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                            ¢Ñ LLL bronchopeumonia·Î ¾à¹°Ä¡·á ÇßÀ¸³ª, È£Àü¾ø¾î ±â°üÁö°æ°Ë»ç ½ÃÇàÇßÀ¸³ª, ¾Ç¼º¼Ò°ß ¾øÀ½.  
                ±Ý³â 1.6    Local Chest X-Ray»óRLL pneumonia º¸ÀÓ.  
                     1.9    Local Chest X-Ray f/u»ó ¾çÆóÇÏ¿±(bothlower lobe) pneumoniaÀ¸·Î ÁøÇà  
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              Chest X-Ray»ó R/O pneumonia·Î ceftriaxone, azithromycin ½ÃÀÛ 
       1.12   #1 R/O bronchial asthma  
                 BLL(both lower lobe) fine crackle & wheezing(+)  
                  -> R/O asthma·Î ventolin & atrovent nebulizer,solu-M30mg bid start  
              #2 Both lower lung pneumonic consolidation  
                 Chest X-Ray»ó pneumonic consolidation ÁøÇà º¸¿© cefepime,cipro change  
                 Respiratory failure·Î ÁßȯÀڽǷΠ¿Å±â°í ±â°ü³»»ð°ü ½ÃÇà.  
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                 1. Extensive and patchy parenchymal opacities in both lungs in a patient withcolon cancer who underwent low anterior resection.  
                     DDx. Bacterial bronchopneumonia, most likely.  
                 2. Bilateral pleural effusions.  
       1.15   Fever, RUL & RLL consolidation Áõ°¡ ->Vancomycin add.  
       1.16   ¢ºChest H.R CT. Bronchiectasis study  
                 1. Progressed disease with increased extent of parenchymal opacities in bothlungs. R/O Diffuse alveolar damage.  
                 2. Increased amount of pleural effusions, bilateral.  
       1.24   ¢ºTracheal Aspiration(1.22°Ë»ç/1.24º¸°í)  
                : #1 Enterococcus faecium, many (R : Vancomycin >=32 µî)¡²Âü°í¡³VRE °ËÃâ  
       1.29   Tracheostomy ½ÃÇà.  
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       2.22   T-cannula Á¦°ÅÇÔ -> O2 1L VNP À¸·Î SpO2 95% À¯Áö  
¡á Âü°í  
