A system for rating the stability and strength of medical evidence
© Treadwell et al; licensee BioMed Central Ltd. 2006
Received: 25 July 2006
Accepted: 19 October 2006
Published: 19 October 2006
Methods for describing one's confidence in the available evidence are useful for end-users of evidence reviews. Analysts inevitably make judgments about the quality, quantity consistency, robustness, and magnitude of effects observed in the studies identified. The subjectivity of these judgments in several areas underscores the need for transparency in judgments.
This paper introduces a new system for rating medical evidence. The system requires explicit judgments and provides explicit rules for balancing these judgments. Unlike other systems for rating the strength of evidence, our system draws a distinction between two types of conclusions: quantitative and qualitative. A quantitative conclusion addresses the question, "How well does it work?", whereas a qualitative conclusion addresses the question, "Does it work?" In our system, quantitative conclusions are tied to stability ratings, and qualitative conclusions are tied to strength ratings. Our system emphasizes extensive a priori criteria for judgments to reduce the potential for bias. Further, the system makes explicit the impact of heterogeneity testing, meta-analysis, and sensitivity analyses on evidence ratings. This article provides details of our system, including graphical depictions of how the numerous judgments that an analyst makes can be combined. We also describe two worked examples of how the system can be applied to both interventional and diagnostic technologies.
Although explicit judgments and formal combination rules are two important steps on the path to a comprehensive system for rating medical evidence, many additional steps must also be taken. Foremost among these are the distinction between quantitative and qualitative conclusions, an extensive set of a priori criteria for making judgments, and the direct impact of analytic results on evidence ratings. These attributes form the basis for a logically consistent system that can improve the usefulness of evidence reviews.
Systematic reviews, technology assessments, and clinical practice guidelines all incorporate evidence-based conclusions. The multifaceted nature of evidence, however, leads to varying degrees of confidence in how well the evidence supports conclusions drawn from it. For example, one is more confident in conclusions drawn from several well-designed randomized controlled trials that find similar effects than in conclusions drawn from a few poorly designed trials with disparate results. Consequently, methods for describing one's confidence in the available evidence are useful for end-users of evidence-based documents. This confidence is embodied in strength-of-evidence ratings.
In this article, we introduce a structured and transparent system for rating the strength of a body of evidence pertaining to a medical technology (see Note 1). We also define the concept of the stability of evidence as distinct from the strength of evidence. We identify the many judgments inherent in the process of performing evidence reviews, and then note how such judgments are incorporated within two prominent rating systems: the U.S. Preventive Services Task Force (USPSTF) system and the Grades of Recommendation Assessment, Development and Evaluation (GRADE) system [1–5]. Next, we describe our system, and detail several of its unique attributes. We present graphical illustrations of how our system provides a logical framework to combine the judgments inherent in evidence reviews. We then provide two complete examples to illustrate the system (one example for an intervention and one for a diagnostic test).
In performing an evidence review, an analyst must make numerous judgments about the available evidence. For many of these judgments, analysts at different centers could reasonably disagree about the status of the evidence. For example, one analyst may view a certain methodological flaw as fatal, whereas another analyst may view that same flaw as minor. This problem may be partially addressed through the use of standardized quality instruments. However, different centers tend to use different instruments, which can lead to different assessments of the quality of trials . In the absence of empirical evidence on the extent to which a particular methodological flaw influences the results, the assessment of study quality necessarily entails judgment.
A Guide to Terminology
Major components of evidence
The extent to which studies are protected from bias
The number of studies and the number of patients
The extent to which different studies found similar results
The extent to which minor alterations in the data do not change conclusions drawn from that data
Magnitude of effect
The effect size
Quantitative and qualitative conclusions
Type of conclusion:
How well does it work?
Does it work?
Type of rating:
Interpretation of rating:
Confidence that future evidence will not indicate a different effect size
Confidence that future evidence will not indicate a different direction of effect
High, Moderate, Low, or Unstable
Strong, Moderate, Weak, or Inconclusive
Judgments Involved in Systematic Reviews
Judgments pertaining to study quality assessment
• What method will be used to assess study quality?
• If a quality scale is to be used, what scoring method will apply?
• What is the threshold for excluding a study from analysis due to poor quality?
• How will the individual study quality ratings be summarized to yield a single overall rating of quality to the evidence base (High, Moderate, or Low)?
Judgment pertaining to sufficient evidence for quantitative estimate
• What is the minimum number of studies required to permit a quantitative estimate?
• What is the minimum percentage of studies reporting accurate information (i.e., calculable effect sizes) required to permit a quantitative estimate?
• What imputation methods will be used for studies that did not report sufficient information for a calculable effect size?
Judgments pertaining to initial meta-analysis
• What effect size measure will be used?
• How will heterogeneity be measured (Q or I2)?
• What is the threshold for considering an evidence base heterogeneous?
• Will the summary effect size estimate be derived from a fixed-effects or random-effects meta-analysis?
Judgments pertaining to quantitative robustness testing
• What robustness tests will be used?
• If a cumulative meta-analysis is one of the robustness tests, will it be a fixed-effects or random-effects model?
• If a cumulative meta-analysis is one of the robustness tests, in what order will studies be entered into the cumulation?
• If a cumulative meta-analysis is one of the robustness tests, how many steps (i.e., study removals) will be examined to determine robustness?
• If a cumulative meta-analysis is one of the robustness tests, what threshold for a change in the summary effect size will be used to determine robustness?
• If publication bias testing is one of the robustness tests, which method of testing for publication bias will be used?
• If confidence interval width is one of the robustness tests, how narrow must the interval be for the summary estimate to be considered robust?
• Will overall robustness be judged based on passing all of the robustness tests, or simply a majority, or what percentage?
Judgments pertaining to meta-regression
• What is the minimum number of studies required to perform meta-regression?
• Which covariates will be included in multiple regression models?
• How many covariates are permitted in any given regression model?
• Does "explaining heterogeneity" require a statistically significant covariate, or the lack of resultant heterogeneity, or both of these?
• What robustness tests will be performed for the meta-regression?
Judgments pertaining to qualitative robustness testing
• What robustness tests will be performed?
