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1.
Tidsskr Nor Laegeforen ; 120(15): 1777-80, 2000 Jun 10.
Article in Norwegian | MEDLINE | ID: mdl-10904666

ABSTRACT

BACKGROUND: The use of still images in an electronic referral makes it possible for patients with uncomplicated skin disorders to receive treatment at their local health clinic by their own physician. The aim of this study was to analyse whether investing in technology to forward still images via telemedicine is cost-effective and to assess how many municipalities in the counties of Troms and Finnmark that have a sufficient workload to reach this requirement. MATERIAL AND METHODS: The additional costs of using still images were compared to patient travel costs to the University Hospital of Tromsø. RESULTS: The results showed that whether the use of still image telemedicine is cost-effective or not, depends on distance and annual workload. Given the assumption in this study, 18 out of 44 municipalities have a sufficient number of patients with a dermatological problem to make telemedicine cost-effective. INTERPRETATION: Less than half of the municipalities in the two northernmost counties have an efficiency potential in using still images. However, telemedicine may be justified because it save time for patients and it increases equal access to care.


Subject(s)
Family Practice/economics , Referral and Consultation/economics , Telepathology/economics , Cold Climate , Cost Savings , Cost-Benefit Analysis , Health Services Accessibility , Humans , Medically Underserved Area , Norway , Travel
2.
Clin J Pain ; 16(1): 22-8, 2000 Mar.
Article in English | MEDLINE | ID: mdl-10741815

ABSTRACT

OBJECTIVE: The goals of this study were to examine agreement and estimate differences in sensitivity between pain assessment scales. DESIGN: Multiple simultaneous pain assessments by patients in acute pain after oral surgery were used to compare a four-category verbal rating scale (VRS-4) and an 11-point numeric rating scale (NRS-11) with a 100-mm visual analog scale (VAS). The sensitivity of the scales (i.e., their ability [power] to detect differences between treatments) was compared in a simulation model by sampling from true pairs of observations using varying treatment differences of predetermined size. RESULTS: There was considerable variability in VAS scores within each VRS-4 or NRS-11 category both between patients and for repeated measures from the same patient. Simulation experiments showed that the VAS was systematically more powerful than the VRS-4 in all simulations performed. The sensitivity of the VAS and NRS-11 was approximately equal. CONCLUSIONS: In this acute pain model, the VRS-4 was less sensitive than the VAS. The simulation results demonstrated similar sensitivity of the NRS-11 and VAS when comparing acute postoperative pain intensity. The choice between the VAS and NRS-11 can thus be based on subjective preferences.


Subject(s)
Pain Measurement/methods , Pain Measurement/standards , Double-Blind Method , Humans , Pain, Postoperative/physiopathology , Reproducibility of Results , Sensitivity and Specificity , Stochastic Processes , Surgery, Oral
3.
Clin Pharmacol Ther ; 66(6): 625-35, 1999 Dec.
Article in English | MEDLINE | ID: mdl-10613619

ABSTRACT

In a randomized double-blind study, 120 patients with moderate to strong pain after surgical removal of wisdom teeth were given the following in single oral doses: 100-mg enteric-coated diclofenac tablets; 1 g acetaminophen (INN, paracetamol); 1 g acetaminophen plus 60 mg codeine; 100-mg enteric-coated diclofenac tablets plus 1 g acetaminophen; or 100-mg enteric-coated diclofenac tablets plus 1 g acetaminophen plus 60 mg codeine. Patients recorded pain intensity and pain relief for 8 hours. Upside assay sensitivity was confirmed because acetaminophen plus codeine was superior to acetaminophen. Diclofenac plus acetaminophen with and without codeine had superior analgesic effect compared with diclofenac, acetaminophen, or acetaminophen plus codeine. Addition of 60 mg codeine increased the degree of side effects. These results support the clinical practice of combining diclofenac with acetaminophen for acute pain. Of clinical importance are superior and prolonged analgesia and fewer side effects after enteric-coated diclofenac tablets plus acetaminophen compared with acetaminophen plus codeine.


