) Module |
Assurance of Confidentiality: The voluntarily provided information obtained in this surveillance system that would permit identification of any individual or institution is collected with a guarantee that it will be held in strict confidence, will be used only for the purposes stated, and will not otherwise be disclosed or released without the consent of the individual, or the institution in accordance with Sections 304, 306 and 308(d) of the Public Health Service Act (42 USC 242b, 242k, and 242m(d)). CDC (57.701) Rev (13.0 December 2024)
Public reporting burden of this collection of information is estimated to average 180 minutes per response, including the time for reviewing instructions, searching existing data sources, gathering, and maintaining the data needed, and completing and reviewing the collection of information. An agency may not conduct or sponsor, and a person is not required to respond to a collection of information unless it displays a currently valid OMB control number. Send comments regarding this burden estimate or any other aspect of this collection of information, including suggestions for reducing this burden to CDC, Reports Clearance Officer, 1600 Clifton Rd., MS H21-8, Atlanta, GA 30333, ATTN: PRA (0920-0666).
Section 2. Glycemic Control |
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Responses to questions in Section 2 are required if “Glycemic Control Module” is checked in Section 1. If unchecked, skip Section 2.
Section 2a. Glycemic Control Program
7. *Does your facility provide leadership support and clinical resources specifically for inpatient glycemic control quality improvement or safety program activities demonstrated by: (Check all that apply.)
Section 2b. Glycemic Control Practices†
Section 2c. Insulin and Hypoglycemia/Hyperglycemia Management Practices‡
9.* Does your facility use the following strategies to implement inpatient glycemic control and insulin management practices. (Check all that apply.)
9a. If this response is selected, please indicate how this protocol is implemented. (Check one.)
9b. If this response is selected, please indicate where these protocols are used. (Check one.)
9c. If this response is selected, please indicate where these protocols are used. (Check one.)
9d. If this response is selected. Please indicate where these protocols are used. (Check one.)
Section 2d. Glycemic Control Software Tools & Additional Information
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Section 3. Opioid-Related Adverse Events |
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Responses to questions in Section 3 are required if “Opioid-Related Adverse Events (ORAE) Module” is checked in Section 1. If unchecked, skip Section 3.
Section 3a. Opioid Prescribing Safety Practices
Section 4b. Education
15a. If your facility has opioid prescribing education programs or practices in place, how frequently is education provided? (Check all that apply.)
15b. If your facility has opioid prescribing education programs or practices in place, what groups of healthcare workers are included in your opioid education programs or practices? (Check all that apply.)
Section 4c. Quality Measurement
16. *What quality metrics are tracked, monitored and/or reported related to opioid safety or quality improvement? (Check all that apply.)
16a. If opioid quality/safety metrics are tracked, monitored, and/or reported, at what level is data trended and/or reported? (Check one.)
16b. What type of opioid-related adverse events are tracked in your facility? (Check all that apply.)
16c. If opioid-related events are tracked, what methods are used to identify potential opioid-related adverse events? (Check all that apply.)
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†Adapted from Society for Hospital Medicine. The Glycemic Control Implementation Guide. 2nd ed. Ed. Maynard G, Berg K, Kulasa K, O’Malley C, Rogers KM. Available at: https://www.hospitalmedicine.org/globalassets/clinical-topics/clinical-pdf/gcmi-guide-m4.pdf. ‡Adapted from the University of California, San Diego Center for Innovation and Improvement Science, with permission from Greg Maynard, MD, MSc |
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File Type | application/vnd.openxmlformats-officedocument.wordprocessingml.document |
Author | Jones, Karen (CDC/DDID/NCEZID/DHQP) (CTR) |
File Modified | 0000-00-00 |
File Created | 2024-11-16 |