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¹Ýµå½Ã °ø½Å·Â ÀÖ´Â ¹®ÇåÀ» ´Ù½Ã Çѹø Âü°í ÇϽñ⠹ٶó¸ç ÀÇ»ç ¶Ç´Â ¾à»çÀÇ ÆÇ´Ü¿¡ µû¶ó Åõ¿©¿©ºÎ°¡ °áÁ¤µÇ¾î¾ß ÇÕ´Ï´Ù.
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°ü»óµ¿¸Æ ½ºÅÙÆ® »ðÀÔ¼ú ÈÄ Ç÷ÀüÁõ°ú Àç ÇùÂø ¹æÁö¸¦ ¸ñÀûÀ¸·Î Åõ¿©ÇÏ´Â Ç×Ç÷¼ÒÆÇ 3Á¦¿ä¹ý (aspirin, clopidogrel, cilostazol) ÀÇ ÀÎÁ¤¹üÀ§
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-¿ø¿Ü󹿳»¿ª(¡®06.8.18) : Ç츣º¥¼¹æÁ¤90mg 1T ---------
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- ¡¯05.2.17: chest painÀ» ÁÖ È£¼Ò·Î ³»¿ø (¡®05.1.31 ÀÌÈÄ 3Â÷·Ê)
nature:squeezing, duration: 5min, agg. factor: µî»ê, °è´Ü ¿À¸¦ ¶§
relieving:resting, radiating pain(+): Lt arm, resting pain(-)
-¡®05.2.18: CAG & PCI(TherapeuticIntervention)
Lt - Lt main(body) : Discrete eccentric stenosis 80%
LCXand LAD : relatively good patency
Rt- No significant luminal stenosis
Balloon angioplasty with Aqua 3.5x15mm 8atm 10" after then suboptimalresult with RS 50%. Stent insertion with Driver 4.0x15mm 14atm 10"
Åð¿ø ¾à(7ÀÏ): Herben 90mg 2T,
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¢Ñ Åð¿ø ÈÄ Çö Áø·áºÐ±îÁö 1³â6°³¿ù°£ 3Á¦¿ä¹ý ó¹æÁß ÀÓ.
¡Û û±¸³»¿ª(¿Ü·¡)
-»óº´¸í : ±âŸ ÇüÅÂÀÇ Çù½ÉÁõ, º»Å¼º°íÇ÷¾Ð, Àν¶¸°ºñÀÇÁ¸¼º ´ç´¢º´
-¿ø¿Ü󹿳»¿ª(¡®06.8.7) : Æ®¸®Å×À̽ºÁ¤ 5mg 1T --------
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º£À̽¼Á¤ 0.3mg 3T l
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¡Û Áø·á³»¿ª(ÀÔ¿ø)
- ¡¯06.3.30: ³»¿ø 20ÀÏÀü resting½Ã 1½Ã°£ °¡·®ÀÇ chest pain ÀÖ¾úÀ¸¸ç ³»¿ø 1ÁÖÀÏ Àü chest painÀÌ ¼öÂ÷·Ê ÀÖ¾úÀ¸³ª NTG¿¡ response¸¦ º¸¿´°í ³»¿ø ´çÀÏ »õº® ÀÚ´Ù°¡ chest pain ÀÖ¾îÀÔ¿øÇÔ.
