Skip to main content

SYSTEMATIC REVIEW article

Front. Neurol., 28 September 2023
Sec. Neuroepidemiology

Prevalence of cerebral palsy comorbidities in China: a systematic review and meta-analysis

Chao Gong&#x;Chao Gong1†Xiaopei Liu,&#x;Xiaopei Liu1,2†Liya FangLiya Fang1Annan LiuAnnan Liu1Beibei LianBeibei Lian1Xunzhong QiXunzhong Qi3Shuyue ChenShuyue Chen4Huiqing LiHuiqing Li4Ming ZhaoMing Zhao5Jin Guo,
Jin Guo1,2*Shaobo Zhou
Shaobo Zhou6*
  • 1College of Rehabilitation Medicine, Jiamusi University, Jiamusi, China
  • 2Jiamusi University Affiliated No. 3 Hospital, Jiamusi, China
  • 3Jiamusi University Affiliated No. 1 Hospital, Jiamusi, China
  • 4College of Basic Medicine, Jiamusi University, Jiamusi, China
  • 5College of Public Health, Jiamusi University, Jiamusi, China
  • 6School of Science, Faculty of Engineering and Science, University of Greenwich, Medway Campus Central Avenue, Chatham Maritime, Kent, England

Objectives: This systematic review aimed to comprehensively understand the comorbidity of cerebral palsy (CP) in China.

Methods: We searched through databases in both Chinese and English until December 2022 to gather cross-sectional studies on the comorbidity of CP in China. After two reviewers independently screened the articles, collected the data, and assessed the bias risk, a meta-analysis was conducted using the Stata 17.0 software.

Results: A total of 73 articles were included. Of these, 16 articles reported total comorbidity, with a prevalence of 79.7% (95% CI: 73.8–85.7%); 56 articles reported epilepsy, with a prevalence of 17.9% (95% CI: 15.4–20.4%); 48 articles reported intellectual disability, with a prevalence of 58.0% (95% CI: 51.8–64.3%); 32 articles reported speech disorders, with a prevalence of 48.0% (95% CI: 41.6–54.4%); 41 articles reported hearing disorders, with a prevalence of 17.2% (95% CI: 13.0–21.4%); and 35 articles reported vision disorders, with a prevalence of 23.1% (95% CI: 16.3–29.8%). The topographical type of CP was the primary source of heterogeneity in the prevalence of epilepsy. Diagnostic criteria for CP, clinical type of CP, GMFCS, publishing time, and topographical type of CP were the primary sources of heterogeneity in the prevalence of intellectual disability. Clinical type of CP and topographical type were the primary sources of heterogeneity in the prevalence of speech disorders. Finally, the region was the primary source of heterogeneity in the prevalence of hearing disorders.

Conclusion: The prevalence of comorbidities in CP is high in China. Comorbidities are related to the characteristics, severity, and risk factors of brain insult and have a particular relationship with regional economic development and medical and health levels.

1. Introduction

Cerebral palsy (CP) is a joint complex and multifactorial chronic neurological disorder that occurs in childhood due to non-progressive abnormalities in postural control, muscle tone, and motor function caused by permanent damage to the brain during early development (1, 2). However, pure motor deficits are rare in CP, and the diversity of neurological insult is inevitably accompanied by many different levels of functional impairment and disease; examples include sensation, perception, cognition, communication, behaviour, epilepsy, and secondary musculoskeletal problems (2).

According to data from high-income nations, CP is frequently accompanied by different levels of related impairment (3, 4). According to a recent study analyzing data from a Norwegian registry of those with the condition, 95% of children with CP had at least one comorbidity (3). The European CP Monitor states that the most frequent comorbidities are speech disorders, intellectual disability, epilepsy, and vision disorders (4). Comorbidities in children with CP are a severe problem. Due to their motor dysfunction, children with CP have impaired motor function. When comorbidities are present, they can substantially hinder rehabilitation training and decrease the likelihood of the child’s survival and quality of life in the future. Our understanding of the complexity of CP can be enhanced by studying the comorbidities, maximizing the health and quality of life of children with CP and informing guidance on coordinated care models, individual and family community involvement, and the direct and indirect costs associated with CP (5, 6).

In 2012, Novak’s team (7) conducted a systematic review of the comorbidities in CP, which revealed that 75% were in pain; 50% had an intellectual disability; 25% could not talk; 25% had epilepsy; 25% had a behavior disorder; 20% had a sleep disorder; 20% dribbled; 10% were blind; 7% were tube-fed; and 4% were deaf. However, the search language was limited to English, so there was no systematic evaluation of CP comorbidity in China. Moreover, there has yet to be a systematic review of the prevalence of CP comorbidities in China. Therefore, the purpose of this study is to conduct a systematic evaluation of the comorbidity of CP in China to provide a thorough understanding of the current state of the comorbidity of CP in China and to help medical researchers gain a comprehensive understanding of the comorbidity of CP in China.

2. Methods

The protocol was registered with the International Prospective Register of Systematic Reviews (PROSPERO; registration number: CRD42023406293).

2.1. Search strategy

Three English databases (PubMed, Embase, and Web of Science) and four Chinese databases (CNKI, Wanfang Database, VIP Database, and Chinese Biomedical Database) were systematically searched to determine all potentially relevant studies on the prevalence of comorbidities of CP reported from the establishment of the database to December 2022. Manual retrieves were conducted of the reference lists of articles considered at the full-text stage and systematic review articles on CP and comorbidities for any additional references pertinent to our systematic review. Using Endnote 20, the retrieved articles were organized, and duplicates were eliminated. The specific search strategy is shown in See Supplementary material S1.

2.2. Inclusion and exclusion criteria

Inclusion criteria: (i) it was directly or indirectly reported in the articles on the prevalence of each comorbidity and total comorbidity in Chinese individuals with CP. The various comorbidities included epilepsy, intellectual disability, speech disorders, hearing disorders, and vision disorders; (ii) English and Chinese articles; (iii) cross-sectional studies with raw data; (iv) Chinese and English articles with clear diagnostic criteria for CP, including the 1988 National Symposium on Pediatric CP in China (8), the 2004 National Symposium on Pediatric CP (9), the 9th National Pediatric CP Rehabilitation Academic Conference in 2006 (10), the 2015 Rehabilitation Guidelines for CP in China (11), and international diagnostic criteria for CP.

Exclusion criteria: (i) review, systematic reviews, meta-analyzes, conference abstracts, comments, or letters; (ii) studies with fewer than 50 participants were excluded to ensure that estimates reflected the intended population; (iii) the full text was not available; (iv) studies’ data were missing, duplicated, or unavailable; (v) to avoid bias in total prevalence, articles from studies that only examined populations with specific CP types was excluded; and (vi) we kept only one article for articles with overlapping collection times and data from the same region.

2.3. Articles screening and data extraction

Two reviewers independently reviewed the titles and abstracts of the retrieved articles to eliminate duplicate and irrelevant studies, and then independently read the full texts of the remaining articles. They then discussed their disagreements with a third senior reviewer to agree. From each article, the first author, year of publication, time of sample collection, the total number of CP individuals, number of comorbid occurrences, prevalence, age, male-to-female ratio, diagnostic criteria for CP, and diagnostic criteria for comorbidities were then separately retrieved. If more information or clarity was required, the study’s authors were contacted. Disagreements were then discussed and resolved by contacting a third senior reviewer.

