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Congenital H-type tracheo-oesophageal fistula: An institutional review of a 10-year period


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Figure 1

X-ray chest and abdomen of one patient showing complete collapse of the left lung, hyperinflation of the right lung and the Chilaiditi sign.
X-ray chest and abdomen of one patient showing complete collapse of the left lung, hyperinflation of the right lung and the Chilaiditi sign.

Figure 2

H-TOF identified in the upper gastrointestinal contrast study.
H-TOF identified in the upper gastrointestinal contrast study.

Figure 3

Bronchoscopy showing H-TOF at the C8–T1 level.
Bronchoscopy showing H-TOF at the C8–T1 level.

Figure 4

Intraoperative image showing the oesophagus and trachea, as well as identification of the fistula.
Intraoperative image showing the oesophagus and trachea, as well as identification of the fistula.

Figure 5

Intraoperative image showing the completed repair.
Intraoperative image showing the completed repair.

Overlapping reasons for previous hospitalisations in all patients with H-TOF

Presenting symptoms No. of patients
Respiratory symptoms Recurrent pneumonias 18
Bouts of coughing and choking after feeds 16
Cyanosis 8
Failure to thrive 14
Abdominal symptoms Abdominal distension 6
Constipation 8

Demographic characteristics of all 18 patients with H-TOF

Total patients with H-TOF 18 out anomalies of total oesophageal (4.2%)
Age at presentation/referral (n=18) <1 year 11
1–3 years 4
3–6 years 2
6–12 years 0
>12 years 1
Gender distribution (n=18) Males 6
Females 12
Number of previous hospitalisations (n=18) 1 8
2 4
3 5
>3 1
Associated anomalies (n=6) ASD 3
VSD and PDA 1
Renal agenesis 1
Radial agenesis 1
eISSN:
2719-535X
Language:
English