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1. |
The Journal in 1992 |
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Australian and New Zealand Journal of Medicine,
Volume 23,
Issue 1,
1993,
Page 1-2
GRAHAM MACDONALD,
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ISSN:0004-8291
DOI:10.1111/j.1445-5994.1993.tb00528.x
出版商:Blackwell Publishing Ltd
年代:1993
数据来源: WILEY
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2. |
Ethics and clinical medicine |
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Australian and New Zealand Journal of Medicine,
Volume 23,
Issue 1,
1993,
Page 3-5
PAUL A. KOMESAROFF,
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ISSN:0004-8291
DOI:10.1111/j.1445-5994.1993.tb00529.x
出版商:Blackwell Publishing Ltd
年代:1993
数据来源: WILEY
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3. |
Culture‐positive tuberculosis at St Vincent's Hospital, Melbourne, 1962–1989 |
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Australian and New Zealand Journal of Medicine,
Volume 23,
Issue 1,
1993,
Page 7-11
J. C. Hurley,
E. M. Uren,
J. H. Andrew,
J. Burdon,
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摘要:
AbstractThe disease types and demography of patients with culture confirmed tuberculosis (TB) diagnosed at St Vincent's Hospital, Melbourne between the years 1962 to 1989 were reviewed. Four hundred and eighty‐two patients with culture‐positive TB were identified whose origins were as follows: Australia 194; Northern Europe 38; The Mediterranean 98; Asia 60 and other or unknown 92. Patients whose country of birth was in Asia or the Mediterranean area accounted for 57% of patients in the 1980s; they presented at a younger age, with a higher proportion of extrapulmonary disease and a more equal sex distribution than did Australian born patients. The main types of extrapulmonary disease also differed for the various ethnic groups. The overall proportion of patients with an isolate resistant to at least one of the anti‐TB drugs was 10.0% but in the Asian born was 21.7%. This survey, the longest series of bacteriologically confirmed cases of TB reported from a single institution in Australasia, has identified several changes in how TB is presenting for diagnosis. (Aust NZ J Med 1993; 23:
ISSN:0004-8291
DOI:10.1111/j.1445-5994.1993.tb00530.x
出版商:Blackwell Publishing Ltd
年代:1993
数据来源: WILEY
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4. |
Medical care and case fatality from myocardial infarction and coronary death in Newcastle and Perth |
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Australian and New Zealand Journal of Medicine,
Volume 23,
Issue 1,
1993,
Page 12-18
A. J. Dobson,
K. D. Jamrozik,
M. Hobbs,
R. F. Heller,
P. L. Steele,
R. Parsons,
P. Thompson,
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摘要:
Abstract:Coronary mortality rates are significantly higher in Newcastle than Perth. In this paper we examine the extent to which this might be due to differences in medical treatment and case fatality.Population‐based disease registers were used to identify all cases of non‐fatal definite myocardial infarction (MI) and coronary death in people aged 25–64 years in the study populations between July 1988 and June 1990.Case fatality (at 28 days from onset of symptoms) was not significantly different between the centres. Thrombolytic therapy was used for one third of all hospitalised events in both centres. Other drugs of proven benefit were, however, used more often in Perth than in Newcastle. For example, during hospitalisation 74% of patients in Perth received β‐blockers compared with 41% in Newcastle (difference=33%, 95% confidence interval (CI): 28%, 37%) and 85% of patients in Perth compared with 72% in Newcastle received aspirin (difference313%, 95% CI: 9%, 17%). Median lengths of stay in a coronary care unit (CCU) and total hospital stay were one day shorter in Perth.As case fatality was similar, the differences in mortality rates can be attributed mainly to differences in attack rates. Greater use of cardio‐active drugs in Perth apparently did not result in improved short‐term outcome although potential long‐term benefits cannot be judged yet. (Aust NZ J Med 19
ISSN:0004-8291
DOI:10.1111/j.1445-5994.1993.tb00531.x
出版商:Blackwell Publishing Ltd
年代:1993
数据来源: WILEY
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5. |
Clinical aspects of malignant mesothelioma in Australia |
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Australian and New Zealand Journal of Medicine,
Volume 23,
Issue 1,
1993,
Page 19-25
T. R. Driscoll,
R. Thompson,
G. J. Baker,
D. A. Ferguson,
S. Daniels,
J. Leigh,
J. Lee,
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摘要:
Abstract:Australia is currently experiencing an epidemic of malignant mesothelioma. The clinical aspects of malignant mesothelioma were investigated in 295 Australian patients as part of a national study of the disease. Most patients were male (91%), with the mean age at diagnosis being 64 years. The predominant cell type was epithelial (38%) and the majority of primary tumours arose from the pleura (94%). Mean survival was poor (17.6 months from first symptom; 11.8 months from diagnosis). Patients with a pleural primary tumour were more likely to present with dyspnoea, chest pain and cough; to have a pleural effusion diagnosed radiologically; and to have metastatic spread. Patients with a peritoneal primary tumour were more likely to present with weight loss, loss of appetite, abdominal pain and ascites; to have radiologic evidence of asbestos exposure; and to have spread along a needle track created during a diagnostic tap. A minority of patients had past thoracic conditions, or radiologic findings, specifically related to previous asbestos exposure. About one fifth of patients had no known asbestos exposure. Forty‐one per cent of subjects received some form of chemotherapy, radiotherapy and/or surgery, but no formal disease staging had been documented for any patient. Proper controlled trials of secondary and tertiary treatments in malignant mesothelioma are now needed. (Aust NZ J Med 1993; 23: 19–
ISSN:0004-8291
DOI:10.1111/j.1445-5994.1993.tb00532.x
出版商:Blackwell Publishing Ltd
年代:1993
数据来源: WILEY
