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Questionnaire PLD‐complaint‐specific assessment identifies need for therapy in polycystic liver disease: A multi‐centric prospective study

BACKGROUND AND AIMS: Polycystic liver disease (PLD) can lead to extensive hepatomegaly. Symptom relief is the primary goal of the treatment. The role of the recently developed disease‐specific questionnaires for identification of the thresholds and the assessment of therapy needs further investigati...

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Autores principales: Billiet, Antoon, Temmerman, Frederik, Coudyzer, Walter, Van den Ende, Natalie, Colle, Isabelle, Francque, Sven, De Maeght, Stephane, Janssens, Filip, Orlent, Hans, Sprengers, Dirk, Delwaide, Jean, Decock, Sofie, De Vloo, Charlotte, Moreno, Christophe, van Malenstein, Hannah, van der Merwe, Schalk, Verbeek, Jef, Nevens, Frederik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10493353/
https://www.ncbi.nlm.nih.gov/pubmed/37278135
http://dx.doi.org/10.1002/ueg2.12387
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author Billiet, Antoon
Temmerman, Frederik
Coudyzer, Walter
Van den Ende, Natalie
Colle, Isabelle
Francque, Sven
De Maeght, Stephane
Janssens, Filip
Orlent, Hans
Sprengers, Dirk
Delwaide, Jean
Decock, Sofie
De Vloo, Charlotte
Moreno, Christophe
van Malenstein, Hannah
van der Merwe, Schalk
Verbeek, Jef
Nevens, Frederik
author_facet Billiet, Antoon
Temmerman, Frederik
Coudyzer, Walter
Van den Ende, Natalie
Colle, Isabelle
Francque, Sven
De Maeght, Stephane
Janssens, Filip
Orlent, Hans
Sprengers, Dirk
Delwaide, Jean
Decock, Sofie
De Vloo, Charlotte
Moreno, Christophe
van Malenstein, Hannah
van der Merwe, Schalk
Verbeek, Jef
Nevens, Frederik
author_sort Billiet, Antoon
collection PubMed
description BACKGROUND AND AIMS: Polycystic liver disease (PLD) can lead to extensive hepatomegaly. Symptom relief is the primary goal of the treatment. The role of the recently developed disease‐specific questionnaires for identification of the thresholds and the assessment of therapy needs further investigation. METHODS: A five‐year prospective multi‐centric observational study in 21 hospitals in Belgium gathered a study population of 198 symptomatic PLD‐patients of whom the disease‐specific symptom questionnaire PLD‐complaint‐specific assessment (POLCA) scores were calculated. The thresholds of the POLCA score for the need for volume reduction therapy were analyzed. RESULTS: The study group consisted of mostly (82.8%) women with baseline mean age of 54.4 years ±11.2, median liver volume expressed as height‐adjusted total liver volume(htLV) of 1994 mL (interquartile range [IQR] 1275; 3150) and median growth of the liver of +74 mL/year (IQR +3; +230). Volume reduction therapy was needed in 71 patients (35.9%). A POLCA severity score (SPI) ≥ 14 predicted the need for therapy both in the derivation (n = 63) and the validation cohort (n = 126). The thresholds to start somatostatin analogues (n = 55) or to consider liver transplantation (n = 18) were SPI scores of ≥14 and ≥ 18 and the corresponding mean htLVs were 2902 mL (IQR 1908; 3964) and 3607 mL (IQR 2901; 4337), respectively. Somatostatin analogues treatment resulted in a decrease in the SPI score −6.0 versus + 4.5 in patients without somatostatin analogues (p < 0.01). Changes in the SPI score were significantly different between the liver transplantation group and no liver transplantation group, +4.3 ± 7.1 versus −1.6 ± 4.9, respectively, (p < 0.01). CONCLUSION: A polycystic liver disease‐specific questionnaire can be used as a guide on when to start a volume reduction therapy and to assess the effect of treatment.
