Anaesthetic considerations in an orphan disease with skeletal anomalies
نویسندگان
چکیده
منابع مشابه
Anaesthetic considerations in an orphan disease with skeletal anomalies
The patient had frontal bossing, micrognathia, depressed nasal bridge, high‐arched palate, multiple impacted supernumerary teeth [Figure 1], barrel‐shaped chest, cup‐shaped distal phalanges and down‐curving nails. Mouth opening was adequate but Mallampati airway grade (MP) was indeterminate. Height (135 cm) was less than 3rd percentile and weight (30 kg) was 10th percentile for her age. She had...
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Incidence of congenital heart disease (CHD) is about 0.8%1 and most of these CHD children (80%) survive to adulthood in developed countries due to early diagnosis and intervention along with improved surgical and anaesthetic techniques. But the situation is different in most of the third world countries, where 90% of these children receive suboptimal or no care2. These patients commonly admitte...
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Cystic hygroma (CH) is a benign tumour composed of large lymph containing cysts. Lymphangiomas of head and neck region frequently present challenges to the anaesthesiologists due to extension in the neck, difficult airway and postoperative complications. We hereby describe the anaesthetic management of a one and a half month old baby presenting with large cystic hygroma on the left side of neck...
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and sometimes non-cooperative patients. A nasogastric tube is often not well tolerated. Whereas intravenous (i.v.) catheterization is considered as invasive, the subcutaneous space is considered as a useful route for fluid diffusion or infusion. Compromised peripheral venous vascularization can be another indication for hypodermoclysis as an alternative to central venous access. Evidence-based ...
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ژورنال
عنوان ژورنال: Indian Journal of Anaesthesia
سال: 2016
ISSN: 0019-5049
DOI: 10.4103/0019-5049.191707