2.4. Article quality evaluation

We used a cross-sectional/prevalence study quality rating scale recommended by the Agency for Healthcare Research and Quality (AHRQ), with 11 entries answered with “yes,” “no,” or “unclear,” and the higher the rating, the higher the quality of the articles (12), which two reviewers evaluated after discussion.

2.5. Data synthesis and analysis

Each comorbidity’s prevalence in CP individuals was statistically estimated using Stata 17.0 (Stata Corp, College Station, TX, United States), providing a 95% CI. To quantify the heterogeneity among the research outcomes, the Q-test and I2 were used. A meta-analysis was conducted after eliminating the impact of significant clinical heterogeneity and further investigating the source of heterogeneity if the level between study outcomes was high (I2 ≥ 50%). Conversely, a fixed-effects model was used. Sensitivity analyzes were performed using a study-by-study removal method to detect each study’s effect on the combined effect. Subgroup analysis and meta-regression analysis were used to investigate the sources of heterogeneity and differences in comorbidity prevalence between groups based on sample source of articles, gross motor function classification system (GMFCS), Chinese diagnostic criteria for CP, regional distribution, year of publication, AHRQ quality score, gender, risk factors, topographical type of CP, and clinical type of CP. Subgroup and meta-regression analysis were used to explore further the source of heterogeneity and the differences in comorbidity among different groups. The test level for the meta-analysis was set at α = 0.05. Moreover, a regression-based Egger’s test was used to assess the effect of small studies and the risk of publication bias. p < 0.05 was considered a significant bias.

3. Results

3.1. Articles screening process and results

In total, 6,889 relevant articles were searched. After 3,167 duplicates were excluded with Endnote 20, 3,533 irrelevant articles were first excluded by reading the titles and abstracts. Then 116 articles were excluded by reading the entire text and applying the inclusion and exclusion criteria. Finally, 73 articles were found to be eligible. Figure 1 depicts the article screening process.

FIGURE 1
www.frontiersin.org

Figure 1. Article screening process and result.

3.2. Characteristics of included articles

The essential characteristics of the included articles are shown in Table 1, in which 16 articles reported total comorbidity, the most involved being epilepsy, intellectual disability, speech disorders, hearing disorders, and vision disorders, Furthermore, 56 articles reported the prevalence of epilepsy, but only 7 (14, 25, 50, 64, 75, 80, 82) mentioned the diagnostic criteria, all referring to the diagnostic criteria established by the International League Against Epilepsy (ILAF) in various years. The prevalence of intellectual disability was reported in 48 articles, with 17 articles mentioning the diagnostic methods, the most frequently used being the Gesell Developmental Scale for children ≤3 years old and the Wechsler Intelligence Scale for Children (WISC) >3 years old (16, 24, 28, 29, 33, 68, 72). Speech disorders were reported in 32 articles, with 8 articles (16, 24, 29, 33, 47, 60, 68, 80) mentioning the diagnostic methods, all of which used the Speech Symbolic Form-Indicative Content (S-S) language delay screening method and the dysarthria screening method adapted by the Chinese Rehabilitation Research Center. A total of 41 articles reported on hearing disorders, of which 19 (16, 24, 2830, 33, 34, 36, 37, 47, 48, 55, 61, 68, 70, 73, 78, 80, 85) mentioned the diagnostic methods, all of these used brainstem auditory evoked potential (BAEP) tests. Finally, 35 articles reported on vision disorders, of which 11 (24, 28, 29, 33, 41, 47, 61, 68, 69, 71, 84) mentioned the diagnostic methods, including routine ophthalmic examinations and Visual Evoked Potential (VEP) tests. See Supplementary material S2 for details.

TABLE 1
www.frontiersin.org

Table 1. Summary of articles.

3.3. Article quality evaluation

After the quality evaluation, each article was found to have a score between 3 and 7, with 16 articles having scores of 3, 15 articles scores of 4, 20 articles scores of 5, 10 articles scores of 6, and 12 articles scores of 7. The mean score was 4.82, showing that the results had a high risk of bias, and the specific article quality evaluation results are shown in Supplementary material S3.

3.4. Results of meta-analysis and publication bias

The meta-analysis results showed high inter-study heterogeneity (I2 ≥ 50%) for all outcome indicators, and therefore all were analyzed using a random-effects model. Articles on the prevalence of total comorbidity involved a total of 6,617 individuals with CP and showed I2 = 98.36, with a prevalence of 79.7% (95% CI: 73.8–85.7%) and some publication bias (p < 0.001). Articles on the prevalence of epilepsy involved a total of 29,020 individuals with CP and showed I2 = 76.59, with a prevalence of 17.9% (95% CI: 15.4–20.4%) and some publication bias (p = 0.002). The articles on the prevalence of intellectual disability involved 430,933 individuals with CP and showed I2 = 99.11, with a prevalence of 58.0% (95% CI: 51.8–64.3%) and some publication bias (p = 0.026). The articles on the prevalence of speech disorders involved 21,426 individuals with CP and showed an I2 = 97.14, with a prevalence of 48.0% (95% CI: 41.6–54.4%) and no significant publication bias (p = 0.135). The articles on the prevalence of hearing disorders involved 429,032 individuals with CP and showed an I2 = 94.75, with a prevalence of 17.2% (95% CI: 13.0–21.4%)and some publication bias (p < 0.001). The articles on the prevalence of vision disorders involved 419,150 individuals with CP and showed I2 = 97.13, with a prevalence of 23.1% (95% CI: 16.3–29.8%) and some publication bias (p < 0.001). These results are shown in Table 2 and Figure 2.

TABLE 2
www.frontiersin.org

Table 2. Summarizes the meta-analysis results and Egger’s test of comorbidities.

FIGURE 2
www.frontiersin.org

Figure 2. Forest plots of meta-analysis of the prevalence of comorbidities. (A) Total Comorbidities, (B) Epilepsy, (C) Intellectual Disability, (D) Speech Disorders, (E) Hearing Disorders, (F) Vision Disorders.

3.5. Sensitivity analysis

A stepwise elimination method was used to investigate the origin of heterogeneity and the results were comparable to the overall detection rate. The following outcome indicators had better stability: total comorbidity (78.4–81.9%), epilepsy (17.4–18.2%), intellectual disability (57.1–59.0%), speech disorders (47.1–49.4%), hearing disorders (16.5–17.9%), and vision disorders (21.6–23.7%). See Supplementary material S4 for details.

3.6. Subgroup analysis and meta-regression analysis

By subgroup analysis and meta-regression analysis, it was found that for total comorbidities, the publishing time was the source of heterogeneity (p = 0.019). For epilepsy prevalence, the topographical type of CP was the source of heterogeneity (p = 0.002). Regarding intellectual disability, the primary sources of heterogeneity were GMFCS (p = 0.004), publishing time (p = 0.047), diagnostic criteria for CP (p = 0.045), clinical type (p = 0.004), and topographical type (p = 0.008). For speech disorders, the topographical type of CP was the primary source of heterogeneity (p = 0.019). For hearing disorders, the region was the primary source of heterogeneity (p = 0.041). These results are shown in Figure 3.

FIGURE 3
www.frontiersin.org

Figure 3. Subgroup analysis and meta-regression analysis of the prevalence of comorbidities. (A) Total Comorbidities, (B) Epilepsy, (C) Intellectual Disability, (D) Speech Disorders, (E) Hearing Disorders, (F) Vision Disorders.