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spelling pubmed-104933532023-09-12 Questionnaire PLD‐complaint‐specific assessment identifies need for therapy in polycystic liver disease: A multi‐centric prospective study Billiet, Antoon Temmerman, Frederik Coudyzer, Walter Van den Ende, Natalie Colle, Isabelle Francque, Sven De Maeght, Stephane Janssens, Filip Orlent, Hans Sprengers, Dirk Delwaide, Jean Decock, Sofie De Vloo, Charlotte Moreno, Christophe van Malenstein, Hannah van der Merwe, Schalk Verbeek, Jef Nevens, Frederik United European Gastroenterol J Hepatobiliary BACKGROUND AND AIMS: Polycystic liver disease (PLD) can lead to extensive hepatomegaly. Symptom relief is the primary goal of the treatment. The role of the recently developed disease‐specific questionnaires for identification of the thresholds and the assessment of therapy needs further investigation. METHODS: A five‐year prospective multi‐centric observational study in 21 hospitals in Belgium gathered a study population of 198 symptomatic PLD‐patients of whom the disease‐specific symptom questionnaire PLD‐complaint‐specific assessment (POLCA) scores were calculated. The thresholds of the POLCA score for the need for volume reduction therapy were analyzed. RESULTS: The study group consisted of mostly (82.8%) women with baseline mean age of 54.4 years ±11.2, median liver volume expressed as height‐adjusted total liver volume(htLV) of 1994 mL (interquartile range [IQR] 1275; 3150) and median growth of the liver of +74 mL/year (IQR +3; +230). Volume reduction therapy was needed in 71 patients (35.9%). A POLCA severity score (SPI) ≥ 14 predicted the need for therapy both in the derivation (n = 63) and the validation cohort (n = 126). The thresholds to start somatostatin analogues (n = 55) or to consider liver transplantation (n = 18) were SPI scores of ≥14 and ≥ 18 and the corresponding mean htLVs were 2902 mL (IQR 1908; 3964) and 3607 mL (IQR 2901; 4337), respectively. Somatostatin analogues treatment resulted in a decrease in the SPI score −6.0 versus + 4.5 in patients without somatostatin analogues (p < 0.01). Changes in the SPI score were significantly different between the liver transplantation group and no liver transplantation group, +4.3 ± 7.1 versus −1.6 ± 4.9, respectively, (p < 0.01). CONCLUSION: A polycystic liver disease‐specific questionnaire can be used as a guide on when to start a volume reduction therapy and to assess the effect of treatment. John Wiley and Sons Inc. 2023-06-05 /pmc/articles/PMC10493353/ /pubmed/37278135 http://dx.doi.org/10.1002/ueg2.12387 Text en © 2023 The Authors. United European Gastroenterology Journal published by Wiley Periodicals LLC on behalf of United European Gastroenterology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Hepatobiliary
Billiet, Antoon
Temmerman, Frederik
Coudyzer, Walter
Van den Ende, Natalie
Colle, Isabelle
Francque, Sven
De Maeght, Stephane
Janssens, Filip
Orlent, Hans
Sprengers, Dirk
Delwaide, Jean
Decock, Sofie
De Vloo, Charlotte
Moreno, Christophe
van Malenstein, Hannah
van der Merwe, Schalk
Verbeek, Jef
Nevens, Frederik
Questionnaire PLD‐complaint‐specific assessment identifies need for therapy in polycystic liver disease: A multi‐centric prospective study
title Questionnaire PLD‐complaint‐specific assessment identifies need for therapy in polycystic liver disease: A multi‐centric prospective study
title_full Questionnaire PLD‐complaint‐specific assessment identifies need for therapy in polycystic liver disease: A multi‐centric prospective study
title_fullStr Questionnaire PLD‐complaint‐specific assessment identifies need for therapy in polycystic liver disease: A multi‐centric prospective study
title_full_unstemmed Questionnaire PLD‐complaint‐specific assessment identifies need for therapy in polycystic liver disease: A multi‐centric prospective study
title_short Questionnaire PLD‐complaint‐specific assessment identifies need for therapy in polycystic liver disease: A multi‐centric prospective study
title_sort questionnaire pld‐complaint‐specific assessment identifies need for therapy in polycystic liver disease: a multi‐centric prospective study
topic Hepatobiliary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10493353/
https://www.ncbi.nlm.nih.gov/pubmed/37278135
http://dx.doi.org/10.1002/ueg2.12387
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