Subject(s)
Acetaminophen/therapeutic use , Analgesics, Non-Narcotic/therapeutic use , Analgesics, Opioid/therapeutic use , Anti-Inflammatory Agents, Non-Steroidal/therapeutic use , Codeine/therapeutic use , Diclofenac/therapeutic use , Molar, Third/surgery , Pain, Postoperative/drug therapy , Tooth Extraction/adverse effects , Acetaminophen/administration & dosage , Acetaminophen/adverse effects , Administration, Oral , Adult , Analgesics, Non-Narcotic/administration & dosage , Analgesics, Non-Narcotic/adverse effects , Analgesics, Opioid/administration & dosage , Analgesics, Opioid/adverse effects , Anti-Inflammatory Agents, Non-Steroidal/administration & dosage , Anti-Inflammatory Agents, Non-Steroidal/adverse effects , Codeine/administration & dosage , Codeine/adverse effects , Diclofenac/administration & dosage , Diclofenac/adverse effects , Double-Blind Method , Drug Combinations , Drug Therapy, Combination , Humans , Linear Models , Pain Measurement , Pain, Postoperative/etiology , Tablets, Enteric-Coated , Treatment Outcome
4.
Eur J Oral Sci ; 106(4): 844-52, 1998 Aug.
Article in English | MEDLINE | ID: mdl-9708687

ABSTRACT

The aims of this study were to test the hypotheses that the type of 3rd molar removal determines baseline pain and that baseline pain influences analgesic assay sensitivity. Three groups of patients were studied: (i) 100 patients that had one fully erupted maxillary 3rd molar extracted; (ii) 95 patients that had one lower impacted 3rd molar surgically removed; and (iii) 98 patients that had two ipsilateral impacted 3rd molars surgically removed. In a randomized, double-blind fashion, the patients received (every third hour, three times) either: (i) paracetamol 1g; (ii) paracetamol 1g plus codeine 60 mg; or (iii) placebo. Baseline pain intensity (100 mm Visual Analogue Scale) was significantly lower after extraction (8 mm (2-20)) (=median (25th -75th percentile) than after surgical removal of one 3rd molar (35 mm (15-57)), which was significantly lower than pain intensity after surgical removal of two 3rd molars (49 mm (24-82)). Analgesic effects of the active test drugs were superior to placebo. Paracetamol with and without codeine could be distinguished in patients after surgical removal of one 3rd molar. In conclusion, baseline pain was related to the degree of surgical trauma, but large inter-individual variation in baseline pain intensity reduced the ability to distinguish between paracetamol with and without codeine.


Subject(s)
Analgesics/therapeutic use , Pain Measurement , Pain, Postoperative/physiopathology , Tooth Extraction/methods , Acetaminophen/administration & dosage , Acetaminophen/therapeutic use , Adolescent , Adult , Analgesics/administration & dosage , Analgesics, Non-Narcotic/administration & dosage , Analgesics, Non-Narcotic/therapeutic use , Analgesics, Opioid/administration & dosage , Analgesics, Opioid/therapeutic use , Codeine/administration & dosage , Codeine/therapeutic use , Double-Blind Method , Female , Humans , Male , Mandible/surgery , Maxilla/surgery , Molar, Third/surgery , Pain, Postoperative/drug therapy , Placebos , Sensitivity and Specificity , Tooth, Impacted/surgery
5.
Methods Find Exp Clin Pharmacol ; 20(8): 719-24, 1998 Oct.
Article in English | MEDLINE | ID: mdl-9922987

