Leitlinienreport S3-Leitlinie Prostatakarzinom | Version 5.0 | April 2018 3

Total Page:16

File Type:pdf, Size:1020Kb

Leitlinienreport S3-Leitlinie Prostatakarzinom | Version 5.0 | April 2018 3 1 1 1 1 Leitlinienreport Interdisziplinäre Leitlinie der Qualität S3 zur Früherkennung, Diagnose und Therapie der verschie- denen Stadien des Prostatakarzinoms Version 5.0 – April 2018 AWMF-Registernummer: 043/022OL © Leitlinienprogramm Onkologie | Leitlinienreport zur S3-Leitlinie Prostatakarzinom | für Version 2.2 Konsulta- tionsfassung, 2. Aktualisierung 2014 2 Inhaltsverzeichnis 1. Informationen zum Leitlinienreport ................................................................. 6 1.1. Autoren des Leitlinienreports ................................................................................................... 6 1.2. Herausgeber ............................................................................................................................ 6 1.3. Federführende Fachgesellschaft ............................................................................................... 6 1.4. Finanzierung der Leitlinie ........................................................................................................ 6 1.5. Kontakt .................................................................................................................................... 6 1.6. Zitierweise des Leitlinienreports .............................................................................................. 7 1.7. Weitere Dokumente zur Leitlinie .............................................................................................. 7 1.8. Abkürzungsverzeichnis ............................................................................................................ 8 2. Geltungsbereich und Zweck der Leitlinie ................................................... 10 2.1. Adressaten ............................................................................................................................ 10 2.2. Zielsetzung ............................................................................................................................ 10 3. Zusammensetzung der Leitliniengruppe .................................................... 11 3.1. Steuergruppe der Leitlinie ...................................................................................................... 11 3.2. Beteiligte Autoren und Mitglieder der Leitliniengruppe .......................................................... 11 3.3. Andere Institutionen .............................................................................................................. 14 3.4. Patientenbeteiligung .............................................................................................................. 15 4. Fragestellungen und Gliederung ..................................................................... 16 5. Methodik ...................................................................................................................... 17 5.1. Evidenzbasierung .................................................................................................................. 17 5.1.1.Erstellung der Leitlinie 2006-2009 .......................................................................................... 17 5.1.2.Erstellung der ersten modularen Aktualisierung 2011 ............................................................. 22 5.1.3.Erstellung der zweiten modularen Aktualisierung 2014 ........................................................... 24 5.1.4.Erstellung der dritten modularen Aktualisierung 2016 ............................................................ 27 5.1.5.Erstellung der vierten modularen Aktualisierung 2017 ............................................................ 28 5.2. Formulierung der Empfehlung und formale Konsensusfindung .............................................. 29 5.2.1.Themenbezogene Gruppenarbeit ............................................................................................ 32 5.2.2.Plenumssitzung mit endgültiger Verabschiedung der Empfehlungen ...................................... 33 5.2.3.Empfehlungen und deren Graduierung .................................................................................... 34 5.2.4.Statements .............................................................................................................................. 34 5.2.5.Expertenkonsens (EK) .............................................................................................................. 34 6. Qualitätsindikatoren ............................................................................................. 35 6.1. 1. Aktualisierung 2011 .......................................................................................................... 35 © Leitlinienprogramm Onkologie | Leitlinienreport S3-Leitlinie Prostatakarzinom | Version 5.0 | April 2018 3 6.2. 2. Aktualisierung 2014 .......................................................................................................... 35 6.3. 3. Aktualisierung 2017 .......................................................................................................... 38 7. Externe Begutachtung und Verabschiedung ............................................. 42 7.1. Erstellung der Leitlinie 2006-2009 ......................................................................................... 42 7.2. 1. Aktualisierung 2011 .......................................................................................................... 42 7.3. 2. Aktualisierung 2014 .......................................................................................................... 42 7.4. 