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     Àü¸³»ùÀÇÁõ½Ä »óº´¿¡ ¾ËÆÄÂ÷´ÜÁ¦(¥á-adrenergic blocker) 2Á¾º´¿ëÅõ¿© ÀÎÁ¤¿©ºÎ(2»ç·Ê)  
¡á û±¸ ¹× Áø·á³»¿ª  
    
  ¡¼Ã»±¸³»¿ª¡½  
     ¡Û »óº´¸í : Àü¸³»ùÀÇÁõ½Ä, ¸¸¼º Àü¸³»ù¿°  
    ¡Û ÁÖ¿ä û±¸³»¿ª  
        259 ÀÚÆ®¶ö¿¢½º¿¤Á¤10mg      1x 60  
        259 ޽ºÇǵåĸ½¶            1x 60  
  ¡¼Áø·á³»¿ª¡½  
   6³âÀü 11.1   CC : Dysuria,fever & chilling (on set : 1day)  
               PH : Renal Tbc, Lt -> ¡Û¡Û´ëº´¿ø 1993³â nephrectomy,Lt  
                    BPH -> Local ºñ´¢±â°ú¿¡¼ medication  
               ROS: fever & chilling (+/+), dysuria(+)  
               PEx: No CVA(costovertebral angle) tenderness  
               Rectal exam: moderate & marked. enlarged prostate   
               IMP: Acute prostatitis  
   2³âÀü 1.25    ÇϷ糯ݼ¿ 0.2mg   1x90  
   Àü³â 8.3     ¢ºBPH °Ë»ç  => Uric acid: 7.9 ¡è,   S-PSA/freePSA : 1.0 / 0.62   
                             UFR(Urine flow rate)c £þ  RU: Qmax117ml/s / 101cc   
                            TRUS(transrectal ultrasonography): prostate volume 44cc <- 24cc   
       8.17   DRE(digital rectal examination)  
                : 1. Symmetry. moderately enlargedprostate  
                  2. Median groove intact  
                  3. Nodule(-/-),  Tenderness(-/-)  
                  4. Regular surface, elastic consistency  
              IPSS(International prostate symptom score) : 16 + 3   
              Med: (ÇϷ糯ݼ¿0.2mg , ÀÚÆ®¶ö¿¢½º¿¤Á¤10mg , ¹Ù¸®¿òÁ¤) 1x35  
       9.20   ROS: good  
              Med: (ÀÚÆ®¶ö¿¢½º¿¤Á¤10mg , ޽ºÇǵåĸ½¶ , ¹Ù¸®¿òÁ¤)1x42  
       11.2   ROS: so so  
              Med: (ÀÚÆ®¶ö¿¢½º¿¤Á¤10mg , ޽ºÇǵåĸ½¶ , ¹Ù¸®¿òÁ¤)1x95  
   ±Ý³â 2.2    Med: (ÀÚÆ®¶ö¿¢½º¿¤Á¤10mg , ޽ºÇǵåĸ½¶ , ¹Ù¸®¿òÁ¤) 1x95  
       4.26   ROS: so so  
              Med: (ÀÚÆ®¶ö¿¢½º¿¤Á¤10mg , ޽ºÇǵåĸ½¶ , ¹Ù¸®¿òÁ¤)1x90  
       6.20   S: ¹è´Â Èûµé´Ù. ¿ä·Î°¡ ¾ÆÇÁ´Ù. ¿ìÃø ¼ÇýºÎµµ.  
              EPS: WBC 10~15/HPF, MQ 0~1/HPF, clumping (-)/HPF  
              ¢º BPH°Ë»ç =>  S-PSA/free PSA: 1.0/0.55   
                            UFRc £þ  RU : Qmax21ml/s / 60cc   
                            TRUS : prostate volume 38cc <- 44cc   
              Med: (Å©¶óºñÆ®Á¤, Å©¸®¸¶ÀÎÁ¤, ¸Þµð¶ô¿¡½ºÀå¿ëݼ¿)3x21  
       7.11   EPS: WBC 10~15/HPF, MQ 0~1/HPF, clumping 0~1/HPF, Many sperm  
              DRE : 1. Symmetry. moderately enlarged prostate  
                    2. Median groove intact  
                    3. Nodule(-/-), Tenderness(-/-)  
                    4. Regular surface, elastic to consistency  
              Med: (ÀÚÆ®¶ö¿¢½º¿¤Á¤10mg , ޽ºÇǵåĸ½¶ , ¹Ù¸®¿òÁ¤)1x30  
        8.8    ROS: so so                                               ¦Â  
              EPS: WBC 3~5/HPF, MQ (-)/HPF, clumping(-)/HPF            ꠛ  * Çöû±¸ºÐ*   
              Med: (ÀÚÆ®¶ö¿¢½º¿¤Á¤10mg  , ޽ºÇǵåĸ½¶  , ¹Ù¸®¿òÁ¤)1x60     ¦Ä  
    