4. Discussion

This study collated and summarized articles on the comorbidity of CP in China over the past 25 years. The results showed that, after excluding articles that did not meet the criteria, 73 articles studied the comorbidity of CP. The sample size of the included articles was extensive. It covered most regions of China, which could reflect the characteristics, development trends, and distribution of comorbidity in CP of China to some extent. However, some of the articles were missing relevant information, and the unequal number of articles included in the subgroup analysis may have affected the comprehensiveness of the results.

Our analysis of CP comorbidity showed that the prevalence of intellectual disability was 58.0%, speech disorders were 48.0%, epilepsy was 17.9%, hearing disorders were 17.2%, and vision disorders were 23.1%. This was different from a population-based study in Australia, which showed that 48% had an intellectual disability, 61% had speech disorders, 28% had epilepsy before the age of 5, 12% had hearing disorders, and 36% had vision disorders (89). We presumed that this was due to differences in ethnicity, geographic and natural environment, and level of health care. In addition, the results showed that the prevalence of epilepsy in this study was lower than the prevalence of 30.5% in Europe and 41% in the United States (90, 91). The reason may be the negligence of early diagnosis in China in the early years, which leads to the failure to diagnose epilepsy in some children with CP early in life because epilepsy occurs mainly in children with CP within 1 year of age and is a marker for early determination of the severity of CP (92, 93). Early diagnosis is vital for rapid etiological assessment, providing early intervention, and preventing complications. The more severe the brain insult, the higher the likelihood of comorbidities (94). In addition, compared to other comorbidities, epilepsy is not directly observed by assessment. It requires a seizure for diagnosis, and most of the included articles obtained the prevalence of epilepsy by reviewing medical history data. Because of the lack of awareness of epilepsy among most Chinese parents, combined with some motor deficits in CP, such as dyskinetic CP with complex partial seizure, parents may consider this a manifestation of CP dyskinesia. When taking a medical history, parents will not think that their child has epilepsy, resulting in an underdiagnosis (93) which may make the prevalence of epilepsy somewhat underestimated. Furthermore, most CP individuals in China are only admitted for short hospital stays and receive rehabilitation in outpatient clinics, making it difficult to accurately and timely document epilepsy when it occurs.

In this study, the prevalence of total comorbidity, epilepsy, hearing disorders, and vision disorders increased after 2011 compared to before 2011. We assume this may be because the diagnostic criteria, tools, and equipment used to detect these comorbidities in China improved and became more sensitive. The idea of early diagnosis is gradually gaining importance. More comorbidities of CP are being correctly diagnosed. However, diagnostic scales for intellectual disability (Gesell Developmental Scale for ≤3 years old, WISC for >3 years old) and speech disorders (S-S speech delay test and dysarthria test adopted by China Rehabilitation Research Center) are the diagnostic tools that most medical institutions in China have used since their introduction from abroad, and the diagnostic criteria have not changed significantly. Moreover, increasing attention and the implementation of early intervention in China may be the reason for the decrease in the prevalence of epilepsy, intellectual disability, and speech disorders in CP after 2011.

Among our included articles, the AHRQ scores ranged from 3 to 7, with extensive range and variable quality. We performed subgroup analyzes based on the AHRQ scores to explore the prevalence of CP comorbidities in different quality articles. This study found that compared with low- and middle-quality articles, the prevalence of most comorbidities in high-quality articles with scores of 6 and 7 was closer to the totalized prevalence in Table 2, suggesting that the totalized results were stable. In contrast, the prevalence of most comorbidities was higher in the articles that scored 5 than in the other two groups, which was caused by the higher prevalence of comorbidities in the multiple articles included.

In this study, we divided it into the clinical type and topographical type for subgroup analysis according to the CP typing criteria of most of the included articles. The results showed that the prevalence of mixed type in clinical type and quadriplegia in topographical type was high. These two types are characterized by relatively severe brain insult, and their GMFCS is often class IV and V. The subgroup analysis of GMFCS found that the prevalence of comorbidities in GMFCS classes IV and V was higher than that in class I-III, which verified that individuals with severe CP were more likely to have comorbidities. Delacy et al. (89) showed that as the GMFCS level increased, the proportion of children with two or more severely related impairments increased from 3% in GMFCS class I to 73% in GMFCS class V. The prevalence of comorbidities increased, with quadriplegia being the group with the highest comorbidities in CP. In addition, we found a higher prevalence of comorbidities in hospital-based studies than in population-based studies, possibly because hospital-based studies tended to include more severe CP individuals. In conclusion, we speculate that the prevalence of comorbidities is related to the severity of CP. Also, it was discovered that the position of the brain insult impacted the occurrence of comorbidity in CP. For example, we found that in terms of the prevalence of epilepsy, intellectual disability, and vision disorders, the spastic type with predominantly cortical brain insult was the highest. In contrast, the dyskinetic type with extrapyramidal insult and the ataxia type with predominantly cerebellar insult were low. However, the prevalence of speech disorders was high in the dyskinetic and ataxia types because the dyskinetic type has dystonia due to extrapyramidal insult, which leads to this dysarthria. The cerebellum mainly controls language processing tasks, so the insult leads to a series of speech disorders.

There is some difference in the prevalence of CP comorbidity by risk factors; for instance, the results of the subgroup analysis show that intracranial hemorrhage was a high prevalence factor for epilepsy. This is because brain insult is more severe in CP with intracranial hemorrhage, which can cause the release of numerous inflammatory factors in the child’s brain cavity, damaging the blood–brain barrier, which can cause functional damage to the child’s ventricles as well as peripheral tissues. Furthermore, it can cause a functional imbalance in glutamate metabolism in the brain, allowing synchronous glutamate firing in the hippocampal neural network and increasing the risk of epilepsy (81). However, risk factors for CP are often multifactorial and confounded, and different risk factors can combine to cause CP, so the results still need to be interpreted cautiously.

To present, the diagnostic criteria for CP have been revised five times in China, with some differences in the diagnostic criteria for CP after each revision, so we analyzed the past four CP guidelines by subgroups (excluding the latest revised Chinese CP guidelines in 2022 (1), which are not currently widely used). The difference in the prevalence of comorbidity was found to be greater in the group based on the 2015 guidelines than in the other groups. This result may be due to a significant change in the diagnostic criteria of the 2015 Chinese CP Guidelines Group. The hypotonic type was removed as a subtype of CP, which was considered to be a transitional form of other CP subtypes, and the type was only defined as a developmental delay in the diagnosis. Furthermore, the low number of articles using the 2015 guideline as the diagnostic criteria may be one of the reasons.

The prevalence of CP comorbidity varies widely among geographic subdivisions. This difference is related to the fact that China is a multi-ethnic country with unbalanced levels of education, economic development, regional healthcare conditions, and CP prevention and treatment measures and capabilities, among other factors (95). In economically developed coastal regions such as South China, where regional development is rapid and the coverage of rehabilitation services is more extensive, early diagnosis and intervention are emphasized and implemented. Hence, the diagnosis rate of epilepsy was higher (28.7%). The prevalence of comorbidities such as hearing disorders (13.9%), vision disorders (18.7%), and speech disorders (45.6%) was lower than in other regions. Although the central and western regions are vast, they are relatively slow to develop and are limited by lower economic conditions and healthcare levels. Prevention and management of CP comorbidities are lacking (96), and the prevalence of comorbidities was higher. However, more studies are needed to verify this in the future because of the small number of included articles in this group.