3. Aktualisierung 2016 .......................................................................................................... 42 7.5. 4. Aktualisierung 2017 .......................................................................................................... 43 8. Redaktionelle Unabhängigkeit und Umgang mit Interessenkonflikten ............................................................................................ 44 9. Verbreitung und Implementierung ................................................................ 45 10. Gültigkeitsdauer der Leitlinie ........................................................................... 46 11. Tabellenverzeichnis ............................................................................................... 46 12. Anhänge ....................................................................................................................... 47 12.1. Schlüsselfragen und Autoren 2009/2011/2014/2016/2017 ................................................. 47 12.2. Methodik und Ergebnisse der Recherchen zur Erstellung der Leitlinie 2009 ........................... 55 12.2.1.Recherche zum Thema Epidemiologie, Risikofaktoren, Prävention und Ernährung ................ 55 12.2.2.Recherche zum Thema Früherkennung und Biopsie .............................................................. 56 12.2.3.Recherche zum Thema Diagnostik und Stadieneinteilung ...................................................... 57 12.2.4.Recherche zum Thema Therapie des nichtmetastasierten Prostatakarzinoms ........................ 60 12.2.5.Recherche zum Thema Lokale Therapie des lokal begrenzten Prostatakarzinoms ................. 61 12.2.6.Recherche zum Thema Lokale Therapie des lokal fortgeschrittenen Prostatakarzinoms ........ 63 12.2.7.Recherche zum Thema Diagnostik und Therapie des rezidivierten oder metastasierten Prostatakarzinoms ....................................................................................................... 66 12.2.8.Recherche zum Thema Rehabilitation und Nachsorge ........................................................... 68 12.2.9.Recherche zum Thema Psychosoziale Aspekte und Lebensqualität ....................................... 68 12.3. Methodik und Ergebnisse der Recherchen zur 1. Aktualisierung 2011 ................................... 69 12.3.1.Recherche zum Thema Stellenwert der Früherkennung/Screening ......................................... 69 12.3.2.Recherche zu den Fragestellungen im Kapitel Diagnostik und Stadieneinteilung ................... 74 12.3.3.Recherche zu Active Surveillance bei lokal begrenztem Prostatakarzinom ............................. 97 12.3.4.Recherche zum Thema Radikale Prostatektomie bei Patienten mit hohem Risikoprofil ........ 110 12.3.5.Recherche zum Thema LDR-Brachytherapie ......................................................................... 118 12.3.6.Recherchen zum Thema perkutane Strahlentherapie ........................................................... 127 12.3.7.Recherchen zum Thema perkutane Strahlentherapie ........................................................... 137 12.3.8.Recherchen zum Thema Protonentherapie .......................................................................... 147 12.3.9.Recherchen zum Thema HIFU .............................................................................................. 152 12.3.10.Recherchen zum Thema Therapie von Knochenmetastasen ............................................... 158 12.3.11.Recherche zum Thema Behandlung des kastrationsresistenten Prostatakarzinoms ........... 164 © Leitlinienprogramm Onkologie | Leitlinienreport S3-Leitlinie Prostatakarzinom | Version 5.0 | April 2018 4 12.4. Methodik und Ergebnisse der Recherchen zur 2. Aktualisierung 2014 ................................. 171 12.4.1.Recherche zum Thema Früherkennung/Screening (Kapitel 3.1 der Leitlinie) ........................ 171 12.4.2.Recherche zum Thema PET-CT/MRT beim PSA-Rezidiv (Empfehlung 3.19 der Leitlinie) ....... 185 12.4.3.Recherche zum Thema
Recommended publications
  • WSAVA List of Essential Medicines for Cats and Dogs
    The World Small Animal Veterinary Association (WSAVA) List of Essential Medicines for Cats and Dogs Version 1; January 20th, 2020 Members of the WSAVA Therapeutic Guidelines Group (TGG) Steagall PV, Pelligand L, Page SW, Bourgeois M, Weese S, Manigot G, Dublin D, Ferreira JP, Guardabassi L © 2020 WSAVA All Rights Reserved Contents Background ................................................................................................................................... 2 Definition ...................................................................................................................................... 2 Using the List of Essential Medicines ............................................................................................ 2 Criteria for selection of essential medicines ................................................................................. 3 Anaesthetic, analgesic, sedative and emergency drugs ............................................................... 4 Antimicrobial drugs ....................................................................................................................... 7 Antibacterial and antiprotozoal drugs ....................................................................................... 7 Systemic administration ........................................................................................................ 7 Topical administration ........................................................................................................... 9 Antifungal drugs .....................................................................................................................