  ¡¼Ã»±¸³»¿ª¡½  
     ¡Û »óº´¸í : Àü¸³»ùÀÇ Áõ½Ä  
    ¡Û ÁÖ¿ä û±¸³»¿ª  
         214 Ä«µÎ¶ó¿¢½º¿¤¼¹æÁ¤4mg       1x90  
         259 ÇϷ糯µðÁ¤0.2mg             1x90  
  ¡¼Áø·á³»¿ª¡½  
   5³âÀü 4.8   CC : Terminaldysuria (D: 15days)  
              PH : 5-6³âÀü ¡Û¡Ûº´¿ø¿¡¼ BPH·Î Ä¡·á  
              ROS: Frequency(+),  nocturia 1 ȸ/night,  weakurinary stream(-)   
              Rectal exam: moderate asymmetry enlarged prostate (Lt< Rt) , notnodule  
   3³âÀü 12.24  No symptom  
               (Ä«µÎ¶ó¿¢½º¿¤¼¹æÁ¤4mg , ¹Ù¸®¿òÁ¤) 1x84  
   2³âÀü 4.15   (Ä«µÎ¶ó¿¢½º¿¤¼¹æÁ¤4mg , ¹Ù¸®¿òÁ¤) 1x84  
        7.15   (Ä«µÎ¶ó¿¢½º¿¤¼¹æÁ¤4mg , ¹Ù¸®¿òÁ¤)1x84,  ÇҽÿÂÁ¤  1x14  
    ±Ý³â 8.24    S: ¿Èê ÀüºÎÅÍ °¡²û¾¿ ÂÇÏ´Ù                       ¦Â  
               P: U/A(ÀÀ±Þ) :WNL                                    ꠛ  * Çöû±¸ºÐ*   
                  Cardura Çϰí Harnal º¹¿ë                           ꠛ  
                  (Ä«µÎ¶ó¿¢½º¿¤¼¹æÁ¤4mg,   ÇϷ糯µðÁ¤0.2mg  ) 1x90     ¦Ä  
¡á Âü°í   
   ¡Û ¾ËÆÄÂ÷´ÜÁ¦ ¹× 5¾ËÆÄȯ¿øÈ¿¼Ò¾ïÁ¦Á¦ÀǽÄǰÀǾàǰ¾ÈÀüûÀå Çã°¡»çÇ×  
   ¡Û Wein: CAMPBELL'sUrology, 9th ed. 2007  
   ¡Û ºñ´¢±â°úÇÐ Á¦4ÆÇ. ´ëÇÑ ºñ´¢±â°úÇÐȸ, 2007. p372-374  
   ¡Û Goldman: Cecil Medicine,23rd ed. 2007. p916-919  
   ¡Û CMDT(Current MedicalDiagnosis & Treatment) 42nd Edition. 2003, pp926-933  
   ¡Û American UrologicalAssociation, Inc. The management of benign prostatic hyperplasia.Baltimore.  2003.(NGC guidline)  
