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Table. 3.

Table. 3.

Level of evidence and grade of recommendation in Korean Clinical Practice Guideline for Stoke (KCPGS) and AHA/ASA guidelines

Korean Clinical Practice Guideline for Stoke
Level of evidence (LOE)
Ia Evidence obtained from meta-analysis of randomized controlled trials
Ib Evidence obtained from at least one randomized controlled trial
IIa Evidence obtained from at least one well-designed controlled study without randomization
IIb Evidence obtained from at least one other type of well-designed quasi-experimental study
III Evidence obtained from well-designed non-experimental descriptive studies, such as comparative studies, correlation studies and case studies
IV Evidence obtained from expert committee reports or opinions and/or clinical experiences of respected authorities

Grade of recommendation (GOR)
A (LOE Ia, Ib) Required: at least one randomized controlled trial as part of the body of literature of overall good quality and consistency addressing specific recommendation
B (LOE IIa, IIb, III) Required: availability of well conducted clinical studies but no randomized clinical trials on the topic of recommendation
C (LOE IV) Required: evidence obtained from expert committee reports or opinions and/or clinical experiences of respected authorities. This grade indicates the absence of directly applicable clinical studies of good quality.
GPP (good practice points) Recommended best practice based on the clinical experience of the guideline development group

AHA/ASA guidelines

Class (Strength) of recommendation (COR)
1 (Strong) Benefit >>> Risk
Is recommended; is indicated/useful/effective/beneficial; should be performed/administered/other
2a (Moderate) Benefit >> Risk
Is reasonable; can be useful/effective/beneficial
2b (Weak) Benefit ≥ Risk
May/might be reasonable; may/might be considered; usefulness/effectiveness is unknown/unclear/uncertain or not well established
3. No benefit (Moderate) Benefit = Risk
Is not recommended; is not indicated/useful/effective/beneficial; should not be performed/administered/other
3. Harm (Strong) Risk > Benefit
Potentially harmful; causes harm; associated with excess morbidity/mortality; should not be performed/administered/other

Level (Quality) of evidence (LOE)
A High-quality evidence from more than 1 RCT;
meta-analyses of high-quality RCTs;
one or more RCTs corroborated by high-quality registry studies
B-R (randomized) Moderate-quality evidence from 1 or more RCTs;
meta-analyses of moderate-quality RCTs
B-NR (nonrandomized) Moderate-quality evidence from 1 or more well-designed, well-executed nonrandomized studies, observational studies, or registry studies;
Meta-analyses of such studies
C-LD (limited data) Randomized or nonrandomized observational or registry studies with limitations of design or execution; meta-analyses of such studies; physiological or mechanistic studies in human subjects
C-EO (expert opinion) Consensus of expert opinion based on clinical experience

RCT, randomized controlled trial; AHA, American Heart Association; ASA, American Stroke Association

Korean J Clin Pharm 2024;34:79-99 https://doi.org/10.24304/kjcp.2024.34.2.79
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