ABSTRACT
Introduction:
It has been reported that serial casting is an effective treatment method in early-onset idiopathic scoliosis, but its role in congenital scoliosis has not been clarified. This study aimed to evaluate the efficacy of serial castings in young children with congenital scoliosis and to discuss whether serial casting can be used effectively to delay surgical procedures.
Methods:
Patients between the ages 2 and 5 years with congenital scoliosis who had a Cobb angle above 25 degrees and had not undergone any surgical treatment between 2016 and 2019 were included in this study. Cast changes were performed at 3-month intervals. Radiographic evaluations were performed on posteroanterior and lateral orthoroentgenograms in the cast on the first day after the cast application and at the last follow-up visit.
Results:
A total of 10 patients (6 female, 4 male) with long congenital curves with mixed type formation or segmentation anomalies were included in the study. The mean number of cast applications was 4 for each patient (range: 3 to 6). The initial casting age was 3.2 (range: 2-4 years). The mean follow-up period was 15.1 months (range: 12-23 months). The mean precasting Cobb angle was 61.9±13.7 degrees (range: 38-76 degrees), which was reduced to 43.4±12.8 degrees (range: 24-58 degrees) after the initial casting, and it was 48.4±12.6 degrees (range: 28-63 degrees) at the latest follow-up. The mean precasting T1-T12 length was 223±27.3 mm (range: 176-271 mm). After the initial cast application, T1-T12 length was 241.8±27.5 mm (range: 189-285 mm). At the last follow-up, the average T1-T12 length was 254±27.6 mm (198, 290 mm).
Conclusion:
In early-onset scoliosis, even when growth-friendly methods were occupied, spontaneous fusion may develop. Serial casting under anesthesia allows for lengthening by controlling the progression of the deformity. This method can provide more time for the patient to delay surgical interventions.
Introduction
Treatment of progressive scoliosis of the immature spine presents several challenges. It has been shown that the rapid growth period of the thoracic spine is from birth to the age of 5 years, with a 50% increase in the spine length during this period (1). If left untreated during this period, progressive curves may result in significant thoracic deformity, resulting in life-threatening cardiopulmonary pathologies (2).
It is accepted in long-term studies that, fusion applied before five-years of age may have adverse effects on pulmonary function via disrupting the growth process of the thoracic cage, thus decreased thoracic spinal height is correlated with reduced forced vital capacity and is associated with low quality of life (3). Therefore, growth-friendly methods have gained popularity in most early-onset progressive scoliosis types, and in congenital deformities to control the progression of curves and to preserve natural growth (4-6). Various growing instruments have been developed which maintain spine alignment while allowing the spine and thoracic cage to grow. For this purpose, conventional and magnetically controlled growing rods and vertical expandable prosthetic titanium rib aim to delay definitive fusion surgery (7). In these methods, complications such as rod fracture, infection, crankshaft phenomenon, rigid and incompatible thoracic wall formation can be observed (7,8). Therefore, non-invasive procedures like serial casting are accepted as an alternative treatment modality in early-onset scoliosis (2). In the literature, it has been shown that serial casting can be used to delay surgery by preventing risks and complications associated with recurrent surgical procedures in growth-friendly methods. Despite the current evidence confirming that the initiation of casting at an early age is an important factor in the success of the treatment, the effect of the curvature etiology on treatment outcomes is not clearly defined in the literature (2).
This study aimed to evaluate the efficacy of serial castings in young children with congenital scoliosis and to discuss whether serial casting can be used effectively to delay surgical procedures.
Methods
Ten patients with congenital scoliosis who underwent serial casting in a single center between 2016 and 2019 were included in the study. Patients under the age of 5-years with a Cobb angle above 25 degrees with congenital scoliosis (falls into three categories; failure of formation, failure of segmentation and mixed), who had not undergone any surgical treatment, and who were followed for at least 12 months were included in the study. A minimum number of three casts were applied to all patients. Patients whose families refused casting treatment and who had a progression of the curvature more than 10 degrees in the course of casting were excluded from the study. Written consent was obtained from the parents of all patients.
Cast application was performed under general anesthesia on a modified Cotrel frame. Mehta modification of the Cotrel-Morel technique was used in cast application (9). The apex points of the kyphotic deformities were well padded to prevent skin lesions. The deformity is gently corrected by traction, derotation, and lateral pressure. The cast is molded over the rib hump to flatten it. An anterior window is made to relieve the chest and abdomen while preventing the lower ribs from rotating. No activity restriction was performed in patients. Casts were changed every 12 weeks. Radiographic evaluations were performed on posteroanterior and lateral orthoroentgenograms in the cast on the first day after the cast application and at the last follow-up visit.