   ¡Û NcVary KT. A review ofcombination therapy in patients with benign prostatic hyperplasia. Clin Ther.2007 Mar;29(3):387-98.  
¡á ½ÉÀdz»¿ë   
   - ¾ç¼ºÀü¸³¼±ºñ´ëÁõ ȯÀÚÀÇ ¾à¹°Ä¡·á¿¡ ´ëÇÏ¿©´Â ±³°ú¼, ÀÓ»óÁø·áÁöħ ¹× °ü·Ã ÇÐȸÀÇ°ß µîÀ» Âü°íÇÒ ¶§ ¾ËÆÄÂ÷´ÜÁ¦(¥á- adrenergic blockers)¿Í 5¾ËÆÄȯ¿øÈ¿¼Ò¾ïÁ¦Á¦(5¥á-reductase inhibitors)°¡ 1Â÷ Ä¡·á¾àÁ¦·Î ±ÇÀåµÇ°í ÀÖÀ¸¸ç, Àü¸³¼±ÀÇ Å©±â°¡ Áõ°¡ÇÑ °æ¿ì¿¡´Â¾ËÆÄÂ÷´ÜÁ¦¿Í 5¾ËÆÄȯ¿øÈ¿¼Ò¾ïÁ¦Á¦ÀÇ º´ÇÕ¿ä¹ýÀÌ Àü¸³¼±ÀÇ Å©±â¸¦ °¨¼Ò½Ã۰í, ÇϺοä·ÎÁõ»óÀÇ °³¼±°ú º´º¯ÀÇ ÁøÇàÀ» ¸·´Âµ¥ È¿°ú°¡ ÀÖ´Ù°í ÇÏ¿´À½.  
     ¶ÇÇÑ, Àü¸³¼±ºñ´ëÁõ¿¡¾ËÆÄÂ÷´ÜÁ¦(¥á- adrenergic blockers) 2Á¾À»º´¿ë Åõ¿©ÇÏ´Â °ÍÀÌ Ä¡·á¿¡ È¿°úÀûÀ̶ó´Â ÀÓ»ó±Ù°Å°¡ ÃæºÐÇÏÁö ¾ÊÀ¸¸ç, ¾ËÆÄÂ÷´ÜÁ¦ ´Üµ¶¿ä¹ýÀ¸·Î Áõ»ó °³¼±µî Ä¡·áÈ¿°ú°¡ ºÎÁ·ÇÑ °æ¿ì¿¡´Â ȯÀÚÀÇ »óÅ µîÀ» °í·ÁÇÏ¿© ¿ë·®À» Áõ°¡Çϰųª ´Ù¸¥ ¾ËÆÄÂ÷´ÜÁ¦ ȤÀº ´Ù¸¥ ±âÀüÀÇ ¾àÁ¦·Î º¯°æÇÏ¿© Åõ¾àÇÏ´Â °ÍÀÌ ¹Ù¶÷Á÷ÇÔ.  
   - µû¶ó¼, µ¿°Ç¿¡¼ Àü¸³»ùÀÇ Áõ½Ä »óº´À¸·Î ¾ËÆÄÂ÷´ÜÁ¦ 2Á¾À» º´¿ë Åõ¿©ÇÑ A~B»ç·Ê¿¡´ëÇØ¼´Â ¾ËÆÄÂ÷´ÜÁ¦ 1Á¾¸¸ ÀÎÁ¤ÇÔ.  
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      Alfuzosin¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸  Alfuzosin acts by inhibiting the postsynaptic alpha(1)-adrenoceptors on vascular smooth muscle. This inhibits the vasoconstrictor effect of circulating and locally released catecholamines (epinephrine and norepinephrine), resulting in peripheral vasodilation. 
     
