№ lp_1_2_09738
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This document outlines the criteria and process for converting intravenous antimicrobial therapy to oral therapy in a clinical setting.
Year:
[effective date]
Region / City:
[Facility Location]
Topic:
Intravenous to Oral Antibiotic Conversion
Document Type:
Policy
Organ / Institution:
[Facility Name]
Author:
[Approving individual or committee]
Target Audience:
Clinical staff, healthcare providers
Period of Effectiveness:
[Effective date]
Approval Date:
[Approval Date]
Date of Changes:
[Date of Changes]
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The product description is provided for reference. Actual content and formatting may differ slightly.
Year:
2023
Region / City:
Canberra, Australia
Topic:
Paediatric intravenous extravasation management
Document Type:
Guideline
Organization:
Canberra Health Services
Author:
Expert clinical reference groups
Target Audience:
Clinicians in paediatric care
Period of validity:
Ongoing
Approval Date:
7 December 2023
Amendment Date:
26 August 2024
Organisation:
Canberra Health Services
Region:
Canberra, Australian Capital Territory, Australia
Healthcare setting:
Hospital in the Home
Clinical area:
Cardiology
Condition:
Congestive cardiac failure
Patient population:
Adults
Type of document:
Clinical procedure
Route of administration:
Intravenous
Treatment:
Furosemide
Admission criteria:
Defined clinical and general eligibility requirements
Source type:
Institutional clinical guideline
Version:
V3.0
Author:
Dr Julia Sikorska, Consultant Haematologist, STSTN Clinical Guidelines Group
Note:
2019
Executive/Divisional sponsor:
Via Hospital Transfusion Committee
Applies to:
All staff involved in the care of patients with Sickle Cell Disease
Date issued:
V3.0 February 2020
Review date:
February 2023
Approval person/Committee:
Hospital Transfusion Committee
Date:
March 2020
Year:
2020
Region / city:
St George’s, UK
Topic:
Hyperhaemolysis management in Haemoglobinopathies
Document type:
Clinical guidelines
Organization / institution:
St George’s University Hospitals NHS
Target audience:
Healthcare staff involved in the care of Sickle Cell Disease patients
Effective period:
February 2020–February 2023
Approval date:
March 2020
Year:
2022
Region / city:
New South Wales, Australia
Theme:
Medical procedure / MRI contrast agent administration
Document Type:
Standing order
Organization / institution:
New South Wales Health
Author:
NSW Health
Target audience:
Medical professionals, particularly those involved in MRI procedures
Period of validity:
Until approval by hospital/district DTC
Approval date:
Not specified
Date of changes:
Not specified
Note:
Contextual description
Year:
2026
Region / city:
Canberra
Topic:
Clinical Procedures, Healthcare, Intravenous Access
Document Type:
Procedure
Organization / institution:
Canberra Health Services
Author:
Not specified
Target audience:
Healthcare professionals at Canberra Health Services
Effective period:
Ongoing
Approval date:
Not specified
Revision date:
Not specified
Document type:
Medication standing order
Clinical area:
Medical imaging and diagnostic radiology
Patient population:
Adults aged 16 years and over
Medication:
Iohexol iodinated contrast media
Route of administration:
Intravenous injection
Indication:
Contrast-enhanced CT imaging studies
Applicable organisations:
NSW public health organisation imaging departments
Exclusions:
Paediatric patients under 16 years of age
Regulatory framework:
NSW State Form SMR060.160 and PD2013_043 Medication Handling in NSW Public Health Facilities
Authorised personnel:
Registered nurses and accredited medical radiation scientists meeting AHPRA and HETI requirements
Contraindications:
Known hypersensitivity to iodinated contrast media; high-risk renal impairment without medical officer approval
Risk considerations:
Contrast-induced acute kidney injury and hypersensitivity reactions
Guideline references:
RANZCR Iodinated Contrast Media Guideline 2018; ACR Manual on Contrast Media 2018
Approval requirements:
Changes require approval by a radiologist or medical officer
Review requirement:
Annual review for currency
Year:
2021
Region / City:
Canberra
Topic:
Medicine / Cardiology
Document Type:
Guideline
Organization / Institution:
Canberra Health Services
Author:
Not specified
Target Audience:
Healthcare professionals working in CHS
Effective Period:
Not specified
Approval Date:
10 September 2021
Amendment Date:
Not specified
Year:
2023
Country:
Australia
Document type:
Clinical guidance
Organization:
Australian Government Department of Health / Blood Service
Target audience:
Healthcare professionals administering IVIg
Scope:
IVIg administration, safety, and monitoring
Effective from:
April 2023
References:
Criteria for the clinical use of intravenous immunoglobulin in Australia, 3rd edition, October 2018; Product information sheets of Privigen®AU, Kiovig®, Flebogamma®, Gammunex®, Octagam®
Appendices:
Product comparison, infusion rate guides
Date:
March 2023
Country:
Australia
Subject:
Intravenous immunoglobulin administration
Document type:
Clinical practice guidance
Healthcare setting:
Hospital and health services
Target audience:
Healthcare professionals involved in IVIg prescribing and administration
Regulatory context:
BloodSTAR authorization and national IVIg criteria
Products referenced:
Privigen®, Kiovig®, Flebogamma®, Gammunex®, Octagam®, Intragam®10
Effective period:
From April 2023
Clinical scope:
Indications, precautions, preparation, infusion, storage, and adverse effects
Source type:
Official guidance
Year:
2023
Region / City:
Liege, Belgium
Field:
Anesthesia, Pharmacology
Document Type:
Clinical Trial Report
Institution:
Department of Anesthesia and Intensive Care Medicine, Liege University Hospital, Liege, Belgium