    [Show full text]
  • The Effects of Osaterone Acetate on Clinical Signs and Prostate Volume in Dogs with Benign Prostatic Hyperplasia
    Polish Journal of Veterinary Sciences Vol. 21, No. 4 (2018), 797–802 DOI 10.24425/pjvs.2018.125601 Original article The effects of osaterone acetate on clinical signs and prostate volume in dogs with benign prostatic hyperplasia P. Socha, S. Zduńczyk, D. Tobolski, T. Janowski Department of Animal Reproduction with Clinic, Faculty of Veterinary Medicine, University of Warmia and Mazury in Olsztyn, Oczapowskiego 14, 10-719 Olsztyn, Poland Abstract A clinical trial was performed to evaluate the therapeutic efficacy of osaterone acetate (OSA) in the treatment of benign prostatic hyperplasia (BPH) in dogs. Osaterone acetate (Ypozane, Virbac) was administered orally at a dose of 0.25 mg/kg body weight once a day for seven days to 23 dogs with BPH. During the 28-day trial, the dogs were monitored five times for their clinical signs and prostate volume. The OSA treatment promoted rapid reduction of clinical scores to 73.2% on day 7 and to 5.9% on day 28 (p<0.05). Osaterone acetate induced the complete clinical remission in approximately 83.0% of the dogs on day 28. The prostate volume regressed to 64.3% of the pretreatment volume after two weeks of the treatment (p<0.05) and to 54.7% at the end of the trial (p<0.05). In conclusion, OSA quickly reduced clinical signs and volume of the prostate glands in dogs with BPH. Key words: dogs, benign prostatic hyperplasia, osaterone acetate, prostate volume Introduction hyperplasia and subsequently transforms to cystic hyperplasia with the formation of multiple small cysts Benign prostatic hyperplasia (BPH) is the most within the prostatic parenchyma.
    [Show full text]
  • 207/2015 3 Lääkeluettelon Aineet, Liite 1. Ämnena I Läkemedelsförteckningen, Bilaga 1
    207/2015 3 LÄÄKELUETTELON AINEET, LIITE 1. ÄMNENA I LÄKEMEDELSFÖRTECKNINGEN, BILAGA 1. Latinankielinen nimi, Suomenkielinen nimi, Ruotsinkielinen nimi, Englanninkielinen nimi, Latinskt namn Finskt namn Svenskt namn Engelskt namn (N)-Hydroxy- (N)-Hydroksietyyli- (N)-Hydroxietyl- (N)-Hydroxyethyl- aethylprometazinum prometatsiini prometazin promethazine 2,4-Dichlorbenzyl- 2,4-Diklooribentsyyli- 2,4-Diklorbensylalkohol 2,4-Dichlorobenzyl alcoholum alkoholi alcohol 2-Isopropoxyphenyl-N- 2-Isopropoksifenyyli-N- 2-Isopropoxifenyl-N- 2-Isopropoxyphenyl-N- methylcarbamas metyylikarbamaatti metylkarbamat methylcarbamate 4-Dimethyl- ami- 4-Dimetyyliaminofenoli 4-Dimetylaminofenol 4-Dimethylaminophenol nophenolum Abacavirum Abakaviiri Abakavir Abacavir Abarelixum Abareliksi Abarelix Abarelix Abataceptum Abatasepti Abatacept Abatacept Abciximabum Absiksimabi Absiximab Abciximab Abirateronum Abirateroni Abirateron Abiraterone Acamprosatum Akamprosaatti Acamprosat Acamprosate Acarbosum Akarboosi Akarbos Acarbose Acebutololum Asebutololi Acebutolol Acebutolol Aceclofenacum Aseklofenaakki Aceklofenak Aceclofenac Acediasulfonum natricum Asediasulfoni natrium Acediasulfon natrium Acediasulfone sodium Acenocoumarolum Asenokumaroli Acenokumarol Acenocumarol Acepromazinum Asepromatsiini Acepromazin Acepromazine Acetarsolum Asetarsoli Acetarsol Acetarsol Acetazolamidum Asetatsoliamidi Acetazolamid Acetazolamide Acetohexamidum Asetoheksamidi Acetohexamid Acetohexamide Acetophenazinum Asetofenatsiini Acetofenazin Acetophenazine Acetphenolisatinum Asetofenoli-isatiini