   
  
   
    Pharmacology 
     
      Alfuzosin¿¡ ´ëÇÑ Pharmacology Á¤º¸  Alfuzosin is an alpha-adrenergic blocking agent used to treat hypertension and benign prostatic hyperplasia. Accordingly, alfuzosin is a selective inhibitor of the alpha1 subtype of alpha adrenergic receptors. In the human prostate, alfuzosin antagonizes phenylephrine (alpha1 agonist)-induced contractions, in vitro , and binds with high affinity to the alpha1c adrenoceptor, which is thought to be the predominant functional type in the prostate. Studies in normal human subjects have shown that alfuzosin competitively antagonized the pressor effects of phenylephrine (an alpha1 agonist) and the systolic pressor effect of norepinephrine. The antihypertensive effect of alfuzosin results from a decrease in systemic vascular resistance and the parent compound alfuzosin is primarily responsible for the antihypertensive activity. 
     
   
  
   
    Metabolism 
    
      Alfuzosin¿¡ ´ëÇÑ Metabolism Á¤º¸  # Phase_1_Metabolizing_Enzyme:Cytochrome P450 3A4 (CYP3A4) 
     
   
  
   
    Protein Binding 
    
      Alfuzosin¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸  82%-90% 
     
   
  
   
    Half-life 
    
      Alfuzosin¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸  10 hours 
     
   
  
   
    Absorption 
    
      Alfuzosin¿¡ ´ëÇÑ Absorption Á¤º¸  Absorption is 50% lower under fasting conditions 
     
   
  
   
    Pharmacokinetics 
    
      Alfuzosin HClÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á  
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    Biotransformation 
    
      Alfuzosin¿¡ ´ëÇÑ Biotransformation Á¤º¸  Hepatic. Alfuzosin undergoes extensive metabolism by the liver, with only 11% of the administered dose excreted unchanged in the urine. Alfuzosin is metabolized by three metabolic pathways: oxidation, O-demethylations, and N-dealkylation. The metabolites are not pharmacologically active. CYP3A4 is the principal hepatic enzyme isoform involved in its metabolism. 
     
   
  
   
    Toxicity 
    
      Alfuzosin¿¡ ´ëÇÑ Toxicity Á¤º¸  Side effects are dizziness (due to postural hypotension), upper respiratory tract infection, headache, and fatigue. 
     
   
  
   
    Drug Interactions 
    
      Alfuzosin¿¡ ´ëÇÑ Drug_Interactions Á¤º¸  Itraconazole	The antifungal increases the effect of alfuzosinKetoconazole	The antifungal increases the effect of alfuzosinRitonavir	Ritonavir increases the effect/toxicity of alfuzosinVardenafil	Risk of significant hypotension with this association 
     
   
  
   
    CYP450  Drug Interaction 
    
      [CYP450 TableÁ÷Á¢Á¶È¸]  
     
   
  
   
    Food Interaction 
    
      Alfuzosin¿¡ ´ëÇÑ Food Interaction Á¤º¸  Take after a meal (always the same meal), product bioavailability is reduced when taken on an empty stomach. 
     
   
  
   
    Drug Target 
    
      
      [Drug Target]  
     
   
  
   
    Description 
    
      Alfuzosin¿¡ ´ëÇÑ Description Á¤º¸  Alfuzosin (INN, provided as the hydrochloride salt) is an alpha-adrenergic blocker used to treat benign prostatic hyperplasia (BPH). It works by relaxing the muscles in the prostate and bladder neck, making it easier to urinate. [Wikipedia] 
     
   
  
   
    Dosage Form 
    
      Alfuzosin¿¡ ´ëÇÑ Dosage_Form Á¤º¸  Tablet, extended release	Oral 
     
   
  
   
    Drug Category 
    
      Alfuzosin¿¡ ´ëÇÑ Drug_Category Á¤º¸  Adrenergic alpha-AntagonistsAntihypertensive Agents 
     
   
  
   
    Smiles String Canonical 
    
      Alfuzosin¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸  COC1=C(OC)C=C2C(N)=NC(=NC2=C1)N(C)CCCNC(=O)C1CCCO1 
     
   
  
   
    Smiles String Isomeric 
    
      Alfuzosin¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸  COC1=C(OC)C=C2C(N)=NC(=NC2=C1)N(C)CCCNC(=O)[C@H]1CCCO1 
     
   
  
   
    InChI Identifier 
    
      Alfuzosin¿¡ ´ëÇÑ InChI_Identifier Á¤º¸  InChI=1/C19H27N5O4/c1-24(8-5-7-21-18(25)14-6-4-9-28-14)19-22-13-11-16(27-3)15(26-2)10-12(13)17(20)23-19/h10-11,14H,4-9H2,1-3H3,(H,21,25)(H2,20,22,23)/f/h21H,20H2 
     
   
  
   
    Chemical IUPAC Name 
    
      Alfuzosin¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸  N-[3-[(4-amino-6,7-dimethoxyquinazolin-2-yl)-methylamino]propyl]oxolane-2-carboxamide 
     
   
    
 
	  
	   
	
	  
       
	    
	      
	        
            
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