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Samenvatting Farmacologie Deel 5 - 2025

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Dit is de samenvatting van deel 5 van het farmacologie voor Bachelor Geneeskunde aan de KU Leuven, geschreven door Jan De Hoon en Minne Casteels. Het document behandelt autacoïden bij inflammatie en allergie, met diepgaande uitleg over eicosanoïden, prostanoïden, leukotriënen, en de rol van COX-enzymen, aangevuld met informatie over ivermectine en andere parasiticiden.

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FARMACOLOGIE DEEL 5
FARMACOTHERAPIE




JAN DE HOON EN MINNE CASTEELS




Inhoudsopgave
INLEIDING: AUTACOÏDEN BIJ INFLAMMATIE EN ALLERGIE..................................3
H1: NSAIDS.................................................................................................... 6
CHEMIE.............................................................................................................................. 6
WERKINGSMECHANISME......................................................................................................... 7
FARMACOKINETIEK................................................................................................................ 8
FAMRACODYNAMIEK.............................................................................................................. 8
INDICATIES.......................................................................................................................... 8
BIJWERKINGEN..................................................................................................................... 8
GI................................................................................................................................. 9
BP................................................................................................................................. 9
Renaal en CV................................................................................................................ 9
Overgevoeligheidsreacties.........................................................................................10
Hepatotoxiciteit en hematologische toxiciteit............................................................10
CONTRA-INDICATIES EN RISICOPOPULATIES...............................................................................10
INTERACTIE....................................................................................................................... 10
PRAKTIJK: KIEZEN VAN NSAID.............................................................................................. 11
VERSCHILLENDE GROEPEN VAN NSAIDS..................................................................................11
salicylaten.................................................................................................................. 11
para-aminofenol derivaten......................................................................................... 12
indool- en arylazijnzuurderivaten...............................................................................13
arylpropionzuurderivaten........................................................................................... 14
oxicams...................................................................................................................... 14
pyrazolonderivaten.................................................................................................... 14
selectieve COX-2 inhibitoren (coxibs).........................................................................15
H2: GLUCOCORTICOÏDEN...............................................................................16
CHEMIE............................................................................................................................ 16
WERKINGSMECHANISME....................................................................................................... 16
FARMACOKINETIEK.............................................................................................................. 17
FARMACODYNAMIEK............................................................................................................ 18
INDICATIES........................................................................................................................ 18
BIJWERKINGEN................................................................................................................... 19
RISICOPOPULATIES.............................................................................................................. 21

,H3: TWEEDELIJNS ANTI-REUMATISCHE GENEESMIDDELEN...............................22
DMARDS......................................................................................................................... 22
csDMARDs.................................................................................................................. 22
bDMARDs................................................................................................................... 23
tsDMARDs.................................................................................................................. 24
IMMUNOSUPPRESSIVA.......................................................................................................... 24
H4: MIGRAINE.............................................................................................. 27
BEHANDELING:................................................................................................................... 27
acute aanval............................................................................................................... 27
profylactische medicatie............................................................................................30
H5: JICHT..................................................................................................... 32
NSAID............................................................................................................................ 33
COLCHICINE...................................................................................................................... 33
GLUCOCORTICOÏDEN........................................................................................................... 33
URICOSTATICA................................................................................................................... 33
URICOSURICA.................................................................................................................... 34
RECOMBINANT URAAT OXIDASE............................................................................................. 35
CANAKINUMAB................................................................................................................... 35
H6: ANTIHISTAMINICA (TYPE I ALLERGIE).......................................................35
HISTAMINE........................................................................................................................ 36
H1-RECEPTORANTAGONISTEN............................................................................................... 38
H7: ASTMA................................................................................................... 42
ANTI-ASTMAGENEESMIDDELEN............................................................................................... 43
ß2-agonist.................................................................................................................. 44
Anticholinergica.......................................................................................................... 45
Corticosteroïden......................................................................................................... 45
Theofylline.................................................................................................................. 46
Leukotriënreceptor-antagonisten...............................................................................47
Andere........................................................................................................................ 47
Aandachtspuntsen...................................................................................................... 48
inhalatiesystemen...................................................................................................... 48
H8: ANAFYLACTISCHE REACTIES....................................................................49
H9: DIABETES MELLITUS...............................................................................50
NORMALE FYSIOLOGIE.......................................................................................................... 51
INSULINE EN ANALOGEN....................................................................................................... 53
ORALE ANTIDIABETICA......................................................................................................... 55
Biguaniden................................................................................................................. 55
Sulfamiden/sulfonylureumderivaten...........................................................................56
Gliniden...................................................................................................................... 57
Thiazolidinedionen of glitazonen................................................................................59
Alfa-gucosidase inhibitoren........................................................................................59
Gliptinen..................................................................................................................... 59
Gliflozinen.................................................................................................................. 60
INCRETINEMIMETICA............................................................................................................ 61