    [Show full text]
  • Reproductive Endocrinology of the Dog
    Reproductive endocrinology of the dog Effects of medical and surgical intervention Jeffrey de Gier 2011 Cover: Anjolieke Dertien, Multimedia; photos: Jeffrey de Gier Lay-out: Nicole Nijhuis, Gildeprint Drukkerijen, Enschede Printing: Gildeprint Drukkerijen, Enschede De Gier, J., Reproductive endocrinology of the dog, effects of medical and surgical intervention, PhD thesis, Faculty of Veterinary Medicine, Utrecht University, Utrecht, The Netherlands Copyright © 2011 J. de Gier, Utrecht, The Netherlands ISBN: 978-90-393-5687-6 Correspondence and requests for reprints: [email protected] Reproductive endocrinology of the dog Effects of medical and surgical intervention Endocrinologie van de voortplanting van de hond Effecten van medicamenteus en chirurgisch ingrijpen (met een samenvatting in het Nederlands) Proefschrift ter verkrijging van de graad van doctor aan de Universiteit Utrecht op gezag van de rector magnificus, prof.dr. G.J. van der Zwaan, ingevolge het besluit van het college voor promoties in het openbaar te verdedigen op dinsdag 20 december 2011 des middags te 12.45 uur door Jeffrey de Gier geboren op 14 mei 1973 te ’s-Gravenhage Promotor: Prof.dr. J. Rothuizen Co-promotoren: Dr. H.S. Kooistra Dr. A.C. Schaefers-Okkens Publication of this thesis was made possible by the generous financial support of: AUV Dierenartsencoöperatie Boehringer Ingelheim B.V. Dechra Veterinary Products B.V. J.E. Jurriaanse Stichting Merial B.V. MSD Animal Health Novartis Consumer Health B.V. Royal Canin Nederland B.V. Virbac Nederland B.V. Voor mijn ouders
    [Show full text]
  • Hexachlorophenum Hexaminolaevulinas Hydrochloridum
    29 Hexachlorophenum Heksaklorofeeni Hexaklorofen Hexachlorophene Hexaminolaevulinas Heksaminolevulinaattihyd- Hexaminolevulinathydro- Hexaminolevulinate hyd- hydrochloridum rokloridi klorid rochloride Hexapropymatum Heksapropymaatti Hexapropymat Hexapropymate Hexobarbitalum Heksobarbitaali Hexobarbital Hexobarbital Hexocyclium Heksosyklium Hexocyklium Hexocyclium Hexoprenalinum Heksoprenaliini Hexoprenalin Hexoprenaline Hexylnicotinatum Heksyylinikotinaatti Hexylnikotinat Hexyl nicotinate Hexylresorcinolum Heksyyliresorsinoli Hexyh-esorcinol Hexylresorcinol Hirudinum Hirudiini Hirudin Hirudin Histamini Histamiinidihydrokloridi Histamindihydroklorid Histamine dihydrochloride dihydrochloridum Histaminum Histamiini Histamin Histamine Histapyrrodinum Histapyrrodiini Histapyrrodin Histapyrrodine Hisb-elinum Histreliini Histrelin Histrelin Homatropini Homati'opiinimetyyli- Homatropinmetylbromid Homatropine methylbromidum