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Biomedical subjects

J K Rosales

Publications and source records attributed to J K Rosales.

16 recordsLinked to original sources

Craniosynostosis: an assessment of blood loss and transfusion practices.

Assessment and accurate replacement of blood loss during primary craniosynostosis repair is difficult due to patient size and surgical technique. Eighty-five charts of all patients undergoing primary craniosynostosis repair over a 15-year period were reviewed to determine blood loss and to assess blood transfusion practices both intraoperatively and postoperatively. Blood loss was calculated on the basis of estimated red cell mass (ERCM). Blood transfusion management was considered appropriate if the postoperative or posttransfusion ERCM was within 15 per cent of the preoperative value. Isolated sagittal craniectomy was the most common operation performed (60 per cent). Mean blood loss for sagittal craniectomies was 24 per cent of estimated blood volume (EBV) or approximately 20 ml.kg-1 and for metopic craniectomies 42 per cent of EBV (P less than 0.05). Intraoperatively, 70 per cent of all patients were appropriately managed with respect to blood transfusion. Postoperatively only 29 per cent of patients receiving transfusions were transfused appropriately. At our institution, intraoperative blood transfusion practices are appropriate, but postoperative transfusions are frequently unnecessary.

Blood Transfusion↗

The haemolytic uraemic syndrome and anaesthesia.

The Haemolytic Uraemic Syndrome is the most important cause of renal failure in infancy and childhood. The disease usually consists of a typical triad of renal failure, haemolytic anaemia, thrombocytopenia. It is, however, a multisystem disorder which may also involve the liver as well as cardiovascular, pulmonary and central nervous systems. We present a case of a female child with Haemolytic Uraemic Syndrome who presented for placement of an arteriovenous shunt to facilitate haemodialysis. The clinical presentation and management of the Haemolytic Uraemic Syndrome is discussed. Anaesthetic management of patients with the Haemolytic Uraemic Syndrome is discussed and recommendations are made.

Anesthesia, General↗

Acute epiglottitis: current management.

Two hundred and sixty-one cases of acute epiglottitis treated at the Montreal Children's Hospital between 1951 and 1980 are reviewed. Clinical features of the disease are described. Treatment protocol at a major children's hospital is presented. Statistics related to age, season and sex are analyzed. The authors compare nasotracheal intubation and tracheostomy as primary treatment. Bacteriology and antibiotic treatment are updated.

Acute Disease↗

Experience with parents' presence during anaesthesia induction in children.

Parents of 50 unpremedicated children were invited to be present during induction of anaesthesia in their children. The presence of the parents resulted in a significant decrease in the number of very upset or turbulent children during the pre-induction and induction periods, when compared to a control group that was induced without the parents' participation. There was no difference in the children's behaviour in the recovery room or at home following surgery. Most parents were calm and supportive during induction, and there were no complications related to their presence. It is concluded that for some preschool children, allowing the parents to support an anxious child during anaesthesia induction can be very effective in relieving anxiety, and minimizes the need for premedication.

Anesthesia↗

Foreign bodies in the tracheobronchial tree--a retrospective study of 217 cases.

This is a retrospective study of 217 cases of foreign body in the tracheobronchial tree. The diagnostic techniques, current management, and statistics related to sex, age, yearly incidence, duration of symptoms, nature of foreign body, location, and duration of hospitalization are discussed. The most common complications resulting from a foreign body in the tracheobronchial tree were atelectasis, subglottic stenosis, and pneumonia.

Anesthesia, Inhalation↗

Anaesthetic considerations in patients with muscular dystrophy undergoing spinal fusion and Harrington rod insertion.

