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1.
Indian J Chest Dis Allied Sci ; 52(1): 55-8, 2010.
Article in English | MEDLINE | ID: mdl-20364617

ABSTRACT

We present the case of a 16-year-old female patient who presented with dyspnoea, cough and noisy breathing that progressed further in hospital with the development of stridor and severe respiratory compromise requiring mechanical ventilatory support. Investigations were consistent with a diagnosis of endotracheal tuberculosis with tracheal and bronchial stenosis. Despite adequate anti-tuberculous therapy and ventilation the patient had high airway pressures, low tidal volumes and hypercapnia, which prevented weaning from mechanical ventilation. Balloon dilatation and stenting of the 4.5cm long, 2.3mm diameter stenotic tracheal segment was performed under radiological guidance. The patient was weaned successfully from the ventilator post-procedure. This report illustrates the successful management of an uncommon presentation of a common disease with modern endoscopic therapy.


Subject(s)
Bronchography , Pregnancy Complications, Infectious/therapy , Respiration, Artificial , Stents , Tracheal Stenosis/therapy , Tuberculosis/complications , Adolescent , Bronchial Diseases/etiology , Bronchial Diseases/therapy , Constriction, Pathologic , Female , Humans , Intubation, Intratracheal , Pregnancy , Tracheal Diseases/complications , Tracheal Stenosis/etiology
2.
Anaesth Intensive Care ; 36(3): 339-50, 2008 May.
Article in English | MEDLINE | ID: mdl-18564794

ABSTRACT

Organophosphate poisoning is common in developing countries. The morbidity and mortality with organophosphate poisoning is relatively high despite the use of atropine as specific antidotal therapy and oximes to reactivate acetylcholinesterase. Several adjunct and alternative therapies have been explored in animal and human studies. We reviewed the literature to ascertain if there was evidence of benefit of such therapies. Adjunct and alternative therapies included treatments to reduce poison absorption by topical application of creams, enhance toxin elimination by haemoperfusion or bioremediation and neutralise the poison by scavenging free organophosphate with cholinesterase-rich human plasma. In addition, magnesium, clonidine, diazepam, N-acetyl cysteine and adenosine receptor agonists have also been used to counteract poison effects. Detailed assessment was limited by the paucity of trials on adjunct/alternative therapies. The limited evidence from the review process suggested potential benefit from the use of human plasma infusion, early initiation of haemoperfusion and intravenous magnesium, in addition to standard therapy with atropine and pralidoxime. There appeared to be no additional benefit with alkalinisation or use of glycopyrrolate instead of atropine in human trials. Diazepam administration has been advocated by military authorities if symptoms developed following exposure to organophosphate. Bioremediation, clonidine, N-acetyl cysteine and adenosine receptor agonists have been evaluated only in animal models. The impact of adjunct and alternate therapies on outcomes in human poisoning needs to be further explored before implementation as standard treatment.


Subject(s)
Antidotes/therapeutic use , Organophosphate Poisoning , Oximes/therapeutic use , Poisoning/drug therapy , Animals , Cholinergic Antagonists/therapeutic use , Cholinesterase Reactivators/therapeutic use , Humans , Organophosphorus Compounds/antagonists & inhibitors , Organophosphorus Compounds/pharmacokinetics
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