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Review 2020 Subject: NEFROLOGIA (English Edition), 42 (2022) 367-389. doi:10.1016/j.nefroe.2022.11.011 Keywords: Author: Elisabet Ars Creator: Elsevier Producer: Acrobat Distiller 11.0 (Windows) CreationDate: Fri Nov 25 09:34:47 2022 CET ModDate: Fri Nov 25 04:07:34 2022 CET Tagged: yes UserProperties: no Suspects: no Form: none JavaScript: no Pages: 23 Encrypted: no Page size: 595.28 x 793.7 pts Page rot: 0 File size: 669876 bytes Optimized: yes PDF version: 1.7 name type encoding emb sub uni object ID ------------------------------------ ----------------- ---------------- --- --- --- --------- HNMHGN+Caecilia-RomanSC Type 1C Custom yes yes yes 974 0 HNMIGP+MTSYB Type 1C Custom yes yes yes 996 0 HNMIJP+Caecilia-Roman Type 1C Custom yes yes yes 997 0 HNMIKA+Caecilia-Italic Type 1C Custom yes yes yes 1015 0 HNMLLN+MTSY Type 1C Custom yes yes yes 1024 0 HNMHGO+Times-Roman Type 1C WinAnsi yes yes no 979 0 HNMHIO+Caecilia-Light Type 1C Custom yes yes yes 980 0 HNMHJP+Caecilia-Bold Type 1C Custom yes yes yes 981 0 HNMHNO+HelveticaLTStd-Bold Type 1C Custom yes yes yes 982 0 HNMHOP+Univers Type 1C Custom yes yes yes 999 0 HNMHPP+Caecilia-Heavy Type 1C Custom yes yes yes 1000 0 HNMIDP+Caecilia-BoldItalic Type 1C Custom yes yes yes 1001 0 HNMIGO+Cmtmib Type 1C Custom yes yes yes 1002 0 HOBDIH+MathematicalPi-One Type 1C Custom yes yes no 564 0 HOGGHH+Helvetica Type 1C Custom yes yes yes 565 0 Jhove (Rel. 1.22.1, 2019-04-17) Date: 2023-06-27 03:30:25 CEST RepresentationInformation: 275179.pdf ReportingModule: PDF-hul, Rel. 1.12.1 (2019-04-17) LastModified: 2023-06-26 14:37:13 CEST Size: 669876 Format: PDF Version: 1.7 Status: Well-Formed and valid SignatureMatches: PDF-hul MIMEtype: application/pdf Profile: Linearized PDF PDFMetadata: Objects: 1094 FreeObjects: 136 IncrementalUpdates: 1 DocumentCatalog: PageLayout: SinglePage PageMode: UseOutlines Language: EN Outlines: Item: Title: Consensus document on autosomal dominant polycystic kindey disease from the Spanish Working Group on Inherited Kindey Dise... Destination: 1 Children: Item: Title: Introduction Destination: 1 Item: Title: Diagnosis Destination: 1 Children: Item: Title: Recommendations Destination: 1 Children: Item: Title: Imaging diagnosis of ADPKD Destination: 1 Item: Title: Recommendations Destination: 1 Item: Title: Genetic diagnosis of ADPKD Destination: 1 Item: Title: Recommendations Destination: 1 Item: Title: Recommendations Destination: 1 Item: Title: Genetic counseling in ADPKD Destination: 1 Children: Item: Title: Recommendations Destination: 1 Item: Title: Management of arterial hypertension and cardiovascular risk Destination: 1 Children: Item: Title: Introduction Destination: 1 Item: Title: Pathogenesis Destination: 1 Item: Title: Treatment Destination: 1 Item: Title: Blood pressure goal Destination: 1 Item: Title: Global cardiovascular risk Destination: 1 Item: Title: Recommendations Destination: 1 Item: Title: Pregnancy in ADPKD Destination: 1 Children: Item: Title: Recommendations Destination: 1 Item: Title: Renal carcinoma Destination: 1 Children: Item: Title: Recommendations Destination: 1 Item: Title: Acute or chronic pain, cystic infection and bleeding Destination: 1 Children: Item: Title: Recommendations Destination: 1 Item: Title: Renal replacement therapy Destination: 1 Children: Item: Title: Recommendations Destination: 1 Item: Title: Polycystic liver disease Destination: 1 Children: Item: Title: Recommendations Destination: 1 Item: Title: Intracranial aneurysms Destination: 1 Children: Item: Title: Recommendations Destination: 1 Item: Title: Autosomal dominant polycystic kidney disease in childhood Destination: 1 Children: Item: Title: Recommendations Destination: 1 Item: Title: Specific treatment of autosomal dominant polycystic kidney disease Destination: 1 Children: Item: Title: Recommendations (see section Recommendations for Assessment in ADPKD Progression) Destination: 1 Item: Title: Assessment of rapid progression in ADPKD Destination: 1 Item: Title: Based on the evidence provided by the TEMPO3/4, TEMPO 4/4 and REPRISE studies, we propose the following criteria to define... Destination: 1 Item: Title: Conflict of interests Destination: 1 Item: Title: Uncited references Destination: 1 Item: Title: Thanks Destination: 1 Info: Title: Consensus document on autosomal dominant polycystic kindey disease from the Spanish Working Group on Inherited Kindey Diseases. Review 2020 Author: Elisabet Ars Subject: NEFROLOGIA (English Edition), 42 (2022) 367-389. doi:10.1016/j.nefroe.2022.11.011 Keywords: Creator: Elsevier Producer: Acrobat Distiller 11.0 (Windows) CreationDate: Fri Nov 25 09:34:47 CET 2022 ModDate: Fri Nov 25 04:37:34 CET 2022 ID: 0xdf72bdbbef30e935f42ed44078f625ae, 0xbeac14a84001d441953b926b442891ec Filters: FilterPipeline: FlateDecode Fonts: Type1: Font: BaseFont: HNMLLN+MTSY FontSubset: true FirstChar: 2 LastChar: 128 FontDescriptor: FontName: HNMLLN+MTSY Flags: Symbolic FontBBox: 0, -954, 1043, 796 FontFile3: true EncodingDictionary: Differences: true ToUnicode: true Font: BaseFont: HNMIGP+MTSYB FontSubset: true FirstChar: 2 LastChar: 2 FontDescriptor: FontName: HNMIGP+MTSYB Flags: Symbolic, ForceBold FontBBox: -16, -935, 1043, 896 FontFile3: true EncodingDictionary: Differences: true ToUnicode: true Font: BaseFont: HNMIJP+Caecilia-Roman FontSubset: true FirstChar: 31 LastChar: 252 FontDescriptor: FontName: HNMIJP+Caecilia-Roman Flags: Serif, Symbolic FontBBox: -167, -270, 1136, 926 FontFile3: true EncodingDictionary: Differences: true ToUnicode: true Font: BaseFont: HNMHOP+Univers FontSubset: true FirstChar: 46 LastChar: 119 FontDescriptor: FontName: HNMHOP+Univers Flags: Symbolic FontBBox: -168, -250, 992, 947 FontFile3: true EncodingDictionary: Differences: true ToUnicode: true Font: BaseFont: HNMHPP+Caecilia-Heavy FontSubset: true FirstChar: 31 LastChar: 243 FontDescriptor: FontName: HNMHPP+Caecilia-Heavy Flags: Serif, Symbolic, ForceBold FontBBox: -170, -277, 1146, 970 FontFile3: true EncodingDictionary: Differences: true ToUnicode: true Font: BaseFont: HNMIDP+Caecilia-BoldItalic FontSubset: true FirstChar: 31 LastChar: 243 FontDescriptor: FontName: HNMIDP+Caecilia-BoldItalic Flags: Serif, Symbolic, Italic, ForceBold FontBBox: -169, -273, 1082, 932 FontFile3: true EncodingDictionary: Differences: true ToUnicode: true Font: BaseFont: HNMIGO+Cmtmib FontSubset: true FirstChar: 44 LastChar: 44 FontDescriptor: FontName: HNMIGO+Cmtmib Flags: Symbolic, ForceBold FontBBox: -117, -263, 1074, 781 FontFile3: true EncodingDictionary: Differences: true ToUnicode: true Font: BaseFont: HNMHGN+Caecilia-RomanSC FontSubset: true FirstChar: 46 LastChar: 117 FontDescriptor: FontName: HNMHGN+Caecilia-RomanSC Flags: Serif, Symbolic, SmallCap FontBBox: -167, -270, 1136, 926 FontFile3: true EncodingDictionary: Differences: true ToUnicode: true Font: BaseFont: HNMHGO+Times-Roman FontSubset: true FirstChar: 32 LastChar: 