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1. |
Introduction |
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Hospital Practice,
Volume 27,
Issue sup2,
1992,
Page 3-4
McLeodGavin X.,
HammerScott M.,
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PDF (214KB)
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ISSN:2154-8331
DOI:10.1080/21548331.1992.11705594
出版商:Taylor&Francis
年代:1992
数据来源: Taylor
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2. |
Monotherapy |
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Hospital Practice,
Volume 27,
Issue sup2,
1992,
Page 5-13
SkowronGail,
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PDF (8029KB)
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摘要:
At present, the nucleoside analogues are the cornerstone of therapy for HIV Infection. Of the three that have been approved for clinical use, AZT is the only one that has clearly proved to prolong survival, ddI is indicated for patients who develop toxicity or resistance to AZT. Current data do not support ddC monotherapy as first-line treatment.
ISSN:2154-8331
DOI:10.1080/21548331.1992.11705595
出版商:Taylor&Francis
年代:1992
数据来源: Taylor
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3. |
Combination Therapy |
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Hospital Practice,
Volume 27,
Issue sup2,
1992,
Page 14-25
McLeodGavin X.,
HammerScott M.,
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PDF (4424KB)
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摘要:
Combination antiretroviral therapy is an important development in the management of HIV infection. AZT with ddC is the first such combination to be approved for clinical use. Several issues remain, however, including the precise clinical benefit and toxicity of combination therapy, its effect on drug resistance, and the development of ever more effective therapeutic strategies.
ISSN:2154-8331
DOI:10.1080/21548331.1992.11705596
出版商:Taylor&Francis
年代:1992
数据来源: Taylor
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4. |
Adverse Effects |
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Hospital Practice,
Volume 27,
Issue sup2,
1992,
Page 26-36
SaagMichael S.,
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PDF (3555KB)
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摘要:
The three approved nucleoside analogues are fairly well tolerated, and only a few patients have to discontinue therapy permanently. However, because clinical experience is limited, especially with ddI and ddC, delayed toxicities are likely to emerge over time. In addition, physicians should be vigilant for overlapping toxicities from combination therapy with these and other medications.
ISSN:2154-8331
DOI:10.1080/21548331.1992.11705597
出版商:Taylor&Francis
年代:1992
数据来源: Taylor
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