№ files_lp_3_process_9_45339
File format: docx
Character count: 2370
File size: 23 KB
Clinical practice guideline outlining the evaluation, differential diagnosis, treatment, monitoring, and potential complications of primary, secondary, and subclinical hypothyroidism.
Condition:
Hypothyroidism (E03.9)
Document Type:
Clinical guideline
Medical Specialty:
Endocrinology
Content Areas:
Subjective assessment, Objective examination, Laboratory and imaging studies, Assessment, Differential diagnosis, Treatment plan, Follow-up
Diagnostic Tests:
TSH, free T4, U/A, CBC, ESR, CMP, anti-TPO antibodies, lipid panel, aPTT, CK, Thyroid ultrasound
Medications Mentioned:
Levothyroxine (Synthroid, Levothroid)
Target Population:
Adult patients with suspected or confirmed hypothyroidism
Associated Conditions:
Thyroiditis, anterior pituitary failure, autoimmune disease, celiac disease
Monitoring Recommendations:
TSH every 6–8 weeks until stable, then annually
Potential Complications:
Myxedema coma, pericardial effusion, heart failure, depression, hyponatremia
Price: 8 / 10 USD
The file will be delivered to the email address provided at checkout within 12 hours.
The file will be delivered to the email address provided at checkout within 12 hours.
Don’t have cryptocurrency yet?
You can still complete your purchase in a few minutes:- Buy Crypto in a trusted app (Coinbase, Kraken, Cash App or any similar service).
- In the app, tap Send.
- Select network, paste our wallet address.
- Send the exact amount shown above.
The final amount may vary slightly depending on the payment method.
The file will be sent to the email address provided at checkout within 24 hours.
The product description is provided for reference. Actual content and formatting may differ slightly.
Year:
Not specified
Region / City:
Not specified
Subject:
Thyroid Disease, TRAb Concentrations
Document Type:
Research Data
Organization / Institution:
Not specified
Author:
Not specified
Target Audience:
Medical Professionals, Researchers
Period of validity:
Not specified
Approval Date:
Not specified
Date of Changes:
Not specified
Year:
2024
Region / City:
European Union
Theme:
Health Technology Assessment
Document Type:
Guidance Document
Author:
HTA Coordination Group (HTACG)
Target Audience:
Health Technology Developers, Regulatory Authorities, Medical Researchers
Period of Validity:
Ongoing
Approval Date:
28 November 2024
Date of Last Change:
N/A
Context:
Guidance document for filling in the joint clinical assessment (JCA) dossier template for medicinal products, intended for use by health technology developers and regulatory bodies.
Year:
2026
Region / City:
Dobbs Ferry
Subject:
Occupational Therapy, Education
Document Type:
Program Curriculum
Institution:
Mercy University
Author:
Not specified
Target Audience:
Prospective students, applicants for Occupational Therapy Doctorate
Period of Validity:
Starting Fall 2026
Approval Date:
Not specified
Modification Date:
Not specified
Institution:
Rural Clinical School Research Centre
Document type:
Research proposal outline
Intended use:
Preliminary presentation of a research idea
Target audience:
Prospective clinical and health researchers
Scope:
Clinical and health research projects
Geographic context:
Australia
Recommended length:
Three to five pages
Required sections:
Title, Background, Aims, Research Question, Research Plan, Dissemination, Project Team, Budget, Timeframe, References
Disciplinary focus:
Medical and health sciences
Note:
Year
Topic:
Clinical Research, Retinal Diseases
Document Type:
Clinical Research Site Information
Organization / Institution:
Jaeb Center for Health Research (JCHR)
Target Audience:
Clinical researchers, Investigators, Healthcare professionals
Authors:
Brendan J. McMullan; Anita J. Campbell; Christopher C. Blyth; Jonathan C. McNeil; Christopher P. Montgomery; Steven Y. C. Tong; Asha C. Bowen
Type of document:
Narrative review article
Topic:
Pediatric Staphylococcus aureus bacteremia
Population:
Neonates, children and adolescents
Medical specialty:
Infectious Diseases
Methods:
Systematic appraisal of published literature
Data sources:
PubMed and Medline
Search period:
January 1960 – 31 December 2018
Geographic context:
High-income countries
Funding source:
No funding received