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6. |
Sheehan's syndrome: clinical profile, pituitary hormone responses and computed sellar tomography |
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Australian and New Zealand Journal of Medicine,
Volume 23,
Issue 1,
1993,
Page 26-31
R. J. Dash,
V. Gupta,
S. Suri,
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摘要:
Abstract:Twenty patients with the typical clinical presentation of Sheehan's syndrome were studied. All had a severe degree of hypopituitarism. The circulating mean basal levels of thyroid hormones, Cortisol and prolactin were significantly lower(p<0.05 to<0.02) compared to those in 50 age matched controls. The provoked pituitary responses to combined pituitary stimulation in 13 patients were markedly lower(p<0.02 to<0.001) than those in ten age matched control subjects. Sellar computed tomography revealed an empty sella in all the patients; partial in five and complete in the remaining. A secondary empty sella is considered a characteristic finding in the classical form of Sheehan's syndrome. (Aust NZ J Med 1993; 23: 26–31
ISSN:0004-8291
DOI:10.1111/j.1445-5994.1993.tb00533.x
出版商:Blackwell Publishing Ltd
年代:1993
数据来源: WILEY
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7. |
Continuous hepatic artery infusion of 5‐fluorouracil for metastatic colorectal cancer localised to the liver |
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Australian and New Zealand Journal of Medicine,
Volume 23,
Issue 1,
1993,
Page 32-34
F. M. Boyle,
R. C. Smith,
J. A. Levi,
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摘要:
Abstract:Continuous regional delivery of chemotherapeutic agents offers the prospect of maximising dose intensity at the site of localised disease, while minimising systemic toxicity. This prospective phase II study evaluates the efficacy and toxicity of hepatic arterial infusion of 5‐Fluorouracil (5‐FU) via an implantable Infusaid™ pump in previously untreated patients with localised but unresectable hepatic metastases from colorectal cancer. In 25 patients the response rate was 56% and median survival was 15 months, comparable to previous reports utilising fluorodeoxy‐uridine (FUDR). Twenty per cent of patients (all responders) survived longer than three years. Systemic toxicity was trivial, and the practice of reducing the intensity of therapy when nausea or a rise in alkaline phosphatase occurred avoided the previously described local toxicity of biliary sclerosis seen frequently with FUDR. In selected patients, particularly those with more limited disease, this form of therapy is effective and well tolerated and warrants further evaluation as an alternative to FUDR. (Aust NZ J Med 1993; 23:
ISSN:0004-8291
DOI:10.1111/j.1445-5994.1993.tb00534.x
出版商:Blackwell Publishing Ltd
年代:1993
数据来源: WILEY
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8. |
Autosomal dominant polycystic kidney disease (ADPKD)—mechanisms of cyst formation and renal failure* |
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Australian and New Zealand Journal of Medicine,
Volume 23,
Issue 1,
1993,
Page 35-41
E. Ritz S. Geberth,
M. Zeier,
S. Gebert,
R. Waldherr,
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摘要:
Abstract:None of the hypotheses proposed so far to explain cyst formation in autosomal dominant polycystic kidney disease (ADPKD) is entirely satisfactory, e.g. the theory of tubular obstruction by intraluminal polyps or dilatation of nephron segments as a consequence of abnormal compliance of the basement membrane. Recentin vitrostudies show that (i) synthesis of basement membrane material is abnormal and that (ii) the direction of transepithelial resorptive flux into a secretory mode is reversed as a consequence of faulty insertion of Na, K‐ATP'ase into the luminal membrane.It remains unclear why cystic transformation of a few percent of nephrons should cause endstage renal failure. Our clinical and experimental studies do not provide evidence to support some hypotheses proposed in the past, i.e. that renal parenchyma is compressed by expanding cysts and that glomeruli are overperfused. Our histological studies show that progression to endstage renal failure is associated with (i) progressive arteriolar lesions (out of proportion to the vascular lesions seen in extrarenal vascular beds; and (ii) progressive interstitial fibrosis. It appears that fibroblasts in ADPKD are particularly sensitive to platelet derived growth factor (PDGF) which is secreted by epithelial cells of the cyst wall in a paracrine fashion.In contrast to previous opinion, which was presumably skewed by ascertainment bias, it appears that not all, and perhaps not even a majority, of ADPKD patients progress to endstage renal failure. Factors related to progression are gender, family history and hypertension. Both abnormal sodium excretion and inappropriate renin secretion play a role in the genesis of hypertension. Elevated blood pressure, albeit within the normotensive range, is demonstrable even in prepubertal children. The involvement of renin in renal vasoconstriction of normotensive ADPKD patients suggests a particular role of ACE inhibitors in the management of these patient
ISSN:0004-8291
DOI:10.1111/j.1445-5994.1993.tb00535.x
出版商:Blackwell Publishing Ltd
年代:1993
数据来源: WILEY
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9. |
The chronic B‐cell leukaemias |
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Australian and New Zealand Journal of Medicine,
Volume 23,
Issue 1,
1993,
Page 42-50
S. P. Mulligan,
D. Catovsky,
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ISSN:0004-8291
DOI:10.1111/j.1445-5994.1993.tb00536.x
出版商:Blackwell Publishing Ltd
年代:1993
数据来源: WILEY
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10. |
Absence of amyloid deposition in gastroduodenal mucosa of uraemic patients undergoing dialysis treatment |
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Australian and New Zealand Journal of Medicine,
Volume 23,
Issue 1,
1993,
Page 51-52
A. WEE,
J. Y. KANG,
A. Y. T. WU,
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ISSN:0004-8291
DOI:10.1111/j.1445-5994.1993.tb00537.x
出版商:Blackwell Publishing Ltd
年代:1993
数据来源: WILEY
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