H10: OSTEOPOROSE.....................................................................................62
NIET-FARMACOLOGISCHE OPTIES............................................................................................ 63

, Calcium + vitamine D................................................................................................63
Vitamine D................................................................................................................. 64
FARMACOLOGISCHE OPTIES................................................................................................... 65
Bisfosfonaten............................................................................................................. 65
SERMs........................................................................................................................ 66
Teriparatide................................................................................................................ 67
Monoclonale AL: denosumab en romosozumab..........................................................67
H11: KANKER............................................................................................... 68
INLEIDING......................................................................................................................... 68
KANKERTHERAPIE............................................................................................................... 69
Principes..................................................................................................................... 69
Terminologie.............................................................................................................. 69
Nevenwerkingen........................................................................................................ 70
Stoffen....................................................................................................................... 70
H12: SUPPORTIEVE THERAPIE BIJ KANKERBEHANDELNG.................................76
RECOMBINANT ERYTHROEPOËTINE.......................................................................................... 76
MELOÏDE GROEIFACTOR, G-CSF............................................................................................ 77
PROFYLACTISCHE ANTI-EMETICA............................................................................................. 78
BOTMETASTASEN................................................................................................................ 78

H13: PALLIATIEVE EN TERMINALE ZORG.........................................................78
INLEIDING......................................................................................................................... 78
SYMPTOOMCONTROLE PALLIATIEVE ZORG.................................................................................79
MEDICATIETOEDIENINGSROUTES............................................................................................ 84
PALLIATIEVE SEDATIE........................................................................................................... 86
EUTHANASIE...................................................................................................................... 86
H14: GI STELSEL........................................................................................... 87
ACID-PEPTIC DISEASE........................................................................................................... 87
H2-receptorantagonisten...........................................................................................87
Protonpompinhibitoren (PPI).......................................................................................88
Misoprostol................................................................................................................. 89
Antacida..................................................................................................................... 89
antibiotica.................................................................................................................. 90
(GASTRO)-PROKINETICA....................................................................................................... 90
Dopamine-2-receptorantagonisten.............................................................................90
Cisapride.................................................................................................................... 91
ANTI-EMETICA.................................................................................................................... 91
PANCREASENZYM-SUBSTITUUT............................................................................................... 92
LAXANTIA......................................................................................................................... 92
ANTI-DIARRHEÏCA............................................................................................................... 93
INFLAMMATOIR DARMLIJDEN (IBD)......................................................................................... 93
BEHANDELING VAN INFESTATIE MET WORMEN...........................................................................94




INLEIDING: AUTACOÏDEN BIJ INFLAMMATIE EN ALLERGIE

 Autacoïden = endogene stoffen die antwoorden op weefselbeschadiging (zelf-
remedie)
o Lokale hormonen

, o Kort halfleven
o Autocrien (op zelfde cel) of paracrien (op nabijgelegen cellen)
o Processen: ontsteking, allergie
o Stoffen
 NT (vb serotonine, histamine)
 Peptiden (vb bradykinine, angiotensine II, VIP)
 Vetzuurderivaten (vb prostanoïden = autocoïden betrokken bij
inflammatie, PAF)
 Anorganische moleculen (NO)
 Eicosanoïden
o = autacoïden gevormd door oxidatie van membraangebonden poly-
onverzadigde vetzuren
o = prostanoïden en leukotriënen
 Via COX: vorming prostanoïden (= prostaglandines en
tromboxanen) uit arachidonzuur
 Via lipoxygenase: vorming leukotriënen
 Prostanoïden
o = prostaglandines en tromboxanen
o Effecten (hieruit kan men bijwerkingen van NSAID’s raden)
 Hersenen
 Verhoging lichaamstemperatuur
 Stimulatie PGE2 door IL-1
 Luchtwegen
 Bronchodilatatie door PGE2 en PGI2
 Bronchoconstrictie door PGF2alfa en TXA2
 Reproductie-orgaan
 Vrouw
o Menstruatie: meer prostaglandins die contractie
veroorzaken  pijn
o Abortus: prostaglandines gebruikt
o Bevalling: contracties en cervixrijping  NSAID:
premature arbeid onderdrukken
 Man
o Prostaglandines in semen  rol conceptie en
infertiliteit
o Erectie: PGE2 via relaxatie van gladde spieren
 Bloedvaten: BALANS
 PGI2: remt BP aggregatie
 TXA2: stimuleert BP aggregatie
 Cave: rokers  onevenwicht: minder PGI2 en meer TXA1
waardoor meer constrictie
 Maag: BESCHERMEND
 PGE2 en PGI2
o Inhibitie maagzuur
o Flow maagwand door vrijstelling NO
o Mucus maagwand
 In utero
 PGE2 en PGI2 zorgen voor normale circulatie tussen linker en
rechter bloedsomloop van ongeboren kind
 Nier
 PGE2 en PGI2: dilatatie afferente arteriolen

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