Physician order reads: Furosemide 60 mg po bid. Available: 40 mg scored tablets. What do you administer to the patient?

Choice A reason: Stopping the enema entirely is premature and unnecessary for cramping, which is a common response to rapid fluid instillation. Documentation of intolerance is only appropriate if the procedure cannot be completed after attempting adjustments. This action fails to address the cramping’s cause, potentially delaying constipation relief and patient comfort.

Choice B reason: Lowering the solution container reduces the flow rate of the enema, decreasing intraluminal pressure in the colon. Cramping often results from rapid fluid instillation stretching the bowel. Slowing the flow allows the colon to accommodate the fluid, alleviating discomfort while continuing the procedure effectively.

Choice C reason: Encouraging the client to bear down is inappropriate as it may cause premature expulsion of the enema fluid, reducing its effectiveness in relieving constipation. Bearing down increases intra-abdominal pressure, potentially exacerbating cramping rather than alleviating it, and does not address the underlying cause of discomfort from fluid instillation.

Choice D reason: Allowing the client to expel fluid prematurely interrupts the enema’s purpose of softening stool and stimulating bowel movement. While it may temporarily relieve cramping, it reduces the procedure’s efficacy, potentially requiring a repeat enema, which increases patient discomfort and procedural risks like rectal irritation.

Choice A reason: Sufficient medication in the PCA syringe does not indicate effective pain management. It may reflect underuse due to inadequate pain control or patient misunderstanding of PCA use. Pain relief is assessed by patient-reported outcomes, not medication volume remaining.

Choice B reason: Sleeping and being difficult to arouse suggests oversedation, a potential adverse effect of PCA, particularly with opioids. This indicates excessive dosing rather than effective pain management, risking respiratory depression or other complications, requiring immediate dose adjustment or monitoring.

Choice C reason: A pain rating of 2 on a 0 to 10 scale indicates effective pain management. PCA allows patients to self-administer doses within safe limits, achieving low pain levels without excessive sedation, reflecting optimal balance of analgesia and patient safety post-trauma.

Choice D reason: Pressing the PCA button shows patient engagement but not pain control effectiveness. Frequent pressing may indicate inadequate relief, while infrequent use could reflect sufficient control or misunderstanding. Patient-reported pain levels are the primary indicator of PCA efficacy.