• If a cumulative meta-analysis is one of the robustness tests, in what order will studies be entered into the cumulation?
• If a cumulative meta-analysis is one of the robustness tests, how many steps (i.e., study removals) will be examined to determine robustness?
• What is the size of a lowest possible effect that is still clinically important?
• What is the p value for statistical significance?
• What is the definition of a large magnitude of effect?
• How will qualitative consistency be defined (based on point estimates, confidence intervals, some percentage of studies, etc)?
In addition to these individual components (i.e., overall quality, quantity, consistency, robustness, and magnitude of effect of all evidence being considered), still another layer of judgment is required: how to combine each of these five components to produce a rating of the overall "strength" of the evidence. Different analysts may disagree about the relative importance of each component and their interplay. For example, if there is one small but well-conducted randomized controlled trial, how should one reconcile the high quality but low quantity of this evidence base to produce an overall strength rating? Or, how should one interpret very large effects observed in suboptimal study designs?
With all the judgments necessary, two different analysts, when faced with exactly the same clinical question and exactly the same evidence base, may have different degrees of confidence in their conclusions. In some instances, this discrepancy could be so large that the two analysts reach different overall conclusions. In a pilot study of inter-reviewer agreement, the GRADE group asked 17 experienced reviewers to rate the strength of the evidence for each of 46 outcomes within 12 systematic reviews . Complete agreement occurred for only three outcomes (6%). The median kappa statistic of agreement was only 0.09, suggesting substantial inter-reviewer differences in evidence ratings. Although this study was conducted when the GRADE system was relatively new (and, therefore, these results may underestimate the true amount of agreement), the results do illustrate that even experienced reviewers can disagree about the strength of the evidence.
The subjectivity of judgments at several points in the systematic review process underscores the need for transparency. With transparent judgments, the end users of the review (including other analysts) can decide for themselves whether the judgments are reasonable.
Currently Available Rating Systems
Numerous rating systems designed to assess the strength of a body of evidence have been proposed. Several of these were reviewed in a 2002 report from the Research Triangle Institute-University of North Carolina Evidence-based Practice Center (RTI-UNC EPC) . This report focused on three components of a rating system: quality, quantity, and consistency. The report incorporated magnitude of effect within the quantity category, and did not mention robustness explicitly. Below, we highlight two major rating systems.
USPSTF System for Evaluating the Quality of Evidence (Harris et al. 2002)
Level of evidence: Individual study
Criteria for judging quality:
• Internal validity – based on a series of separate, specific criteria for systematic reviews, RCTs, cohort studies, case-control studies, and diagnostic accuracy studies
• External validity – degree to which the study is generalizable to the population of interest and conditions of typical clinical practice
Level of evidence: Linkage (key question) in the analytic framework
Criteria for judging quality:
• Aggregate internal validity of studies addressing the linkage
• Aggregate external validity of studies addressing the linkage
• Coherence/consistency of studies addressing the linkage
Level of evidence: Entire preventive service
Criteria for judging quality:
• Quality of the evidence for each linkage in the analytic framework
• Degree to which a complete chain of linkages supported by adequate evidence connects the preventive service to health outcomes
• Degree to which the complete chain of linkages "fit" together a
• Degree to which the evidence connecting the preventive service and health outcomes is "direct" b
The GRADE System for Grading Quality of Evidence and Strength of Recommendations[2,5]
Quality of evidence for each outcome (high, moderate, or low) – based on the following criteria:
• Study design– grade of high or low assigned based on design (RCT = high, observational study = low)
• Study quality– Detailed study methods and execution.
1) Limitations in quality can decrease grade one or two levels.
2) Evidence of reporting bias can also decrease grade one level.
3) Grade can be increased one level if all plausible confounders would have reduced the treatment effect.
• Consistency of results– The level of similarity of estimates of effects across studies.
1) Important inconsistency can decrease grade one level.
• Directness of evidence– the extent to which the people, interventions, and outcome measures are similar to those of interest.
1) Some or major uncertainty about directness lowers the grade one or two levels.
• Other considerations
1) Magnitude of effect can increase the grade of evidence. Strong evidence of association (significant relative risk of >2 or <0.5 based on consistent evidence from 2 or more observational studies with no plausible confounders) increases the grade by one level. Very strong evidence of association (significant relative risk of >5 or <0.2 based on direct evidence with no major threats to validity) increases the grade by two levels.
2) Evidence of a dose-response gradient increases the grade by one level.
3) Imprecise or sparse data can lower the grade by one level.
Relative importance of outcomes – included outcomes should be critical or important (but not critical) to a decision
Overall quality of evidence – judged across outcomes based on the lowest quality of evidence for any of the critical outcomes
Balance of benefits and harms – classified as net benefits, trade-offs, uncertain trade-offs, or no net benefits based on the important health benefits and harms
Balance of net benefits and costs – are incremental health benefits worth the costs?
Strength of recommendation – the extent to which one can be confident that adherence to a recommendation will do more good than harm
Within the various increments and decrements in GRADE, several implicit judgments are necessary. For example, what is a "serious" limitation in study quality or an "important" inconsistency among effect sizes? Such judgment is an inevitable part of performing systematic reviews, as discussed earlier, and the GRADE group readily acknowledges the need for judgment. Further, a key motivation behind the GRADE effort was a need for "explicit definitions" and "sequential, explicit judgments," and the GRADE system represents an importance advance towards transparency.
An explicit system for combining these judgments (i.e., a point system) is a particular strength of the GRADE approach. This system defines precisely how the various aspects of the evidence are combined to arrive at an overall grade of the evidence for each outcome. Thus, if a user made different judgments than the analyst, then the user could apply the GRADE point system accordingly, and possibly arrive at a different rating of the evidence. For example, suppose an analyst judged that there were important inconsistencies in the data for a certain outcome, but a user examined the same data and believed that the inconsistency was unimportant. Using the GRADE system, the user could then increase the final grade by one level.
In addition to USPSTF and GRADE, several other prominent systems for rating the strength of evidence have been proposed by the American College of Chest Physicians (ACCP) , the Australian National Health and Medical Research Council (ANHMRC) , the Oxford Centre for Evidence-Based Medicine (OCEBM) , the Scottish Intercollegiate Guidelines Network (SIGN) , and the U.S. Task Force on Community Preventive Services (USTFCPS) . Each of these systems were reviewed by the GRADE group, which concluded that these systems all have important shortcomings .