The obtained data included age, Cobb angles of congenital coronal curves (angle formed by the intersection of two lines, one parallel to the endplate of the superior end vertebra and the other parallel to the endplate of the inferior end vertebra), sagittal deformity magnitude, coronal balance (measuring the distance between the central sacral vertical line and the plumb line), sagittal balance (measuring the distance between the posterosuperior aspect of the S1 vertebral body and the plumb line), thoracic height (The T1-T12 height was measured on full-length posteroanterior radiographs of the spine using the vertical distance from the middle of), number of cast applications, follow-up time and complications.
The study was approved by Metin Sabancı Baltalimanı Bone Diseases Training and Research Hospital Ethics Committee (decision no: 254, date: 12.11.2018).
Statistical Analysis
SPSS 15.0 for Windows (IBM Corporation, Chicago, IL, USA) was used for statistical analyses. The descriptive statistic was expressed as numbers and percentages for categorical variables. The mean and the standard deviation were used as a numerical variable for normally distributed data. The mean of T1-S1 length, Cobb angle, Kyphosis angle, coronal and sagittal balance at the preoperative period, early postoperative period, and the late postoperative period were analyzed with Repeated measures ANOVA with a Greenhouse-Geisser correction. Post hoc tests using Bonferroni correction determined differences among preoperative, early postoperative, or late postoperative period. A p value of <0.05 was considered to indicate significance. Inter-observer agreement was assessed using the “κ” statistical test. A kappa value between 0.8 and 1 was considered a perfect agreement.
Results
A total of 10 patients (6 female, 4 male) with long congenital curves with mixed type formation or segmentation anomalies were included in the study. The mean number of cast applications was 4 for each patient (range: 3 to 6). The initial casting age was 3.2 (range: 2-4 years). The mean follow-up period was 15.1 months (range: 12-23 months). In two patients, the decision to perform a growing rod was made. In one of them, curve progression exceeded more than 10 degrees within the cast, and for the other, the parents of the patient refused further cast application.
The mean pre-casting Cobb angle was 61.9±13.7 degrees (range: 38 to 76 degrees), which was reduced to 43.4±12.8 degrees (range: 24 to 58 degrees) after the initial casting, and it was 48.4±12.6 degrees (range: 28-63 degrees) at the latest follow-up. When the pre-casting and after the initial casting values have been compared, we found that there was a statistically significant improvement (p=0.001), but statistical significance was impaired when initial correction magnitude and last follow up values were compared (p=0.275). The mean pre-casting T1-T12 length was 223±27.3 mm (range: 176-271 mm). After the initial cast application, T1-T12 length was 241.8±27.5 mm (range: 189-285). At the last follow-up, the mean T1-T12 length was found to be 254±27.6 mm (range: 198-290 mm). When the pre-casting, initial cast application, and last follow up values were compared, we found that statistically significant elongation was achieved (p=0.001).
The mean pre-casting kyphosis angle was 28.8±8.2 degrees (range: 20-45 degrees). It was reduced to 25.2±5.1 degrees (range: 15-32 degrees) after the initial cast application and was measured as 26.7±6.2 degrees (range: 17-38 degrees) at the last follow-up. We observed no significant change in the kyphosis angle (p=0.242).
The mean pre-casting after initial casting and last follow-up lumbar lordosis angles were 37.1±11.4, 34.3±12.2, and 34.8±12.5, respectively (p=0.799). We did not observe a statistically significant improvement in coronal and sagittal balance values (p=0.622 and p=0.066) (Table 1).
None of the patients had a neurological deficit or thoracic wall deformity. Two patients had mild skin irritation and improved with local wound care. In one patient, the cast treatment was temporarily terminated due to pneumonia and continued after the infection was resolved. The treatment of patients continues. Curvature was kept under control during one-year period, and no surgical treatment was required (Figure 1). Only in one patient, scoliosis progressed, and cast treatment was discontinued.
Discussion
Congenital spinal deformities have a broad spectrum ranging from mild asymptomatic curves to deformities that are concomitant with neurological and cardiopulmonary pathologies. The course of the deformity varies according to the localization and type of malformation and the age of the patient (10). Although the studies are limited, patients with congenital anomalies have been reported to have limited lung capacity, which can cause severe disability and even death if left untreated (5). Conservative treatment methods in congenital scoliosis are thought to be ineffective due to the rigid nature of the deformity but may have a corrective effect only on compensatory curves. Therefore, it has been reported that surgical treatment should be preferred if there is a high risk of progression in this patient group (5,11). In selected patients with congenital scoliosis, convex hemiepiphysiodesis has been used as a growth-friendly surgical method for many years, but it has been shown that hemiepiphysiodesis may have unpredictable outcomes (12). However, hemiepiphysiodesis is still an invasive procedure regardless of technique and may not always result in the resolution of the deformity.
