Document
57.106
ICR 201908-0920-004 · OMB 0920-0666 · Object 94117201.
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Document Metadata
| File Type | application/vnd.openxmlformats-officedocument.wordprocessingml.document |
|---|---|
| File Title | 57.106 |
| Subject | NHSN OMB FORM 2018 |
| Keywords | NHSN, PS, Monthly, Reporting, Plan |
| Author | CDC/NCZEID/DHQP |
| Last Modified By | Writer |
| File Modified | 2018-09-25 |
| File Created | 2026-10-10 |
| Conversion State | complete |
Extracted Text
Patient Safety Monthly Reporting Plan Page 1 of 2 *required for saving Facility ID: _____________________________ *Month/Year: ___________ /______ □ No NHSN Patient Safety Modules Followed this Month Device-Associated Module Locations CLABSI VAE CAUTI CLIP PedVAP PedVAE _________________________________ □ □ □ □ □ □ _________________________________ □ □ □ □ □ □ _________________________________ □ □ □ □ □ □ _________________________________ □ □ □ □ □ □ _________________________________ □ □ □ □ □ □ _________________________________ □ □ □ □ □ □ _________________________________ □ □ □ □ □ □ _________________________________ □ □ □ □ □ □ _________________________________ □ □ □ □ □ □ _________________________________ □ □ □ □ □ □ Procedure-Associated Module Procedures SSI IN OUT _________________________________ □ □ _________________________________ □ □ _________________________________ □ □ _________________________________ □ □ _________________________________ □ □ _________________________________ □ □ _________________________________ □ □ _________________________________ □ □ _________________________________ □ □ Antimicrobial Use and Resistance Module Locations Antimicrobial Use Antimicrobial Resistance _________________________________ □ □ _________________________________ □ □ _________________________________ □ □ _________________________________ □ □ _________________________________ □ □ 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)). Public reporting burden of this collection of information is estimated to average 15 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, Project Clearance Officer, 1600 Clifton Rd., MS D-74, Atlanta, GA 30333, ATTN: PRA (0920-0666). CDC 57.106(Front) Rev. 5, v9.2 Patient Safety Monthly Reporting Plan Page 2 of 2 MDRO and CDI Module +Locations Specific Organism Type ±LabID Event ±LabID Event (Circle one) All Specimens Blood specimens only FacWideIN FacWideOUT ______________ □ □ FacWideIN FacWideOUT ______________ □ □ FacWideIN FacWideOUT ______________ □ □ FacWideIN FacWideOUT ______________ □ □ Process and Outcome Measures Locations Specific Organism Type Infection Surveillance §AST Timing §AST Eligible Incidence Prevalence LabID Event HH GG __________ ________ □ Adm Both All NHx □ □ □ □ □ __________ ________ □ Adm Both All NHx □ □ □ □ □ __________ ________ □ Adm Both All NHx □ □ □ □ □ __________ ________ □ Adm Both All NHx □ □ □ □ □ __________ ________ □ Adm Both All NHx □ □ □ □ □ + FacWideIN = Facility-wide Inpatient FacWideOUT = Facility-wide Outpatient NHx = Only patients tested are those who have no documentation at the admitting facility in the previous 12 months of MDRO-colonization or infection at the time of admission. ± LabID Event = Laboratory-identified Event § For AST, circle one choice to indicate time of testing and one choice to indicate type of patients eligible for testing. Timing: Adm = Admission Both = Both Admission and Discharge/Transfer Patients Eligible: All patients tested