A nurse is providing discharge instructions to a client who has been prescribed Lithium for bipolar disorder. Which of the following statements by the client indicates a need for further teaching?
"I should maintain a consistent sodium intake in my diet."
"I should have regular blood tests to monitor my lithium levels."
"It's important to restrict my fluid intake while taking this medication."
"I need to report any signs of nausea, vomiting, or diarrhea to my doctor."
The Correct Answer is C
A. "I should maintain a consistent sodium intake in my diet.": Sodium levels directly affect lithium levels in the body. Fluctuations in sodium intake can lead to lithium toxicity or subtherapeutic effects. A consistent sodium intake helps maintain stable lithium blood levels.
B. "I should have regular blood tests to monitor my lithium levels.": Lithium has a narrow therapeutic range and can become toxic if levels rise too high. Regular monitoring is essential to ensure safe and effective treatment, especially during dose adjustments or illness.
C. "It's important to restrict my fluid intake while taking this medication.": This statement is incorrect and indicates a need for further teaching. Fluid restriction can lead to dehydration, increasing lithium reabsorption in the kidneys and raising the risk of toxicity. Clients should maintain adequate hydration, especially during hot weather or illness.
D. "I need to report any signs of nausea, vomiting, or diarrhea to my doctor.": These are early signs of lithium toxicity. Prompt reporting is crucial so that lithium levels can be checked and treatment adjusted to prevent progression to severe toxicity.
Nursing Test Bank
Naxlex Comprehensive Predictor Exams
Related Questions
Correct Answer is B
Explanation
A. Cardiotoxicity: While NSAIDs can contribute to cardiovascular risks such as hypertension and fluid retention, nephrotoxicity is the more direct explanation for the elevated kidney function tests and potassium level. Cardiotoxicity typically presents with symptoms like heart failure or arrhythmias rather than kidney-related lab abnormalities.
B. Nephrotoxicity: NSAIDs inhibit prostaglandin synthesis, which plays a key role in maintaining renal blood flow, especially in older adults or those with preexisting renal impairment. Chronic NSAID use can reduce glomerular filtration, leading to elevated creatinine, hyperkalemia, and worsening blood pressure control, all of which are evident in this patient.
C. Neurotoxicity: Neurotoxic effects are not commonly associated with NSAID use. Symptoms of neurotoxicity include confusion or seizures, which are not relevant to the clinical findings in this scenario.
D. Hepatotoxicity: NSAID-induced liver injury is rare and would typically present with elevated liver enzymes (AST, ALT), not elevated creatinine or potassium. The current lab findings and blood pressure changes are more consistent with kidney involvement.
Correct Answer is B
Explanation
A. Second-generation antihistamines have shorter half-lives and require more frequent dosing compared to first-generation antihistamines: Second-generation antihistamines typically have longer half-lives, allowing once-daily dosing. They are designed for sustained action with improved compliance and fewer side effects.
B. First-generation antihistamines block both histamine and muscarinic receptors, while second-generation antihistamines primarily block histamine receptors: First-generation agents, such as diphenhydramine, cross the blood-brain barrier and exert anticholinergic effects by blocking muscarinic receptors. Second-generation antihistamines are more selective for peripheral H1 receptors, resulting in fewer CNS and anticholinergic side effects.
C. First-generation antihistamines are less likely to cause sedation compared to second-generation antihistamines: First-generation antihistamines are more likely to cause sedation because they easily penetrate the blood-brain barrier and affect central H1 receptors, unlike second-generation agents.
D. Second-generation antihistamines cross the blood-brain barrier, causing significant central nervous system effects: These medications are designed not to cross the blood-brain barrier significantly, which is why they are much less sedating and have minimal CNS effects compared to first-generation antihistamines.
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