bromidi methylbromide Homatropinum Homatropiini Homatropin Homatropine Hormonum parathyroidum Paratyroidihormoni Parathormon Parathyroid hormone (rdna) (rdna) Hyaluronidasum Hyaluronidaasi Hyaluronidas Hyaluronidase Hydralazinum Hydralatsiini Hydralazin Hydralazine Hydrochlorothiazidum Hydroklooritiatsidi Hydroklortiazid Hydrochlorothiazide Hydrocodonum Hydrokodoni Hydrokodon Hydrocodone Hydrocortisonum Hydrokortisoni Hydrokortison Hydrocortisone Hydroflumethiazidum Hydroflumetiatsidi Hydroflumetiazid Hydroflumethiazide Hydromorphonum Hydromorfoni Hydromorfon Hydromorphone Hydrotalcitum Hydrotalsiitti Hydrotalcit Hydrotalcite
    [Show full text]
  • Lääkealan Turvallisuus- Ja Kehittämiskeskuksen Päätös
    Lääkealan turvallisuus- ja kehittämiskeskuksen päätös N:o xxxx lääkeluettelosta Annettu Helsingissä xx päivänä maaliskuuta 2016 ————— Lääkealan turvallisuus- ja kehittämiskeskus on 10 päivänä huhtikuuta 1987 annetun lääke- lain (395/1987) 83 §:n nojalla päättänyt vahvistaa seuraavan lääkeluettelon: 1 § Lääkeaineet ovat valmisteessa suolamuodossa Luettelon tarkoitus teknisen käsiteltävyyden vuoksi. Lääkeaine ja sen suolamuoto ovat biologisesti samanarvoisia. Tämä päätös sisältää luettelon Suomessa lääk- Liitteen 1 A aineet ovat lääkeaineanalogeja ja keellisessä käytössä olevista aineista ja rohdoksis- prohormoneja. Kaikki liitteen 1 A aineet rinnaste- ta. Lääkeluettelo laaditaan ottaen huomioon lää- taan aina vaikutuksen perusteella ainoastaan lää- kelain 3 ja 5 §:n säännökset. kemääräyksellä toimitettaviin lääkkeisiin. Lääkkeellä tarkoitetaan valmistetta tai ainetta, jonka tarkoituksena on sisäisesti tai ulkoisesti 2 § käytettynä parantaa, lievittää tai ehkäistä sairautta Lääkkeitä ovat tai sen oireita ihmisessä tai eläimessä. Lääkkeeksi 1) tämän päätöksen liitteessä 1 luetellut aineet, katsotaan myös sisäisesti tai ulkoisesti käytettävä niiden suolat ja esterit; aine tai aineiden yhdistelmä, jota voidaan käyttää 2) rikoslain 44 luvun 16 §:n 1 momentissa tar- ihmisen tai eläimen elintoimintojen palauttami- koitetuista dopingaineista annetussa valtioneuvos- seksi, korjaamiseksi tai muuttamiseksi farmako- ton asetuksessa kulloinkin luetellut dopingaineet; logisen, immunologisen tai metabolisen vaikutuk- ja sen avulla taikka terveydentilan
    [Show full text]
  • Benign Prostate Hyperplasia
    Vet Times The website for the veterinary profession https://www.vettimes.co.uk BENIGN PROSTATE HYPERPLASIA Author : Henry L’Eplattenier Categories : Vets Date : April 4, 2011 Henry L’Eplattenier considers this common condition in older dogs and discusses its symptoms and treatment THE prostate is the only major accessory sex gland in the dog. It is a bilobed structure that completely encircles the proximal portion of the urethra. In young animals, the prostate lies entirely within the pelvic cavity, but with sexual maturity it increases in size and assumes an abdominal position. Histologically, the prostate has an epithelial and a stromal component. The epithelial cells form tubuloalveoli that