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

• Published in: Healthcare (Basel) Vol. 12; no. 1; p. 13
• Main Authors: Płomiński, Janusz, Olesińska, Jolanta, Kamelska-Sadowska, Anna Malwina, Nowakowski, Jacek Józef, Zaborowska-Sapeta, Katarzyna
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 20-12-2023; MDPI
• Subjects: Age; Amniotic fluid; Asymmetry; Babies; Birth defects; Care and treatment; Childbirth; children; Children & youth; Congenital diseases; Diagnosis; Genetic disorders; Health aspects; Hip dislocation; Infants; Ischemia; Medical research; Medicine, Experimental; Newborn babies; perinatal risk factors; Pregnancy; Prenatal development; Risk factors; sternocleidomastoid muscle; Torticollis; Trauma; Ultrasonic imaging; Poland; perinatal risk factors; children; torticollis; sternocleidomastoid muscle
• ISSN: 2227-9032; 2227-9032
• DOI: 10.3390/healthcare12010013

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°. 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.
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.
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.
The data revealed that CMT is less common in female infants (
= 51, 46%) compared to male (
= 61, 54%) infants, in whom a greater birth weight was reported (
< 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.