   ¡Û º¸°Çº¹ÁöºÎ °í½Ã Á¦2007-77È£(2007.8.30) ꡒÀÚ4-1 Çϱ⵵Áõ±âÈíÀÔÄ¡·áÀÎÁ¤±âÁØꡓ  
   ¡Û ½É»çÁöħ (2002.1.28)ꡒÀΰøÈ£Èí±â¿¡¿¬°áÇÏ¿© ½Ç½ÃÇÑ Çϱ⵵Áõ±âÈíÀÔÄ¡·á ÀÎÁ¤¿©ºÎꡓ  
   ¡Û º¥Å丰ÈíÀÔ¾×, ¾ÆÆ®·Îº¥Æ®ÈíÀÔ¾×À¯µðºñ½ÄǰÀǾàǰ¾ÈÀüûÀå Çã°¡»çÇ×  
   ¡Û Dennis L. Kasper, et al.Harrison'S Principles of Internal Medicine, 16th edition, 2005.  
   ¡Û Cecil textbook ofmedicine, 22nd edition, 2004, p519-522  
   ¡Û Alan F. Barker, M.D.Bronchiectasis. N Engl J Med, Volume 346:1383-1393, May 2, 2002.  
   ¡Û Aetna :Nebulizers (2006.11.13)  
   ¡Û °ü·Ã ¼ö°¡ ¹× ¼ö°¡Çؼ³  
¡á ½ÉÀdz»¿ë  
   - ÀÚ4-1 Çϱ⵵Áõ±âÈíÀÔÄ¡·á ÀÎÁ¤±âÁØ(°í½Ã Á¦2007-77È£¡®07.8.30)Àº  ꡒõ½ÄÀ̳ª¸¸¼ºÆó¼â¼º ÆóÁúȯÀÇ ±Þ¼º¾Çȱâ, ±Þ¼º¼¼±â°üÁö¿°ÀÇ È£Èí°ï¶õÄ¡·áꡓ¿¡½Ç½Ã ½Ã ÀÎÁ¤Çϰí ÀÖÀ¸¸ç, ÀΰøÈ£Èí±â¿¡ Nebulizer±â±¸µîÀ» ¿¬°áÇÏ¿© Çϱ⵵ Áõ±âÈíÀÔÄ¡·á ½Ã µ¿ ¼ö°¡¸¦ º°µµ·Î ÀÎÁ¤ÇÏÁö ¾Ê°í ÀÖÀ½.  
   - µ¿ °Ç(³²/85¼¼)Àº Æó·Å »óº´À¸·Î º¥Å丰 ÈíÀÔ¾×°ú ¾ÆÆ®·Îº¥Æ® ÈíÀÔ¾×À¯µðºñ ¾àÁ¦¹× ÀÚ4-1 Çϱ⵵ Áõ±âÈíÀÔÄ¡·á°¡ û±¸µÈ »ç·Ê·Î,  
      Áø·á³»¿ª ¹× ÀÇ»ç¼Ò°ß¼¿¡ ÀÇÇϸé 9³âÀü ±â°üÁöÈ®ÀåÁõ Áø´ÜÀ» ¹ÞÀº ÈÄ Ä¡·áÁßÀΠȯÀÚ·Î, ±Ý³â 1¿ù 10ÀÏ x-ray»ó¾çÆóÇÏ¿± Æó·ÅÀ¸·Î ÁøÇàµÇ¾î 44Àϰ£ ÀÔ¿øÄ¡·á Áß 1¿ù 12ÀÏ¿¡ ½ÃÇàÇÑ Chest HRCT»ó bacterial bronchopneumonia ¼Ò°ß°ú ¾çÆóÇÏ¿±¿¡¼wheezingÀÌ Ã»ÁøµÇ¾î õ½Ä ÀÇÁõÇÏ¿¡ ventolin & atroventnebulizer(ÃÑ42ÀÏ)¸¦ ½ÃÇàÇÏ¿´À¸¸ç, ±â°ü³»»ð°ü ÈÄ¿¡ ÀΰøÈ£Èí±â Ä¡·á Áß(ÃÑ23ÀÏ) Áß nebulizer¸¦»ç¿ëÇÑ °ÍÀ¸·Î È®ÀεÊ.  
      ¸¸¼ºÆó¼â¼ºÆóÁúȯ(COPD)¶Ç´Â õ½Ä(Asthma) ±âÀúÁúȯÀÌ ¾ø´õ¶óµµ Ä¡·á ÁßwheezingÀÌ Ã»ÁøµÇ´Â °æ¿ì bronchial spasm¿¡ ÀÇÇÑ ÀÌÂ÷ÀûÀÎ Áõ»óÀ¸·Î nebulizerÀÇ »ç¿ëÀÌ ÇÊ¿äÇϹǷΠ±â°üÁöÈ®ÀåÁõÀÇ ±Þ¼º ¾Çȱ⿡ ½ÃÇàÇÑ Çϱ⵵ Áõ±âÈíÀÔÄ¡·á´Â ÇöÇà ÀÎÁ¤±âÁعüÀ§³»·Î ÆÇ´ÜµÇ¹Ç·Î ÀÎÁ¤ÇϵÇ, ÀΰøÈ£Èí±â ÀåÂø ±â°£À» Á¦¿ÜÇÑ 19Àϸ¸ÀÎÁ¤ÇÔ.  
   - µû¶ó¼, ±³°ú¼³ªÀÓ»ó³í¹®¿¡¼µµ ±â°üÁöÈ®ÀåÁõ Ä¡·á ½Ã Áõ»ó ¿Ïȸ¦ À§ÇØ nebulizerÀÇ ½ÃÇàÀ» Á¦½ÃÇϰí ÀÖÀ¸¹Ç·Î ±â°üÁöÈ®ÀåÁõÀDZ޼º ¾Çȱ⿡ õ½ÄÁõ»óÀÌ ¹ß»ýÇÏ´Â °æ¿ì¿¡´Â »ç·Êº°·Î ÀÎÁ¤Å°·Î ÇÔ.  
[2008.2.4 Áø·á½É»çÆò°¡À§¿øÈ¸]  
 
