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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.
[2008.6.2 Áø·á½É»çÆò°¡À§¿øÈ¸]
DUR °ü·Ã °í½Ã
[º´¿ë¿¬·É±Ý±â ÀǾàǰ / ÀӺαݱâ ÀǾàǰ / ºñ¿ëÈ¿°úÀû ÇÔ·® ÀǾàǰ / ¾ÈÀü¼º °ü·Ã ±Þ¿©ÁßÁö ÀǾàǰ]
ÇмúÁ¤º¸
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DUR (ÀǾàǰ»ç¿ëÆò°¡)
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[cobicistat silicon dioxide (as cobicistat)+elvitegravir+emtricitabine+tenofovir alafenamide fumarate (as tenofovir alafenamide)]
[nirmatrelvir+ritonavir]
[»óÈ£ÀÛ¿ë/º´¿ë±Ý±â°Ë»ö]
¿¬·É´ë±Ý±â :
°í½ÃµÈ ¿¬·É±Ý±â ³»¿ëÀº ¾ø½À´Ï´Ù.
[¿¬·É´ë±Ý±â»ó¼¼°Ë»ö]
Mechanism of Action
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
ÀÛ¿ë¹ßÇö½Ã°£ :
¾ç¼º Àü¸³¼±ºñ´ëÁõ : 1.5 ½Ã°£
°íÇ÷¾Ð : 1.5 ½Ã°£
ÃÖ´ëÈ¿°ú ¹ßÇö½Ã°£ : ¾ç¼º Àü¸³¼±ºñ´ëÁõ : 4-6ÁÖ
Èí¼ö : À§Àå°üÀ¸·ÎºÎÅÍ ½Å¼ÓÇÏ°Ô Èí¼öµÈ´Ù.
»ýü³»ÀÌ¿ë·ü : ¾à 65%
ºÐÆ÷¿ëÀû : 2.5 L/kg
´Ü¹é°áÇÕ : 90%
´ë»ç : °£´ë»ç Å
¹Ý°¨±â : ¾à 5½Ã°£ (¹üÀ§ : 3-9 ½Ã°£)
Ç÷ÁßÃÖ°í³óµµ µµ´Þ½Ã°£ : 1-2 ½Ã°£
¼Ò½Ç :
ÁÖ·Î ´ë»çü·Î¼ ´ëº¯À» ÅëÇØ ¹è¼³µÈ´Ù.
¹Ìº¯Èü·Î ¾à 11%, ´ë»çü·Î¼ 30%±îÁö ¼Òº¯À» ÅëÇØ ¹è¼³µÈ´Ù.
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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