In addition, the results of this study are more reflective of the prevalence rate of comorbidity of CP in medical institutions, as 87.2% of the included studies were medical institution-based studies. Theoretically, patients with CP in medical institution-based studies are more likely to be admitted to rehabilitation for severe conditions. In contrast, patients with CP who have relatively mild symptoms and are from low-income families may not be admitted to rehabilitation, thus, the final results may overestimate the comorbidity of CP (97). In 1998, Surveillance of Cerebral Palsy in Europe (SCPE) became the world’s first CP surveillance network, consisting of 14 CP management centers in eight countries. By 2018, it had expanded to 23 centers in 20 countries, registering 21,043 children with CP born from 1976 to 2018. SCPE coordinated the European CP registry management centers to cooperate and develop a central database to provide uniform standards and criteria for collaborative research (98). Although Japan and Korea have not established a CP surveillance system, nationwide health insurance systems covering the whole country can monitor the prevalence of CP, understand comorbidities and risk factors, and provide prevention strategies, thus serving as a database for policy development and playing an essential role in the prevention, treatment, and rehabilitation of CP (99, 100). In China, only some provinces and cities have built CP child detection systems and information platforms, and no reports have established national or multi-regional collaborative CP monitoring systems and information platforms (95). So far, only Henan Province has published relevant articles through data from the CP child registration management monitoring network built in 2020 (80), and no related research has been reported in other provinces and cities. In China, one can consult SCPE and the Australian Cerebral Palsy Register (ACPR) (101) as information platforms to establish a standard of unified data collection table. For example, through many parts of the country, at hospitals, rehabilitation centers, and special education schools, CP individuals are registered through an online and/or paper-based registration system, which specialized agencies and personnel then administer. However, it is still difficult to establish a CP registry in China because China has a wide geographical area, uneven economic development, and numerous institutions accepting CP children, so it needs gradual development and establishment. It is of great significance to establish a sound national CP register and understand the epidemic characteristics and trends of CP over time through a network monitoring system and information data platforms for the formulation of effective prevention and treatment strategies for CP.

The limitations of this study are as follows. (i) This study is a meta-analysis of a single rate group, with enormous heterogeneity among studies. (ii) The included CP cases were of varying severity, and the different confounding risk factors and severity of CP may produce some differences in the results. (iii) The inclusion of an extensive age range and low age may have some influence on the final results, due to the reason that some comorbidities often develop with age, and younger children with CP comorbidities may be difficult to diagnose (102), so the older the CP patient is at the time of recording, the less likely it is that the diagnosis will be missed (103). (iv) The substantial between-study heterogeneity limits the interpretability and clinical applicability of the reported prevalence figures.

In conclusion, the prevalence of CP comorbidity is high in China. Comorbidity is related to brain insult characteristics, severity, and risk factors. It has a particular relationship with regional economic development and medical and health levels. Future studies on the prevention of CP comorbidity to improve the survival and quality of life of CP individuals should pay attention to these factors.

Data availability statement

The original contributions presented in the study are included in the article/Supplementary material, further inquiries can be directed to the corresponding authors.

Author contributions

CG, JG, and SZ were responsible for the conception and design of the article, the revision of the article, and the overall responsibility of the article. CG, LF, and MZ were responsible for the implementation and feasibility analysis of the study and statistical processing. BL, AL, and SC were responsible for the articles search, data collection, and organization. CG, SZ, LF, and XL were responsible for analyzing and interpreting the results. CG, JG, and AL were responsible for the writing and proofreading the article. HL and XQ participated in the revision of the article.

Funding

The Heilongjiang Provincial Natural Science Foundation Project (No. LH2020H006) and Fund Basic Scientific Research Operating Expenses of Provincial Institutions of Higher Learning in Heilongjiang Province (No. 2019-KYYWF-1366 and No. 2022-KYYWF-0653) supported this study.

Acknowledgments

We would like to thank all the authors involved in this study, especially Prof. Zhou, for polishing the language of our article and for his valuable comments in the revision process.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Supplementary material

The Supplementary material for this article can be found Available at: https://www.frontiersin.org/articles/10.3389/fneur.2023.1233700/full#supplementary-material

References

1. Children’s Rehabilitation Professional Committee of China Rehabilitation Medical Association, Children’s Cerebral Palsy Rehabilitation Professional Committee of China Rehabilitation Association for the Disabled, Children’s Rehabilitation Professional Committee of Rehabilitation Physician Branch of Chinese Medical Doctor Association, Editorial Board of Chinese Cerebral Palsy Rehabilitation Guide . (2022). Chinese rehabilitation guidelines for cerebral palsy (2022) chapter 1: Introduction. Zhong Hua Shi Yong Er Ke Lin Chuang Za Zhi 2022, No. 37. pp. 887–892. doi: 10.3760/cma.j.cn101070-20220505-00500

CrossRef Full Text | Google Scholar

2. Rosenbaum, P , Paneth, N , Leviton, A , Goldstein, M , Bax, M , Damiano, D, et al. A report: the definition and classification of cerebral palsy April 2006. Dev Med Child Neurol. (2007) 109:8–14.

PubMed Abstract | Google Scholar

3. Hollung, SJ , Bakken, IJ , Vik, T , Lydersen, S , Wiik, R , Aaberg, KM, et al. Comorbidities in cerebral palsy: a patient registry study. Dev Med Child Neurol. (2020) 62:97–103. doi: 10.1111/dmcn.14307

PubMed Abstract | CrossRef Full Text | Google Scholar

4. SCPE Collaborative Group . Surveillance of cerebral palsy in Europe: a collaboration of cerebral palsy surveys and registers. Dev Med Child Neurol. (2000) 42:816–24. doi: 10.1017/s0012162200001511

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Szpindel, A , Myers, KA , Ng, P , Dorais, M , Koclas, L , Pigeon, N, et al. Epilepsy in children with cerebral palsy: a data linkage study. Dev Med Child Neurol. (2022) 64:259–65. doi: 10.1111/dmcn.15028

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Duke, RE , Torty, C , Okorie, U , Kim, MJ , Eneli, N , Edadi, U, et al. Pattern of comorbidities in special school-aged children with cerebral palsy in Cross River state, Nigeria. BMC Pediatr. (2021) 21:165. doi: 10.1186/s12887-021-02637-9

CrossRef Full Text | Google Scholar

7. Novak, I , Hines, M , Goldsmith, S , and Barclay, R . Clinical prognostic messages from a systematic review on cerebral palsy. Pediatrics. (2012) 130:e1285–312. doi: 10.1542/peds.2012-0924

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Lin, Q . Definition, diagnostic criteria and classification of cerebral palsy in children. Zhong Hua Er Ke Za Zhi. (1989) 27:162.

