临床决策分析(clinical decision analysis,CDA)

临床决策分析(clinical decision analysis,CDA)


相关考题:

临床决策分析(clinical decision analysis,CD A)(名词解释)

临床证据手册(handbook of clinical evidence)(名词解释)

clinical pharmacy

临床药剂学的英文是A.Industrial pharmacyB.Physical pharmacyC.PharmacokineticsD.Clinical pharmacyE.Biopharmacy

下列摩托罗拉Handover参数中,哪些是接收质量切换门限参数() A.decision_1_n5B.decision_1_p5C.decision_1_n6D.decision_1_p6E.decision_1_n7F.decision_1_p7

下列摩托罗拉PowerControl参数中,哪些是接收质量功率控制门限参数() A.decision_1_p1B.decision_1_p2C.decision_1_p3D.decision_1_p4

共用题干Clinical Trials1. Many clinical trials are done to see if a new drug or device is safe and effective for people to use.Sometimes clinical trials are used to study different ways to use the standard treatments so they will be more effective,easier to use,and/or decrease side effects.Sometimes,studies are done to learn how to best use the treatment in a different population,such as children,in whom the treatment was not previously tested.2. It is important to test drugs and medical products in the people they are meant to help.It is also important to conduct research in a variety of people because different people may respond differently to treatments.Some people participate in clinical trials because they have exhausted standard treatment options .Other people participate in trials because they want to contribute to the ad-vancement of medical knowledge.3. The FDA(食品及药物管理局)works to protect participants in clinical trials and to ensure that people have reliable information as they decide whether to join a clinical trial.Although efforts are made to control the risks to clinical trial participants,some risks may be unavoidable because of the uncertainty inherent(内在的)in medical research studies involving new medical treatments.4. People should learn as much as possible about the clinical trials that interest them.They should also feel comfortable discussing their questions and concerns with members of the health care team. Prospective(预期的)participants should understand what happens during the trial ,the type of health care they will receive,and any costs to them.Anyone considering a clinical trial should also know that there are benefits and risks associated with participating. Paragraph 2______A: Are clinical trials safe?B: What are clinical trials?C: What should people know before participating in a clinical trial?D: Who should consider clinical trials and why?E: Where are clinical trials conducted?F: Why are clinical trials done?

共用题干Clinical Trials1 Many clinical trials are done to see if a new drug or device is safe and effective for people to use .Sometimes clinical trials are used to study different ways to use the standard treatments so they will be more effective,easier to use,and/or decrease side effects. Sometimes,studies are done to learn how to best use the treatment in a different group, such as children,in whom the treatment was not previously tested.2 It is important to test drugs and medical products in the people they are meant to help,It is also important to conduct research in a variety of people because different people mayrespond differently to treatments.Some people participate in clinical trials because they have exhausted standard treatment options.Other people participate in trials because they want to contribute to the advancement of medical knowledge.3 The FDA(食品及药物管理局)works to protect participants in clinical trials and to ensure that people have reliable information as they decide whether to join a clinical trial. Although efforts are made to control the risks to clinical trial participants,some risks may be unavoidable because of the uncertainty inherent(内在的)in medical research studies involving new medical treatments.4 People should learn as much as possible about the clinical trials that interest them.They should also feel comfortable discussing their questions and concerns with members of thehealth care team. Prospective(预期的)participants should understand what happens during the trial,the type of health care they will receive,and any costs to them.Anyone considering a clinical trial should also know that there are benefits and risks associated with participating. Reliable information should be available to_________.A: for some patientsB: before participationC: in humansD:medical knowledgeE: during the trialF: candidates for clinical trials

共用题干Clinical Trials1. Many clinical trials are done to see if a new drug or device is safe and effective for people to use.Sometimes clinical trials are used to study different ways to use the standard treatments so they will be more effective,easier to use,and/or decrease side effects.Sometimes,studies are done to learn how to best use the treatment in a different population,such as children,in whom the treatment was not previously tested.2. It is important to test drugs and medical products in the people they are meant to help.It is also important to conduct research in a variety of people because different people may respond differently to treatments.Some people participate in clinical trials because they have exhausted standard treatment options .Other people participate in trials because they want to contribute to the ad-vancement of medical knowledge.3. The FDA(食品及药物管理局)works to protect participants in clinical trials and to ensure that people have reliable information as they decide whether to join a clinical trial.Although efforts are made to control the risks to clinical trial participants,some risks may be unavoidable because of the uncertainty inherent(内在的)in medical research studies involving new medical treatments.4. People should learn as much as possible about the clinical trials that interest them.They should also feel comfortable discussing their questions and concerns with members of the health care team. Prospective(预期的)participants should understand what happens during the trial ,the type of health care they will receive,and any costs to them.Anyone considering a clinical trial should also know that there are benefits and risks associated with participating. Learn as much as you can about a clinical trial______.A: candidates for clinical trialsB: during the trialC: medical knowledgeD: in humansE: before participationF: for some patients

In modern clinical practice, doctors personally assess patients in order to ______, treat, and prevent disease using clinical judgment.A.remedyB.diagnoseC.infectD.judge

哮喘可分为三期()。A、急性发作期(acute exacerbation)B、慢性持续期(chronic persistent)C、临床缓解期(clinical remission)D、以上都对

短期经营决策分析主要包括()A、生产经营决策分析B、定价决策分析C、销售决策分析D、战略决策分析E、战术决策分析

冠心病监护病房为()。A、intensive care unitB、coronary care unitC、acute myocardial infarctionD、Clinical common crisisE、Clinical Intensive Care

Clinical Practice Guidelines代表()A、临床操作规程指南B、评价研究证据C、临床实践指南D、病例对照研究

下列摩托罗拉Handover参数中,哪些是接收质量切换门限参数()A、decision_1_n5B、decision_1_p5C、decision_1_n6D、decision_1_p6E、decision_1_n7F、decision_1_p7

临床实践指南(clinical practice guideline)

多中心临床试验(multicenter clinical trial)

临床试验(clinical trial)

临床证据手册(handbook of clinical evidence)

名词解释题临床血液学和血液检验(clinical hematology and hematologic examinations)

单选题Clinical Practice Guidelines代表()A临床操作规程指南B评价研究证据C临床实践指南D病例对照研究E系统评价

名词解释题多中心临床试验(multicenter clinical trial)

名词解释题临床决策分析(clinical decision analysis,CDA)

单选题Clinical Practice Guidelines代表()A临床操作规程指南B评价研究证据C临床实践指南D病例对照研究

多选题短期经营决策分析主要包括()A生产经营决策分析B定价决策分析C销售决策分析D战略决策分析E战术决策分析

名词解释题临床证据手册(handbook of clinical evidence)

名词解释题药物临床试验(drug clinical trial)