Charts of nine patients with Duchenne and one with Becker's muscular dystrophy who had undergone spinal fusion and Harrington rod insertion for scoliosis were reviewed retrospectively. The mean age was 15 years and mean angle of scoliosis was 69 degrees. Preoperative pulmonary function studies showed a restrictive defect with a mean vital capacity of 1.3 +/- 0.69 litres, 35 +/- 20 per cent of predicted value, 33 +/- 20 ml . kg-1 and a mean inspiratory capacity of 0.99 +/- 0.5 litres, 23 +/- 13 ml . kg-1. There were no anaesthetic complications during operation and obstructive cardiomyopathy, hyperpyrexia, hyperkalaemia and rhabdomyolysis were not problems. Succinylcholine was avoided. One patient developed an arrhythmia postoperatively and one patient whose postoperative problems included tracheostomy, pneumonia and sepsis could not be weaned from the ventilator and died 11 weeks after operation. As assessing risk and survival of the operation depends on objective pulmonary function, a vital capacity of at least 20 ml . kg-1 in the range of 30 per cent of predicted volume with an inspiratory capacity of at least 15 ml . kg-1 would appear to be adequate in patients with muscular dystrophy requiring Harrington rod insertion. Other factors including the rapidity of progression of the muscular disease, other respiratory and cardiovascular problems, and disease such as obesity should also be considered.

Adolescent↗

Subcutaneous facial emphysema complicating dental anaesthesia.

A 20 year-old female developed swelling and protrusions of the tongue and marked facial swelling while under general anaesthesia for dental restoration and gigivectomy. The initial diagnosis was angioedema; however x-rays showed marked subcutaneous emphysema more extensive in the perimandibular area with a minimal amount in the neck. There was no evidence of pneumomediastinum or pneumothorax. The iatrogenic subcutaneous emphysema was felt to be due to air-driven dental equipment. Tracheal intubation was maintained for 21 hours to prevent airway obstruction. The patient was treated with oxygen and antibiotics. Subcutaneous emphysema may occur following root canal therapy, tooth extraction, periodontal surgery and operative dentistry, due to the use of air-driven dental equipment. It has the potential to cause obstruction.

Adult↗

Anaesthesia for correction of oesophageal stricture in a patient with recessive epidermolysis bullosa dystrophica: case report.

Epidermolysis bullosa dystrophica is a rare hereditary disorder which presents significant anaesthetic problems. These include malnutrition and anaemia; electrolyte imbalance in severe cases; renal failure and amyloidosis in progressive disease; association with porphyria; a history of steroid therapy. Technical problems associated with the necessity to avoid trauma to the skin and mucous membranes include those related to management of the airway and avoidance of regional techniques. Venepuncture may be difficult and oesophageal stricture increases the risk of regurgitation and aspiration. Anaesthetic management of a patient with epidermolysis bullosa dystrophica with oesophageal stricture presenting for colonic interposition is described and the problems associated with this disease are discussed.

Anesthesia, Endotracheal↗

Acute epiglottitis: current management and review.

Forty-seven patients treated for acute epiglottitis by nasotracheal intubation under general anaesthesia following a preset protocol are presented. The results are compared with 61 cases treated by tracheostomy following induction of general anaesthesia and intubation in the same institution. Both groups were followed clinically, and 13 of the children treated by nasotracheal intubation alone had a follow-up endoscopic examination of the larynx. There was no mortality in either group, but the morbidity was significantly higher in the children who had tracheostomy. Details of the management protocol are presented. Only inhalation anaesthetic agents are recommended and it is concluded that children with acute epiglottitis should always have an artificial airway inserted. Nasotracheal intubation seems to be associated with less morbidity than tracheostomy in experienced hands.

Acute Disease↗

Congenital tracheal diverticulum. A case report.

A six-month-old female with a history of recurrent bronchopulmonary infections was admitted to the Montreal Children's Hospital in severe respiratory distress. Cardiac arrest ensued and although ventilation by mask was always possible during the resuscitation procedure, there was a confusing inability to aerate the lungs after successful intubation. A right-sided tracheal diverticulum was identified at autopsy. It was assumed, in retrospect, that the intubating tube entered and abutted against the wall of the diverticulum, thus obstructing its distal lumen. The embryology, morphology and pathophysiology of congenital tracheal diverticuli are discussed. This rare diagnosis should be entertained when successful intubation leads to ineffectual ventilation

Bronchopneumonia↗