°ú°Å·Â) ´ç´¢: À̹ø¿¡ óÀ½À¸·Î Áø´Ü¹ÞÀ½ (¾Æ¸¶¸±Á¤ 2§·*1, º£À̽¼Á¤ 0.3§·*3)
°¡Á··Â) ¾Æ¹öÁö: AMI(+), ¾î¸Ó´Ï CABG Hx(+)
- ¡¯06.3.31: CAG & PCI(TherapeuticIntervention)
CAG>Lt- pLAD, mLCX : minimal stenosis, mLAD : diffuse irregular stenosis 30-75%
pLCX: tubular eccentric stenosis 30%, dLCX :tubular eccentric stenosis 40%
Rt-No luminal stenosis
Balloon angioplasty with Aqua 2.5x20mm 4atm 4atm 6atm 10" Stent implantationwith Cypher 2.75x33mm 8atm 14atm 10" (stent indication : suboptimal resultwith RS 60%)
Åð¿ø ¾à(7ÀÏ): Æ®¸®Å×À̽ºÁ¤5mg 1T, ¾Æ¸¶¸±Á¤2mg 1T, º£À̽¼Á¤0.3mg 3T
Ç㺥Á¤ 90mg 2T, º£½ºÆ¼µòÁ¤20mg 2T,
¾Æ½ºÇǸ°ÇÁ·ÎÅØÆ®Á¤100mg 2T, Çöóºò½ºÁ¤ 1T, ÇÁ·¹Å»Á¤100mg 2T
¢Ñ Åð¿ø ÈÄ Çö Áø·áºÐ±îÁö 5°³¿ù°£ 3Á¦¿ä¹ý ó¹æÁß ÀÓ.
¡á Âü°í
¡Û EBH Æò°¡º¸°í¼(2008.12.4)
¡Û ´ëÇѽÉÀåÇÐȸ Àǰß
¡Û Comparison of TripleVersus Dual Antiplatelet Therapy After Drug-Eluting Stent Implantation (fromthe DECLARE-Long trial) Lee SW, Am J Cardiol. 2007 Oct 1;100(7):1103-8
¡Û Reduced 6-monthresource use and costs associated with cilostazol in patients after successfulcoronary stent implantation: Results from the Cilostazol for RESTenosis (CREST)trial Zefeng Zhang, Am Heart J 2006;152:770-6
¡Û Triple Versus Dual Antiplatelet Therapy after Coronary Stenting-Impact on stent Thrombosis
Seung-Whab Lee, J Am CollCardiol 2005;46:1833-7
¡Û Coronary stentrestenosis in patients treated with cilostazol. Douglas JS Jr, Circulation. 2005; 112:2826-2832.
¡á ½ÉÀdz»¿ë
- °ü»óµ¿¸Æ½ºÅÙÆ®»ðÀÔ¼ú ÈÄ ½ºÅÙÆ®Ç÷ÀüÁõ ¹× Àç ÇùÂø ¹æÁö¸¦ ¸ñÀûÀ¸·Î ½ÃÇàÇÏ´Â Ç×Ç÷¼ÒÆÇ 3Á¦¿ä¹ý(aspirin, clopidogrel, cilostazol)ÀÇÀû¿ë´ë»ó ¹× Åõ¿©±â°£¿¡ ´ëÇÏ¿© ³íÀÇÇÑ °á°ú, Àӻ󿬱¸¹®Çå ¹× °ü·ÃÇÐȸ ÀÇ°ß µî¿¡¼ ½ºÅÙÆ®»ðÀÔ¼ú °ü·ÃÇÑ Àç ÇùÂø ¹ß»ý µîÀÌ ³ôÀº °í À§Ç豺Àº ¡®´ç´¢, Long stenting, small lesion,multi-stenting¡¯µîÀ¸·Î º¸°í ÀÖÀ¸¸ç, EBH Æò°¡º¸°í¼¿¡¼ ¡°°ü»óµ¿¸Æ½ºÅÙÆ® ½Ã¼úÈÄ »ç¿ëÇÑ ½Ç·Î½ºÅ¸Á¹À» Æ÷ÇÔÇÑ Ç×Ç÷¼ÒÆÇ 3Á¦¿ä¹ýÀº ÀÓ»óÀû À¯¿ë¼º Ãø¸é¿¡¼ ±âÁ¸ÀÇ 2Á¦¿ä¹ý°ú ºñ±³ÇÒ ¶§ ÁÖ¿ä½ÉÀå»ç°Ç(MACE) ¹× Ç¥Àûº´º¯Àç½Ã¼ú, Ç¥ÀûÇ÷°üÀç½Ã¼ú, Àç ÇùÂø·ü, Èıâ¼Õ½ÇÀÇ À§ÇèÀ» ÁÙÀ̴µ¥ ´õ ¿ì¿ùÇÑ °á°ú¡±¸¦ º¸¿´´Ù°í ÇÔ.
