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ISSN 2348 – 0319 International Journal of Innovative and Applied Research (2015), Volume 3, Issue (1): 42- 46
42
Journal home page: http://www.journalijiar.com INTERNATIONAL JOURNAL OF INNOVATIVE AND APPLIED RESEARCH
RESEARCH ARTICLE
Incidence and Patterns of Clubfoot Deformity at Gajra Raja Medical College, Gwalior
*Dr. Ashish Sirsikar1 and Dr. Nitin Kiradiya
2
1. Assistant Professor, Department of Orthopaedics, Gajra Raja Medical College, Gwalior (M. P.).
2. Senior Resident, Department of Orthopaedics, Gajra Raja Medical College, Gwalior (M. P.).
……………………………………………………………………………………………………… Abstract:
Background: Congenital Talipes Equinovarus (CTEV), also referred to as Clubfoot, occurs in 1 in 1000 live births
and is one of the most common birth defects involving the musculoskeletal system. The objective of this study was
to evaluate the incidence and pattern of presentation of this deformity at Gajra Raja Medical College, Gwalior.
Methods: A prospective study was carried out from June 2011 to March 2014 of all the clubfoot patients, presenting
at the clubfoot clinic in the Department of Orthopaedics at Gajra Raja Medical College, Gwalior. The patterns of
clubfoot with respect to gender, laterality, presence of other congenital anomalies and maternal obstetric history
were recorded.
Results: The total number of patients with clubfoot deformity recorded was 98, and the estimated incidence of
clubfoot in our study is 1 in 1210 live births, or 0.8 per 1000 live births. The male to female sex ratio was 1.7: 1.
Fifty seven (58 %) of the patients had bilateral clubfeet. Among the rest of 41 patients with unilateral affection, the
left side was involved in 22 (23 %) of the patients. Nineteen (19%) patients had other associated congenital
anomalies. Arthrogryposis Multiplex Congenita and Neural tube defects were the commonest anomalies associated
with clubfeet.
Interpretation: There is requirement of more studies in order to establish the true incidence and pattern of
presentation of this deformity in our region.
Key Words: Clubfoot, congenital anomalies, CTEV.
Abbreviation
CTEV: Congenital Talipes Equinovarus.
………………………………………………………………………………………………………
Introduction Congenital Talipes Equinovarus (CTEV), also referred to as clubfoot, occurs in 1 in 1000 live births
1 and is
one of the most common birth defects involving the musculoskeletal system. It is recognizable at birth and is readily
distinguishable from positional foot anomalies because the foot is rigid and does not correct with passive movement.
In contrast to metatarsus adductus and calcaneovalgus foot anomalies, both positional in nature, there is less
evidence to suggest that CTEV results from intrauterine crowding or positional effects1.
CTEV can present in 2 forms. In severe syndromic CTEV, other malformations are present such as spina
bifida, spinal muscular atrophy, sacral agenesis, or arthrogryposis. Associated features may also include joint laxity,
congenital dislocation of the hip, tibial torsion, ray anomalies of the foot, and the absence of some tarsal bones. In
previous series the prevalence of associated anomalies in patients with CTEV varied from 11 to 48%, depending on
the population and method of study1,2,3
.
In idiopathic CTEV—the more common form—the anomaly is isolated or may be associated with minor
malformations. There may be a family history of foot anomalies.
The purpose of our study was to determine the overall incidence of Clubfoot deformity and its pattern of
presentation with respect to gender, laterality, presence of other congenital anomalies and maternal obstetric history.
Material & Methods All the patients of Clubfoot presenting at the clubfoot clinic in the Department of Orthopaedics at Gajra
Raja Medical College, Gwalior from June 2011 to March 2014 were prospectively enrolled in this study.
Institutional Review Board approval was obtained for this research and informed consent was obtained from parents.
A Postgraduate resident recorded the details of the patients on the Clubfoot Proforma. The Case information
ISSN 2348 – 0319 International Journal of Innovative and Applied Research (2015), Volume 3, Issue (1): 42- 46
43
included age at presentation, gender, laterality, other associated congenital anomalies and maternal obstetric history,
which included birth order, mode of delivery, gestational age.