Google Scholar

9. Lin, Q . Summary of 2004 National Symposium on cerebral palsy in children. Zhong Hua Er Ke Za Zhi. (2005) 43:261. doi: 10.3760/j.issn:0578-1310.2005.04.006

CrossRef Full Text | Google Scholar

10. Chen, XJ . Definition, classification and diagnostic criteria of cerebral palsy in children. Zhong Hua Wu Li Yi Xue Yu Kang Fu Za Zhi. (2007) 29:309. doi: 10.3760/j:issn:0254-1424.2007.05.026

CrossRef Full Text | Google Scholar

11. Li, XJ , Tang, JL , and Ma, BX . Chinese rehabilitation guideline for cerebral palsy (2015): part I. Zhong Guo Kang Fu Yi Xue Za Zhi. (2015) 30:749–50. doi: 10.3969/j.issn.1001-1242.2015.07.028

CrossRef Full Text | Google Scholar

12. Stang, A . Critical evaluation of the Newcastle-Ottawa scale for the assessment of the quality of nonrandomized studies in meta-analyses. Eur J Epidemiol. (2010) 25:603–5. doi: 10.1007/s10654-010-9491-z

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Yu, R . Clinical analysis of 98 cases of cerebral palsy in children. Qing Dao Yi Yao Wei Sheng. (1997) 1:5–6.

Google Scholar

14. Kwong, KL , Wong, SN , and So, KT . Epilepsy in children with cerebral palsy. Pediatr Neurol. (1998) 19:31–6. doi: 10.1016/S0887-8994(98)00011-3

CrossRef Full Text | Google Scholar

15. Liu, DY , Tang, JL , Ding, ND , and Li, W . CT examination of cerebral palsy and its clinical significance. An Hui Yi Ke Da Xue Xue Bao. (2000) 1:62–3. doi: 10.19405/j.cnki.issn1000-1492.2000.01.026

CrossRef Full Text | Google Scholar

16. Cao, JG , Guo, XZ , He, XR , and Lu, HY . Clinical study of cerebral palsy complications. Zhong Guo Kang Fu Yi Xue Za Zhi. (2001) 1:21–3. doi: 10.3969/j.issn.1001-1242.2001.01.006

CrossRef Full Text | Google Scholar

17. Dong, XL , and Li, CG . Clinical observation of high risk factors and complications of cerebral palsy in children. Hua Xi Yi Xue. (2002) 3:353. doi: 10.3969/j.issn.1002-0179.2002.03.042

CrossRef Full Text | Google Scholar

18. He, XY . Risk factors of cerebral palsy in children. Zhong Guo Kang Fu Li Lun Yu Shi Jian. (2002) 8:48–51. doi: 10.3969/j.issn.1006-9771.2002.08.020

CrossRef Full Text | Google Scholar

19. Huang, Y . Clinical study of cerebral palsy with ocular dysfunction in children. Hai Nan Yi Xue. (2002) 3:8–9. doi: 10.3969/j.issn.1003-6350.2002.03.006

CrossRef Full Text | Google Scholar

20. Gao, L , Meng, Y , Zhao, SY , Zhou, CJ , Yuan, CZ , Wang, YH, et al. Epidemiological investigation of cerebral palsy in children in Henan province. Zhong Guo Shi Yong Er Ke Za Zhi. (2003) 8:464–7. doi: 10.3969/j.issn.1005-2224.2003.08.008

CrossRef Full Text | Google Scholar

21. Hong, SX , Li, S , Wang, TM , Zhao, FL , and Lin, Q . Clinico-epidemiological analysis of cerebral palsy complicated diseases in children. Zhong Hua Er Ke Za Zhi. (2003) 41:468–9. doi: 10.3760/j.issn:0578-1310.2003.06.023

PubMed Abstract | CrossRef Full Text | Google Scholar

22. Wang, SJ , Shi, BP , Yang, H , and Shi, W . High risk factors and neurological dysfunction in children with cerebral palsy: analysis of 265 cases. Zhong Guo Lin Chuang Kang Fu. (2004) 33:7484–5. doi: 10.3321/j.issn:1673-8225.2004.33.076

CrossRef Full Text | Google Scholar

23. Zheng, JY . Analysis of etiology and clinical related factors of 112 children with cerebral palsy. Zhe Jiang Lin Chuang Yi Xue. (2004) 3:170–2. doi: 10.3969/j.issn.1008-7664.2004.03.066

CrossRef Full Text | Google Scholar

24. Yao, BZ , Xia, LP , Ling, W , Wang, JL , and Jiang, D . Clinical analysis of common complications of cerebral palsy in children. Zhong Guo Kang Fu. (2005) 5:31–3. doi: 10.3870/j.issn.1001-2001.2005.05.011

CrossRef Full Text | Google Scholar

25. Lai, YQ , and Chen, JH . Clinical analysis of 25 children with cerebral palsy and epilepsy. Zhong Guo Re Dai Yi Xue. (2005) 9:1901–2. doi: 10.3969/j.issn.1009-9727.2005.09.064

CrossRef Full Text | Google Scholar

26. Liao, JX . Clinical analysis of 55 children with cerebral palsy. Hua Xia Yi Xue. (2005) 1:77–8. doi: 10.3969/j.issn.1672-688X.2010.03.022

CrossRef Full Text | Google Scholar

27. Chan, HS , Lau, PH , Fong, KH , Poon, D , and Lam, CC . Neuroimpairment, activity limitation, and participation restriction among children with cerebral palsy in Hong Kong. Hong Kong Med J. (2005) 11:342–50.

PubMed Abstract | Google Scholar

28. Zheng, H , Wang, XH , Han, TL , and Zou, LP . Analysis of complications in 195 children with cerebral palsy. Zhong Guo Kang Fu Li Lun Yu Shi Jian. (2006) 10:837–8. doi: 10.3969/j.issn.1006-9771.2006.10.005

CrossRef Full Text | Google Scholar

29. Li, HY , Ma, HX , Li, XX , Xu, L , Sang, L , Huang, Y, et al. The relationship between gross motor function and cerebral palsy types and complications in children with cerebral palsy. Zhong Guo Kang Fu Li Lun Yu Shi Jian. (2006) 10:833–4. doi: 10.3969/j.issn.1006-9771.2006.10.003

CrossRef Full Text | Google Scholar

30. Liu, QM , Zhu, R , Guo, X , Li, DY , Cai, HQ , Chen, T, et al. Analysis of audiological characteristics in 118 children with cerebral palsy. Zhong Guo Er Tong Bao Jian. (2006) 4:352–4. doi: 10.3969/j.issn.1008-6579.2006.04.012

CrossRef Full Text | Google Scholar

31. Wang, XK , Wang, GX , Liu, JJ , and Hu, YY . Analysis of strabismus in 220 children with cerebral palsy. Zhong Guo Kang Fu Li Lun Yu Shi Jian. (2006) 7:545–6. doi: 10.3969/j.issn.1005-2224.2006.07.025

CrossRef Full Text | Google Scholar

32. Cao, LH , Pang, BD , Liu, Y , and Dong, Y . Clinical analysis of 500 cases of cerebral palsy. Zhong Guo Fu You Bao Jian. (2007) 5:617–8. doi: 10.3969/j.issn.1001-4411.2007.05.039

CrossRef Full Text | Google Scholar

33. Zhang, XH , Wang, WD , and Ding, G . Clinical analysis of common complications of cerebral palsy in children. Zhong Guo Ji Ceng Yi Yao. (2007) 14:1966–7. doi: 10.3760/cma.j.issn.1008-6706.2007.12.014

CrossRef Full Text | Google Scholar

34. Liu, YM , Zhang Feng Hu, J , and Yao, YZ . Clinical characteristics of 74 children with cerebral palsy. Yi Xue Chuang Xin Yan Jiu. (2007) 4:22–3.