drain into the urethra. The prostate is surrounded by a capsule containing smooth muscle fibres that extend into the organ, dividing the alveolar tissue into dis tinct lobules. Blood supply to the prostate is supplied by the prostatic artery, which arises from the pudendal or umbilical artery. Anastomoses can be found between the prostatic vessels and the urethral artery, and the cranial and caudal rectal artery. Venous blood returns via the prostatic vein to the internal iliac vein. Lymph drains into the iliac lymph nodes. Sympathetic innervation is provided by the hypogastric nerve, which stimulates the active secretory process and expulsion of secretions by smooth muscle contractions. Parasympathetic innervation with fibres from the pelvic nerve also contributes to smooth muscle contraction1. 1 / 5 Fluid secreted by the prostate forms more than 90 per cent of the total volume of the ejaculate2 and is expulsed in the first and third fractions of the ejaculate.
    [Show full text]
  • Audition Publique « Auteurs De Violences Sexuelles : Prévention, Évaluation, Prise En Charge »
    Audition publique « Auteurs de violences sexuelles : prévention, évaluation, prise en charge » Rapports des experts et du groupe bibliographique Tome 3 : Évaluation Préface : Mathieu LACAMBRE, Sabine MOUCHET-MAGES Auteurs : François ARNAUD, Roland COUTANCEAU, Julien DA COSTA, Emmanuelle DUSACQ, Bruno GRAVIER, Ivan GUITZ, Hanin HEDJAM, Pierre LAMOTHE, Cédric LE BODIC, Nora LETTO, Frédéric MEUNIER, Valérie MOULIN, Thierry PHAM, Pierre ROUVIERE Suivi de « Synthèse du rapport de la commission d’audition. 35 propositions concrètes pour lutter efficacement contre les violences sexuelles » Edition collector à l’occasion du 10ème Congrès International Francophone sur l’Agression Sexuelle (CIFAS, Montpellier, 2019) ISBN : 978-2-491142-02-5 © FFCRIAVS - 2019 Audition publique « Auteurs de violences sexuelles : prévention, évaluation, prise en charge » Paris, juin 2018 AUDITION Publique «AUTEURS DE VIOLENCES SEXUELLES : PRÉVENTION, ÉVALUATION, PRISE EN CHARGE» Préface Dans le champ des violences sexuelles, nous disposons en France d’un héritage clinique, théorique et conceptuel particulièrement riche ainsi que de dispositifs législatifs inédits (injonction de soins, contrainte pénale…) mais aussi institution- nels permettant une articulation étroite entre la Santé et la Justice autour du pa- tient-condamné. Ainsi, des équipes pluriprofessionnelles originales ont vu le jour à partir de 20061 au sein de Centres Ressources pour les intervenants auprès d’Auteurs de Violences Sexuelles (CRIAVS). Près de 200 professionnels de tout horizon (secré- taire, documentaliste, juriste, sociologue, criminologue, psychologue, éducateur, assistant de recherche clinique, psychiatre, sexologue…) se sont réunis dans chaque région pour incarner les CRIAVS et porter haut nos missions : la prévention, la forma- tion, la documentation, l’information, le soutien aux équipes de terrain, la recherche et l’animation des réseaux Santé-Justice.
