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Intravascular

Cytokines, eg, interferons, interleukins, tumor necrosis factor (TNF), and certain growth factors, could have antitumor activity directiy, or may modulate cellular mechanisms of antitumor activity (2). Cytokines may be used to influence the proliferation and differentiation of T-ceUs, B-ceUs, macrophage—monocyte, myeloid, or other hematopoietic cells. Alternatively, the induction of interferon release may represent an important approach for synthetic—medicinal chemistry, to search for effective antiinflammatory and antifibrotic agents. Inducers of interferon release may also be useful for lepromatous leprosy and chronic granulomatous disease. The potential cytokine and cytokine-related therapeutic approaches to treatment of disease are summarized in Table 4. A combination of cytokines is a feasible modaUty for treatment of immunologically related diseases however, there are dangers inherent in such an approach, as shown by the induction of lethal disserninated intravascular coagulation in mice adrninistered TNF-a and IFN-y. [Pg.41]

Low Osmolality Contrast Media. An ideal intravascular CM possesses several properties high opacity to x-rays, high water solubihty, chemical stabihty, low viscosity, low osmolahty, and high biological safety. Low cost and patentabihty are also important for commercial agents. The newer nonionic and low osmolar agents represent an advanced class of compounds in the development of x-ray contrast media. [Pg.462]

N Generic une Trade Company name Concen -tration, b mg/mL Osmolahty, mOsm/kg H2O Intravascular, mice g/kg Intracistemal, rats mg/kg Partition coefficient, octanol / water, X 10 ... [Pg.463]

Although blood pressure control follows Ohm s law and seems to be simple, it underlies a complex circuit of interrelated systems. Hence, numerous physiologic systems that have pleiotropic effects and interact in complex fashion have been found to modulate blood pressure. Because of their number and complexity it is beyond the scope of the current account to cover all mechanisms and feedback circuits involved in blood pressure control. Rather, an overview of the clinically most relevant ones is presented. These systems include the heart, the blood vessels, the extracellular volume, the kidneys, the nervous system, a variety of humoral factors, and molecular events at the cellular level. They are intertwined to maintain adequate tissue perfusion and nutrition. Normal blood pressure control can be related to cardiac output and the total peripheral resistance. The stroke volume and the heart rate determine cardiac output. Each cycle of cardiac contraction propels a bolus of about 70 ml blood into the systemic arterial system. As one example of the interaction of these multiple systems, the stroke volume is dependent in part on intravascular volume regulated by the kidneys as well as on myocardial contractility. The latter is, in turn, a complex function involving sympathetic and parasympathetic control of heart rate intrinsic activity of the cardiac conduction system complex membrane transport and cellular events requiring influx of calcium, which lead to myocardial fibre shortening and relaxation and affects the humoral substances (e.g., catecholamines) in stimulation heart rate and myocardial fibre tension. [Pg.273]

Diagnosis and treatment of disseminated intravascular coagulation, a severe hemorrhagic disorder. [Pg.425]

Plasma proteins are contraindicated in those with a history of allergic reactions to albumin, severe anemia, or cardiac failure in the presence of normal or increased intravascular volume and in patients on cardiopulmonary bypass. Plasma protein fractions are used cautiously in patients who are in shock or dehydrated and in those with congestive cardiac failure or hepatic or renal failure. These solutions are Pregnancy Category C drugp and are used cautiously during pregnancy and lactation. [Pg.635]

Miniaturized catheter-type ISE sensors, such as the implantable probe shown in Figure 5-20 represent the preferred approach for routine clinical in-vivo monitoring of blood electrolytes. For these intravascular measurements the reference electrode is placed outside die artery (in die external arm of die catheter), tints obviating biocompatability and drift problems associated with its direct contact with the blood. [Pg.164]

