Nursing Medication Card - Ramipril (Kor/Eng)
Nursing Medication Card – Ramipril
약물명 (Drug Name): Ramipril (라미프릴)
상품명 (Brand Name): Altace (알타제)
약물분류 (Class): Antihypertensive / ACE Inhibitor (혈압강하제 / 안지오텐신 전환효소 억제제)
1. Indications (적응증)
- Hypertension (고혈압)
- Heart failure post-myocardial infarction (심근경색 후 심부전)
- Risk reduction of myocardial infarction, stroke, and death in high-risk patients
(고위험 환자의 심근경색, 뇌졸중, 심혈관 사망 위험 감소)
2. Therapeutic Effects (치료 효과)
- Lowers blood pressure (혈압 감소)
- Improves survival after MI (심근경색 후 생존율 향상)
- Reduces progression of heart failure (심부전 진행 억제)
- Vasodilation and reduced workload on the heart (혈관 확장 및 심장 부담 감소)
3. Absorption (흡수)
- Oral bioavailability: ~50–60% (경구 흡수율 약 50–60%)
- Food may delay absorption but does not reduce effect (음식이 흡수 지연 가능성은 있으나 효과 감소는 없음)
4. Distribution (분포)
- Does not significantly enter breast milk
(모유로 거의 전달되지 않음)
5. Metabolism & Excretion (대사 및 배설)
- Prodrug converted to active metabolite (ramiprilat) in the liver
→ 간에서 활성 대사체(ramiprilat)로 전환 - Excreted via urine and feces
→ 소변과 대변으로 배설 - Half-life: 13–17 hours (반감기: 13–17시간)
6. Adverse Effects (부작용)
Common:
- Hypotension (저혈압)
- Dizziness (어지러움)
- Cough (기침)
Serious (rare):
- Angioedema (혈관부종)
- Hyperkalemia (고칼륨혈증)
- Neutropenia/agranulocytosis (호중구감소증/무과립구증)
7. Dose (용량)
- Hypertension:
PO: 2.5–5 mg once daily, up to 10 mg/day (1–2 divided doses) - Heart failure post-MI:
PO: Start 2.5 mg BID, increase as tolerated (최대 10 mg/day) - Adjust dose in renal impairment
(신장 기능 저하 시 용량 조절 필요)
8. Nursing Considerations (간호 고려사항)
- Monitor blood pressure regularly (혈압 자주 모니터링)
- Monitor renal function (BUN, creatinine) and electrolytes (특히 potassium)
→ 신장 기능 및 전해질 (특히 칼륨) 수치 확인 - Watch for signs of angioedema: facial/lip swelling, difficulty breathing
→ 얼굴, 입술 붓기, 호흡 곤란 시 즉시 보고 - Instruct patient not to use potassium supplements or salt substitutes containing potassium
→ 칼륨 보충제 또는 칼륨 함유 소금 대체제 사용 자제 - May cause persistent dry cough
→ 지속적인 마른 기침 유발 가능성 있음
Ramipril
antihypertensives/ACE inhibitors
● Indications: management of HTN, reduction of risk of death or development of HF following MI
● Therapeutic effects: lowering of BP, improved symptoms in patients w/ HF, lower risk of MI, stroke or death from CVD causes in high-risk patients
● Absorption: 50-60% ac PO
● Distribution: doesn’t enter breast milk
● Protein binding:
● Metabolism&Excretion: converted by liver to ramiprilat, active metabolite
● ADE: CV; hypotension GI; taste disturbances Hemat; agranulocytosis Resp; cough Misc; angioedema
● Dose: PO; HTN-2.5-5 mg/day upto 40mg/day in 1-2 divided doses, IV; HTN-0.625-1.25mg Q6H (upto 5mg every 6hr)