Google Scholar

35. Zhou, QR , Bai, YQ , and Ma, XL . High risk factors and clinical features of 285 cases of children with cerebral palsy. Zhong Guo Kang Fu. (2007) 6:423–4. doi: 10.3870/j.issn.1001-2001.2007.06.025

CrossRef Full Text | Google Scholar

36. Wang, W , Wan, G , and Wang, J . Analysis of the reasons of cerebral palsy children's hearing loss. Lin Chung Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. (2007) 21:450–2. doi: 10.3969/j.issn.1001-1781.2007.10.006

CrossRef Full Text | Google Scholar

37. Huang, Y , Li, RH , and Que, LS . Clinical analysis of 258 cases of cerebral palsy in children. Guang Dong Yi Xue. (2008) 10:1715–6. doi: 10.3969/j.issn.1001-9448.2008.10.056

CrossRef Full Text | Google Scholar

38. Li, R , Liu, XM , Yang, ZX , Deng, XQ , and Wang, JP . Clinical analysis of 35 children with cerebral palsy and epilepsy. Xu Zhou Yi Xue Yuan Xue Bao. (2008) 11:763–4. doi: 10.3969/j.issn.1000-2065.2008.11.028

CrossRef Full Text | Google Scholar

39. Sun, X . Li L, Qin M, Analysis of clinical types, concomitant diseases, complications and treatment of cerebral palsy in children. Zhong Guo You Sheng Yu Yi Chuan Za Zhi. (2008) 7:114–5.

Google Scholar

40. Hou, WM , Yang, HH , Wu, HL , and Zhang, LF . Clinical analysis of 258 cases of cerebral palsy in children. Nao Yu Shen Jing Ji Bing Za Zhi. (2001) 9:295–5. doi: 10.3969/j.issn.1006-351X.2001.05.035

CrossRef Full Text | Google Scholar

41. Liu, Y , and Liu, ZH . Clinical analysis of visual dysfunction in children with cerebral palsy. Zhong Guo Er Tong Bao Jian. (2007) 1:71–2. doi: 10.3969/j.issn.1008-6579.2007.01.031

CrossRef Full Text | Google Scholar

42. Zhang, J , and Han, X . Clinical and EEG characteristics of cerebral palsy with epilepsy. Zhong Guo Shi Yong Yi Kan. (2009):93–4. doi: 10.3760/cma.j.issn.1674-4756.2009.16.059

CrossRef Full Text | Google Scholar

43. Zhou, Z , Ma, B , Du, XB , and Li, HW . Analysis of clinical data of 680 hospitalized children with cerebral palsy. Zhong Guo Fu You Bao Jian. (2009) 24:5011–3.

Google Scholar

44. Li, M . Analysis of strabismus in children with cerebral palsy. Yi Yao Lun Tan Za Zhi. (2009) 30:22–3.

Google Scholar

45. Liu, WY , Hou, YJ , Wong, AM , Lin, PS , Lin, YH , and Chen, CL . Relationships between gross motor functions and health-related quality of life of Taiwanese children with cerebral palsy. Am J Phys Med Rehabil. (2009) 88:473–83. doi: 10.1097/PHM.0b013e3181a0de3a

PubMed Abstract | CrossRef Full Text | Google Scholar

46. Wen, XS , Deng, FP , and Zhang, JM . Clinical and prognosis of cerebral palsy with epilepsy. Zhong Guo Shang Can Yi Xue. (2010) 18:25–7. doi: 10.3969/j.issn.1673-6567.2010.01.015

CrossRef Full Text | Google Scholar

47. Wang, SL , Li, WY , and Dou, TF . Clinical retrospective analysis of cerebral palsy with dysfunction in children. Zhong Hua Quan Ke Yi Xue. (2010) 8:1550–1.

Google Scholar

48. Rui, F . Analysis of clinical types and etiology, auxiliary examination, complications and curative effect of gross motor in children with cerebral palsy. An Hui Yi Ke Da Xue. (2010). doi: 10.7666/d.D128836

CrossRef Full Text | Google Scholar

49. Chu, CH , and Lo, EC . Oral health status of Chinese teenagers with cerebral palsy. Community Dent Health. (2010) 27:222–6.

PubMed Abstract | Google Scholar

50. Zhu, DN , Wang, J , Jia, YJ , Niu, GH , Sun, L , Xiong, HC, et al. Clinical analysis of 322 cases of non-epileptic cerebral palsy. Zhong Guo Dang Dai Er Ke Za Zhi. (2010) 12:933–5. doi: 10.1016/S1876-3804(11)60004-9

CrossRef Full Text | Google Scholar

51. Hou, M , Sun, DR , Shan, RB , Wang, K , Yu, R , Zhao, JH, et al. Comorbidities in patients with cerebral palsy and their relationship with neurologic subtypes and gross motor function classification system levels. Zhong Hua Er Ke Za Zhi. (2010) 48:351–4.

Google Scholar

52. Huang, ST , Hurng, SJ , Liu, HY , Chen, CC , Hu, WC , Tai, YC, et al. The oral health status and treatment needs of institutionalized children with cerebral palsy in Taiwan. J Dent Sci. (2010) 5:75–89. doi: 10.1016/S1991-7902(10)60012-8

CrossRef Full Text | Google Scholar

53. Li, Y . Case analysis of 208 children with cerebral palsy. Ji Lin Da Xue. (2011)

Google Scholar

54. Wang, JY , Zhang, HJ , Tang, QB , Qin, R , Yan, H , Xiong, MW, et al. Correlation analysis of risk factors and complications of cerebral palsy in children. Zhong Guo Bing An. (2011) 12:30–1. doi: 10.3969/j.issn.1672-2566.2011.02.018

CrossRef Full Text | Google Scholar

55. Tang, XR , Huang, LH , Li, HH , Yang, Y , Lin, N , and Zhou, XY . Audiological characteristics and risk factors of children with cerebral palsy and hearing loss. Ting Li Xue Ji Yan Yu Ji Bing Za Zhi. (2011) 19:512–4. doi: 10.3969/j.issn.1006-7299.2011.06.007

CrossRef Full Text | Google Scholar

56. Wu, ZF , Jiang, K , Liu, WH , Zhang, YH , Yang, W , Du, X, et al. Logistic regression analysis of sleep disorders and influencing factors in children with cerebral palsy. Zhong Guo Er Tong Bao Jian. (2011) 19:48–50.

