Postoperative care after craniofacial surgery: evaluation of routine laboratory testing
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Published on: January 17, 2018
R J van Krugten1, A P Bos, M Offringa
1Department of Pediatric Surgery, Sophia Children's Hospital, Rotterdam, The Netherlands.
Insights
Routine laboratory testing after craniofacial surgery offers limited value. Indiscriminate testing did not predict complications, while targeted testing improved management and reduced costs.
Area of Science:
- Pediatric Surgery
- Medical Diagnostics
Background:
- Postoperative monitoring of children following major craniofacial surgery is crucial for detecting complications.
- Previous monitoring protocols relied heavily on repetitive laboratory testing, raising questions about their efficiency and impact.
Purpose of the Study:
- To compare the efficacy and value of two distinct postoperative monitoring protocols for children undergoing major craniofacial surgery.
- To evaluate whether routine laboratory testing predicts complications or influences clinical management.
Main Methods:
- A comparative study involving two groups of children post-craniofacial surgery.
- Protocol 1: Repetitive laboratory testing over 2 years (37 children).
- Protocol 2: Adapted protocol with initial routine testing and further testing based on clinical symptoms or abnormal results over 5 years (98 children).
Main Results:
- Repetitive laboratory testing in Protocol 1 did not predict complications or alter management.
- Protocol 2 significantly reduced the mean number of tests per patient (42.5 to 7.0).
- In Protocol 2, abnormal test results frequently led to changes in clinical management (84%), unlike Protocol 1.
Conclusions:
- Indiscriminate routine laboratory testing is of limited value in the postoperative period after craniofacial surgery.
- A targeted testing approach, guided by clinical symptoms or initial results, is more effective and efficient.
- Optimizing monitoring protocols can reduce healthcare costs without compromising patient care or complication rates.
Abstract:
In this study, two protocols for monitoring children after major craniofacial surgery were compared. The first protocol consisted of repetitive laboratory testing in 37 children to detect surgical and medical complications during a 2-year period. None of the complications were predicted by abnormal test results, and abnormal results of routinely performed tests never led to a change in management. The second protocol, an adapted version of the first protocol, was continued for 5 years as a prospective study in 98 children: Patients were routinely tested only once, and further testing was initiated either after an abnormal test result or because of clinical symptoms. Clinical management and the incidence of postoperative complications did not differ between groups. The second protocol considerably reduced the mean number of tests per patient from 42.5 to 7.0, but in contrast with the first protocol, 84 percent of abnormal test results led to changes in clinical management. In conclusion, in the first group the test results were not used and were not predictive of complications. In the second group, tests were more apt to have abnormal results and often initiated treatment. This shows that indiscriminate routine laboratory testing is of limited value in covering the postoperative period after craniofacial surgery.
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