- µû¶ó¼, Ç×Ç÷¼ÒÆÇ 3Á¦¿ä¹ýÀ»ÀÎÁ¤ÇÏ´Â °í À§Ç豺ÀÇ Àû¿ë¹üÀ§´Â ¡°´ç´¢º´ ȯÀÚ, ÀçÇùÂø º´º¯, ´ÙÇ÷°üÇùÂø¿¡ ´ëÇÑ ½ºÅÙÆ® ½Ã¼ú(multi-stenting)¡±·Î ÇϵÇ, Åõ¿©±â°£Àº 6°³¿ù±îÁö ÀÎÁ¤Å°·Î ÇÔ.
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CYP450 Drug Interaction
[CYP450 TableÁ÷Á¢Á¶È¸]
Description
Aspirin¿¡ ´ëÇÑ Description Á¤º¸ The prototypical analgesic used in the treatment of mild to moderate pain. It has anti-inflammatory and antipyretic properties and acts as an inhibitor of cyclooxygenase which results in the inhibition of the biosynthesis of prostaglandins. Aspirin also inhibits platelet aggregation and is used in the prevention of arterial and venous thrombosis. (From Martindale, The Extra Pharmacopoeia, 30th ed, p5)
Dosage Form
Aspirin¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Gum OralLiquid OralPowder OralSolution / drops OralSuppository RectalTablet OralTablet, chewable OralTablet, coated OralTablet, delayed release Oral
Drug Category
Aspirin¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anti-Inflammatory Agents, Non-SteroidalAnticoagulantsCyclooxygenase InhibitorsFibrinolytic AgentsPlatelet Aggregation InhibitorsSalicylates
Smiles String Canonical
Aspirin¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CC(=O)OC1=CC=CC=C1C(O)=O
Smiles String Isomeric
Aspirin¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ CC(=O)OC1=CC=CC=C1C(O)=O
InChI Identifier
Aspirin¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C9H8O4/c1-6(10)13-8-5-3-2-4-7(8)9(11)12/h2-5H,1H3,(H,11,12)/f/h11H
Chemical IUPAC Name
Aspirin¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ 2-acetyloxybenzoic acid
Drug-Induced Toxicity Related Proteins
ASPIRIN ÀÇ Drug-Induced Toxicity Related ProteinÁ¤º¸Replated Protein :VimentinDrug :aspirin Toxicity :aspirin-induced gastric mucosal microvessels injury . [¹Ù·Î°¡±â] Replated Protein :Angiopoietin-related protein Drug :aspirin Toxicity :damage to microvessels. rupture of capillary walls. necrosis of endothelial cells. damage to endothelial organelles. deposition of fibrin. adherence of platelets to damaged endothelium. [¹Ù·Î°¡±â] Replated Protein :Myeloperoxidase Drug :aspirin Toxicity :haemorrhagic erosions. [¹Ù·Î°¡±â] Replated Protein :Thromboxane A2 receptorDrug :aspirin Toxicity :thrombotic complications. [¹Ù·Î°¡±â] Replated Protein :Integrin beta-3Drug :Aspirin Toxicity :Antiplatelet effect. [¹Ù·Î°¡±â] Replated Protein :Integrin alpha-IibDrug :Aspirin Toxicity :Antiplatelet effect. [¹Ù·Î°¡±â] Replated Protein :Nuclear factor NF-kappa-B p105 subunit Drug :aspirin Toxicity :apoptosis in human colon cancer cells. [¹Ù·Î°¡±â]
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