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Short-term effect and effect on rate of lung function decline after surgery for neuromuscular or syndromic scoliosis
Esther S Veldhoen1, Anneloes de Vries1, Tom P C Schlosser2
1Pediatric Intensive Care Unit, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands.
Insights
Scoliosis surgery did not stabilize lung function in children with neuromuscular or syndromic conditions. Lung function tests showed a decline in neuromuscular patients post-surgery, with inconclusive effects on the rate of decline.
Area of Science:
- Pediatric Orthopedics
- Pulmonology
- Medical Engineering
Background:
- Scoliosis surgery in children with neuromuscular diseases or dysmorphic syndromes requires careful patient counseling regarding potential impacts on lung function.
- Understanding the postoperative trajectory of lung function is crucial for managing expectations and optimizing patient outcomes.
Purpose of the Study:
- To prospectively compare lung function test (LFT) results before and after scoliosis surgery in pediatric patients with neuromuscular diseases or dysmorphic syndromes.
- To evaluate whether scoliosis surgery leads to stabilization or alters the rate of lung function decline in these patient populations.
Main Methods:
- Prospective study including 43 children with neuromuscular or syndromic scoliosis capable of performing LFTs.
- Analysis of forced vital capacity ([F]VC), FEV1/FVC ratio, and peak expiratory flow (PEF) preoperatively and 3-4 months postoperatively.
- Comparison of the mean monthly change in LFTs up to 2 years post-surgery with preoperative trends using linear mixed-effects models.
Main Results:
- No significant change in absolute LFT values ( [F]VC, FEV1/FVC, PEF) was observed immediately after surgery.
- A significant decrease in median standardized lung function was noted in neuromuscular patients post-surgery (VC: 43% to 33%, FVC: 42% to 31%, PEF: 51% to 40%).
- Syndromic patients showed a smaller decrease in median FVC (68% to 65%), and the rate of FVC change remained non-significantly altered in both groups.
Conclusions:
- Scoliosis surgery does not appear to stabilize lung function in children with neuromuscular or syndromic scoliosis and restrictive lung disease.
- The long-term effect of scoliosis surgery on the rate of lung function decline in these pediatric populations remains inconclusive based on this study.
Introduction:
Understanding the impact of scoliosis surgery on lung function is important for counseling patients about risks and benefits of surgery. We prospectively compared the trends in lung function test (LFT) results before and after scoliosis surgery in children with neuromuscular diseases or dysmorphic syndromes. We hypothesized a stabilization.
Methods:
We prospectively included children with neuromuscular or syndromic scoliosis able to perform LFTs. We studied (forced) vital capacity ([F]VC), ratio of forced expiratory volume in 1 s (FEV1 ) and FVC, and peak expiratory flow (PEF). Preoperative LFT results were compared with results 3-4 months after surgery. The mean monthly change in LFT results up to 2 years after surgery was compared with the preoperative natural history using linear mixed-effects models.
Results:
We included 43 patients. No significant change was observed in absolute values of (F)VC, FEV1 /FVC, and PEF before and after surgery. In 23 neuromuscular patients median standardized VC, FVC, and PEF decreased significantly after surgery from 43% to 33%, 42% to 31%, and 51% to 40%, respectively. In 20 syndromic patients, median FVC decreased from 68% to 65%. The monthly rate of change in FVC did not change significantly in both groups with a mean difference of 0.18% (95% CI: -0.27, -0.61) and -0.44% (95% CI: -1.05, 0.16).
Conclusion:
No stabilization of lung function 3-4 months after scoliosis surgery was observed in children with neuromuscular and syndromic scoliosis with restrictive lung function disease. The effect on the rate of lung function decline remains inconclusive.
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