Dantrolene should be repeated after 5—8 hr. Bicarbonate, procaine amide, and other drugs should be repeated as needed. Treatment of disseminated intravascular coagulation is symptomatic. Early diagnosis and treatment ofMH is essential. After effective treatment, the patient should be watched closely in the intensive care unit for recurrence of MH, myoglobinuric renal failure, disseminated intravascular coagulation, muscle weakness, and electrolyte imbalance. [Pg.407]

As is the case with tryptase, chymase is also stored in mast cell granules. This mediator can activate the angiotensin system converting angiotensin I to angiotensin II. With this action it compensates the intravascular loss of volume and the permeability... [Pg.127]

Once diagnosed, patients with AlA should avoid aspirin and any other NSAIDs strongly inhibiting COX-1 their education is of utmost importance. They should receive a list of contraindicated and well-tolerated analgesics (table 2). Even topical administration (intravascular or by iontophoresis) of a NSAID may cause an asthma attack and should be avoided. [Pg.175]


See other pages where Intravascular is mentioned: [Pg.198]    [Pg.58]    [Pg.269]    [Pg.460]    [Pg.462]    [Pg.462]    [Pg.462]    [Pg.464]    [Pg.473]    [Pg.473]    [Pg.484]    [Pg.165]    [Pg.166]    [Pg.170]    [Pg.171]    [Pg.177]    [Pg.178]    [Pg.178]    [Pg.121]    [Pg.205]    [Pg.111]    [Pg.272]    [Pg.273]    [Pg.274]    [Pg.406]    [Pg.431]    [Pg.204]    [Pg.419]    [Pg.425]    [Pg.432]    [Pg.151]    [Pg.273]    [Pg.229]    [Pg.86]    [Pg.47]    [Pg.80]    [Pg.83]    [Pg.149]    [Pg.150]    [Pg.168]    [Pg.186]   
See also in sourсe #XX -- [ Pg.34 , Pg.40 ]

See also in sourсe #XX -- [ Pg.11 , Pg.34 , Pg.55 , Pg.134 ]




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Administration intravascular

Antimicrobial polyurethanes for intravascular medical devices

Brain intravascular volumes

Coronary artery intravascular ultrasound image

Disseminated Intravascular Coagulation (DIC) Model

Disseminated intravascular

Disseminated intravascular clotting

Disseminated intravascular coagulation

Disseminated intravascular coagulation anticoagulants

Disseminated intravascular coagulation clinical presentation

Disseminated intravascular coagulation diagnosis

Disseminated intravascular coagulation model

Disseminated intravascular coagulation pathophysiology

Disseminated intravascular coagulation treatment

Disseminated intravascular coagulation, stroke

Disseminated intravascular coagulopathy

Disseminated intravascular concentrate

Disseminated intravascular heparin

Disseminated intravascular incidence

Drug administration intravascular

Endotoxin disseminated intravascular coagulation

Hemolysis, intravascular

Injection intravascular

Intravascular Coagulation

Intravascular catheter

Intravascular complications

Intravascular device-related infections

Intravascular device-related infections polymers

Intravascular device-related infections prevention

Intravascular devices

Intravascular devices infections

Intravascular devices infections associated with

Intravascular enhancement

Intravascular fluid

Intravascular fluid compartment

Intravascular fluid volume

Intravascular fragment

Intravascular glucose sensors

Intravascular haemolysis

Intravascular lead extraction

Intravascular lymphoma

Intravascular magnetic resonance

Intravascular magnetic resonance imaging

Intravascular metabolism

Intravascular neurosurgery

Intravascular oxygenator

Intravascular persistence

Intravascular procedure

Intravascular retention

Intravascular tubing

Intravascular ultrasound

Intravascular volume

Intravascular volume expansion, excessive

Microcatheters intravascular

Pathogenesis of intravascular device-related infections

Pharmacokinetics intravascular administration

Plaques, intravascular

Pregnancy disseminated intravascular coagulation

Prevention of intravascular device-related infections

Prothrombin complex disseminated intravascular

Sepsis disseminated intravascular coagulation

Water-soluble intravascular iodinated

Water-soluble intravascular iodinated contrast agents

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