Authors:
G Van Munster, F Beck, PY Hardy, M Carella, V Bonhomme
Target Audience:
Medical professionals, researchers in anesthesia
Period of Study:
October 21, 2021 – April 8, 2022
Approval Date:
2021
Modification Date:
N/A
Funding:
Department of Anesthesia and Intensive Care Medicine, Liege University Hospital, Liege, Belgium
Ethics Approval:
Comité d’Ethique Hospitalo-Facultaire Universitaire de Liège (study number 2021/190)
Clinical Trial Registration:
EudraCT: 2021-002824-19
Methodology:
Randomized, Double-blind, Placebo-controlled
Conclusion:
MS does not effectively reduce propofol requirements for hypnosis in general anesthesia during thyroidectomy
Year:
2019
Region / City:
Global
Topic:
Medical Research
Document Type:
Research Study
Institution:
Various research institutions
Author:
Multiple authors
Target Audience:
Healthcare professionals, researchers
Period of Validity:
Ongoing
Approval Date:
2019
Date of Changes:
Not specified
Main Outcome:
Return of spontaneous circulation, survival to hospital discharge, favorable neurological outcome
Comparative Intervention:
Intraosseous vs. Intravenous drug administration during cardiac arrest
Additional Considerations:
Cost, feasibility, health equity
Assessment:
Observational studies
Desirable Effects:
Potential for faster drug delivery
Undesirable Effects:
Risk of reduced drug effectiveness, complications
Certainty of Evidence:
Very low
Resources Required:
No specific study on resource comparison
Cost-Effectiveness:
No included studies
Equity:
IO access may increase health inequity in low-resource settings
Acceptability:
Likely acceptable to stakeholders
Feasibility:
Likely feasible to implement
Program:
Medicare IVIG Demonstration
Administering Agency:
Centers for Medicare & Medicaid Services (CMS)
Country:
United States
Legal Basis:
Medicare IVIG Access and Strengthening Medicare and Repaying Taxpayers Act of 2012
Extended Under:
Disaster Tax Relief and Airport and Airway Extension Act of 2017
Further Extension:
Consolidated Appropriations Act, 2021
OMB Control Number:
0938-1246
CMS Form Number:
CMS-10518
Subject:
Application for beneficiary participation in the IVIG Demonstration
Target Population:
Medicare Part B beneficiaries with primary immune deficiency disease (PIDD)
Enrollment Cap:
6,500 beneficiaries (originally 4,000)
Funding Limit:
$45 million including administrative and evaluation costs
Coverage Scope:
Bundled payment for medically necessary supplies and services for in-home IVIG administration
Application Requirement:
Mandatory signed application by beneficiary and provider
Submission Methods:
Mail or fax
Languages Available:
English and Spanish
Period of Demonstration:
Through December 31, 2023 or until statutory limits are met
Participation Status:
Voluntary; may be terminated by beneficiary at any time
TERMS AND CONDITIONS FOR THE SUPPLY, STORAGE, AND MANAGEMENT OF INTRAVENOUS FLUIDSLICENSED MEDICINES
Year:
2022
Region / city:
London
Topic:
Contractual terms and conditions for the supply and management of intravenous fluids and licensed medicines
Document type:
Contract
Agency / institution:
Department of Health and Social Care
Author:
The Secretary of State for Health and Social Care
Target audience:
Healthcare suppliers, contractors
Period of validity:
From [insert date] to [insert date]
Approval date:
[insert date]
Amendment date:
[insert date]
Year:
2021
Region / City:
Elk City, Oklahoma
Topic:
Transportation, Infrastructure
Document Type:
Technical Report
Organization:
Oklahoma Transportation
Author:
Office of Research and Implementation, Oklahoma Transportation
Target Audience:
Transportation professionals, highway engineers, government agencies
Period of validity:
N/A
Approval Date:
March 2021
Date of Changes:
N/A
Contextual Description:
Technical report detailing the design and implementation of a Diverging Diamond Interchange (DDI) in Elk City, Oklahoma, part of a broader transportation innovation initiative.
Year:
2015
Month:
October
Organization:
Washington State Department of Transportation (WSDOT)
Document Type:
Methods and Assumptions Template
Related Report:
Interchange Justification Report (IJR)
Intended Audience:
Project support team, stakeholders, FHWA, local agencies
Document Purpose:
Establish and record methods and assumptions used in IJR studies
Signatory Parties:
WSDOT HQ Access, WSDOT HQ ASDE, FHWA (if applicable), Traffic Representative, other stakeholders
Project Phase:
Study phase
Reference Materials:
WSDOT Design Manual Chapter 550, Highway Capacity Manual (HCM), Highway Safety Manual (HSM)
Content Elements:
Project description, background, traffic studies, analysis years, operational and collision analysis, alternatives assessment
Year:
2011
Region / City:
United States
Document Type:
Release Notes
Organization / Institution:
Department of Veterans Affairs
Author:
Department of Veterans Affairs
Target Audience:
Veterans Administration staff, healthcare professionals, and IT personnel
Period of Action:
August 2011
Approval Date:
August 2011
Date of Changes:
Not specified
Year:
2011
Region / city:
United States
Topic:
Male Reproductive System, Disability Benefits
Document type:
Guidelines, Technical Document
Organization / institution:
Department of Veterans Affairs
Author:
REDACTED
Target audience:
Veterans, Healthcare Providers, Medical Examiners
Effective period:
Ongoing (as of document date)
Approval date:
April 2011
Revision history:
Multiple updates in 2011
Year:
2011
Region / City:
United States
Topic:
Prostate Cancer, Disability Benefits
Document Type:
Questionnaire
Author:
REDACTED
Target Audience:
Veterans, Healthcare Providers
Period of Validity:
Not specified
Approval Date:
11/02/2010
Revision Date:
4/1/2011, 4/7/2011