Published online Sep 26, 2011. doi: 10.5662/wjm.v1.i1.12
Revised: September 5, 2011
Accepted: September 19, 2011
Published online: September 26, 2011
“Who shall decide when doctors disagree?” This question, raised by Alexander Pope in 1732, must have been a very common one in Pope’s day, since medical practice at that time was based largely on tradition and opinion, not science. In the 21st century, medicine should be considered at least a combination of art and science. Consequently, careful clinical research should provide clear answers that stand the test of time and the scrutiny of additional investigations. This is the theory behind evidence-based, data-driven scientific medicine[1-3].
In scientific terms, when focused strictly on the evaluation of clinical variables, Pope’s question challenges reproducibility, in particular interobserver reproducibility[4-8]. It relates to the common experience where two independent observers provide different results, with this disagreement implying a sort of uncertainty about the truth. From the patient’s point of view, it may appear that his/her condition is not an objective one and that each clinician is allowed to have his/her own opinion. This may be very frustrating and cause the patient to lack trust in medicine.
In addition to interobserver reproducibility there is also intraobserver reproducibility, i.e. the ability of a single observer to provide the same opinion regarding a patient’s condition if he/she is questioned again later. In fact, self-disagreements occur more frequently than might be expected, in particular if the question posed has more than two mutually exclusive answers (categorical variables).
An example of efforts to better clarify intra- and interobserver reproducibility is the BI-RADS score system for breast lesions. Based mainly on the appearance at mammography, radiologists may apply one of the following scores: (0) Incomplete, when mammograms do not give the radiologist enough information to make a clear diagnosis; (1) Negative, when there is nothing to comment on; (2) Benign, in presence of a definite benign finding; (3) Probably benign, in presence of findings that have a high probability of being benign; (4) Suspicious abnormality, in presence of a lesion not characteristic of breast cancer, but with reasonable probability of being malignant; and (5) Highly suspicious of malignancy, in presence of a lesion that has a high probability of being malignant.
Because of their different experience in reading mammograms, two independent observers may apply two different scores to the same image (lack of interobserver reproducibility). On the other hand, the learning curve of an individual radiologist, may mean that he/she will apply a score to a single mammogram different to that applied during a previous reading (lack of intraobserver reproducibility).
Intra- and interobserver reproducibility not only apply to categorical and ordinal variables but also, and more strictly, to quantitative (continuous) variables. Examples include cardiac ventricle volumes, a vessel diameter, arterial blood pressure, and body temperature. From the observer’s point of view, the numerical values observed for such variables are obtained by mean of “instruments”, i.e. technical systems, based on a physical principle, that are sensitive to the quantity to be measured. Many of these instruments are now available as software algorithms implemented on computers used for imaging techniques.
Even if the use of a technical instrument may lead an observer the believe the measurement to be an objective process without uncertainty, we must remember that this process does not proceed by itself and that it needs the observer’s intervention. This intervention may apply at any level and certainly impacts on the final observed value. For example, the measurement of a vessel diameter based on a magnetic resonance image needs the observer to place a ruler between two distant points (the vessel boundaries) and the repetition of this action rarely provides the same value as that previously obtained.Furthermore, an independent observer may perform this measurement by placing the ruler at another part of the vessel course, i.e. on another slice of the magnetic resonance scan. Therefore, as for categorical variables, the measurement of continuous variables also is characterized by intra- and interobserver variability.
Reproducibility and variability are two complementary concepts: the larger the variability, the lower the reproducibility, and vice versa. Thus, we may think of them as interchangeable, even though statistical techniques have been developed for estimating variability. Moreover, intra- and interobserver variability are only two of the possible sources of the total variability of a measurement obtained using imaging techniques. In general, if an examination on a patient is repeated after a treatment, the total variability associated with the measurements will consist of the following components: (1) The intraobserver variability of the radiologist who performed the measurement prior the treatment; (2) Intraobserver variability of the radiologist who performed the measurement after treatment; (3) The interobserver variability between those radiologists; (4) The interstudy variability, due to the repetition of the examination; (5) The inter-instrumentation variability, due to the possible use of two different machines; and (6) The biological variability, due to changes in the patient’s health status during the time elapsed between the two examinations (the effect of treatment may also be a part of this variability).
Why do we need to know the variability of measurements of categorical and continuous variables? The most important and simplest answer is because we need to know the reliability of measured values before taking decisions based on those measurements! Recalling the previous example, if we observe a difference between the values measured before and after the treatment, can we establish that the patient’s health status is changed, or is that difference within the overall variability? Of course, the only way to answer that question is to know the overall variability.
In theory, one way to estimate the measurement variability is to repeat a measurement many times, to calculate the mean value and the 95%-confidence interval. However, this approach has three important limitations. Firstly, it no longer holds if the measurements are taken by different observers, adding interobserver variability. Secondly, in clinical practice there is little or no time available for repeating the same measurement. Thirdly, although this allows estimation of the variability associated to a particular value, that variability cannot be applied to all possible values. Therefore, it is more practical to perform a preliminary analysis of at least intra- and interobserver variability.
The statistical techniques suitable for the estimation of the intra- and interobserver variability depend only on the type of the measured variables. Two main methods are available: Cohen k statistics for categorical variables and Bland-Altman statistics for continuous variables[7,8]. Here, I will not go into the mathematical details of these methods (a complete description may be found in references), but I would like to highlight the main difference between them. The Cohen k method provides a coefficient of agreement that lies within the range (-1, 1), where k = 1 indicates perfect agreement, k = 0 absolutely no agreement, and k = -1 the “perfect disagreement”.Conversely, Bland-Altman analysis results in a value expressed with the same measurement units as the measured variable.
The estimation of the intra- and interobserver variability may be performed in parallel. In clinical settings, a suitable protocol would include two observers with different experience in the measurement under evaluation. The less experienced observer should measure the variable of interest twice for each patient, with the more experienced observer making only one measurement per patient. The intraobserver variability may be estimated using the pairs of values obtained by the first observer, while the interobserver variability may be estimated using the first value of the first observer and the single value obtained by the second observer.
Let me conclude with an example taken from my own experience as an author. In 2008 we demonstrated that the interobserver variability in the measurement of the left ventricle ejection fraction on magnetic resonance imaging may be as large as 17%, in absolute units! This means that if an observer obtains a value of, for example, 50% for a patient’s ejection fraction, a second observer may obtain a value of between 33% to 67% for the same patient. Considering such variability, I can only smile when I see continuous variables expressed to two or three decimals places.