    [Show full text]
  • Canine Prostate Disease
    Canine Prostate Disease Bruce W. Christensen, DVM, MS KEYWORDS Prostate Benign prostatic hyperplasia (BPH) Prostatitis Prostatic neoplasia Canine prostate-specific arginine esterase (CPSE) KEY POINTS All intact, male dogs eventually develop benign prostatic hyperplasia and a subset will develop clinical signs associated with subfertility, discomfort, or infection. Any male dog may develop neoplasia associated with the prostate, with a higher propor- tion of neutered males being affected. Ultrasound imaging and prostatic tissue cytology remain the most reliable diagnostic tests for canine prostate disease, but canine prostate-specific arginine esterase shows value as a supporting diagnostic test. Older recommendations to treat prostatitis for 4 to 8 weeks with appropriate antibiotics have been updated to now recommend a truncated 4-week treatment regime for acute cases. Medical treatments for benign prostatic hyperplasia have variable effects on prostate size and function, and may affect androgen production. Video content accompanies this article at http://www.vetsmall.theclinics.com/. INTRODUCTION The prostate is the only accessory sex organ in dogs. Diseases of the canine prostate are relatively common. The canine prostate is constantly developing and growing un- der androgenic influence throughout the life of the intact male dog. This androgenic influence seems to have a protective effect in the case of neoplastic disease,1–3 but the increase in size under androgens also predisposes the canine prostate to infection and cystic disease.4–6 The consequences of these diseases range from mild discom- fort to varying effects on semen quality to very painful or life-threatening illness. An evolving understanding of the way the canine prostate functions has led to expanded diagnostic options and recent changes in treatment recommendations for some of these conditions.
    [Show full text]
  • Associations Between Canine Male Reproductive Parameters And
    Associations between Canine Male Reproductive Parameters and Serum Vitamin D and Prolactin Concentrations by Adria Julianne Kukk A Thesis presented to The University of Guelph In partial fulfillment of requirements for the degree of Doctor of Veterinary Science in Population Medicine Guelph, Ontario, Canada ¤ Adria Julianne Kukk, December, 2011 ABSTRACT ASSOCIATIONS BETWEEN CANINE MALE REPRODUCTIVE PARAMETERS AND SERUM VITAMIN D AND PROLACTIN CONCENTRATIONS Adria Julianne Kukk Advisor: University of Guelph, 2011 Professor C.J. Gartley Maintaining reproductive health and diagnosing and treating conditions of infertility in stud dogs is important in canine theriogenology. However, there is still a great deal to be learned about reproductive physiology and factors that affect reproductive organs and semen quality in dogs. This thesis is an investigation of two factors in the male dog; serum 25-hydroxy Vitamin D (25OHVD) and prolactin (PRL) concentrations, and their possible associations with benign prostatic hyperplasia (BPH), prostate volume and/or sperm morphology and motility characteristics. 28 (Vitamin D Study) and 29 (28 plus one for the Prolactin study) client dogs of various breeds from the Ontario Veterinary College and Graham Animal Hospital in Southwestern Ontario, Canada were enrolled in the study from March to December 2009. Of these dogs 22 were successfully collected for semen. BPH was diagnosed using prostate volume measured by ultrasound, as well as clinical signs including blood in the ejaculate. Semen analysis was performed
    [Show full text]
  • WO 2020/0951S3 A1 14 May 2020 (14.05.2020) I 4 P Cl I P C T
