This news release looks at a program to introduce a quality improvement initiative aimed at reducing complications and deaths among frail older adults undergoing major elective surgery.
The release contained a welcome summary of the findings–the quantified benefits are very clear. But we wanted to know more about the screening tool used to determine how frail patients were, as well as the implementation plans: Is this a brand-new concept, or are there similar efforts out there? How much did the program cost? The news release also could have been more clear about the limitations of the study, such as the lack of a control group.
Given how successfully the intervention apparently worked to reduce deaths, this study is likely to be read with wide interest.
No costs are mentioned.
This is a very strong point for the release. It states clearly that absolute reductions were seen before and after the intervention: i.e.: “overall 30-day mortality decreased from 1.6 percent (84 of 5,275 patients) to 0.7 percent (26 of 3,878 patients) after FSI implementation. Improvement was greatest among frail patients (12.2 percent to 3.8 percent), although mortality rates also decreased among the robust patients (1.2 percent to 0.3 percent).”
Given that this was a study about a quality improvement initiative, we’ll rate this N/A. However, it might have been worth raising the question of whether the time and emphasis placed on this screening test by clinicians detracted from other work they could have been doing to improve patient care and outcomes.
More was needed on the limitations of the study. For example, the abstract said that the causal connections between the use of the screening tool and mortality outcomes required “additional investigation” to be confirmed–but the news release contained no such important caveat.
And also from the study: “Most important, although we were able to control for frailty, we were unable to account for patients who screened as frail and did not undergo surgery. This limitation may be a source of significant selection bias, although it is clear that surgeons continued to operate on frail patients. Further research using a randomized controlled design will be necessary to establish the causal connection between the FSI and mortality outcomes.”
No obvious disease mongering in this release.
We learn that the study “was supported by a grant from the U.S. Department of Veterans Affairs, Veterans Health Administration, Office of Research and Development, Health Services Research and Development. We did not detect any conflicts of interest that should have been disclosed.
The release mentions no alternatives to this screening program but presumably there are other methods and techniques that are used to reduce harm done on frail people who undergo elective surgery. Since this is a “before-after” trial presumably there would be some kind of frailty assessment, even an informal one, that happens prior to surgery?
It is not clear if the screening index and action plans for surgery among frail patients are readily available for other institutions to use.
The release establishes what’s novel by stating: ““This study reveals the feasibility of facility-wide frailty screening in elective surgical populations.” We would have liked a bit more information on the risk analysis indicator used to assess frailty–is this a well-established tool or being used uniquely here?
There is no unjustifiable language in the news release.
Systematic, Criteria-Driven
Take all the issues enmeshed in any cancer screening story and amplify it with the liquid biopsy issue. @AP's @CarlaKJohnson. did a solid job here. https://apnews.com/article/science-business-health-hodgkin-lymphoma-oregon-ca899bb9c4c7f1859d4e9ce16a1cf78d
Come on, NY Times; you must do better than this. Important research doesn’t need hype and the “breaking news” BS doesn’t help readers or patients. https://www.healthnewsreview.org/2022/03/nyt-proclaims-breaking-news/
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