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Chemotherapy, infections,

Treatment with flndarabine resnlts in prolonged immunosuppression lasting over 6 months (15). Patients who are immunocompromised are at risk of infection with chemotherapy. Infection with JC vrrns, a hnman polyoma virus, occurred in two patients after flndarabine treatment of a low-grade lymphoma, which led to a progressive multifocal leukoencephalopathy (16). In one series of 27 patients who received flndarabine, serions infections developed in 24 (17). [Pg.1392]

Much of the development of the chemistry of sulfanilamidoselenazole derivatives is a result of the important role played by sulfonamides in chemotherapy and more particularly the good activity of sulfathiazoie against bacterial infections. Backer and De Jonge (441 prepared these derivatives by reaction of 2-amino-4-methyl- and 2-aminO-4-phenyl-selenazoles with A -acetylsulfanilic acid chloride in pyridine.. Alkaline... [Pg.248]

The immunorestorative potential of inosiplex has been evaluated in several clinical conditions, including post-surgical trauma, cancer patients with concurrent viral infections, and cancer patients receiving radiotherapy or chemotherapy. For example, most (84%) of the surgery patients remained immunologicaHy depressed, but 56% of the inosiplex-treated surgery patients had complete restoration of normal skin test reactivity (probability level < 0.0005). The use of inosiplex as an adjuvant to chemotherapy or radiotherapy appears to be valuable in the prophylaxis against opportunistic infections. [Pg.36]

Impla.nta.ble Ports. The safest method of accessing the vascular system is by means of a vascular access device (VAD) or port. Older VAD designs protmded through the skin. The totally implanted ports are designed for convenience, near absence of infection, and ease of implantation. Ports allow dmgs and fluids to be deUvered directiy into the bloodstream without repeated insertion of needles into a vein. The primary recipients of totally implanted ports are patients receiving chemotherapy, bolus infusions of vesicants, parenteral nutrition, antibiotics, analgesics, and acquired immune disease syndrome (AIDS) medications. [Pg.184]

Clinically, GM-CSF or G-CSF have been used to accelerate recovery after chemotherapy and total body or extended field irradiation, situations that cause neutropenia and decreased platelets, and possibly lead to fatal septic infection or diffuse hemorrhage, respectively. G-CSF and GM-CSF reproducibly decrease the period of granulocytopenia, the number of infectious episodes, and the length of hospitalization in such patients (152), although it is not clear that dose escalation of the cytotoxic agent and increased cure rate can be rehably achieved. One aspect of the effects of G-CSF and GM-CSF is that these agents can activate mature cells to function more efficiently. This may, however, also lead to the production of cytokines, such as TNF- a, that have some toxic side effects. In general, both cytokines are reasonably well tolerated. The side effect profile of G-CSF is more favorable than that of GM-CSF. Medullary bone pain is the only common toxicity. [Pg.494]

CarbocycHc 2/3 -didehydro-2/3 -dideoxyguanosine [118353-05-2] (carbovk, CBV, 66), C H 2N502, synthesized in 1988 (177), is a promising candidate for the chemotherapy of AIDS. CBV inhibits HIV repHcation and HIV-induced cytopathic effects in a variety of human T-lymphoblastoid ceU lines at concentrations approximately two hundred- to four hundredfold below its cytotoxic concentrations (177). CBV is as effective as AZT and DDC in reducing the expression of vkal antigen in HIV-infected CEM ceUs (177). The antivkal potency and selectivity of carbovk is comparable to the anti-HIV-1 potency and selectivity of 2/3 -dideoxyadenosine (178). The exact mode of antivkal action of carbovk has not yet been elucidated, but may be the modulating effect of intraceUular nucleotides on 5 -nucleotidase activity (179). [Pg.314]

Infusion devices have been used for diabetes, cancer chemotherapy, pain control (patient-controUed analgesia, ie, PGA), infection, Alzheimer s disease, Parkinson s, nausea, thalassemia, thromboembolism, and to treat severe spasms resulting from spiaal cord iajury (140—143). [Pg.233]

