Het volume van chirurgische ingrepen en de impact ervan op ... - KCE
Het volume van chirurgische ingrepen en de impact ervan op ... - KCE
Het volume van chirurgische ingrepen en de impact ervan op ... - KCE
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216 Volume Outcome <strong>KCE</strong> reports 113<br />
• In cardiology, the Belgian Working Group for Interv<strong>en</strong>tional Cardiology<br />
(BWGIC) disposes of data for CABG and PCI, and, although we did not<br />
link MCD data to BWGIC registry due to time constraints, this type of<br />
linkage has already be<strong>en</strong> performed in the past and could be redone.<br />
• For orth<strong>op</strong>aedic procedures, only very rec<strong>en</strong>t the National Institute for<br />
Health and Disability Insurance (NIHDI) started the electronic registry<br />
ORTHOpedic (Prosthesis Id<strong>en</strong>tification Data ORTHOpri<strong>de</strong>) which will<br />
inclu<strong>de</strong> all prostheses of hip and knee. 343 Such initiatives will <strong>de</strong>finitely be<br />
of b<strong>en</strong>efit to the quality of future studies.<br />
We cannot rule out confounding by unmeasured characteristics of pati<strong>en</strong>ts in our study.<br />
Nevertheless, we do not believe that limitations related to risk adjustm<strong>en</strong>t threat<strong>en</strong> our main<br />
conclusions about the association betwe<strong>en</strong> <strong>volume</strong> and outcome.<br />
5. Appr<strong>op</strong>riate statistical methods should be used. Regression mo<strong>de</strong>ls are<br />
available that respect the hierarchical nature of the data (pati<strong>en</strong>ts nested<br />
within surgeons, surgeons nested within c<strong>en</strong>tres), and account for the<br />
correlations within these clusters. The failure to inclu<strong>de</strong> any type of<br />
adjustm<strong>en</strong>t for those correlations would lead to falsely high statistically<br />
significant effects. G<strong>en</strong>eralized Estimating Equations (GEE) and G<strong>en</strong>eralized<br />
Linear Mixed Mo<strong>de</strong>ls (GLMM) and are two examples of methods that can be<br />
used to analyze hierarchical data.<br />
6. The graphical pres<strong>en</strong>tation of results. The funnel plot is a good and “easy to<br />
use” tool. It avoids spurious ranking of institutions, spurious stigmatization of<br />
low <strong>volume</strong> c<strong>en</strong>tres, and allows for an informal assessm<strong>en</strong>t of any <strong>volume</strong><br />
outcome relationship.<br />
7. S<strong>en</strong>sitivity analyses and robustness of the results. Results should be<br />
transpar<strong>en</strong>t. In our study, effects of <strong>volume</strong> were always pres<strong>en</strong>ted with and<br />
without adjustm<strong>en</strong>t for case mix (based on administrative data only or based<br />
on all clinical data available) so that one can assess the influ<strong>en</strong>ce of case mix<br />
on the <strong>volume</strong> effect. S<strong>en</strong>sitivity analyses were also performed wh<strong>en</strong> there<br />
were huge <strong>volume</strong> outliers, where it is difficult to differ<strong>en</strong>tiate the effect of<br />
the <strong>volume</strong> or other characteristics of that c<strong>en</strong>tre.<br />
8. Problem of missing data on cancer stage: on average 30% missing data,<br />
sometimes 40% in small <strong>volume</strong> hospitals. The fact that mortality rate was<br />
not substantially higher in the pati<strong>en</strong>ts whose stage was missing in the BCR<br />
seems to indicate, that, in this study, these pati<strong>en</strong>ts are randomly divi<strong>de</strong>d into<br />
the four disease stages. I<strong>de</strong>ally, though, this assumption should have be<strong>en</strong><br />
checked with the help of s<strong>en</strong>sitivity analyses, but this was not done due to<br />
time constraints.<br />
In addition, we noticed that many hospitals – low-<strong>volume</strong> as well as high<strong>volume</strong><br />
– missed data on stage and that the perc<strong>en</strong>tage of missing data varied<br />
among these hospitals. Despite the failure to retrieve information on disease<br />
stage, this problem did not restrain us from drawing conclusions on the<br />
<strong>volume</strong> outcome association. Nevertheless, this problem of missing data on<br />
disease stage (and other variables useful for risk adjustm<strong>en</strong>t) supports the<br />
need for complete and accurate data collection.<br />
9. Sample size is sometimes not suffici<strong>en</strong>t in one year: analysis of several years<br />
for rare tumours or procedures (pancreas, oes<strong>op</strong>hagus, heart transplant) is<br />
required.