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1. |
In this Issue |
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Medical Journal of Australia,
Volume 165,
Issue 4,
1996,
Page 178-178
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ISSN:0025-729X
DOI:10.5694/j.1326-5377.1996.tb124916.x
出版商:Wiley
年代:1996
数据来源: WILEY
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2. |
Sudden infant death syndrome |
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Medical Journal of Australia,
Volume 165,
Issue 4,
1996,
Page 179-180
Susan M Beal,
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摘要:
If all infants were to sleep supine, in conditions which ensured that the head could not become covered, the incidence of SIDS in Australia could fall to less than 0.4 per 1000 live births
ISSN:0025-729X
DOI:10.5694/j.1326-5377.1996.tb124917.x
出版商:Wiley
年代:1996
数据来源: WILEY
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3. |
Motor neurone disease and the life of motor neurones |
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Medical Journal of Australia,
Volume 165,
Issue 4,
1996,
Page 180-181
Garth A Nicholson,
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摘要:
Upsetting the balance of the regulators of cell survival and cell death may lead to motor neurone Joss
ISSN:0025-729X
DOI:10.5694/j.1326-5377.1996.tb124918.x
出版商:Wiley
年代:1996
数据来源: WILEY
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4. |
Outpatient chemotherapy: there's no place like home — sometimes |
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Medical Journal of Australia,
Volume 165,
Issue 4,
1996,
Page 182-182
John R Zalcberg,
Jim Siderov,
Mark Petty,
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摘要:
Despite some apparent advantages of home chemotherapy, clinical trials of its outcomes are necessary before it can be advocated
ISSN:0025-729X
DOI:10.5694/j.1326-5377.1996.tb124919.x
出版商:Wiley
年代:1996
数据来源: WILEY
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5. |
Hyperparathyroidism: a management dilemma |
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Medical Journal of Australia,
Volume 165,
Issue 4,
1996,
Page 183-183
Solomon Posen,
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摘要:
Can surgery be justified for all patients with this disorder?
ISSN:0025-729X
DOI:10.5694/j.1326-5377.1996.tb124920.x
出版商:Wiley
年代:1996
数据来源: WILEY
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6. |
Home chemotherapy for cancer patients: cost analysis and safety |
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Medical Journal of Australia,
Volume 165,
Issue 4,
1996,
Page 184-187
Raymond M Lowenthal,
Anne Piaszczyk,
Gillian E Arthur,
Sue O'Malley,
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摘要:
ObjectiveTo assess the safety and to analyse the cost‐effectiveness of home treatment, including cytotoxic chemotherapy, for cancer patients.DesignA restrospective overview of a home oncology nursing service over its first five years (1989‐1994), and a detailed cost analysis over 12 months, firstly, by comparing direct costs of chemotherapy administration at home or in the hospital's day treatment ward and, secondly, by assessing the marginal cost of treating home care program patients in the hospital versus the total cost of the home care program.Patients and settingPatients of the Haematology/Oncology Unit of a metropolitan teaching hospital treated either at home by an experienced oncology nurse, or in the hospital day care ward.InterventionPatients were offered treatments, including chemotherapy, at home rather than in hospital.Main outcome measuresSafety, assessed by the rate of major complications (i.e., requiring any patient to be admitted to hospital), and cost‐effectiveness, assessed by comparing expenditure in the home and hospital settings.ResultsOver five years, there were 5444 home visits to 424 patients, including 1688 chemotherapy administrations to 179 patients. Only two of the 424 patients decided against continuing in the home program once it had begun. There were no major complications. The average cost of home chemotherapy administration (excluding drugs) was $49.91, compared with $116.00 in hospital. The cost of treating patients at home was $5.09 per patient more than the “marginal cost” of treating these patients in the hospital.ConclusionsHome anticancer chemotherapy is a safe and economically realistic alternative to traditional in‐hospital treatment. Efforts should be made to overcome budgetary and administrative barriers to more widespread adoption of this model of care.