Google Scholar

57. Qin, SH , Ge, JZ , and Chen, JW . Statistical analysis of surgical treatment of 1090 cases of cerebral palsy. Zhong Hua Gu Yu Guan Jie Wai Ke Za Zhi. (2011) 4:374–9. doi: 10.3969/j.issn.1674-1439.2011.05.007

CrossRef Full Text | Google Scholar

58. Huang, XL , Zhang, YH , Liu, WJ , Cai, GL , and Xiao, FF . The clinical data of 273 children with cerebral palsy were retrospectively analyzed. Xian Dai Yi Yuan. (2012) 12:41–4. doi: 10.3969/j.issn.1671-332X.2012.07.017

CrossRef Full Text | Google Scholar

59. Song, ZX . Risk factors and clinical characteristics of cerebral palsy in children. Zheng Zhou Da Xue. (2012)

Google Scholar

60. Zhou, Z , Ma, BX , and Zhang, C . Clinical observation of behavior-related damage in 530 children with cerebral palsy. Zhong Guo Zhong Yi Yao Yuan Cheng Jiao Yu. (2013) 11:43–5. doi: 10.3969/j.issn.1672-2779.2013.03.028

CrossRef Full Text | Google Scholar

61. Xiong, YJ , Liu, J , Zhou, HT , Wang, PQ , Qin, R , and Zhang, HJ . Comparison of types and comorbidities of cerebral palsy between preterm and term infants. Zhong Guo Kang Fu Li Lun Yu Shi Jian. (2012) 18:910–2. doi: 10.3969/j.issn.1006-9771.2012.10.006

CrossRef Full Text | Google Scholar

62. Wu, GL , and Li, HJ . The correlation between clinical characteristics and rehabilitation efficacy of 196 hospitalized children with cerebral palsy. Zhong Guo Fu You Bao Jian. (2012) 27:841–3.

Google Scholar

63. Peng, GL , Hu, SX , Li, YL , Wang, YD , and Cai, SY . Analysis of risk factors for epilepsy in children with cerebral palsy. Zhong Guo Er Tong Bao Jian. (2013) 21:726–8. doi: 10.3969/j.issn.1673-5110.2016.17.0

CrossRef Full Text | Google Scholar

64. Sun, DR , Hou, M , Li, J , Li, Y , and Sun, AJ . Investigation on intelligence level of preSpecial school children with cerebral palsy. Zhong Guo Kang Fu Li Lun Yu Shi Jian. (2013) 19:874–7. doi: 10.3969/j.issn.1006-9771.2013.09.022

CrossRef Full Text | Google Scholar

65. Jia, J . Retrospective analysis of 182 cases of cerebral palsy and discussion on the pathogenesis of traditional Chinese medicine. He Nan Zhong Yi Xue Yuan. (2014)

Google Scholar

66. Guo, JY . Clinical research progress of cerebral palsy comorbidity. Guang Dong Zhong Yi Yao Da Xue. (2013) 21:717–8.

Google Scholar

67. Li, X , and Liu, LW . Huang J, Shi Y, Analysis of complications of cerebral palsy in children. Gui Zhou Yi Yao. (2015) 39:542–3. doi: 10.3969/j.ISSN.1000-744X.2015.06.027

CrossRef Full Text | Google Scholar

68. Wang, S . Effects of different TCM classification, clinical classification and GMFcs classification on the comorbidity of cerebral palsy in children. Liao Ning Zhong Yi Yao Da Xue. (2016)

Google Scholar

69. Lin, BR , Xu, GX , Liu, JR , Yang, J , and Xiang, QY . Visual impairment in children with cerebral palsy. Zhong Guo Kang Fu Yi Xue Za Zhi. (2016) 31:979–83. doi: 10.3969/j.issn.1001-1242.2016.09.010

CrossRef Full Text | Google Scholar

70. Chen, ZH , and Li, X . Correlation analysis of cytomegalovirus infection and hearing impairment in children with cerebral palsy. Chong Qing Yi Xue. (2016) 45:394–6. doi: 10.3969/j.issn.1671-8348.2016.03.034

CrossRef Full Text | Google Scholar

71. Li, XJ , Peng, QH , Tian, YZ , and Wu, QY . Clinical analysis of common visual impairment in children with cerebral palsy. Guo Ji Yan Ke Za Zhi. (2016) 16:392–4. doi: 10.3980/j.issn.1672-5123.2016.2.55

CrossRef Full Text | Google Scholar

72. Guan, LJ , Mu, YP , Wang, XY , Wang, S , Qu, D , Li, RJ, et al. Investigation on the current situation of children with cerebral palsy aged 3-14 years in Liaoning Province. Zhong Guo Yi Shi Jin Xiu Za Zhi. (2017) 40:724–8. doi: 10.3760/cma.j.issn.1673-4904.2017.08.014

CrossRef Full Text | Google Scholar

73. Shu, JJ , and Zhang, XH . Clinical analysis of 34 children with cerebral palsy and hearing impairment. Beng Bu Yi Xue Yuan Xue Bao. (2017) 42:1524–6.

Google Scholar

74. Xie, F , and Tian, S . Analysis of influencing factors of mental retardation in preSpecial school children with cerebral palsy. Xian Dai Yi Qi Yu Yi Liao. (2017) 23:54–5. doi: 10.11876/mimt201704022

CrossRef Full Text | Google Scholar

75. Study on the nutritional and cellular immune status of children with cerebral palsy. Zheng Zhou Da Xue, (2016).

Google Scholar

76. He, P , Chen, G , Wang, Z , Guo, C , and Zheng, X . Children with motor impairment related to cerebral palsy: prevalence, severity and concurrent impairments in China. J Paediatr Child Health. (2017) 53:480–4. doi: 10.1111/jpc.13444

CrossRef Full Text | Google Scholar

77. Ke, HY . Epidemiological study of cerebral palsy in children in Hangzhou, Zhejiang Province. Zhe Jiang Zhong Yi Yao Da Xue. (2018)

Google Scholar

78. Yang, HX . Clinical characteristics and early intervention analysis of hearing impairment in children with cerebral palsy. Zhong Guo Lin Chuang Yi Xue. (2018) 10:53–4. doi: 10.3969/j.issn.1674-7860.2018.12.023

CrossRef Full Text | Google Scholar

79. Chiang, KL , Kuo, FC , Cheng, CY , and Chang, KP . Prevalence and demographic characteristics of comorbid epilepsy in children and adolescents with cerebral palsy: a nationwide population-based study. Childs Nerv Syst. (2019) 35:149–56. doi: 10.1007/s00381-018-3920-9

PubMed Abstract | CrossRef Full Text | Google Scholar

80. Yuan, JY , Wang, YE , Wang, J , Liu, J , Cui, B , Cai, ZJ, et al. Construction and data analysis of registration management and monitoring network for children with cerebral palsy in Henan Province. Zhong Guo Kang Fu Li Lun Yu Shi Jian. (2020) 26:885–91. doi: 10.3969/j.issn.1006-9771.2020.08.003

CrossRef Full Text | Google Scholar

81. Wang, YM , Zhang, MM , and Zhang, L . Related factors of epilepsy in children with cerebral palsy. Yi Yao Lun Tan Za Zhi. (2022) 43:44–6.

Google Scholar

82. Niu, GH , Xie, JY , Zhu, DN , Wang, J , Liu, HX , Wang, X, et al. Risk factors for epilepsy in children with cerebral palsy. Zhong Guo Er Tong Bao Jian Za Zhi. (2022) 30:1241–5. doi: 10.11852/zgetbjzz2022-0646

CrossRef Full Text | Google Scholar

83. Yang, L , Lin, WY , Guri, A , and Xu, MN . Analysis of the characteristics of children with cerebral palsy in Ili prefecture and the influencing factors of rehabilitation status. Chang Chun Zhong Yi Yao Da Xue Xue Bao. (2022) 38:910–4. doi: 10.1007/978-3-030-22009-9_1051

CrossRef Full Text | Google Scholar

84. Lin, N , Sun, XQ , Deng, RZ , Li, YZ , and Lv, F . Analysis of visual impairment characteristics of children and adolescents with cerebral palsy in Kashgar, Xinjiang. Zhong Guo Yan Shi Guang Xue Yu Shi Jue Ke Xue Za Zhi. (2022) 24:263–9.

