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Biomedical subjects

D M Justins

Publications and source records attributed to D M Justins.

18 recordsLinked to original sources
PubMed1999

The use of stop signals to reduce the pain and distress of patients undergoing a stressful medical procedure: an exploratory clinical study.

The present study investigates stop signals and their effects on the pain and distress of patients undergoing a stressful medical procedure. Thirty-six chronic pain patients (17 men, 19 women) attending an out-patient operating theatre for diagnostic nerve blocks/local anaesthetic injections were allocated to one of two conditions (experimental and control). All patients received a standard information leaflet concerning the forthcoming injections. Additional information was given to those in the experimental group on four occasions (three orally, one written) before the injections which stated that they could halt the procedure at any time by saying 'stop'. Subjective measures of anxiety, pain, distress, sense of control over the procedure as well as observer ratings of patient distress and pain behaviour were obtained before, during and after the injections. After initial differences in pre-injection pain were controlled for the experimental group, patients rated themselves as less distressed during the injections and recorded lower state anxiety following treatment. In view of various methodological limitations of the present study its findings may only be accorded 'pilot study' status. These limitations are explored in the discussion along with their implications for a more robust replication study. Nevertheless the present findings provide tentative support for the hypothesis that the use of stop signals can reduce the stressful nature of diagnostic nerve blocks.

Adult↗
PubMed1996

Inpatient vs. outpatient pain management: results of a randomised controlled trial.

Inpatient and outpatient cognitive behavioural pain management programmes for mixed chronic pain patients were compared. Patients were randomly allocated to the 4 week inpatient programme or to the 8 half day per week outpatient programme, or to a waiting list control group. Staff, teaching materials, and setting were the same for the two treatment groups. Patients were assessed pre-treatment, and at 1 month after discharge, and treated patients also at 6 months and 1 year after discharge, by assessors blind to treatment group; assessments included physical, functional and psychological measures, and medication use. In total, 121 mixed chronic pain patients (mean age 50 years; mean chronicity 8.1 years) were included in the study, following medical examination to ensure that no further medical treatment was appropriate. There was no change in the control group; inpatients and outpatients, comparable before treatment, both made significant improvements in physical performance and psychological function, and reduced medication use. Inpatients made greater gains, and maintained them better at 1 year; they also used less health care than outpatients. There were no outstanding predictors of improvement other than treatment group.

Ambulatory Care↗
PubMed1993

Evaluation of a cognitive behavioural programme for rehabilitating patients with chronic pain.

The aim of this prospective longitudinal study was to evaluate an inpatient cognitive behavioural pain management programme for patients with chronic pain. A physical and psychological assessment of patients was carried out before and after treatment, and at one and six months follow up. A total of 212 patients with disabling chronic pain of mean duration 10.5 years, for whom no further medical or psychiatric treatment was appropriate or available, were admitted; their mean age was 50 years and 65% were women. The four week programme was delivered by a multidisciplinary team of two psychologists, a physiotherapist, nurse, occupational therapist and anaesthetist. The main components of therapy included: education, teaching behavioural and cognitive skills, a stretch and exercise programme, medication reduction, goal setting and pacing, and relaxation training. Outcome measures assessed quality of life, physical performance (for example walking speed), pain intensity and distress, depression severity and confidence. Assessment immediately after treatment revealed significant improvements on all measures. Improvements were well maintained at six month follow up. Cognitive behavioural treatment can be of value in improving the day-to-day functioning and quality of life of patients with chronic pain for whom conventional medical treatments have apparently failed.

Adult↗
PubMed1991

Clinical management of acute pain.

The clinical management of acute pain has been impeded by traditions and misconceptions which have resulted in suboptimal application to the patient of the currently available methods of pain control. The search for new drugs and exotic ways to deliver them has further obscured many of the basic principles which should guide management. Standard regimens fail because of the wide, unpredictable variability in pain intensity, patient characteristics, and pharmacological responses. Treatment needs to be individualized for each patient. Unrelieved acute pain produces psychological, physiological and socioeconomic consequences. Pre-emptive analgesia may damp down the development of both immediate and long-term pain following surgery and adequate psychological preparation can improve coping abilities. The delivery of opioid analgesics can be improved using patient controlled analgesia or spinal administration in some cases. Regional analgesia, often using simple techniques, can produce excellent pain relief. Overall management and staff education should be delegated to an acute pain service.

Acute Disease↗
PubMed1989

Paravertebral somatic nerve block: a clinical, radiographic, and computed tomographic study in chronic pain patients.