A New System
Our system is designed to rate the stability and strength of evidence for each outcome an analyst chooses to evaluate (see Note 2), and is not intended to produce overall recommendations for (or against) a technology. By contrast, both USPSTF and GRADE rate the strength of the overall evidence for the technology (which is often based on several outcomes), and the strength of a recommendation about the technology. The first involves assessing the overall net benefit by balancing the benefits and harms. The second entails more judgments (listed in the USPSTF methods article) about the importance and impact of cost, ethics, law, patient expectations, and societal expectations . Also, unlike GRADE and USPSTF, our evidence rating system focuses on only the internal validity of the evidence. Questions about generalizability can be addressed outside the scope of the rating system. We are currently examining how well our evidence rating system can be applied within the overall GRADE framework.
Quantitative and Qualitative Conclusions
Our system draws a distinction between two types of conclusions: quantitative and qualitative (see the bottom half of Table 1). The quantitative conclusion addresses the question, "How well does it work?", and we refer to the corresponding rating as a "stability" rating. By contrast, the qualitative conclusion addresses the more general question, "Does it work?", and we refer to the rating of the evidence pertaining to this conclusion as a "strength" rating. Thus, a quantitative conclusion characterizes the size of the effect, whereas a qualitative conclusion characterizes the direction of the effect.
This key distinction allows one to draw a strong qualitative conclusion in the face of quantitatively heterogeneous data. Such a situation arises when the results of all studies included in an evidence base demonstrate efficacy, but the magnitude of measured treatment effect differs considerably across studies.
Another important purpose of differentiating quantitative from qualitative conclusions is to acknowledge the different needs of those who utilize systematic reviews. Some users are primarily interested in obtaining an estimate of the amount of benefit (or harm) associated with a technology. Other users are simply interested in whether the technology provides any benefit at all. If a systematic review provides both kinds of conclusions, then both needs are met.
No other system for rating medical evidence distinguishes explicitly between quantitative and qualitative conclusions. We believe the distinction is critical to ensure that systematic reviews provide a full picture of the evidence. The GRADE group defines their ratings as the likelihood that further evidence will change one's confidence in the size of the effect, which appears to be a purely quantitative definition. The USPSTF system does not state whether its ratings refer to quantitative conclusions, qualitative conclusions, or both.
In our system, stability and strength ratings are not independent. Logically, evidence that permits a "highly stable" estimate of treatment effect (e.g., an odds ratio of 3.25 in favor of treatment) must also permit a "strong" conclusion about the direction of effect (e.g., that the odds ratio favors treatment). Thus, one built-in feature of our system is that the stability rating sets a lower bound on the strength rating. This means that "moderate" stability can be accompanied by a strength rating no lower than "moderate", and "low" stability can be accompanied by a strength rating no lower than "weak."
Crucial to understanding the results of a systematic review is understanding whether the results are clinically important; statistically significant results do not necessarily represent a clinically important effect. This has been mentioned in many systematic reviews [14–18], and our quantitative/qualitative distinction provides an analytic approach. To address clinical importance in our system, one first defines precisely the magnitude of effect that is considered clinically important (e.g., a difference of 0.5% in HbA1c in treatments for diabetes). Then, clinical importance can be addressed as a qualitative question: "Is the difference clinically important?" This question is addressed analytically via a comparison of effect sizes to an effect size predefined as clinically important.
Extensive A PrioriCriteria for Judgments
Most systematic reviews use a priori inclusion criteria to reduce the potential for bias in judgments about which studies to include. Some also make an a priori judgment about which instrument will be used to assess study quality. However, many other judgments are still susceptible to bias. To reduce this potential, our system specifies the use of a priori judgments wherever possible. For example, the system requires that one specify a priori quantitative definitions of "consistent" and "robust" effects. Also, the analyst must pre-specify the minimum percentage of included studies that reported the outcome of interest in order to permit a meta-analytic estimate of effect size. If only a small percentage of included studies reported the outcome, selective outcome reporting may have occurred, thereby biasing the meta-analytic summary statistic. For study quality, the analyst must identify not only the instrument to be used, but also the scoring system (if used) and the thresholds that define study quality categories (high, moderate, or low quality). Even the threshold for statistical significance (which does not have to be the conventional 0.05 in all contexts because some clinical contexts may warrant greater or lesser concern about Type 1 errors) must be specified beforehand. To address the question of clinical importance, the minimum level considered to be clinically important must also be determined a priori. These definitions, and others, are discussed further in the section entitled "How the System Works".
Consequences of Meta-Analysis and Sensitivity Analysis
Many systematic reviews report the results of meta-analyses, and some also describe sensitivity analyses. Often, however, the results of these statistical analyses are not explicitly tied to ratings of the evidence. In this section, we describe how our system links analytic results to both stability and strength ratings.
The purpose of meta-analysis is not just to obtain a summary estimate of treatment effect, but also to test the data for consistency (heterogeneity testing). This latter purpose is typically accomplished using the Q-statistic, and more recently, I2 [19, 20] If important heterogeneity is detected, our system requires that, whenever appropriate (e.g., when the evidence base is large enough), the analyst explore potential sources of this heterogeneity using meta-regression. If heterogeneity cannot be explained by meta-regression, then our system precludes one from presenting a single summary estimate of treatment effect (i.e., a stability rating of "Unstable") (see Note 3). Some investigators advocate the use of a random effects summary statistic in this situation. However, unexplained heterogeneity could be due to differences in patient populations, and/or the way a treatment is administered. Our view is that computing a single summary estimate is not warranted when the evidence demonstrates the existence of multiple estimates.
Although our system precludes the use of random-effects models in determining a single summary estimate of treatment effect, the use of these models does have an important role. This role involves a summary of the evidence to support a qualitative conclusion. Even if there is substantial unexplained heterogeneity, the evidence may still indicate a consistent direction of effect. The confidence interval (CI) around the random effects summary statistic, which incorporates both within-study and between-study variance, may lie fully above 0 or below 0 (see Note 4). This CI, therefore, is suitable for determining whether the data suggest a clear direction of effect.