Google Scholar

85. Zhu, Q , Li, XJ , Huang, YZ , Wang, T , and Yang, F . Characteristics of hearing impairment in children with cerebral palsy and its effect on development. Zhong Guo Kang Fu Yi Xue Za ZHi. (2021) 36:1384–9. doi: 10.3969/j.issn.1001-1242.2021.11.010

CrossRef Full Text | Google Scholar

86. Bax, MCO . Terminology and classification of cerebral palsy. Dev Med Child Neurol. (1964) 6:295–7. doi: 10.1111/j.1469-8749.1964.tb10791.x

PubMed Abstract | CrossRef Full Text | Google Scholar

87. Bax, M , Goldstein, M , Rosenbaum, P , Leviton, A , Paneth, N , Dan, B, et al. Proposed definition and classification of cerebral palsy. Dev Med Child Neurol. (2005) 47:571–6. doi: 10.1017/S001216220500112X

PubMed Abstract | CrossRef Full Text | Google Scholar

88. Koman, LA , Smith, BP , and Shilt, JS . Cerebral palsy. Lancet. (2004) 363:1619–31. doi: 10.1016/S0140-6736(04)16207-7

CrossRef Full Text | Google Scholar

89. Delacy, MJ , and Reid, SM . The Australian cerebral palsy register group profile of associated impairments at age 5 years in Australia by cerebral palsy subtype and gross motor function classification system level for birth years 1996 to 2005. Dev Med Child Neurol. (2016) 58:50–6. doi: 10.1111/dmcn.13012

PubMed Abstract | CrossRef Full Text | Google Scholar

90. Christensen, D , Naarden, V , Braun, K , Doernberg, NS , Maenner, MJ , Arneson, CL, et al. Prevalence of cerebral palsy, co-occurring autism spectrum disorders, and motor functioning - autism and developmental disabilities monitoring network, USA, Dev. Med Child Neurol 2014. (2008) 56:59–65. doi: 10.1111/dmcn.12268

CrossRef Full Text | Google Scholar

91. Delobel-Ayoub, M , Klapouszczak, D , van Bakel, MME , Horridge, K , Sigurdardottir, S , Himmelmann, K, et al. Prevalence and characteristics of autism spectrum disorders in children with cerebral palsy. Dev Med Child Neurol. (2017) 59:738–42. doi: 10.1111/dmcn.13436

PubMed Abstract | CrossRef Full Text | Google Scholar

92. Beckung, E , Hagberg, G , Uldall, P , and Cans, C . Probability of walking in children with cerebral palsy in Europe. Pediatrics. (2008) 121:e187–92. doi: 10.1542/peds.2007-0068

CrossRef Full Text | Google Scholar

93. Zelnik, N , Konopnicki, M , Bennett-Back, O , Castel-Deutsch, T , and Tirosh, E . Risk factors for epilepsy in children with cerebral palsy. Eur J Paediatr Neurol. (2010) 14:67–72. doi: 10.1016/j.ejpn.2009.06.002

CrossRef Full Text | Google Scholar

94. Kakooza-Mwesige, A , Forssberg, H , Eliasson, AC , and Tumwine, JK . Cerebral palsy in children in Kampala, Uganda: clinical subtypes, motor function and co-morbidities. BMC Res Notes. (2015) 8:166. doi: 10.1186/s13104-015-1125-9

CrossRef Full Text | Google Scholar

95. Yang, DT , Li, XJ , Li, QH , and Wang, H . Epidemiological characteristics and early prevention of cerebral palsy in children. Zhong Guo Kang Fu Yi Xue Za Zhi. (2022) 37:1406–11. doi: 10.3969/j.issn.1001-1242.2022.10.021

CrossRef Full Text | Google Scholar

96. Li, XJ . The current situation, challenges and development strategies of cerebral palsy rehabilitation in China. Zhong Guo Kang Fu Yi Xue Za Zhi. (2016) 31:6–8. doi: 10.3969/j.issn.1001-1242.2016.01.002

CrossRef Full Text | Google Scholar

97. Khandaker, G , Muhit, M , Karim, T , Smithers-Sheedy, H , Novak, I , Jones, C, et al. Epidemiology of cerebral palsy in Bangladesh: a population-based surveillance study. Dev Med Child Neurol. (2019) 61:601–9. doi: 10.1111/dmcn.14013

CrossRef Full Text | Google Scholar

98. Arnaud, C , Hollung, S , and Himmelmann, K . Surveillance of cerebral palsy in Europe(SCPE) scientific report 1998–2018. Europe: European Study (2018).

Google Scholar

99. Toyokawa, S , Maeda, E , and Kobayashi, Y . Estimation of the number of children with cerebral palsy using nationwide health insurance claims data in Japan. Dev Med Child Neurol. (2017) 59:317–21. doi: 10.1111/dmcn.13278

PubMed Abstract | CrossRef Full Text | Google Scholar

100. Kim, SW , Jeon, HR , Shin, JC , Youk, T , and Kim, J . Incidence of cerebral palsy in Korea and the effect of socioeconomic status: a population-based Nationwide study. Yonsei Med J. (2018) 59:781–6. doi: 10.3349/ymj.2018.59.6.781

PubMed Abstract | CrossRef Full Text | Google Scholar

101. The Australian Cerebral Palsy Register Report . (2013). Available at: https://www.cerebralpalsy.org.au/timeposts/the-australian-cerebral-palsy-register-report-2013 (Accessed Sep 20, 2014).

Google Scholar

102. Påhlman, M , Gillberg, C , and Himmelmann, K . One-third of special school-aged children with cerebral palsy have neuropsychiatric impairments in a population-based study. Acta Paediatr. (2019) 108:2048–55. doi: 10.1111/apa.14844

PubMed Abstract | CrossRef Full Text | Google Scholar

103. Sellier, E , Uldall, P , Calado, E , Sigurdardottir, S , Torrioli, MG , Platt, MJ, et al. Epilepsy and cerebral palsy: characteristics and trends in children born in 1976-1998. Eur J Paediatr Neurol. (2012) 16:48–55. doi: 10.1016/j.ejpn.2011.10.003

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: cerebral palsy, comorbidities, epilepsy, prevalence, meta-analyzes, China

Citation: Gong C, Liu X, Fang L, Liu A, Lian B, Qi X, Chen S, Li H, Zhao M, Guo J and Zhou S (2023) Prevalence of cerebral palsy comorbidities in China: a systematic review and meta-analysis. Front. Neurol. 14:1233700. doi: 10.3389/fneur.2023.1233700

Received: 02 June 2023; Accepted: 25 August 2023;
Published: 28 September 2023.

Edited by:

Paolo Ragonese, University of Palermo, Italy

Reviewed by:

Mile Vuković, University of Belgrade, Serbia
Kuo-Liang Chiang, Kuang Tien General Hospital, Taiwan

Copyright © 2023 Gong, Liu, Fang, Liu, Lian, Qi, Chen, Li, Zhao, Guo and Zhou. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Jin Guo, Z3VvamluODAwMkAxNjMuY29t; Shaobo Zhou, cy56aG91QGdyZWVud2ljaC5hYy51aw==

These authors share first authorship

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.