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       [¿¬·É´ë±Ý±â»ó¼¼°Ë»ö]
       
       
        
        
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    | Mechanism of Action | 
    
       Salbutamol¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Salbutamol is a beta(2)-adrenergic agonist and thus it stimulates beta(2)-adrenergic receptors. Binding of albuterol to beta(2)-receptors in the lungs results in relaxation of bronchial smooth muscles. It is believed that salbutamol increases cAMP production by activating adenylate cyclase, and the actions of salbutamol are mediated by cAMP. Increased intracellular cyclic AMP increases the activity of cAMP-dependent protein kinase A, which inhibits the phosphorylation of myosin and lowers intracellular calcium concentrations. A lowered intracellular calcium concentration leads to a smooth muscle relaxation. Increased intracellular cyclic AMP concentrations also cause an inhibition of the release of mediators from mast cells in the airways. 
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    | Pharmacology | 
     
       Salbutamol¿¡ ´ëÇÑ Pharmacology Á¤º¸ Salbutamol (INN) or albuterol (USAN), a moderately selective beta(2)-receptor agonist similar in structure to terbutaline, is widely used as a bronchodilator to manage asthma and other chronic obstructive airway diseases. The R-isomer, levalbuterol, is responsible for bronchodilation while the S-isomer increases bronchial reactivity.  The R-enantiomer is sold in its pure form as Levalbuterol.  The manufacturer of levalbuterol, Sepracor, has implied (although not directly claimed) that the presence of only the R-enantiomer produces fewer side-effects. 
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    | Half-life | 
    
       Salbutamol¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 1.6 hours 
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    | Absorption | 
    
       Salbutamol¿¡ ´ëÇÑ Absorption Á¤º¸ Systemic absorption is rapid following aerosol administration. 
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    | Pharmacokinetics | 
    
       SalbutamolÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á 
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    | Biotransformation | 
    
       Salbutamol¿¡ ´ëÇÑ Biotransformation Á¤º¸ Hydrolyzed by esterases in tissue and blood to the active compound colterol. The drug is also conjugatively metabolized to salbutamol 4'-O-sulfate. 
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    | Toxicity | 
    
       Salbutamol¿¡ ´ëÇÑ Toxicity Á¤º¸ LD50=1100 mg/kg (orally in mice) 
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    | Drug Interactions | 
    
       Salbutamol¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Not Available 
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    CYP450  Drug Interaction | 
    
      [CYP450 TableÁ÷Á¢Á¶È¸] 
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    | Drug Target | 
    
      
      [Drug Target]
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    | Description | 
    
       Salbutamol¿¡ ´ëÇÑ Description Á¤º¸ A racemic mixture with a 1:1 ratio of the r-isomer, levalbuterol, and s-albuterol. It is a short-acting beta2-adrenergic agonist with its main clinical use in asthma. [PubChem] 
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    | Dosage Form | 
    
       Salbutamol¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Aerosol, metered	Respiratory (inhalation)Liquid	OralPowder	Respiratory (inhalation)Solution	IntramuscularSolution	IntravenousSolution	OralSolution	Respiratory (inhalation)Tablet	Oral 
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    | Drug Category | 
    
       Salbutamol¿¡ ´ëÇÑ Drug_Category Á¤º¸ Adrenergic beta-AgonistsBronchodilator AgentsTocolytic Agents 
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    | Smiles String Canonical | 
    
       Salbutamol¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CC(C)(C)NCC(O)C1=CC(CO)=C(O)C=C1 
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    | Smiles String Isomeric | 
    
       Salbutamol¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ CC(C)(C)NC[C@H](O)C1=CC(CO)=C(O)C=C1 
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    | InChI Identifier | 
    
       Salbutamol¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C13H21NO3/c1-13(2,3)14-7-12(17)9-4-5-11(16)10(6-9)8-15/h4-6,12,14-17H,7-8H2,1-3H3 
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    | Chemical IUPAC Name | 
    
       Salbutamol¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ 4-[2-(tert-butylamino)-1-hydroxyethyl]-2-(hydroxymethyl)phenol 
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    | Drug-Induced Toxicity Related Proteins | 
    
      SALBUTAMOL ÀÇ Drug-Induced Toxicity Related ProteinÁ¤º¸ Replated Protein:Beta-2 adrenergic receptor Drug:Salbutamol  Toxicity:desensitization, cardiovascular effects.  [¹Ù·Î°¡±â] 
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