Other systems, such as GRADE and USPSTF, are largely silent on the role of meta-analysis in systematic reviews. Our system uses meta-analysis and meta-regression (when clinically appropriate) to increase statistical power and employ precise study weights; furthermore, the system is unique in incorporating the results of these analyses into evidence ratings.
We now turn to the role of sensitivity analysis in our system. In this context, consider that the goal of rating evidence is to assess the likelihood that future evidence will indicate something different than what current evidence indicates. If a large amount of consistent evidence has already accumulated, then future evidence is unlikely to alter the overall strength or stability. Conversely, conclusions based on only a small amount of accumulated evidence may easily change when a single new study is published.
Considered from this perspective, we argue that sensitivity analysis (see Note 5) can substitute for certain judgments about quantity. The idea is that if the conclusion from a meta-analysis depends critically on only one or a few studies in that analysis (or if there is reason to suspect that not all relevant studies are available), then the conclusion may not be robust. Such dependence suggests that a future study may alter conclusions based on currently available studies. Consequently, our system downgrades the stability or strength ratings accordingly. Although there is a widespread sense that sensitivity analysis should be incorporated into an analysis, the system is unique in offering explicit rules for how to gauge the impact of the results of sensitivity analyses on one's confidence in the available evidence.
Sensitivity analysis can obviate the need for certain subjective judgments about the magnitude of effect. Some rating systems (e.g., GRADE) employ such judgments, and if the observed effect is very large, the evidence receives a higher strength rating. Presumably, this is because a very large effect is less likely to be overturned by future evidence and is therefore more robust. However, if there are sufficient studies to perform direct robustness tests via sensitivity analyses, then we advocate doing so, in lieu of making judgments about effect sizes. A meta-analytic sensitivity analysis incorporates effect sizes and confidence intervals from all studies, so that the test is empirically-based.
As with consistency, the quantitative/qualitative distinction helps clarify two notions of robustness. Quantitative robustness concerns the degree to which the summary effect size from meta-analysis tends to change based on relatively small alterations in the data. To assess quantitative robustness, one can perform successive meta-analyses and observe the relative changes in the summary estimate. If the changes in the estimate exceed a predetermined tolerance level, then the original summary estimate is not quantitatively robust. Qualitative robustness refers to whether the evidence base yields the same qualitative general conclusion upon alterations of the data. To assess it, one can again perform successive meta-analysis, but in this case the issue is whether the confidence intervals around summary statistics consistently indicate the same direction of effect.
How the System Works
The system is shown graphically in five figures:
An important feature of this system is that every question illustrated in the figures requires a set of a priori criteria. Nearly all of these a priori criteria are operational definitions that are quantitative. The use of a priori criteria helps to reduce bias and subjectivity, as discussed above, and the use of quantitative definitions increases transparency. This system assumes that the assessor has already applied appropriate inclusion/exclusion criteria and has excluded from the analysis any study with fatal flaws.
The initial entry into the system occurs with an assessment of the quality of the evidence for a specific outcome (Figure 1), which we consider to be the most important aspect of the evidence. Quality sets an upper bound on the stability and strength ratings (e.g., moderate strength is only possible for data that is, at minimum, moderate quality). Although quality evaluation can be performed with a checklist or scale, any reasonable method for separating the evidence base into different categories of quality will suffice. After an evaluation of individual study quality, studies are judged to be high, moderate, low, or very low quality. Studies of very low quality are always excluded from the evidence base, and the analyst may also choose to exclude low or even moderate quality studies as well. The analyst must choose a method for aggregating the quality of the individual studies to obtain an overall quality rating for the evidence base and then enter the high, moderate, or low quality arm of the system. Within these arms, the system further assesses the quantity, consistency, robustness, and (in some instances) magnitude of effect to determine the stability and strength of the evidence.
Figure 2 through Figure 5 detail the high quality arm of the system. The top half of each figure includes all of the questions and decisions that impact stability ratings (and quantitative conclusions), while the bottom half includes all of the questions and decisions that impact strength ratings (and qualitative conclusions). The moderate and low quality arms of the system are not shown because all aspects of this system are already displayed in the high quality arm.
At the top of these pathways, one first considers whether the evidence base is sufficient to provide a single quantitative estimate of the effect size. We generally require at least three studies, but other investigators may wish to set this criterion higher (e.g., five studies). Additionally, the system requires that a certain percentage of the studies (e.g., 80% or more) must have calculable effect sizes (that can be determined without imputation). If these criteria are not met, then one proceeds to Figure 5 (small evidence base). If these criteria are met, then one tests the quantitative consistency of the data using a heterogeneity measure such as Q or I2. Under homogeneity, one proceeds to Figure 3, whereas under heterogeneity, one proceeds to Figure 4.
In the homogeneous pathway (Figure 3), one performs a meta-analysis to combine the study results. If the meta-analytic summary statistic is not informative, then no conclusions are reached. If the summary statistic is informative, one tests the robustness of the findings through sensitivity analysis (e.g., removal of one study at a time). If the meta-analytic summary statistic passes the robustness tests, the estimate is quantitatively robust. This produces a high stability rating for the quantitative estimate, which leads directly to a strong qualitative conclusion. The logic behind this implication is that if one is confident in the specific estimate of the effect, one is automatically confident in the general direction of that effect.
Continuing within Figure 3, if the findings are not quantitatively robust, one re-examines the sensitivity analyses to determine qualitative robustness (e.g., do any of the last three analyses in a cumulative meta-analysis of a given data set lead to a different qualitative conclusions?). Additional sensitivity analyses that can be used include removing each study separately or changing the effect size statistic (e.g., using Cohen's h instead of an odds ratio). We also consider tests for publication bias to be a form of sensitivity analysis, although publication bias testing requires a minimum number of available studies. Whether the findings are qualitatively robust determines whether one reaches a strong or moderate qualitative conclusion. Also, one can only reach a strong conclusion from a high quality evidence base. In the moderate and low quality arms, the qualitative conclusion can never be stronger than moderate or weak, respectively.