ISSN:0025-729X
DOI:10.5694/j.1326-5377.1996.tb124921.x
出版商:Wiley
年代:1996
数据来源: WILEY
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7. |
Survey of haemolytic‐uraemic syndrome in Queensland 1979–1995 |
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Medical Journal of Australia,
Volume 165,
Issue 4,
1996,
Page 188-191
Youichi Mizusawa,
Lydia A Pitcher,
John R Burke,
Michael C Falk,
Waichiro Mizushima,
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摘要:
ObjectiveTo review the clinical course of haemolytic‐uraemic syndrome (HUS) in children admitted to Brisbane children's hospitals between April 1979 and October 1995.DesignRetrospective case survey.SettingRoyal Children's Hospital and Mater Misericordiae Children's Hospital (the two major children's hospitals in Brisbane).SubjectsAll children hospitalised for HUS.Outcome measuresClinical and laboratory features on presentation (including typical [diarrhoea‐positive, D+] or atypical [diarrhoea‐negative, D‐]presentation), clinical course, treatment and features on subsequent outpatient follow‐up (1, 3, 6 and 12 months later), renal outcome on long term follow‐up (3‐16 years later).Results55 children (aged 2 months to 13 years) were hospitalised for HUS, but no epidemic was detected. Seven children (13%) had D‐ presentations, including three (5%) with T‐activation caused by pneumococcal pneumonia. Thrombocytopenia was more severe and prolonged in D‐ patients (P<0.01). Major complications occurred only in the D+ group (one patient died, and two had recurrences). Chronic renal failure was significantly more likely in patients with prolonged oliguria or hypertension in the acute illness and proteinuria or hypertension on follow‐up.ConclusionsThe clinical course and outcome in childhood HUS vary greatly and D‐ HUS is not invariably associated with a poorer prognosis than D+ HUS. Pneumococcal‐associated T‐activation is an important cause of D‐ HUS and should be actively sought to allow for appropriate therapy.
ISSN:0025-729X
DOI:10.5694/j.1326-5377.1996.tb124922.x
出版商:Wiley
年代:1996
数据来源: WILEY
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8. |
Asthma and atopy in four rural Australian Aboriginal communities |
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Medical Journal of Australia,
Volume 165,
Issue 4,
1996,
Page 192-196
Antony J Veale,
Jennifer K Peat,
Euan R Tovey,
Cheryl M Salome,
John E Thompson,
Ann J Woolcock,
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摘要:
ObjectiveTo determine the prevalence and nature of asthma in four rural Australian Aboriginal communities.DesignCross‐sectional population study.SettingFour Aboriginal communities in Queensland, the Northern Territory and South Australia, Australia.SubjectsData were collected from 1252 subjects aged 5‐84 years in August 1990 and August/September 1991.Main outcome measuresRespiratory symptoms, measured by interviewadministered questionnaire; airway hyperresponsiveness (AHR), measured by histamine challenge; and allergy, measured by skin‐prick tests. AHR was a PD20FEV1of histamine of less than or equal to 3.9 μmol.ResultsThe prevalence of AHR in the four communities ranged from 2.2% to 7.5% and significantly increased with age (χ2trend test: P<0.05). The prevalence of current asthma was 0.5% among 8‐12 year old children and 3.3% among adults. The overall prevalence of atopy in the four communities ranged from 21% to 34%. Allergy to cats, house dust mites or cigarette smoking was a risk factor for AHR, and cat allergy was a risk factor for current asthma.ConclusionsThe prevalence of asthma in rural Aboriginal adults is low in comparison with the prevalence among non‐Aboriginal Australians, and asthma in Aboriginal children is almost non‐existent. The low prevalence of asthma is possibly due to environmental factors that influence the acquisition of atopy and AHR.
ISSN:0025-729X
DOI:10.5694/j.1326-5377.1996.tb124923.x
出版商:Wiley
年代:1996
数据来源: WILEY
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9. |
Surgically proven primary hyperparathyroidism with a suppressed intact parathyroid hormone |
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Medical Journal of Australia,
Volume 165,
Issue 4,
1996,
Page 197-198
Paul Glendenning,
Peter T Pullan,
David Gulland,
Anthony J Edis,
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摘要:
A patient with hypercalcaemia had persistently suppressed serum intact parathyroid hormone levels (measured by immunochemiluminometric assay). However, other biochemical tests and open‐neck exploration confirmed a diagnosis of primary hyperparathyroidism.
ISSN:0025-729X
DOI:10.5694/j.1326-5377.1996.tb124924.x
出版商:Wiley
年代:1996
数据来源: WILEY
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10. |
Correction |
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Medical Journal of Australia,
Volume 165,
Issue 4,
1996,
Page 198-198
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PDF (138KB)
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ISSN:0025-729X
DOI:10.5694/j.1326-5377.1996.tb124925.x
出版商:Wiley
年代:1996
数据来源: WILEY
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