Midterm Flashcards

1
Q

regenerative medicine?

A

using bodies own materials to heal or fix

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2
Q

Webster Chapter One: what 3 categories of health technologies are considered to be innovative?

A

Pharmaceuticals
Medical Devices
Healthcare Services/Processes

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3
Q

Length Time Bias

A

This bias arises when screening is more likely to detect slower-growing (less aggressive) forms of a disease than aggressive forms. As a result, the overall survival statistics may be misleadingly favorable. Bias of when sample is taken

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4
Q

What is a systematic review (research synthesis)?

A

A systematic review is a comprehensive and structured evaluation of all relevant research studies on a specific question, aimed at summarizing the evidence and drawing reliable conclusions.

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5
Q

2 Barriers in Canada to digital health

A

Barrier 1: Payment models can limit the adoption of digital health care tools
Barrier 2: Licensing requirements across provinces and territories

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6
Q

Webster Chapter two: concept of social scaffold

A

A “social scaffold” refers to the network of institutions, organizations, and social norms that support the development and implementation of biomedical innovations

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7
Q

is germ line gene therapy legal in canada

A

no, cant use embroynic cells either

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8
Q

Describe Rogers’ theories of technology adoption

A

Innovation
Communication Channels.
Time:
Social System

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9
Q

PICO framework?

A

Patient or problem being addressed (P)
❖Intervention or exposure being considered (I)
❖Comparison intervention or exposure (when relevant) or area of interest (C)
❖Outcomes of interest (O)

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10
Q

Lead time bias?

A

This bias occurs when the early detection of a disease through diagnostic technology (such as screening) makes it appear that patients are living longer with the disease, even though the actual time of survival has not changed.

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11
Q

Kaplan: Define pseudodisease

A

subclinical disease that would not become overt before the patient dies of other causes

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12
Q

what is a retrovirus

A

retrovirus is a virus with an RNA genome, sometimes used in gene therapy, not always safe

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13
Q

2 types of cdss (clinical descision support system)

A

The two types of CDSS are knowledge-based systems, which use pre-defined rules and medical guidelines, and non-knowledge-based systems, which rely on machine learning to analyze data and make predictions.

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14
Q

different gene therapies?

A

viral vectors- viruses injected to deliver genetic material
homologous recombination- DNA instered into specific location
selective reverse mutation- inducing specific mutations in a gene and then selecting for cells that have reverted to the wild-type (normal) state.
regulation- methods that control gene activity in the cells

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15
Q

What aspects of research evidence are evaluated? in HTA

A

Clinical efficacy and safety data from clinical trials.
Comparative effectiveness against existing treatments.
Economic evaluations, including cost-effectiveness analysis.
Patient-reported outcomes and quality of life measures.
Ethical, legal, and social implications.

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16
Q

Stanimirovic: failures/fallacies related to e-health
according to

A

Interoperability
Universal Access and Healthcare Disparities
Digital Literacy and User Training
Data Privacy and Security

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17
Q

Rogers: How can technology adopters be classified?

A

Innovators, early adopters, early majority, late majority, laggards

18
Q

Overdiagnosis bias

A

same as pseudodisease

19
Q

Webster chapter two: The Holy Trinity of Evidence-Based Medicine”

A

Clinical Expertise
Best Research Evidence
Patient Values and Preferences

20
Q

some barriers of health infrstructure?

A

lack of tech, standards, cultural barriers, human factor issues, etc

21
Q

health informatics

A

the scientific field that deals with the storage, retrieval, and optimal use of health information, data, and knowledge for problem solving and decision making

22
Q

Kohn et Al: challenges of gene therapies

A

Delivery of Gene Therapies
Durability of the Therapeutic Effect
Immune Responses
Insertional Mutagenesis
Cost and Accessibility

23
Q

What is HTA

A

multidisciplinary process that uses explicit methods to determine the value of a health technology at different points in its lifecycle

24
Q

what are adenoids

A

Viruses that carry their genetic material in the form of double-stranded DNA, show promise in treating cancer

25
Q

Regulatory bodies vs CDA?

A

reg- is it safe
cda- is it effective

26
Q

Describe Rogers’ theories of technology diffusion

A

Relative advantage.
Compatibility
Complexity
Trialability
Observability

27
Q

Stanimirovic: What is technological solutionism

A

belief that technology alone can solve complex problems, ignoring the need for policy, behavior, and system changes

28
Q

Kohn et Al: First Group of Disorders Treated Successfully with Gene Therapy

A

The first group of disorders successfully treated with gene therapy includes monogenic diseases, where a single gene mutation causes the disease

29
Q

The Four Generative Mechanisms of NPT

A

Coherence, Cognitive Participation, Collective Action, Reflexive Monitoring

30
Q

most common type of vector

A

viruses

31
Q

What did the HTA on proton beam therapy find

A

Mixed evidence, High costs

32
Q

toti, pluri, uni, multipotency?

A

toti- zygote, any cells can be made
pluri- any cells no gametes,
uni- one kind (somatic)
multi- adult stem cells, some variation

33
Q

What is compared when looking at new HT’s?

A

Cost vs benefit

34
Q

Kohn et Al: Performance Criteria for Genetic Modifications to Enhance T-Cell Potency

A

Specificity
Persistence
Proliferation
Safety

35
Q

Kohn et Al: History of XSCID Treatment with Gene Therapy

A

XSCID was one of the first diseases treated by gene therapy, with trials dating back to the 1990s. Early trials involved inserting the correct gene (IL2RG) into hematopoietic stem cells using retroviral vectors. However, the approach led to severe side effects in some patients, including the development of leukemia
In later approaches, safer vectors like lentiviruses have been used to reduce the risk of insertional mutagenesis

36
Q

2 types of pseudodiseases

A

type 1-disease does not progress
type 2. the other in which the disease does progress – but so slowly that it never becomes clinically evident to the patient

37
Q

monogenic disorder

A

caused by a single allele of a gene AND are inherited in families, easiest to treat

38
Q

Miller: torque of nosologic change

A

genetic information displaces a more traditional diagnosis, based primarily on clinical signs and symptoms, and asserts a genetic logic of disease definition. Individual patients and their families can get caught in the ‘‘torque’’ of such nosologic change, creating uncertainties about what disease they ‘‘have’’

39
Q

Kohn et Al: Allogenic vs. Autologous Approaches to Gene Therapy

A

Allogenic Gene Therapy: This approach involves using donor cells or tissues for the therapy.
Autologous Gene Therapy: In this approach, the patient’s own cells are used. These cells are harvested, genetically modified (correcting the disease-causing mutation), and then reintroduced into the patient.

40
Q

DIfferent scanning tech?

A

x ray, CAT (multiple xrays), MRI (slices), mammogram, PET (uses radiation)

41
Q

Electronic Health Record vs Electronic Medical Record

A

EMR- A digital version of a patient’s medical history and treatment from a specific provider or practice.
EHR- A comprehensive digital record that contains a patient’s health information across different healthcare settings.

42
Q

basic process of gene therapy

A

correct copy” gene is provided or inserted, carrier called a vector must be used to deliver