32 FontDescriptor: FontName: HNMHGO+Times-Roman Flags: Serif, Nonsymbolic FontBBox: -168, -218, 1000, 898 FontFile3: true Encoding: WinAnsiEncoding Font: BaseFont: HNMHIO+Caecilia-Light FontSubset: true FirstChar: 48 LastChar: 133 FontDescriptor: FontName: HNMHIO+Caecilia-Light Flags: Serif, Symbolic FontBBox: -164, -266, 1130, 908 FontFile3: true EncodingDictionary: Differences: true ToUnicode: true Font: BaseFont: HOBDIH+MathematicalPi-One FontSubset: true FirstChar: 2 LastChar: 2 FontDescriptor: FontName: HOBDIH+MathematicalPi-One Flags: Symbolic FontBBox: -30, -210, 1000, 779 FontFile3: true EncodingDictionary: Differences: true Font: BaseFont: HNMHJP+Caecilia-Bold FontSubset: true FirstChar: 40 LastChar: 121 FontDescriptor: FontName: HNMHJP+Caecilia-Bold Flags: Serif, Symbolic, ForceBold FontBBox: -166, -273, 1141, 938 FontFile3: true EncodingDictionary: Differences: true ToUnicode: true Font: BaseFont: HOGGHH+Helvetica FontSubset: true FirstChar: 2 LastChar: 128 FontDescriptor: FontName: HOGGHH+Helvetica Flags: Symbolic FontBBox: -166, -225, 1000, 931 FontFile3: true EncodingDictionary: Differences: true ToUnicode: true Font: BaseFont: HNMHNO+HelveticaLTStd-Bold FontSubset: true FirstChar: 69 LastChar: 241 FontDescriptor: FontName: HNMHNO+HelveticaLTStd-Bold Flags: Symbolic, ForceBold FontBBox: -170, -228, 1003, 962 FontFile3: true EncodingDictionary: Differences: true ToUnicode: true Font: BaseFont: HNMIKA+Caecilia-Italic FontSubset: true FirstChar: 37 LastChar: 243 FontDescriptor: FontName: HNMIKA+Caecilia-Italic Flags: Serif, Symbolic, Italic FontBBox: -166, -270, 1053, 915 FontFile3: true EncodingDictionary: Differences: true ToUnicode: true XMP: application/pdf 10.1016/j.nefroe.2022.11.011 Consensus document on autosomal dominant polycystic kindey disease from the Spanish Working Group on Inherited Kindey Diseases. Review 2020 Elisabet Ars Carmen Bernis Gloria Fraga Mnica Furlano Vctor Martnez Judith Martins Alberto Ortiz Maria Vanessa Prez-Gmez Jos Carlos Rodrguez-Prez Laia Sans Roser Torra en nombre del grupo de trabajo de Enfermedades Renales Hereditarias de la Sociedad Espaola de Nefrologa ADPKD Autosomal dominant polycystic kidney disease Recommendations Management Progression Consensus NEFROLOGIA (English Edition), 42 (2022) 367-389. doi:10.1016/j.nefroe.2022.11.011 Sociedad Española de Nefrología journal NEFROLOGIA (English Edition) © 2021 Sociedad Española de Nefrología. Published by Elsevier España, S.L.U. 2013-2514 42 4 July-August 2022 367-389 367 389 10.1016/j.nefroe.2022.11.011 http://dx.doi.org/10.1016/j.nefroe.2022.11.011 VoR 10.1016/j.nefroe.2022.11.011 noindex Elsevier 2022-11-25T08:34:47Z 2022-11-25T08:37:34+05:30 True True Acrobat Distiller 11.0 (Windows) uuid:5cab0f85-2715-4a1f-a8b3-6f2895b508ba uuid:e85bb9ef-5c8a-441e-a3b8-ca457e2affb8 http://creativecommons.org/licenses/by-nc-nd/4.0/ Pages: Page: Label: 1 Annotations: Annotation: Subtype: Link Rect: 281, 797, 402, 803 Flags: Print Annotation: Subtype: Link Rect: 277, 703, 405, 709 Flags: Print Annotation: Subtype: Link Rect: 161, 564, 180, 571 Flags: Print Destination: 904 Annotation: Subtype: Link Rect: 255, 564, 274, 571 Flags: Print Destination: 904 Annotation: Subtype: Link Rect: 337, 564, 355, 571 Flags: Print Destination: 904 Annotation: Subtype: Link Rect: 435, 564, 454, 571 Flags: Print Destination: 904 Annotation: Subtype: Link Rect: 535, 564, 553, 571 Flags: Print Destination: 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