Figure 4 illustrates the branch followed when an evidence base has enough studies with calculable effect sizes to potentially reach a quantitative effect estimate, but the heterogeneity test indicates significant differences among the studies. If this heterogeneity can be explained using meta-regression, one can still reach a quantitative conclusion. The quantitative conclusion is the conclusion reached about the regression coefficients, including the intercept. For example, if gender is the variable that explains heterogeneity, one might have a conclusion such as "treatment X improved symptoms twice as effectively in women as in men". If meta-regression is not possible or does not explain heterogeneity, no quantitative conclusion is possible. However, one can still perform a random-effects meta-analysis which, if informative, may allow a qualitative conclusion.
Figure 5 illustrates what occurs when the evidence base is too small or otherwise insufficient to allow a quantitative conclusion. Some studies may not report effects sizes and standard errors (nor sufficient information for the analyst to calculate both measures). The analyst must acknowledge and adjust for the existence of such studies. This adjustment may require the estimation or imputation of effect sizes in certain studies . The full evidence base is then assessed in a random-effects meta-analysis to determine if a qualitative conclusion can be reached.
If there are only two studies and both have calculable effect sizes, one performs a random-effects meta-analysis which, if informative, allows a qualitative conclusion. Of note, meta-analysis of a two-study evidence base is not required in the moderate quality arm, where a conclusion would require both studies to have a statistically significant effect. In the low quality arm, a minimum of three studies is required to reach any conclusion. A qualitative conclusion is also possible for two studies with imprecise effect sizes (that cannot be combined) if both studies are informative and show qualitatively consistent results. If two studies are qualitatively inconsistent or not informative when combined, the findings are inconclusive. If there is only one study, a large effect size is required to allow a weak qualitative conclusion (note that one cannot reach a conclusion if the single study is of moderate or low quality).
In this section, we provide two example applications of our evidence rating system. In addition to illustrating various aspects of the system, we show how the system can be used in conjunction with simple declarative conclusions that are tied to the stability and strength ratings. The first example involves drug-eluting stents (DESs) for the treatment of coronary artery disease, and the second example involves positron emission tomography (PET) in the staging of lymphoma.
Example #1: Comparison between Drug-Eluting Stents and Bare-Metal Stents for the Treatment of Coronary Artery Disease
In a 2006 report, we examined the evidence comparing the safety and efficacy of drug-eluting stents (DESs) and bare-metal stents for the treatment of angina .
We included 14 randomized trials that compared drug-eluting stents to bare metal stents and reported the percentage of patients in each group who underwent target lesion revascularization (TLR) after stent implantation. The trials enrolled a total of 7,006 patients. We addressed the quantitative issue of the size of the difference in overall TLR rates and also the qualitative issue of whether there was any difference in overall TLR rates between the two types of stents.
Study quality assessment
To assess the quality of the studies, we applied a quality rating scale, and determined (using a priori definitions of high, medium, and low quality) that the evidence base was of high quality.
Sufficient data for quantitative estimate
In order to attempt a quantitative estimate of the effect, we required a priori that there must be at least three studies, and at least half of the included studies reported sufficient information for us to calculate effect sizes and confidence intervals. All 14 studies reported such information, so we attempted to make a quantitative estimate.
A priori, we defined quantitative consistency based on thresholds for Q and I2. These thresholds were a p value for the Q statistic less than 0.10 (which would mean quantitative inconsistency) and I2 < 50% (which would also mean quantitative inconsistency). We used a p value of 0.10 because of the known low power of Q. We used a threshold of 50% for I2 because this value represents moderate heterogeneity [19, 20] For this evidence base, we performed a meta-analysis using Cohen's h and found substantial heterogeneity (I2 = 78%, Q = 59, p value for Q was less than 0.000001).
Meta-regressions to explain heterogeneity
Given the heterogeneity of effect sizes, we performed meta-regressions in an attempt to explain why study results differed. Not all potential covariates could be examined because not all studies reported some covariates. The three covariates we could examine were drug type (paclitaxel or sirolimus), mean target vessel diameter, and mean target lesion length. None of these three factors were sufficient to explain the observed heterogeneity. Therefore, we did not draw a quantitative conclusion for the outcome of TLR rates. However, we proceeded to a qualitative analysis using a random-effects model to determine whether the evidence permitted a qualitative conclusion.
We rated the stability of the evidence as Unstable, due to the unexplained heterogeneity among effect sizes.
We performed a random-effects meta-analysis using Cohen's h. The summary statistic was statistically significant (lower TLR rates among patients who received DESs) and clinically important (because TLR is an important patient-oriented outcome, we defined clinical importance a priori as any statistically significant effect). This meant that the evidence was informative.
Qualitative robustness testing
A priori, we defined a quantitatively robust evidence base as one in which the confidence intervals of the last three cumulative, random-effects meta-analyses remained fully on the same side of zero after; 1) removal of the study with the smallest weight (i.e., the lowest precision), and, 2) after the additional removal of the study with the second smallest weight in the meta-analysis. Because the evidence base met both of these criteria, we deemed the evidence base to be qualitatively robust.
The strength rating of the evidence for a qualitative difference in TLR rates was Strong, because the meta-analysis was of high quality studies, and was informative and qualitatively robust.
Wording of conclusions
The conclusions for this outcome were phrased in the following manner:
The use of DESs (Cypher and TAXUS stents) leads to lower overall TLR rates than use of bare-metal stents in patients with angina at 6 to 12 months following stent implantation. (Strength of evidence: Strong)
• Due to unexplainable differences among the findings of different trials, one cannot accurately determine how much lower these rates are at 6 to 12 months following implantation of a DES.
Example #2: Positron Emission Tomography for the Staging of Lymphoma
In a 2006 report prepared by ECRI's Health Technology Assessment Information (HTAIS) under contract to TRICARE Management Activity (see Note 7), we assessed the use of positron emission tomography (PET) in the staging of lymphoma. The reference standard for determining whether lymphoma has reached Stage IV is a bone marrow biopsy typically taken from the iliac crest. PET may potentially help patients avoid the invasiveness of bone marrow biopsy, depending on how accurately it detects bone marrow infiltration.
