Paediatric injection medialisation laryngoplasty: Recent Great Ormond Street Hospital experience.

Introduction: Unilateral vocal fold paresis may significantly impair the vocal quality and laryngeal competence of a child. Relatively little literature relates to injection medialisation laryngoplasty (IML) in children and previous reports have involved small numbers of heterogenous cases.

Methods: A retrospective review was conducted of paediatric patients managed by our multidisciplinary specialist voice clinic undergoing IML for unilateral vocal fold paresis.

A study of laryngeal mask inflation. Pressures exerted on the pharynx.

Laryngeal mask airway cuff inflation pressures were measured when inflated with the same volume of gas firstly in free space and then in position in the pharynx. A large difference in these pressures was observed and this was related to pharyngeal mucosal perfusion pressure. This study shows that it may be easy to produce pressures on the pharyngeal mucosa in excess of the critical perfusion pressure and thus potentiate mucosal trauma.

Bleeding time: is it a useful clinical tool?

The bleeding times of five volunteers were assessed individually by each of 12 observers. The reliability of the measurements obtained was examined by comparing statistically the variability between subjects and between observers. This variability was found to be similar for both groups.

Identification of epidural space by drip method.

In 100 pregnant women, identification of the epidural space was performed by a modified drip method. A saline infusion was prepared, leaving the distal 40 cm of infusion tubing full of air, and then attached to the hub of a Tuohy needle. Accurate identification of the epidural space was accomplished in less than one minute in 95% of cases.

The effect of micropore filters on the aspiration test in epidural analgesia.

Continuous epidural analgesia may be complicated by intravascular or subarachnoid injection of local analgesic, with disastrous consequences. One of the techniques described to prevent these complications is the aspiration test. It is the current standard of practice to employ a micropore bacterial filter for epidural infusions.

Anaesthetic management of caesarean section for a mother with pre-eclampsia, the Klippel-Feil syndrome and congenital hydrocephalus.

A mother with the Klippel-Feil syndrome, congenital hydrocephalus and increased intracranial pressure presented for delivery by Caesarean section at 33 weeks because of pre-eclampsia. Anaesthetic management comprised awake intubation using the fibreoptic bronchoscope, followed by induction and maintenance of general anaesthesia for the delivery of a live male infant. This case report describes the problems arising under these circumstances and the relative merits of different anaesthetic techniques.

Maternal inspired oxygen concentration and neonatal status for caesarean section under general anaesthesia. Comparison of effects of 33% or 50% oxygen in nitrous oxide.

The relationship between maternal FIO2 and umbilical venous PO2, PCO2, pH and neonatal Apgar and TSR (time to sustained respiration) scores was studied in 35 patients undergoing Caesarean section under general anaesthesia. Patients were allocated randomly to breathe an FIO2 of either 0.5 or 0.

Fentanyl-droperidol supplementation of rapid sequence induction in the presence of severe pregnancy-induced and pregnancy-aggravated hypertension.

Twenty-six patients manifesting severe pregnancy-induced (PIH) or pregnancy-aggravated (PAH) hypertension who presented for emergency Caesarean section under general anaesthesia were studied. All patients came from a previously identified high risk group--namely greater than 25 yr, multiparous and with diastolic arterial pressures sustained at greater than 120 mm Hg. Our standard accelerated induction technique for the management of severely hypertensive mothers was modified to include the use of fentanyl and droperidol before induction.

Comparison of midazolam and thiopental for rapid sequence anesthetic induction for elective cesarean section.

Sixty healthy mothers undergoing elective cesarean section received at random either midazolam 0.2 mg/kg or thiopental 3.5 mg/kg with succinylcholine 1 mg/kg for rapid sequence intravenous anesthetic induction.

Inflation pressure, gastric insufflation and rapid sequence induction.

An investigation was carried out into the relationship between the inflation pressures of normally compliant lungs and the airways pressure necessary to produce the insufflation of gas to the stomach. This relationship was examined during manual ventilation with a mask, using a rapid sequence induction technique. In the absence of cricoid pressure the lungs of all the patients could be ventilated "gently" satisfactorily by hand without gas entering the stomach.

Fresh gas flow requirements using the ADE anaesthetic system during late pregnancy.

Thirty-two pregnant patients at term undergoing elective Caesarean section were ventilated with a non-co-axial ADE anaesthetic system (E mode) supplied with fresh gas flows (FGF) of either 70 or 100 ml kg-1 min-1, on a random basis. Ventilation with an FGF of 70 ml kg-1 min-1 produced mean PaCO2 and PE' CO2 values of 6.48 +/- 1.

Pulmonary aspiration during unsuccessful cardiopulmonary resuscitation.

The incidence of pulmonary aspiration in a group of patients who did not respond to cardiopulmonary resuscitation (CPR) was assessed at autopsy and found to be 29%. This figure is undoubtedly an underestimate of the total problem, and some indication of the potential for aspiration during CPR is revealed by the fact that 46% of the patients studied had full stomaches at autopsy. Clearly this fact has implications for CPR methods as suggested by Cummings and Eisenberg.

Cricoid pressure with or without the "cricoid yoke".

The performance of cricoid pressure was studied in three groups of medical personnel likely to be involved in its application using the cricoid yoke and a test rig. The instrument enabled individuals who had no previous experience in the application of cricoid pressure to achieve results as good as those obtained by experienced anaesthetic staff. Furthermore, the instrument improved the consistency of the applied force in all groups, particularly if cricoid pressure was required for sustained periods of 30 s or more.

The cricoid yoke--a device for providing consistent and reproducible cricoid pressure.

An instrument is described which, when used during the accelerated induction technique, ensures that consistent and adequate cricoid pressure can be applied. Mothers undergoing general anaesthesia for elective Caesarean section were studied in order to illustrate the clinical application of the instrument. The consequences to intubating conditions of applying adequate cricoid pressure, and an assessment of the instrument's control over the incidence of regurgitation during operation were investigated.