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Pediatric Clinics of North America - CIPERJ

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300 O’BRIEN<br />

cost-effectiveness and cost-utility analyses. The database describes each<br />

study and appraises study quality, strengths, and weaknesses.<br />

Evaluating the decision analysis literature<br />

The number <strong>of</strong> published decision analysis articles has increased steadily<br />

over the past 2 decades. Also, the demand for economic evaluations in health<br />

care has increased the use <strong>of</strong> modeling tools to assess the cost-effectiveness<br />

<strong>of</strong> new drug therapies and treatment strategies [11]. Therefore, it is important<br />

for all physicians to be able to analyze the results <strong>of</strong> these studies critically.<br />

An excellent guide to interpreting a clinical decision analysis has been published<br />

by Richardson and Detsky, as part <strong>of</strong> the Users’ Guides to the Medical<br />

Literature series in the Journal <strong>of</strong> the <strong>America</strong>n Medical Association [22,34].<br />

This section briefly summarizes those recommendations.<br />

First, readers must be able to assess the validity <strong>of</strong> a decision analysis<br />

model. The structure <strong>of</strong> any decision tree should mirror as closely as possible<br />

a real-life clinical dilemma. All available and important clinical strategies<br />

should be considered, and the strategies need to have competing benefits<br />

and risks in order for the dilemma to be meaningful and worth studying.<br />

Just as with a systematic review, the investigators <strong>of</strong> a clinical decision analysis<br />

should describe how they searched and reviewed the literature to estimate<br />

probabilities, and this methodology should be explicit and reproducible. Analysts<br />

should describe how they judged the quality <strong>of</strong> the available data and if<br />

and how any data were transformed. For example, 5-year DVT recurrence<br />

rates may have been adjusted to fit a model with a 2-year timeline. Investigators<br />

also should report the source <strong>of</strong> cost and utility estimates. The most credible<br />

utility ratings come from the following sources: (1) direct measurements<br />

from a large group <strong>of</strong> patients who had the disease in question or the general<br />

public or (2) published studies <strong>of</strong> quality-<strong>of</strong>-life ratings from patients who<br />

had the disease in question. Finally, readers always should assess how the investigators<br />

determined the impact <strong>of</strong> uncertainty in the model. All probability,<br />

cost, and utility estimates should be tested in at least a one-way sensitivity<br />

analysis, and readers should take note <strong>of</strong> which variables, if any, altered the<br />

optimal strategy. The more robust the model, the more confident readers can<br />

be that a recommended strategy is in fact the optimal choice.<br />

In the second part <strong>of</strong> the series, Richardson and Detsky [22] describe how<br />

to interpret the results and generalizability <strong>of</strong> a clinical decision analysis. In<br />

a decision analysis, any one clinical strategy can be chosen as a preferred<br />

strategy or there may be a toss-up between two or more strategies. Readers<br />

must decide if the difference between strategies is important clinically. Previous<br />

studies have suggested that a gain in life expectancy or QALYs <strong>of</strong> 2 or<br />

more months can be considered significant [35,36]. Another rule <strong>of</strong> thumb in<br />

decision analysis, as discussed previously, is that an intervention costing less<br />

than $50,000 to $100,000 per QALY gained typically is considered cost effective.<br />

Finally, readers need to ensure that their patients are similar to the

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