We included five diagnostic cohort studies that performed PET as well as bone marrow biopsy and also reported sufficient information for the calculation of sensitivity and specificity. The studies reported data on a total of 243 patients. Because our research question was to determine a quantitative estimate of diagnostic accuracy, we did not attempt to draw a qualitative conclusion. Therefore, the text below refers only to the stability rating, not to a strength rating.
Study quality assessment
To assess the quality of the studies, we applied a quality rating scale, and determined (using a priori definitions of high, moderate and low quality) that the evidence base was of moderate quality. To rate the strength and stability of this evidence, we used the moderate quality branch of the system, which is not included in this paper, but is structurally very similar to the high quality arm. The key difference is an across-the-board decrease in both stability and strength ratings (e.g., "Strong" in the high quality branch corresponds to "Moderate" in the moderate quality branch).
Sufficient data for quantitative estimate
A priori, we decided that an evidence base could be considered sufficient to permit a quantitative estimate if there were at least three studies and also if at least 75% of the included studies had reported effect sizes or had provided sufficient information for the calculation of effect sizes. In this case, there were five studies, and both sensitivity and specificity were calculable for all five studies. Therefore, we proceeded with the quantitative analysis.
A priori, we defined quantitatively consistent results as an I2 of less than 50% (see above). We computed the diagnostic odds ratio for each of the five studies, and the heterogeneity test revealed no heterogeneity (I2 = 0%). Therefore, based on the definition of quantitative consistency, we deemed these findings to be quantitatively consistent. There was a threshold effect in the data, however, as evidenced by a plot of the data in ROC space and a strong negative correlation between sensitivity and specificity. We used the method of Littenberg and Moses  to construct a symmetric summary ROC curve, and computed a summary diagnostic odds ratio of 12.7 (95% confidence interval 5.5 to 29.7). At the mean threshold in the included studies, this estimate corresponded to a sensitivity of 64% and a specificity of 88%.
When evaluating this diagnostic, we attempted to reach only quantitative conclusions, not qualitative conclusions. Therefore, we did not consider informativeness, and we automatically proceeded to quantitative robustness testing for the summary diagnostic odds ratio (DOR).
Quantitative robustness testing
A priori, we defined a quantitatively robust evidence base as one that met both of the following two conditions: 1) the confidence interval around the summary DOR did not contain a DOR 50% higher or lower than the summary point estimate, and 2) a cumulative meta-analysis in which studies were entered by precision (highest precision study first) found that all of the last three analyses produced summary effects that were within 5% of the overall summary diagnostic odds ratio. In this case, the evidence base met neither of these conditions; therefore, we deemed the estimate to be not robust.
Using the system, we assigned a stability rating of Low to the estimated diagnostic odds ratio of 12.7 (95% CI 5.5 to 29.7). This rating was based on the fact that the studies were of moderate quality, and the estimate was not quantitatively robust.
Wording of conclusions
The conclusion was phrased in the following manner:
For the detection of bone marrow infiltration, at mean threshold PET has a sensitivity of 64% (95% CI: 43% to 80%), and a specificity of 88% (95% CI: 76% to 95%). Stability of estimate: Low.
The rating system described in this paper has several unique attributes. First, it distinguishes quantitative stability ratings from qualitative strength ratings. Second, it makes extensive use of a priori judgments to avoid bias. Third, it makes explicit the consequences of the results of meta-analysis and sensitivity analyses for both stability ratings and strength ratings. We have linked these attributes, and many others, into a logically consistent system intended to improve the process of systematic review.
Our system recognizes the fundamental role of judgment in summarizing evidence. The system is best viewed as a logical way to organize one's own judgments, not a predefined list of required judgments. Because different analysts can have different judgments, however, there is a critical need for transparency. This allows the user to trace the path of judgments that lead to a stability or strength rating. In fact, to use our system without making judgments explicit would constitute a misuse of the system.
Explicitness in judgments has been advocated by the GRADE group , but explicitness is not sufficient. Wherever possible, judgments should be made a priori and should be empirically-based. A priori judgments, a natural extension of a priori inclusion criteria, may help reduce bias by avoiding the influence of observed data on operational definitions. Also, basing judgments on empirical analyses, rather than opinion alone, may reduce bias. For example, judgments about quantity can be made empirically-based via formal sensitivity analysis.
While our system allows different analysts to make different judgments, it does place certain boundaries on judgments. If there are only one or two studies, for example, the evidence base must be judged insufficient to permit a quantitative estimate of the effect size. Further, if these one or two studies are of low quality, then no conclusion is possible. If there is only one study, then it must have been a high quality study observing a large effect in order to permit any conclusion. These limitations for small evidence bases are grounded in the principle of independent replication of scientific findings.
The GRADE system also places certain boundaries on the kinds of judgments permitted. In GRADE, one must give high priority to randomization: RCTs are initially judged as two levels stronger than observational studies, and three levels stronger than other study designs. Also, GRADE defines a "strong" association as a relative risk between 2 and 5 (or between 0.2 and 0.5) and a "very strong" association as a relative risk greater than 5 (or less than 0.2) (see Note 8). Other judgments are left up to the analyst, although GRADE recommends that all judgments be made explicit.
We next note some potential limitations of the system described in this paper. First, the system is complex. Understanding how it works, and more importantly why it works that way, requires careful study. Second, the system is resource-intensive, mostly because of the numerous a priori judgments. The analyst is responsible for making reasonable judgments before analyzing the data. For example, the a priori definition of a "clinically significant effect" is a critical judgment that can greatly impact the conclusions of the review. One strategy we have employed is to have additional clinicians and methodologists examine the analyst's a priori judgments for their reasonableness, and then to resolve disagreements in conference. These consensus judgments are then employed throughout the step-by-step system to produce evidence ratings. Whatever judgments are agreed upon, however, should be made fully explicit in the review. Such transparency, as emphasized throughout this paper, can enhance the flexibility and usefulness of the review.
In summary, explicit judgments and formal combination rules, as advocated by the GRADE group, represent two important steps on the path to a fully reliable system for rating medical evidence. Throughout this paper, we have argued that many additional steps must be taken. Foremost among these are distinguishing between quantitative and qualitative conclusions, making a priori judgments to avoid bias, and directly linking analytic results to evidence ratings.
