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Tarangnan Community Hospital · Quality Management System integrated with LUIB (read-only)
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Home / Documents / F-QM-POST-002-A-V0

F-QM-POST-002-A-V0 — Critical Value & Notifiable Disease Notification Log

Type: Form · Version: V0 · Status: DRAFT — UNAPPROVED · Served read-only from the bundled QMS copies. The Drive master is untouched.

Parent document: LAB-QM-POST-002 — Reporting of Critical Values and Notifiable Diseases Policy (parent is encoded in the form number)

Rendered in-browser from the project's Word file F-QM-POST-002-A-V0-critical-and-urgent-results-notification-log.docx (policies-docx / forms-docx — the file Junry reviews). Formatting is faithful, not pixel-perfect; the DOCX is the official copy.

Document #F-QM-POST-002-A-V0Parent DocumentLAB-QM-POST-002 — Reporting Critical Values Policy

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Part 1 — Life-Threatening Critical (Panic) & Urgent Results Verbal Communication Log

Policy Mandate: Call the attending physician, ER physician, or charge nurse by phone as soon as the result is verified (within 15 minutes). Require the recipient to read back the patient full name, hospital number, test name, and critical value word for word before ending the call.

Log No.Date & Time VerifiedPatient Full NameHospital No. (MRN)Ward / ER / OPDTest Name & Result (with Units)Category: [C] Critical / [U] UrgentRecipient Name & RoleRead-Back Confirmed?Notification Time & Elapsed MinReporting MT SignatureRemarks / Attending MD Orders
1[ ] C [ ] U[ ] Yes [ ] NoHH:MM (___ min)
2[ ] C [ ] U[ ] Yes [ ] NoHH:MM (___ min)
3[ ] C [ ] U[ ] Yes [ ] NoHH:MM (___ min)
4[ ] C [ ] U[ ] Yes [ ] NoHH:MM (___ min)
5[ ] C [ ] U[ ] Yes [ ] NoHH:MM (___ min)
6[ ] C [ ] U[ ] Yes [ ] NoHH:MM (___ min)

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Part 2 — Unusual Laboratory Findings & Extreme Delta-Check Technical Escalation Record

Use this record when a finding differs sharply from prior data, an extreme delta check fails, or microscopic morphology is unexpectedly abnormal.

Escalation Ref No.Date & TimePatient Full NameHospital No. (MRN)Analyte InvolvedCurrent ValuePrevious Value & Date
ESC-YYYY-____YYYY-MM-DD HH:MM

2.1 Technical Investigation Checklist

2.2 Pathologist Technical Evaluation & Authorization

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Part 3 — Notifiable Infectious Disease Case Report & Surveillance Log (RA 11332)

Mandatory Reporting Protocol: Under Republic Act No. 11332, reactive findings for Dengue Duo, Hepatitis B (HBsAg), and Syphilis (RPR) require duplicate confirmatory repeat from the primary tube, clinician notification, reporting to Tarangnan RHU / Samar PHO, and 6-month frozen (-20°C) retention of the reactive sample.

Case Ref #Detection DatePatient Full NameAge / SexResidential Address (Barangay / Municipality)Notifiable Disease / ExaminationTest Method & Kit Lot No.Initial ResultConfirmatory Repeat ResultIPC & Clinician NotifiedRHU / PHO Transmittal No.Freezer Storage Location (-20°C)MT Initials
1YYYY-MM-DDDengue Duo (NS1/IgM/IgG)RDT / Lot: ________ReactiveReactive[ ] YesRef: ________Box: ___ Pos: ___
2YYYY-MM-DDHepatitis B (HBsAg)RDT / Lot: ________ReactiveReactive[ ] YesRef: ________Box: ___ Pos: ___
3YYYY-MM-DDSyphilis (RPR Flocculation)RPR / Lot: ________Titer: 1:____Titer: 1:____[ ] YesRef: ________Box: ___ Pos: ___
4YYYY-MM-DD[ ] YesRef: ________Box: ___ Pos: ___

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Part 4 — Monthly Supervisory Review & Sign-Off

4.1 Medical Technologists

We confirm that 100% of critical values were communicated with read-back verification and all reactive notifiable conditions were confirmed by duplicate repeat.

Technologist NamePRC License NumberDateSignature

4.2 Chief Medical Technologist / Laboratory Quality Manager

4.3 Pathologist / Head of Laboratory