The drug that should be routinely evaluated for possible toxicity is digoxin.
<h3>What is toxicity?</h3>
The term toxicity refers to the point that a drug could lead to harm in a patient. This often stems from the use of the drug.
Given that the drug digoxin has been traditionally used to treat heart conditions an could lead to toxicity, it ought to be evaluated for possible toxicity.
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Answer:
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Explanation:
To depict the recurrence of weight ulcer hazard appraisal in pediatric patients and weight ulcer avoidance intercession utilize by and large and by healing center unit sort, a clear auxiliary examination was performed of information submitted to the National Database for Nursing Quality Indicators (NDNQI) for at slightest 3 of the 4 quarters in 2012.
Significant information on weight ulcer hazard from 271 clinics over the Joined together States extricated from the NDNQI database included understanding skin and weight ulcer hazard evaluation on confirmation, time since the final weight ulcer hazard appraisal, strategy utilized to survey weight ulcer hazard, and chance status.
Extricated information on weight ulcer anticipation included skin evaluation, pressure-redistribution surface utilize, schedule repositioning, wholesome bolster, and dampness administration. These information were organized by unit sort and consolidated with information on clinic characteristics for the investigation.
The frequency of prevention intervention use among those at risk ranged from 99.2% for skin assessment to 70.7% for redistribution surface use.
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Answer:
b) blastic red blood cell (RBC).
Explanation:
In excess of 340 blood group antigens have now been described that vary between individuals. Thus, any unit of blood that is nonautologous represents a significant dose of alloantigen. Most blood group antigens are proteins, which differ by a single amino acid between donors and recipients. Approximately 1 out of every 70 individuals are transfused each year (in the United States alone), which leads to antibody responses to red blood cell <u>(RBC) alloantigens</u> in some transfusion recipients. When alloantibodies are formed, in many cases, RBCs expressing the antigen in question can no longer be safely transfused. However, despite chronic transfusion, only 3% to 10% of recipients (in general) mount an alloantibody response. In some disease states, rates of alloimmunization are much higher (eg, sickle cell disease). For patients who become alloimmunized to multiple antigens, ongoing transfusion therapy becomes increasingly difficult or, in some cases, impossible. While alloantibodies are the ultimate immune effector of humoral alloimmunization, the cellular underpinnings of the immune system that lead to ultimate alloantibody production are complex, including antigen consumption, antigen processing, antigen presentation, T-cell biology.