Considered as a whole, our system constitutes a flexible tool for incorporating the full complexity of the evidence. Despite this complexity, the system outputs straightforward conclusions and ratings for medical decision makers to employ as they encounter difficult evidence-based decisions.
• Systematic reviewers inevitably make judgments about the quality, quantity, consistency, robustness, and magnitude of effects observed in the studies identified
• This paper introduces a formal system for combining these judgments in a logical, consistent framework
• Unique aspects of the system include the distinction between quantitative and qualitative conclusions, extensive a priori criteria for judgments, and the direct impact of meta-analysis and sensitivity analysis on evidence ratings
• Stability ratings refer to the likelihood that future evidence will indicate a different size of effect
• Strength ratings refer to the likelihood that future evidence will overturn conclusions about whether a device, drug or procedure is effective (or harmful)
1 – Throughout this paper, the word "technology" is used generically to refer to drugs, devices, or procedures.
2 – The specific outcome could be a surrogate outcome or a patient-oriented outcome.
3 – The presence of heterogeneity is a violation of the assumption of fixed-effects models: that the available data are sampled from a single distribution that describes a single summary estimate of treatment effect.
4 – The use of 0 assumes that the effect size metric is centered around 0 (e.g., the standardized difference between means). Other effect size metrics (e.g., relative risk, odds ratio) are centered around 1, and for these one would determine whether the random-effects confidence interval were fully above 1 or below 1.
5 – We refer to an entire family of procedures designed to assess the sensitivity of one's conclusions to certain aspects of the data or certain analytic assumptions. Many of these were listed in a paper by Olkin, and some examples include publication bias testing, [27–29] cumulative meta-analysis, [21, 30] and the removal of specific subsets of the data.
6 – Although not illustrated in the figure, there are possible effect sizes corresponding to A through D that would fall on the left side of the graph (below zero). Some of these possibilities would lead to a conclusion that the treatment was either harmful or inferior to a comparison treatment.
7 – TRICARE is the government agency under the Department of Defense responsible for administering the health benefits for the U.S. armed forces and their dependants.
8 – Note that the GRADE system's treatment of effect magnitude does not specifically mention the confidence interval around the effect. Instead the system addresses imprecise or sparse data in a separate manner. Our system considers an effect size and its confidence interval simultaneously.
Funding for this project was provided by ECRI, Plymouth Meeting, Pennsylvania, USA. We thank Wendy Bruening, Ph.D., Richard Chapell, Ph.D., David Doggett, Ph.D., Matthew Mitchell, Ph.D., David Snyder, Ph.D., and Karen Tappe, M.A., for their contributions to the development of this rating system. We also appreciate the comments of peer reviewers, whose comments enhanced the quality of the manuscript.
- Harris RP, Helfand M, Woolf SH, Lohr KN, Mulrow CD, Teutsch SM, Atkins D: Current methods of the U.S. Preventive Services Task Force. A review of the process. Am J Prev Med. 2001, 20 (3 Suppl): 21-35. 10.1016/S0749-3797(01)00261-6.View ArticlePubMedGoogle Scholar
- Atkins D, Best D, Briss PA, Eccles M, Falck-Ytter Y, Flottorp S, Guyatt GH, Harbour RT, Haugh MC, Henry D, Hill S, Jaeschke R, Leng G, Liberati A, Magrini N, Mason J, Middleton P, Mrukowicz J, O'Connell D, Oxman AD, Phillips B, Schunemann HJ, Edejer TT, Varonen H, Vist GE, Williams JW, Zaza S: Grading quality of evidence and strength of recommendations. BMJ. 328 (7454): 1490-2004 Jun 19;, [http://bmj.bmjjournals.com/cgi/reprint/328/7454/1490]
- Atkins D, Eccles M, Flottorp S, Guyatt GH, Henry D, Hill S, Liberati A, O'Connell D, Oxman AD, Phillips B, Schunemann H, Edejer TT, Vist GE, Williams JW, GRADE Working Group: Systems for grading the quality of evidence and the strength of recommendations I: critical appraisal of existing approaches The GRADE Working Group. BMC Health Serv Res. 4 (1): 38-10.1186/1472-6963-4-38. 2004 Dec 22;Google Scholar
- Atkins D, Briss PA, Eccles M, Flottorp S, Guyatt GH, Harbour RT, Hill S, Jaeschke R, Liberati A, Magrini N, Mason J, O'Connell D, Oxman AD, Phillips B, Schunemann H, Edejer TT, Vist GE, Williams JW, GRADE Working Group: Systems for grading the quality of evidence and the strength of recommendations II: pilot study of a new system. BMC Health Serv Res. 5 (1): 25-10.1186/1472-6963-5-25. 2005 Mar 23;Google Scholar
- Guyatt G, Gutterman D, Baumann MH, Addrizzo-Harris D, Hylek EM, Phillips B, Raskob G, Lewis SZ, Schunemann H: Grading strength of recommendations and quality of evidence in clinical guidelines: report from an american college of chest physicians task force. Chest. 2006, 129 (1): 174-81. 10.1378/chest.129.1.174.View ArticlePubMedGoogle Scholar
- Brouwers MC, Johnston ME, Charette ML, Hanna SE, Jadad AR, Browman GP: Evaluating the role of quality assessment of primary studies in systematic reviews of cancer practice guidelines. BMC Med Res Methodol. 5 (1): 8-10.1186/1471-2288-5-8. 2005 Feb 16;Google Scholar