Various methods have been described for the cast application in scoliosis. The casting was first proposed 50 years ago by Cotrel and Morel for the treatment of scoliosis. Cotrel and Morel’s EDF (elongation, derotation, flexion) correction technique is a frequently used conservative treatment modality (13). Cotrel and Morel stated that the technique is suitable not only to prevent progression but also to regress structural vertebral and thoracic deformities (13). One of the most commonly used methods is the Risser casting method applied from three points (14). This technique cannot adequately intervene in rotational abnormalities and can cause significant rib deformations and chest constriction, especially in younger children with the flexible bone (15). Due to the problems that emerged in growth-friendly surgical treatment modalities, serial casting treatment has gained popularity once more, and it has been shown that serial casting can provide successful results in idiopathic and non-idiopathic deformities (2,16). Fletcher et al. (16) reported that spinal growth was sustained during the casting treatment in 12 idiopathic and 17 non-idiopathic scoliosis patients, and 39 months delay for the surgery had been achieved and 72.4% of the patients avoided growing rod surgery. In their series of 39 patients including 17 non-idiopathic scoliosis patients, Baulesh et al. (2) concluded that non-idiopathic deformities had less resolution of the deformity when compared to idiopathic deformities, on the other hand, the thoracic growth was sustained and the initial surgical procedure for the growing rod was delayed by an average of two years. In our study, the mean pre-casting T1-S1 length was 223±27.3 mm (range: 176-271 mm). After initial casting, T1-S1 lengths were 241.8±27.5 mm (range: 189-285). At the last follow-up, the mean T1-S1 length was measured to be 254±27.6 mm (range: 198-290 mm). When we compared pre-casting, initial casting, and last follow-up values, we concluded that the growth was similar to other studies in the literature and was statistically significant (p<0.05).
In their study of 16 early-onset scoliosis (EOS) patients (8 idiopathic, 8 syndromic), Waldron et al. (17) stated that the Cobb angle decreased from 73 degrees to 45 degrees, and progression to surgery was observed in 31% of the patients and complications due to casting in 19%. In their study, Demirkiran et al. (5) stated that the correction was obtained after the first cast application and was maintained during the treatment period, and the majority of the correction was provided during the first cast application, and the magnitude of the deformity correction was similar to the growing rod application. In our study, Cobb angle was 61.9±13.7 degrees (range: 38-76 degrees), which was corrected to 43.4±12.8 degrees (range: 24-58 degrees) after the initial casting, and it was 48.4±12.6 degrees (range: 28-63 degrees) at the latest follow-up. When we compared pre-casting and early post-casting values, we found that there was a statistically significant improvement (p<0.05), but we found that statistical significance was impaired when we compared initial casting and last follow-up values (p=0.275). Although the improvement achieved with the first casting was somewhat lost in the subsequent casts, the present correction could be preserved and saved us time for surgical treatment. In only one patient, due to the progression of the curvature, we switched to a growing rod, and we did not encounter any severe complications.
A potential disadvantage of the casting treatment is that it may have adverse effects on pulmonary function due to the advanced deformity of the rib cage, especially in patients with congenital scoliosis. Despite the deterioration of pulmonary parameters after the initial cast application, it was reported in the literature that it returned to the baseline values after the second cast application (18). In our study, we did not evaluate pulmonary functions before and after cast applications, but in our patient group, cast application was well tolerated in terms of pulmonary functions, and we did not encounter any problems. In one patient, the cast treatment was temporarily terminated due to pneumonia and continued after the infection had resolved. Two patients had mild skin irritation due to the insufficiency of skin and subcutaneous tissues. Between the cast changes, one week of rest and local care was given, and the skin irritation was resolved without any problems.
Although modern cast application requires general endotracheal anesthesia, it is far from surgical trauma, infection risk, and neurological complications that surgical treatment methods may cause. With cast treatment, the goal is to delay the surgery until sufficient vertebral growth has been achieved for satisfactory respiratory function (4). The purpose of treatment in EOS is to control the progression of deformity to delay or eliminate the need for spinal fusion without compromising normal spinal, thoracic, and pulmonary growth (6). Serial casting is an effective growth protection technique and is less invasive than the growth-friendly surgical techniques described. We estimate that most of the children in this study will be followed up with a growth-preserving surgical method following serial cast treatment. Regardless of the severity of the etiology of the deformity, we assume that serial cast treatment should be considered as an alternative method to delay growth-sparing surgery. The limitation of our study is the low number of patients and incomplete cast treatments.
Conclusion
We concluded that serial casting treatment is an effective alternative for delaying surgical interventions and avoiding surgical risks in congenital scoliosis patients.