Congenital Muscular Torticollis-Current Understanding and Perinatal Risk Factors: A Retrospective Analysis

被引:2
|
作者
Plominski, Janusz [1 ,2 ]
Olesinska, Jolanta [3 ,4 ]
Kamelska-Sadowska, Anna Malwina [5 ,6 ]
Nowakowski, Jacek Jozef [7 ]
Zaborowska-Sapeta, Katarzyna [5 ,6 ]
机构
[1] Prof Adam Gruca Independent Publ Clin Hosp CMKP, PL-05400 Otwock, Poland
[2] Ctr Postgrad Med Educ, PL-01813 Warsaw, Poland
[3] Coll Rehabil, Dept Physiotherapy, PL-01234 Warsaw, Poland
[4] Prof Jan Bogdanowicz Childrens Hosp, Dept Physiotherapy, PL-03924 Warsaw, Poland
[5] Univ Warmia & Mazury, Sch Med, Dept Rehabil & Orthoped, Coll Med, PL-10719 Olsztyn, Poland
[6] Reg Specialised Childrens Hosp, PL-10561 Olsztyn, Poland
[7] Univ Warmia & Mazury, Dept Ecol & Environm Protect, PL-10719 Olsztyn, Poland
关键词
torticollis; sternocleidomastoid muscle; children; perinatal risk factors; STERNOCLEIDOMASTOID MUSCLE; INFANTS; ULTRASONOGRAPHY; FIBROSIS; CHILDREN;
D O I
10.3390/healthcare12010013
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Introduction: Congenital muscular torticollis (CMT) is an asymmetrical head position resulting from structural changes in the sternocleidomastoid (SCM) muscle that occurs early during a child's development or due to perinatal trauma. Children with CMT exhibit a marked imbalance in tension between the SCMs. In a typical clinical picture, an ultrasound scan is performed to reveal characteristic lesions, such as tissue fibrosis or post-traumatic changes. An early diagnosis of CMT in newborns and the implementation of treatment offer the chance of a complete resolution. Torticollis treatment aims to restore the SCM's normal function. Surgical treatment is performed when conservative methods fail to improve the patient's condition. The indications that surgery is needed include a marked shortening of the SCM, persistent fibrosis in the muscle, constant head and facial asymmetry, and rotation or lateral flexion in the cervical spine restricted by >15(degrees). Of all the newborn and infant anomalies, congenital torticollis is the third most common after hip dysplasia and equinovarus deformities. Some authors demonstrate that torticollis coexists with hip dysplasia. Aim: The aim of this study was to collect data on infants referred to paediatric rehabilitation and to identify the risk factors associated with CMT in this group of patients, as well as to assess demographic and clinical characteristics concerning risk factors. Materials and methods: The target population for this retrospective study consisted of 111 infants aged 0 to 5 months born in Poland and diagnosed with and undergoing treatment due to CMT. The following were determined: the relationship between the side of the CMT location and the type of delivery (caesarean section vs. vaginal), the relationship between the body weight at birth and the side of the CMT location, the relationship between the extent of SCM thickening and the type of delivery, and the incidence of CMT depending on the order of delivery. Results and conclusions: The data revealed that CMT is less common in female infants (n = 51, 46%) compared to male (n = 61, 54%) infants, in whom a greater birth weight was reported (p < 005). Seventy-six percent (76%) of the paediatric patients with CMT were the offspring of primipara mothers. More often, children born via vaginal delivery had left-sided torticollis with a more significant broadening of the SCM, as shown on ultrasound scans, than right-sided torticollis. Theories of torticollis development pathophysiology should be deepened and systematised, and further research is needed.
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页数:14
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