- West S, King V, Carey TS, Lohr KN, McKoy N, Sutton SF, Lux L: Systems to rate the strength of scientific evidence. (Prepared by Research Triangle Institute – University of North Carolina Evidence-based Practice Center under Contract no. 290-97-0011). AHRQ Publication no. 02-E016. 2002, Rockville (MD): Agency for Healthcare Research and Quality (AHRQ), 199-(Evidence report/technology assessment; no. 47).Google Scholar
- Guyatt G, Schunemann H, Cook D, Jaeschke R, Pauker S, Bucher H: Grades of recommendation for antithrombotic agents. Chest. 2001, 119 (1 Suppl): 3S-7S. 10.1378/chest.119.1_suppl.3S.View ArticlePubMedGoogle Scholar
- National Health and Medical Research Council (NHMRC): How to use the evidence: assessment and application of scientific evidence. 2000, Canberra (Australia): National Health and Medical Research Council (NHMRC), 91-(NHMRC handbook series on preparing clinical practice guidelines; no. CP69).Google Scholar
- Levels of evidence and grades of recommendation. [internet]. Oxford Centre for Evidence-Based Medicine, University Department of Psychiatry, Warneford Hospital, 4-[cited 2003 Apr 8], [http://www.cebm.net/levels_of_evidence.asp]
- Harbour R, Miller J: A new system for grading recommendations in evidence based guidelines. BMJ. 323: 334-6. 10.1136/bmj.323.7308.334. 2001 Aug 11;Google Scholar
- Briss PA, Zaza S, Pappaioanou M, Fielding J, Wright-De Aguero L, Truman BI, Hopkins DP, Mullen PD, Thompson RS, Woolf SH, Carande-Kulis VG, Anderson L, Hinman AR, McQueen DV, Teutsch SM, Harris JR: Developing an evidence-based Guide to Community Preventive Services– methods. The Task Force on Community Preventive Services. Am J Prev Med. 2000, 18 (1 Suppl): 35-43. 10.1016/S0749-3797(99)00119-1.View ArticlePubMedGoogle Scholar
- ECRI: Drug-eluting stents for the treatment of coronary artery disease. 2006, Plymouth Meeting (PA):ECRI Health Technology Assessment Information Service, 124-(Windows on medical technology; no. 134).Google Scholar
- Fleming C, Whitlock EP, Beil TL, Lederle FA: Screening for abdominal aortic aneurysm: a best-evidence systematic review for the U.S. Preventive Services Task Force. Ann Intern Med. 142 (3): 203-11. 2005 Feb 1;Google Scholar
- Hartmann K, Viswanathan M, Palmieri R, Gartlehner G, Thorp J, Lohr KN: Outcomes of routine episiotomy: a systematic review. JAMA. 293 (17): 2141-8. 10.1001/jama.293.17.2141. 2005 May 4;Google Scholar
- McAlister FA, Ezekowitz JA, Wiebe N, Rowe B, Spooner C, Crumley E, Hartling L, Klassen T, Abraham W: Systematic review: cardiac resynchronization in patients with symptomatic heart failure. Ann Intern Med. 141 (5): 381-90. 2004 Sep 7;Google Scholar
- Wilt T, Nair B, MacDonald R, Rutks I: Early versus deferred androgen suppression in the treatment of advanced prostatic cancer. Cochrane Database of Systematic Reviews 2001 [internet]. 2001, Hoboken (NJ): John Wiley & Sons, Ltd., 2001 Oct 23 [updated 2001 Aug 16]. [cited 2006 Jul 10]. [Art. No.: CD003506]. Available: DOI: 10.1002/14651858. CD003506., 4, [internet]View ArticleGoogle Scholar
- Kane RL, Saleh KJ, Wilt TJ, Bershadsky B, Cross WW, MacDonald RM, Rutks I: Total knee replacement. (Prepared by Minnesota Evidence-based Practice Center, Minneapolis, MN). AHRQ Pub. No. 04-E006-2. 2003, Rockville (MD): Agency for Healthcare Research and Quality, 150-(Evidence report/technology assessment; no. 86).Google Scholar
- Higgins JP, Thompson SG: Quantifying heterogeneity in a meta-analysis. Stat Med. 21 (11): 1539-58. 10.1002/sim.1186. 2002 Jun 15;Google Scholar
- Higgins JP, Thompson SG, Deeks JJ, Altman DG: Measuring inconsistency in meta-analyses. BMJ. 327 (7414): 557-60. 10.1136/bmj.327.7414.557. 2003 Sep 6;Google Scholar
- Lau J, Schmid CH, Chalmers TC: Cumulative meta-analysis of clinical trials builds evidence for exemplary medical care. J Clin Epidemiol. 1995, 48 (1): 45–57-59–60. 10.1016/0895-4356(94)00106-Z.View ArticlePubMedGoogle Scholar
- ECRI: Bulimia nervosa: efficacy of available treatments [technology assessment report]. 2006, Plymouth Meeting (PA): ECRI Health Technology Assessment Information Service, 623-[http://www.ecri.org/Patient_Information/Patient_Reference_Guide/Default.aspx]Google Scholar
- Armitage P, Berry G: Statistical methods in medical research. 1994, Oxford, England: Blackwell Scientific, 620-3Google Scholar
- Pudar Hozo S, Djulbegovic B, Hozo I: Estimating the mean and variance from the median, range, and the size of a sample. BMC Med Res Methodol. 5 (1): 13-10.1186/1471-2288-5-13. 2005 Apr 20;Google Scholar
- Moses LE, Shapiro D, Littenberg B: Combining independent studies of a diagnostic test into a summary ROC curve: data-analytic approaches and some additional considerations. Stat Med. 12 (14): 1293-316. 1993 Jul 30;Google Scholar
- Olkin I: Diagnostic statistical procedures in medical meta-analysis. Stat Med. 18 (17–18): 2331-41. 1999 Sep 15;Google Scholar
- Begg CB, Mazumdar M: Operating characteristics of a rank correlation test for publication bias. Biometrics. 1994, 50 (4): 1088-101. 10.2307/2533446.View ArticlePubMedGoogle Scholar
- Duval SJ, Tweedie RL: A non-parametric 'trim and fill' method of assessing publication bias in meta-analysis. J Am Stat Assoc. 2000, 95 (449): 89-98. 10.2307/2669529.Google Scholar
- Egger M, Davey Smith G, Schneider M, Minder C: Bias in meta-analysis detected by a simple, graphical test. BMJ. 315 (7109): 629-34. 1997 Sep 13;Google Scholar
- Ioannidis JP, Contopoulos-Ioannidis DG, Lau J: Recursive cumulative meta-analysis: a diagnostic for the evolution of total randomized evidence from group and individual patient data. J Clin Epidemiol. 1999, 52 (4): 281-91. 10.1016/S0895-4356(98)00159-0.View ArticlePubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2288/6/52/prepub
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