Results Incidence
The number of patients with Clubfoot deformity presenting to us during the study period was 98. The total
number of live births during this study period was 1,18,654. This gave an estimated incidence of clubfoot of 1 in
1210 live births, or 0.8 per 1000 live births.
Patterns of Clubfeet deformity
Out of the total 98 patients, 62 (63 %) of patients with clubfoot were male and 36 (37 %) were female
(Male Female ratio= 1.7: 1). 57 (58 %) out of the total 98 patients, had bilateral clubfeet. Among the rest of 41 (42
%) patients with unilateral affection, the right side was involved in 19 (19 %) and left side in 22 (23 %) of the
patients.
Associated Congenital anomaly
79 (81 %) patients had primary idiopathic clubfoot, whereas the remaining 19 (19 %) patients had clubfoot
deformity associated with other congenital anomalies. Arthrogryposis Multiplex Congenita and Neural tube defects
were the commonest anomalies associated with clubfeet.
Table 1: Demographic data of patients with idiopathic and non-idiopathic CTEV
Idiopathic Non-idiopathic
Number of Patients (%) 79 (81) 19 (19)
Male / Female 56/23 6/13
Bilateral (%) 45/79 (57) 12/19 (63)
Unilateral- Right (%) 15/79 (19) 4/19 (21)
Unilateral- Left (%) 19/79 (24) 3/19 (16)
Table 2: Presence of Associated Congenital Anomalies
S. No. Associated Congenital Anomaly Frequency
1. Arthrogryposis Multiplex Congenita 5
2. Neural Tube Defect 4
3. Bilateral Constriction Bands of Leg & Syndactyly 3
4. Syndactyly 1
5. Maldeveloped Feet & 4 toes on Right Foot 1
6. Hexadactyly All 4 limbs 1
7. Genu Recurvatum 1
8. Tongue Tie Bilateral Webbing of Fingers 1
9. Imperforate Anus 1
10. Cleft Palate & Facial Nerve Palsy 1
Figure I. Non- idiopathic CTEV associated with Arthrogryposis Multiplex Congenita
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Figure II. Non- idiopathic CTEV associated with Neural Tube Defect
Figure III. Non- idiopathic CTEV associated with Constriction Band Syndrome
Birth order
The birth order of the child is shown below in the chart.
Mode of Delivery
Among the 98 patients with clubfeet, 87 were normal delivery, 11 delivered by Caesarean Section.
0
5
10
15
20
25
30
35
40
45
Gravida 1 Gravida 2 Gravida 3 Gravida 4 Gravida 5 Gravida 6
4238
13
31 1
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45
Gestation Period
5 out of 98 patients with clubfeet were preterm, 2 had idiopathic clubfeet and 3 had clubfeet associated with
other congenital anomalies. 92 children with clubfeet were born at term, whereas one patient was post-term and
associated with microcephalus & autism.
Discussion The overall incidence of clubfeet deformity in our study is 0.8 per 1000 live births. Studies among black
South Africans showed that the incidence of congenital clubfoot is between 1.5 per 1000 and 3.5 per 1000 live
births4,5
. Amongst Caucasian populations the incidence of congenital clubfoot is between 0.64 and 2.5 per 1000 live
births6,7
.
The deformity was most often bilateral, and if unilateral, more often involved the left side. Previous studies
have found the prepondance of right over left side (Grunett et al 20088, Dobbs et al 2009
9, Parker et al 2009
10).
Moreover, our study confirmed that boys are more frequently involved as compared to girls, which also supports
previous studies (Byron-Scott et al 200511
, Carey et al 200512
, Dickinson et al 200813
).
Patients with clubfoot associated with other congenital anomalies comprise for 19% of all cases. The most
common congenital anomaly associated with clubfoot deformity includes arthrogryposis and neural tube defects.
Conclusion Although the vast majority of patients with CTEV are idiopathic, in our tertiary clinic, 19% were non-idiopathic.
Non-idiopathic CTEV is associated with a long list of associated congenital anomalies, majority of which include
arthrogryposis multiplex congenital, neural tube defect and constriction band syndrome. More studies in order to
establish the true incidence and pattern of presentation of this deformity in our region is recommended.
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