ABSTRACT

Contrary results have been reported from studies comparing horizontal and vertical orientations of the visual analogue scale (VAS) in non-dental pain states. The vertical orientation of the VAS has been used in our department for several years while the horizontal orientation is the most commonly used in other acute pain models. The present study investigated whether a horizontally oriented VAS is as sensitive as a vertically oriented VAS in the assessment of present pain after oral surgery. Seventy-four patients recorded their pain intensity hourly and half-hourly 15 times during 11 hours after surgery on a horizontal and on a vertical 100 mm VAS. Slightly lower mean and median values were observed at 2/3 of the observation time points for the vertical VAS compared to the horizontal VAS. The results from the two scales were compared with analysis of variance for repeated measures. No significant differences between the horizontal and the vertical VAS-values were found (p = 0.099). Distributions (Kolmogorov-Smirnov test) and dispersions of data were also similar with the two orientations of the VAS. This study shows that a vertically oriented VAS is equally sensitive as a horizontally oriented VAS in assessing present pain intensity after oral surgery.


Subject(s)
Molar, Third/surgery , Pain Measurement/methods , Acetaminophen/therapeutic use , Adolescent , Adult , Codeine/therapeutic use , Female , Humans , Male , Oral Surgical Procedures , Pain, Postoperative/drug therapy , Sensitivity and Specificity
6.
Tidsskr Nor Laegeforen ; 117(23): 3359-62, 1997 Sep 30.
Article in Norwegian | MEDLINE | ID: mdl-9411887

ABSTRACT

328 surgical "errors" reported to the Norwegian System of Compensation for Injuries to Patients were analysed in order to find out how the errors can be exploited for the purpose of quality improvement. In 8% of the cases the patients had been treated as emergency cases. 7% of the patients had been treated as out-patients. 30% of the patients had become more than 15% permanently disabled as a consequence of the "error". The Norwegian System of Compensation for Injuries to Patients operates with five different categories of errors defined by medical specialty, of which surgery is one. We found that among "surgical errors" 16% of the patients had been treated by an anaesthetist or by a specialist in internal medicine, and 13% had been treated by a gynaecologist. There were several recurring "errors" such as nerve injuries and complications related to general atherosclerosis. A system for categorising errors with a view to quality improvement should be different from other systems of categorisation. We suggest a system based on not only five but all medical specialties. Data from such a system could be used to prepare "pedagogic reports" that can be sent to the managers of services and education in each medical specialty. Thus, by turning surgical errors into "medical treasures", the errors can be exploited to promote quality improvement.


Subject(s)
Intraoperative Complications , Medical Errors , Postoperative Complications , Quality Assurance, Health Care , Clinical Competence , Female , Humans , Insurance Claim Review , Intraoperative Complications/classification , Intraoperative Complications/diagnosis , Intraoperative Complications/epidemiology , Male , Norway/epidemiology , Postoperative Complications/classification , Postoperative Complications/diagnosis , Postoperative Complications/epidemiology , Registries , Specialties, Surgical/standards
7.
Tidsskr Nor Laegeforen ; 117(28): 4099-102, 1997 Nov 20.
Article in Norwegian | MEDLINE | ID: mdl-9441446

ABSTRACT

Claims for compensation for surgical injuries submitted to the Norwegian System of Compensation for Injuries to Patients were analysed with respect to the written documentation of the case, patient information and the medical experts involved. Documentation of the indication for treatment, the surgical procedures and the injury were good, and acceptable in more than 90% of the case reports. Preoperative information on the patient was only documented in the report in 5% of the cases. There has been some discussion on the way in which medical experts used in the evaluation of patients claims are selected. In order to increase the legitimation of the medical experts we suggest that the Norwegian System of Compensation for Injuries to Patients and the Norwegian Board of Health should consider using the same set of rules for selecting experts. To improve the quality of patients' treatment and for security reasons, the System of Compensations of Injuries to Patients' data on documentation of patient information and categorized reports on the medical errors should be periodically reported to the hospitals.


Subject(s)
Insurance Claim Review , Surgical Procedures, Operative/adverse effects , Clinical Competence , Expert Testimony , Humans , Malpractice , Medical Errors , Medical Records , Norway , Patient Education as Topic , Registries
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