Conflict of interest:
None declared
Clinical scope:
Community-acquired and healthcare-associated bacteremia
Note:
Year
Year:
2023
Region / city:
Canberra
Topic:
Healthcare, Peritoneal Dialysis
Document Type:
Clinical Procedure
Organization / institution:
Canberra Health Services
Author:
Not specified
Target audience:
Healthcare staff, including Registered and Enrolled Nurses, Medical Officers, Consultants, Nephrology Advance Trainee Registrar (ATR), Students under direct supervision
Period of validity:
Not specified
Approval date:
Not specified
Date of amendments:
Not specified
Year:
2026
Institution:
Nova Southeastern University, Ft. Lauderdale
Course:
Neuromuscular Systems II
Credits:
2
Duration:
12 weeks, first semester of third year
Contributors:
Suzana Simoes PT, DPT, NCS; Kim B. Smith PT, DPT; Jennifer Canbek, PT, PhD, NCS
Target audience:
Physical therapy students
Activity type:
Laboratory learning activity with volunteer patients
Focus:
Clinical decision making using ICF model for Parkinson’s disease
Learning objectives:
Assessment of PD cases, development of PT problem list, formulation of patient-centered plan of care, implementation of treatment interventions, evaluation of treatment outcomes
Materials:
Assigned readings from Schenkman & McCulloch (2002), Schenkman et al. (2010)
Methods:
Lab sessions with patient volunteers, outcome measures, treatment sessions, video documentation, SOAP note assignments
Assessment:
Rubric-based evaluation of outcome measures, ICF model application, problem list, plan of care, goals, treatment, and documentation
Year:
2021
Region / City:
Not specified
Topic:
Clinical practice guidelines, rehabilitation, stroke
Document Type:
Interview transcript
Organization / Institution:
Academy of Neurologic Physical Therapy, Jefferson College of Rehabilitation Sciences, Boston University
Authors:
Dr. Therese Johnston, Dr. Lisa Brown
Target Audience:
Clinicians, rehabilitation professionals, researchers
Period of Validity:
Not specified
Approval Date:
Not specified
Date of Changes:
Not specified
Note:
Year
Region / City:
Canberra
Subject:
Female Genital Cutting (FGC), Clinical Guidelines, Healthcare
Document Type:
Clinical Guideline
Organization / Institution:
Canberra Health Services
Target Audience:
Healthcare staff (medical officers, nurse practitioners, registered nurses, midwives, allied health, students)
Contextual Description:
Clinical guideline outlining the management and prevention of female genital cutting (FGC) for healthcare providers at Canberra Health Services.
Year:
2004
Region / City:
USA
Subject:
Healthcare, Medical Software, Procedures
Document Type:
Technical Manual
Organization / Institution:
Department of Veterans Affairs
Author:
REDACTED
Target Audience:
Medical Professionals, IT Staff
Period of Validity:
Ongoing
Approval Date:
April 2004
Date of Changes:
December 2018
Year:
2022
Region / City:
Canberra
Subject:
Clinical Records Management
Document Type:
Procedure
Organization:
Canberra Health Services
Author:
Unknown
Target Audience:
CHS staff involved in clinical record management
Period of Validity:
Indefinite
Approval Date:
2022
Amendment Date:
2022
Year:
2016
Region / city:
Canberra
Subject:
Hip Fracture Care
Document Type:
Clinical Guideline
Organization:
Canberra Health Services
Author:
Australian Commission on Safety and Quality in Health Care
Target Audience:
Healthcare professionals involved in hip fracture management
Period of validity:
Not specified
Approval Date:
22 October 2021
Amendment Date:
Not specified
Jurisdiction:
Australia
Regulatory framework:
Therapeutic Goods Administration (TGA) Clinical Trial Notification scheme
Document type:
Regulatory notification form
Scope:
Clinical trials involving medicines, biologicals, medical and therapeutic devices
Trial phases covered:
Phase I–IV, bioavailability/bioequivalence, device studies
Subjects:
Human participants
Ethics oversight:
Human Research Ethics Committee (HREC)
Approving authority:
Relevant institutional authority
Geographic coverage:
Australian trial sites with optional international sites
Responsible party:
Lead Investigator
Fee responsibility:
Lead Investigator
Related institution:
La Trobe University
Submission requirement:
Completed form and ethics approval