    (12) INTERNATIONAL APPLICATION PI;BLISHED I. NDER THE PATENT COOPERATION TREATY (PCT) (19) World intellectual Propertv Organraation llIIlIIlllIlIlllIlIllIllIllIIIIIIIIIIIIIIIIIIIIIIllIlIlIlIllIlllIIllIlIIllllIIIIIIIIIIIIIIIIIII International Bureau (10) International Publication Number (43) International Publication Date WO 2020/0951S3 A1 14 May 2020 (14.05.2020) I 4 P Cl I P C T (51) International Patent Classification: MC. MK, MT. M., NO, PL, PT, RO, RS. SE. SI. SK. SM, A6JK3J/4166 (2006.01) A6/K&/5/t)6 (200G 01) TR). OAPI (BF, BJ, CF, CG, CI. CYI. GA, GN, GQ. GW. AGJK39/00(2006 01) C07K/6/28 (2006 01) KM,:vIL. MR, NE. SN, TD, TG) A6JP35/00(200G 01) AGJK38/68 (2019 Ol) Published: (21) International Application tiumber: »iili nrternatinrral seair 6 repurt 14rt 2113&i PCT/IB2019/059459 m Alar/ and &ilnte, the mternat»rrral app/icramn as fihrl (22) International Filing Date: crmiamerl en/«i rrr grevscale a&irl is rivrnhihiefur d«ii nlrrarl 04 November 2019 (04,11.2019) /rum P) TES"/;ST'OPE (25) Filing Langurrge: Enghsh (26) Public&stion Language: Enghsh (30) Priority Data: (&2/755.944 05 Not en&ber 2018105.11 20)8) US (i2/882.424 02 Auknrst 2019 (02 08.2019) US (71) Applicants: PFIZER INC. [US/L S], 233 East 42nd Street. Neve York. Ncw York 10017 (US). MERCK PATENT GMBH [DE/DE], Frankfurter Strasse 250, G4293 Dmm- stadi (DE) NEKTAR THERAPEUTICS [US/US]. 435 Nlission Ba) Boulmard South. Suite 100. San Francis- co, California 94158 (US). ASTELLAS PHARMA INC. f JP/JP], 2-5-1. Nihonbashi-Honcho, Chuo-Ku, Tokv o (JP) (72) Inventors: BOSHOFF, Christoffel Hendrik; c/o PFIZER INC, 235 East 42nd Street Neu York.
    [Show full text]
  • Aktualne Metody Farmakologicznego Leczenia Łagodnego Przerostu Prostaty U Psów
    Med. Weter. 2015, 71 (6), 335-340 335 Artykuł przeglądowy Review Aktualne metody farmakologicznego leczenia łagodnego przerostu prostaty u psów JOANNA PASIKOWSKA, WOJCIECH NIŻAŃSKI Katedra Rozrodu z Kliniką Zwierząt Gospodarskich, Wydział Medycyny Weterynaryjnej, Uniwersytet Przyrodniczy we Wrocławiu, pl. Grunwaldzki 49, 50-366 Wrocław Otrzymano 07.07.2014 Zaakceptowano 21.07.2014 Pasikowska J., Niżański W. Methods of pharmacological treatment of benign prostatic hyperplasia in dogs: An update Summary Benign prostatic hyperplasia (BPH) is the most common disease of the prostate in dogs. It can be treated by surgical or pharmacological methods. Surgical methods are used in non-breeder males or males with pathological changes in the testis. Pharmacological treatment is an alternative for breeder males and old animals with associated diseases. Substances that can be used for medical treatment are GnRH analogues, GnRH antagonists, estrogens, progestogens, antiandrogens, inhibitors of 5α-reductase, antiestrogens, and VDR agonists. This paper presents short characteristics of pharmacological substances that we have used in BPH treatment. Keywords: benign prostatic hyperplasia, dogs, GnRH analogues, GnRH antagonists, antiandrogens Łagodny przerost prostaty (BPH – benign prostatic Najczęstsze objawy towarzyszące BPH to okre- hyperplasia) to najczęstsza choroba dotycząca gruczołu sowe wypływy z cewki moczowej, makroskopowe krokowego u psów. krwawienia podczas oddawania moczu oraz zmiany BPH stwierdza się u 16% psów powyżej drugiego w ejakulacie (krew w nasieniu i zwiększona ilość III roku życia, u 80% psów powyżej 5. roku życia i prak- frakcji nasienia) (20, 35). tycznie u 100% pacjentów powyżej 8. roku życia. Stosunkowo często BPH towarzyszą także problemy BPH diagnozowane jest u psów wszystkich ras oraz z oddawaniem kału – zaparcia, częste i bolesne parcia, mieszańców (14).
    [Show full text]