Enhancing understanding and optimizing outcomes: insights from selective dorsal rhizotomy in pediatric cerebral palsy
Letter to the Editor

Enhancing understanding and optimizing outcomes: insights from selective dorsal rhizotomy in pediatric cerebral palsy

Rui Wang1# ORCID logo, Wenbin Jiang1# ORCID logo, Min Wei1, Junlu Wang1, Xidan Yu2, Bo Xiao3* ORCID logo, Qijia Zhan1* ORCID logo

1Department of Neurosurgery, Shanghai Children’s Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China; 2Department of Rehabilitation, Shanghai Pubin Children’s Hospital, Shanghai, China; 3Department of Neurosurgery, Shanghai Children’s Medical Center, School of Medicine, Shanghai Jiao Tong University, Shanghai, China

#These authors contributed equally to this work as co-first authors.

*These authors contributed equally to this work.

Correspondence to: Qijia Zhan, MD, PhD. Department of Neurosurgery, Shanghai Children’s Hospital, School of Medicine, Shanghai Jiao Tong University, No. 355, Luding Rd., Putuo District, Shanghai 200062, China. Email: hanbing_1125@163.com; Bo Xiao, MD, PhD. Department of Neurosurgery, Shanghai Children’s Medical Center, School of Medicine, Shanghai Jiao Tong University, No. 1678, Dongfang Rd., Pudong New Area, Shanghai 200127, China. Email: xiao977@hotmail.com.

Response to: Strobl W, Finsterer J. Before selective dorsal rhizotomy can be judged as beneficial for cerebral palsy, long-term results and controlled studies are needed. Transl Pediatr 2024;13:875-5.


Submitted Mar 20, 2024. Accepted for publication Apr 07, 2024. Published online May 27, 2024.

doi: 10.21037/tp-24-106


We would like to extend our gratitude to Dr. Walter Strobl and colleagues for their thoughtful and constructive critique of our recent clinical study titled “Short-term change of tibial torsion in children with spastic cerebral palsy after selective dorsal rhizotomy”, which was published in the Translational Pediatrics (1).

Regarding the first point raised by Dr. Strobl et al. (2), we acknowledge that selective dorsal rhizotomy (SDR) involves cutting not only Ia and Ib fibers but also type II and III fibers, which could potentially lead to sensory disturbances. In our cohort, we observed that 60–70% of patients experienced transient hyperpathia postoperatively. However, these abnormal sensations resolved within one to four weeks after the SDR surgery in all cases. We attribute the absence of long-term sensory disturbances to two main factors:

The implementation of a novel intraoperative neurophysiological method to guide the selection of rootlets for cutting during SDR (3). This method results in a low rhizotomy ratio, meaning that fewer rootlets are cut, which may reduce the likelihood of irreversibly damaging type II and III fibers.

The relatively young age of our patients (average 6.0±2.2 years), which may allow for greater neural plasticity and the resolution of sensory complaints over time.

We reviewed our data and discovered that the 21% of cases that demonstrated significant improvements in transmalleolar angle (TMA) following SDR were considerably younger than those who improved less (4.8±1.0 vs. 6.6±2.1 years, P<0.0001). This suggests that SDR may be more effective in younger patients before the development of severe contractures, corroborating the advantages of early intervention (4).

Regarding the necessity for long-term follow-up, we agree that further studies with extended follow-up periods are essential to validate our findings. Nevertheless, we wish to emphasize that a minimum two-year post-SDR intensive rehabilitation program is crucial to sustain and enhance the initial benefits achieved through SDR (5,6). Considering the significant increase in body weight during puberty, we advocate for performing SDR before the age of 6–8 years, which could make the subsequent two-year rehabilitation therapy more effective.

We appreciate the opportunity to discuss these points, which have provided valuable insights into our study and will undoubtedly inform our future research. It is our sincere hope that this dialogue will contribute to the advancement of treatment options for children with spastic cerebral palsy.


Acknowledgments

Funding: The work was supported by the Science and Technology Commission of Shanghai Municipality (20Y11905800), Shanghai Children’s Hospital (2020YGZQ05), and Shanghai Jiao Tong University (YG2021QN117).


Footnote

Provenance and Peer Review: This article was commissioned by the editorial office, Translational Pediatrics. The article did not undergo external peer review.

Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at https://tp.amegroups.com/article/view/10.21037/tp-24-106/coif). The authors have no conflicts of interest to declare.

Ethical Statement: The authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.

Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.


References

  1. Wang R, Jiang W, Wei M, et al. Short-term change of tibial torsion in children with spastic cerebral palsy after selective dorsal rhizotomy. Transl Pediatr 2023;12:2131-41. [Crossref] [PubMed]
  2. Strobl W, Finsterer J. Before selective dorsal rhizotomy can be judged as beneficial for cerebral palsy, long-term results and controlled studies are needed. Transl Pediatr 2024; [Crossref]
  3. Zhan Q, Tang L, Wang Y, et al. Feasibility and effectiveness of a newly modified protocol-guided selective dorsal rhizotomy via single-level approach to treat spastic hemiplegia in pediatric cases with cerebral palsy. Childs Nerv Syst 2019;35:2171-8. [Crossref] [PubMed]
  4. Zhan Q, Yu X, Jiang W, et al. Whether the newly modified rhizotomy protocol is applicable to guide single-level approach SDR to treat spastic quadriplegia and diplegia in pediatric patients with cerebral palsy? Childs Nerv Syst 2020;36:1935-43. [Crossref] [PubMed]
  5. Bolster EA, van Schie PE, Becher JG, et al. Long-term effect of selective dorsal rhizotomy on gross motor function in ambulant children with spastic bilateral cerebral palsy, compared with reference centiles. Dev Med Child Neurol 2013;55:610-6. [Crossref] [PubMed]
  6. Park TS, Liu JL, Edwards C, et al. Functional Outcomes of Childhood Selective Dorsal Rhizotomy 20 to 28 Years Later. Cureus 2017;9:e1256. [Crossref] [PubMed]
Cite this article as: Wang R, Jiang W, Wei M, Wang J, Yu X, Xiao B, Zhan Q. Enhancing understanding and optimizing outcomes: insights from selective dorsal rhizotomy in pediatric cerebral palsy. Transl Pediatr 2024;13(5):873-874. doi: 10.21037/tp-24-106

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