The spread of solution after a standardized paravertebral injection was studied to determine the precision and predictability of paravertebral spread. The spread of 5 ml of a solution of radiological contrast medium (sodium iothalamate) and local anesthetic mixture after 45 (34 thoracic, 11 lumbar) paravertebral injections was studied in 31 patients by radiography and computed tomography and correlated with the clinical effects. Spread confined to the paravertebral area occurred after only eight (18%) injections. Spread was epidural after 31 (70%) injections and exclusively so in 14 (31%) injections. Mean sensory loss was greater after epidural spread, but a wide range of sensation loss was observed with all patterns of spread. Intrapleural spread occurred after three injections, as did spread into the psoas muscle. In addition, measurements were made of 114 paravertebral spaces in 20 patients by means of computed tomography. Dimensional factors identified as possibly leading to complications of a paravertebral injection included narrow width of the thoracic transverse processes (mean, 3.18 cm; range, 2.1-4.2 cm) and the wide range in paravertebral dimensions. The distance from bony landmarks to pleura frequently fell outside the limits recommended by many standard texts. We conclude that the spread of a small volume of solution after paravertebral injection is imprecise and unpredictable. Neurolytic and diagnostic paravertebral injections performed without the aid of radiological imaging and contrast media should be regarded as hazardous and interpreted with extreme caution.

Analgesia, Epidural↗
PubMed1988

Delayed contralateral sympathetic blockade following chemical sympathectomy--a case history.

A young girl with an idiopathic degenerative nervous system disease developed delayed contralateral sympathetic blockade each time following lumbar paravertebral sympathetic block of either side. Bilateral sympathetic blockade developed on each occasion despite observed ipsilateral containment of X-ray contrast on injection. The aetiological mechanisms of this phenomenon are discussed.

Adolescent↗
PubMed1985

Epidural fentanyl in labour. An evaluation of the systemic contribution to analgesia.

In a randomized double-blind trial in the first stage of labour, 20 patients given fentanyl 80 micrograms in the epidural test dose of bupivacaine, were compared with 20 patients receiving an intravenous infusion designed to produce comparable plasma fentanyl concentrations, at the same time as their epidural test dose. Despite slightly higher plasma fentanyl concentrations in the intravenous fentanyl group, epidural fentanyl produced analgesia which was more complete, more rapid in onset and slightly longer lasting. Supplementary doses of bupivacaine were needed to produce analgesia in 75% of the intravenous and 30% of the epidural fentanyl group. It is clear that epidural fentanyl produces satisfactory pain relief when added to the epidural test dose, but that the presence of fentanyl in the systemic circulation makes a negligible contribution to analgesia.

Adult↗
PubMed1983

Epidural versus intramuscular fentanyl. Analgesia and pharmacokinetics in labour.

In a randomised double blind trial, 36 patients in the first stage of labour received either epidural or intramuscular fentanyl at the same time as the epidural test dose of bupivacaine. Analgesia was more rapid in onset and more complete in the epidural fentanyl group. Supplementary doses of bupivacaine were required within the first hour in 62% of the intramuscular fentanyl group compared with only 16% in the epidural group. Plasma fentanyl concentrations showed wide interindividual variation, but after epidural fentanyl the peak occurred earlier. There was no correlation between analgesia and plasma fentanyl concentration, and epidural fentanyl produced superior analgesia but a systemic contribution to this effect cannot be ruled out.

Adult↗
PubMed1982

A controlled trial of extradural fentanyl in labour.

In a double-blind trial carried out on patients in the first stage of labour, either fentanyl 80 micrograms (n = 35) or physiological saline (n = 33) was added to the test dose of bupivacaine and administered extradurally. Thereafter analgesia was maintained as necessary with 0.5% bupivacaine alone. Supplementary bupivacaine (a further dose within 1 h) was required to produce satisfactory analgesia in eight patients in the fentanyl group and in 26 patients in the control group. Analgesia was more rapid in onset and more complete in the fentanyl group, and the duration from first dose to first top-up was 2.36 h, compared with 1.66 h (supplements notwithstanding) in the control group. No serious side-effects were encountered in either group, although eight patients in the fentanyl group experienced mild itching, compared with one in the control group.

Adult↗
PubMedDate not supplied

Chronic pain management.

Patients with chronic pain often present with complex multidimensional problems. Satisfactory management requires attention to the various components of the pain as well as to the resulting disability and the psychosocial dimensions of the problem.

Analgesia↗