№ lp_1_2_43505
File format: docx
Character count: 3348
File size: 25 KB
Year:
2020
Region / City:
Not specified
Subject:
Healthcare, Patient Care
Document Type:
EHR Process/Instruction
Organization / Institution:
Not specified
Author:
Not specified
Target Audience:
Healthcare Providers, Medical Practitioners
Period of Action:
Not specified
Approval Date:
Not specified
Date of Changes:
Not specified
Price: 8 / 10 USD
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The product description is provided for reference. Actual content and formatting may differ slightly.
Year:
2022
Region / city:
Denmark
Topic:
Electronic Health Record System Requirements
Document type:
Requirements specification
Organization / institution:
IT University of Copenhagen
Author:
Soren Lauesen
Target audience:
IT developers, IT consultants, project managers
Period of validity:
Not specified
Approval date:
February 2022
Date of changes:
February 2022
Year:
2023
Region / City:
United States
Topic:
Electronic Health Records (EHR), Health Information Management
Document Type:
Practice Brief
Organization / Institution:
AHIMA
Author:
AHIMA
Target Audience:
Health Information Management Professionals
Effective Period:
Not specified
Approval Date:
Not specified
Amendment Date:
Not specified
Year:
2026
Organization:
EHR Go
Document Type:
Activity List
Audience:
Students and Faculty in Healthcare Education
Scope:
Multi-disciplinary healthcare training
Update Frequency:
Continuous
Contact:
[email protected]
Year:
2026
Region / City:
United States
Topic:
Electronic Health Record (EHR) Activities
Document Type:
Activity List
Organization / Institution:
EHR Go
Author:
EHR Go Team
Target Audience:
Healthcare students, educators, and practitioners
Period of validity:
Ongoing
Approval Date:
Not specified
Modification Date:
Not specified
Context:
A list of activities in EHR Go, categorized by discipline and activity type, including orientation, knowledge, skills, and application activities for healthcare education.
Note:
Year
Subject:
Blood Borne Virus Testing, HIV, Hepatitis B, Hepatitis C
Document Type:
Procedure
Organization / Institution:
Canberra Health Services
Target Audience:
Medical Officers, nurses, midwives, students under supervision
Version:
1.5.0.0
Protocol Posting Date:
June 2024
CAP Laboratory Accreditation Program Protocol Required Use Date:
March 2025
Authors:
Gulisa Turashvili, MD, PhD; Uma G. Krishnamurti, MD, PhD; Barbara A. Crothers, DO; Giovanna A. Giannico, MD; Krisztina Hanley, MD; Anna Plotkin, MD; Anthony N. Karnezis, MD, PhD.
Note:
Accreditation Requirements
Date of Protocol Posting:
June 2024
Date of Required Use:
March 2025
Year:
2021
Region / City:
United Kingdom
Subject:
Assistance Dogs, Emergency Ambulance Services
Document Type:
Procedure
Organization / Institution:
South East Coast Ambulance Service NHS Foundation Trust
Author:
Not specified
Target Audience:
Ambulance Service Staff
Period of Validity:
Not specified
Approval Date:
Not specified
Date of Changes:
Not specified
Year:
2026
Version:
NENC v2.0
Date published:
22 January 2026
Planned review date:
October 2027
Region:
North East and North Cumbria
Healthcare system:
NHS
Clinical area:
Neurology
Condition:
Amyotrophic lateral sclerosis
Medicine:
Riluzole
Document type:
Shared care protocol
Indication:
Extension of survival or time to mechanical ventilation in ALS
Target population:
Adults
Intended audience:
NHS healthcare professionals
Initiating authority:
Neurological specialist services
Regulatory reference:
NICE Technology Appraisal TA20
Prescribing setting:
Secondary to primary care transfer
Monitoring requirements:
Liver function tests, full blood count, urea and electrolytes
Route of administration:
Oral or enteral
Licensing status:
Licensed for ALS only
Year:
2024
Region / City:
Australia
Document Type:
Regulatory submission for PBS listing
Organization:
Biogen Australia Pty Ltd
Drug Name:
Omaveloxolone (Skyclarys®)
Indication:
Friedreich’s ataxia in adults and adolescents aged 16 years and older
Dosage Form:
Capsule 50 mg, oral administration
Regulatory Status:
Orphan drug status granted by TGA, EMA and FDA approvals
Submission Date:
26 June 2024
PBAC Meeting:
March 2025
Population:
Patients aged 16 years and older with Friedreich’s ataxia
Treatment Phase:
Initial and continuing treatment
Prescriber Type:
Dental, Medical Practitioners, Nurse Practitioners, Optometrists
Restriction Type:
Authority Required (telephone/online PBS Authorities system)
Clinical Criteria:
Genetic confirmation of FXN mutation, presence of clinical symptoms, management under a specialist or consultation with specialized unit if needed
Treatment Criteria:
Must be given with best supportive care, hemodynamically stable in case of cardiac history
Administrative Advice:
Queries directed to Services Australia, prescribing information available online
Year:
2023
Region / city:
Australia
Topic:
Chronic hyperkalaemia, kidney disease, sodium zirconium cyclosilicate
Document Type:
Submission to PBAC
Agency / organization:
AstraZeneca Pty Ltd
Author:
Not specified
Target audience:
Medical practitioners, healthcare professionals
Period of validity:
Ongoing, based on PBAC recommendation and PBS listing
Approval date:
1 September 2023
Date of amendments:
Not specified
Year:
2024
Region / city:
Humber and North Yorkshire ICB
Theme:
Hydroxychloroquine treatment protocol
Document type:
Clinical guideline
Organization / institution:
NHS
Author:
RDTC
Target audience:
NHS healthcare professionals
Effective period:
From the initiation date until March 2028
Approval date:
March 2025
Date of changes:
November 2023
Next review date:
March 2028
Year:
2018
Region / City:
British Columbia
Theme:
Medical Supplies Coverage for Gender Affirmation and Surgery
Document Type:
Guidelines
Organization:
Ministry of Social Development and Poverty Reduction
Author:
Unknown
Target Audience:
Medical practitioners (MDs, NPs)
Effective Date:
August 28, 2018
Approval Date:
August 28, 2018
Revision Date:
None
Acute Inpatient Psychiatric Admission Form for Patients Aged 10–17 with Neurodevelopmental Disorders
Patient Name:
____________________________________________
Date of Birth:
____________________
Home Address:
_________________________________________________________________________
Parent/Guardian Name/Phone/Email:
______________________________________________________
Expected Admission Type:
Voluntary / Involuntary
Referral for:
Acute Inpatient Psychiatric Treatment, approximately 30 days
Target Population:
Patients aged 10–17 with autism spectrum disorder, intellectual disability, or related neurodevelopmental disability
Current Psychiatric Provider:
UNC Psychiatry Outpatient (if applicable)
Diagnoses:
_____________________________________________________________________________
Current Medications:
____________________________________________________________________
Medical Problems:
______________________________________________________________________
Isolation Precautions:
No / Yes
Past Medical Hospitalizations or Surgeries:
__________________________________________________
Previous Psychiatric Treatment:
___________________________________________________________
Substance Use:
_________________________________________________________________________
Post-Treatment Residence Confirmed:
No / Yes
Department of Social Services / Child Protective Services Involvement:
_________________________
Consent for Medical Treatment:
___________________________________________________________
Last COVID Test:
___________________
Laboratory Results:
Within normal limits / Not done / Any abnormalities: ______________________
Pregnancy Status:
No / Yes
Seizure History:
No / Yes, well-controlled / Yes, uncontrolled
Last Vital Signs:
T______ P______ BP______ RR______ O2 Sat _____ Weight______ Height_______ BMI_________
Pending/Past Legal Problems:
_____________________________________________________________
ADL Support:
Independent / Needs Assistance with Eating, Hygiene, Walking (specify assist device)
Communication Method:
Verbally (sentences/words/phrases), Sign language, Pictures, Device, Gestures
Sensory Needs:
Hearing impaired / Visually impaired / Over/undersensitive to ____________________
Year:
2025
Region / City:
United Kingdom
Topic:
COVID-19 treatment, lateral flow device tests
Document Type:
Service Specification
Organization / Institution:
NHS England
Author:
NHS England
Target Audience:
Pharmacy contractors, healthcare professionals
Period of Validity:
Ongoing, from 6 November 2023
Date of Approval:
May 2025
Date of Changes:
01 May 2025
Standard Operating Procedure: iMATCH tissue collection from HPB patients (Adapted from iMatch WP2.2)
Version:
1.0
Date of issue:
18/1/22
Date of next review:
21/2/22
Year:
2022
Region / City:
UK
Subject:
Tissue collection, bio-bank, clinical trials
Document Type:
Standard Operating Procedure
Organization / Institution:
MFT
Author:
Dominique Jones
Target Audience:
Clinical staff involved in tissue collection and surgery
Period of validity:
From 18/1/22 until further revision
Approval Date:
18/1/22
Modification Date:
21/2/22
Year:
2023
Region / City:
N/A
Topic:
Manuscript preparation guidelines
Document Type:
Template
Institution:
JFAS
Author:
JFAS
Target Audience:
Authors submitting manuscripts to JFAS
Effective Period:
N/A
Approval Date:
N/A
Modification Date:
N/A
Year:
2023
Region / city:
Australia
Topic:
Oncology, Pharmaceuticals
Document Type:
Resubmission
Institution:
Australian Government, Pharmaceutical Benefits Advisory Committee
Author:
AstraZeneca Pty Ltd.
Target Audience:
Healthcare professionals, regulatory bodies
Effective Period:
Ongoing
Approval Date:
November 2021
Date of Changes:
November 2021
Year:
2022
Region / city:
Europe
Topic:
Postoperative delirium
Document type:
Guideline update
Institution:
European Society of Anaesthesiology and Intensive Care Medicine (ESAIC)
Author:
Aldecoa C, Bettelli G, Bilotta F, Sanders RD, Spies CD et al.
Target audience:
Medical professionals, anaesthesiologists, intensive care specialists
Period of validity:
2022-ongoing
Approval date:
February 2022
Modification date:
Not specified
Contextual description:
This is an updated guideline on postoperative delirium for adult patients, covering risk factors, preventive measures, neuromonitoring, and treatment outcomes, based on the latest evidence and consensus.
Year:
2021
Region / City:
N/A
Topic:
Health Information Exchange, Interface Configuration
Document Type:
Technical Specification
Organization / Institution:
athenahealth, Inc.
Author:
athenahealth, Inc.
Target Audience:
Healthcare organizations, IT staff, athenahealth interface users
Period of validity:
N/A
Approval Date:
N/A
Date of Changes:
N/A