Chemotherapy is the control and treatment of disease by synthetic drugs. Most of these are organic compounds, often of remarkably simple structure. Sulfanilamide is one example of an organic compound synthesized by chemists for the treatment of bacterial infections. [Pg.434]

However, several situations can be anticipated in which support of the immune system is required. These include congenital defects in the immune repertoire, acquired immune deficiencies such as in HIV infection, but also situations in which the immune system is compromised after treatment of patients, e.g., after radiation or chemotherapy. [Pg.616]

Kaposi sarcoma (KS) - an angiogenic-inflammatory neoplasm - is the most prevalent cancer in HIV-infected patients and its appearance is preceded by infection with human Heipesvitus-8 (HHV-8). Although chemotherapy has become the treatment of choice approved by the FDA, there are also good response rates in patients treated with IFN-a. Fortunately, today highly active antiretroviral therapy (HAART) has dramatically decreased the incidence of KS in AIDS patients. [Pg.645]

MA M10 M10.056 Aeruginolysin Target for vaccine development, and chemotherapy of bacterial infection... [Pg.879]

Schinazi RF (1991) Combined therapeutic modalities for viral infections - rationale and clinical potential. In Chou TC, Rideout DC (eds) Synergism and antagonism in chemotherapy. Academic, Orlando, FL, pp 110-181... [Pg.50]

Smee DE, Bailey KW, Morrison AC, SidweU RW (2002) Combination treatment of influenza A virus infections in ceU culture and in mice with the cyclopentane neuraminidase inhibitor RWJ-270201 and ribavirin. Chemotherapy 48 88-93... [Pg.152]

Helicase has also been a focal point for the development of antiviral chemotherapy of the coronavirus associated with severe acute respiratory syndrome (SARS) in humans. Although several experimental compounds with nucleic acid binding activity showing effective inhibition of SARS-CoV helicase were reported in 2005, there have been no reports of any further development since that time (Kesel 2005). It remains to be seen whether the S ARS-CoV compounds will be developed further, especially since no new infections have been observed in recent years. [Pg.164]

Hammond JN, Leavitt MC, Rudy JJ, Isaacson JS, Hertogs K, Larder BA, Pattick AK (2003) Long-term virological response to capravirine in HIV-infected NNRTI-experienced patients. In 43rd interscience conference on antimicrobial agents and chemotherapy. Chicago, IL, Abstract H-871... [Pg.172]

Mycobacterium tuberculosis is the causal organism of tuberculosis in humans. Allied strains cause infections in animals, e.g. bovine tuberculosis and tuberculosis in rodents. Due to the waxy nature of the cell wall this organism will resist desiccation and will survive in sputum. Tuberculosis has been largely eliminated by immunization and chemotherapy. [Pg.32]

Griseofulvin is adminisfered orally in the form of tablets. It is not totally absorbed when given orally, and one method of increasing absorption is to reduce the particle size of the drug. Griseofulvin is deposited in the deeper layers of the skin and in hair keratin, and is therefore employed in chemotherapy of fungal infections of these areas caused by susceptible organisms. [Pg.114]

Neutrophil Segs 40%-60% Bands 3%-5% Phagocytic Leukocytosis Bacterial infections Fungal infections Physiologic stress Tissue injury (e.g. myocardial Infarction) Medications (e.g. corticosteroids) Leukopenia Long-standing infection Cancer Medications (e.g., chemotherapy)... [Pg.1024]


See other pages where Chemotherapy, infections, is mentioned: [Pg.602]    [Pg.219]    [Pg.602]    [Pg.219]    [Pg.203]    [Pg.25]    [Pg.268]    [Pg.476]    [Pg.217]    [Pg.538]    [Pg.262]    [Pg.313]    [Pg.444]    [Pg.151]    [Pg.195]    [Pg.478]    [Pg.233]    [Pg.581]    [Pg.435]    [Pg.429]    [Pg.18]    [Pg.157]    [Pg.169]    [Pg.174]    [Pg.77]    [Pg.130]    [Pg.137]    [Pg.197]    [Pg.198]    [Pg.198]    [Pg.474]    [Pg.1050]   


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