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Symptom relief and not cyst reduction determines treatment success in aspiration sclerotherapy of hepatic cysts

OBJECTIVE: To assess whether quantitative assessment of symptom reduction is a better outcome parameter than cyst volume reduction for treatment success in patients treated by aspiration sclerotherapy. METHODS: We included patients with symptomatic, large (> 5 cm), hepatic cysts from a randomized...

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Autores principales: Neijenhuis, Myrte K., Wijnands, Titus F. M., Kievit, Wietske, Ronot, Maxime, Gevers, Tom J. G., Drenth, Joost P. H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6510865/
https://www.ncbi.nlm.nih.gov/pubmed/30542749
http://dx.doi.org/10.1007/s00330-018-5851-y
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author Neijenhuis, Myrte K.
Wijnands, Titus F. M.
Kievit, Wietske
Ronot, Maxime
Gevers, Tom J. G.
Drenth, Joost P. H.
author_facet Neijenhuis, Myrte K.
Wijnands, Titus F. M.
Kievit, Wietske
Ronot, Maxime
Gevers, Tom J. G.
Drenth, Joost P. H.
author_sort Neijenhuis, Myrte K.
collection PubMed
description OBJECTIVE: To assess whether quantitative assessment of symptom reduction is a better outcome parameter than cyst volume reduction for treatment success in patients treated by aspiration sclerotherapy. METHODS: We included patients with symptomatic, large (> 5 cm), hepatic cysts from a randomized controlled trial (NCT02048319). At baseline and 6 months after treatment, symptoms were assessed with the polycystic liver disease questionnaire (PLD-Q) and we measured cyst volume using ultrasonography. Patient-reported change in health was assessed on a 5-point Likert scale (much worse to much better) after 6 months. We tested whether PLD-Q scores and cyst volumes changed after aspiration sclerotherapy (responsiveness). Changes in PLD-Q scores and cyst volume were compared with change in health as a measure of treatment success (discriminative ability). As secondary analysis, we compared baseline characteristics between responders (improved) and non-responders (not improved). RESULTS: We included 32 patients. Six months after treatment, 23 patients (72%) improved. Both PLD-Q score and cyst volume significantly decreased (median 38 to 18 points, p < 0.001, and 479 to 68 mL, p < 0.001). Larger improvement in PLD-Q score was associated with a positive change in health (p = 0.001), while larger proportional reduction in cyst volume was not significantly associated with health improvement after treatment (p = 0.136). Responders had larger baseline cyst volumes compared to non-responders (median 624 mL [IQR 343–1023] vs. 322 mL [IQR 157–423] p = 0.008). CONCLUSION: Cyst diameter reduction does not reflect treatment success in aspiration sclerotherapy from patients’ perspective, while symptoms measured with the PLD-Q can be used as a reliable outcome measure. KEY POINTS: • Cyst diameter reduction poorly reflects treatment success in aspiration sclerotherapy. • Symptoms measured by the polycystic liver disease questionnaire (PLD-Q) is a better outcome measure than cyst volume reduction for treatment success after aspiration sclerotherapy. • Particularly patients with larger cysts (≥ 529 mL) benefit from aspiration sclerotherapy. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00330-018-5851-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-65108652019-05-28 Symptom relief and not cyst reduction determines treatment success in aspiration sclerotherapy of hepatic cysts Neijenhuis, Myrte K. Wijnands, Titus F. M. Kievit, Wietske Ronot, Maxime Gevers, Tom J. G. Drenth, Joost P. H. Eur Radiol Gastrointestinal OBJECTIVE: To assess whether quantitative assessment of symptom reduction is a better outcome parameter than cyst volume reduction for treatment success in patients treated by aspiration sclerotherapy. METHODS: We included patients with symptomatic, large (> 5 cm), hepatic cysts from a randomized controlled trial (NCT02048319). At baseline and 6 months after treatment, symptoms were assessed with the polycystic liver disease questionnaire (PLD-Q) and we measured cyst volume using ultrasonography. Patient-reported change in health was assessed on a 5-point Likert scale (much worse to much better) after 6 months. We tested whether PLD-Q scores and cyst volumes changed after aspiration sclerotherapy (responsiveness). Changes in PLD-Q scores and cyst volume were compared with change in health as a measure of treatment success (discriminative ability). As secondary analysis, we compared baseline characteristics between responders (improved) and non-responders (not improved). RESULTS: We included 32 patients. Six months after treatment, 23 patients (72%) improved. Both PLD-Q score and cyst volume significantly decreased (median 38 to 18 points, p < 0.001, and 479 to 68 mL, p < 0.001). Larger improvement in PLD-Q score was associated with a positive change in health (p = 0.001), while larger proportional reduction in cyst volume was not significantly associated with health improvement after treatment (p = 0.136). Responders had larger baseline cyst volumes compared to non-responders (median 624 mL [IQR 343–1023] vs. 322 mL [IQR 157–423] p = 0.008). CONCLUSION: Cyst diameter reduction does not reflect treatment success in aspiration sclerotherapy from patients’ perspective, while symptoms measured with the PLD-Q can be used as a reliable outcome measure. KEY POINTS: • Cyst diameter reduction poorly reflects treatment success in aspiration sclerotherapy. • Symptoms measured by the polycystic liver disease questionnaire (PLD-Q) is a better outcome measure than cyst volume reduction for treatment success after aspiration sclerotherapy. • Particularly patients with larger cysts (≥ 529 mL) benefit from aspiration sclerotherapy. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00330-018-5851-y) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2018-12-12 2019 /pmc/articles/PMC6510865/ /pubmed/30542749 http://dx.doi.org/10.1007/s00330-018-5851-y Text en © The Author(s) 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Gastrointestinal
Neijenhuis, Myrte K.
Wijnands, Titus F. M.
Kievit, Wietske
Ronot, Maxime
Gevers, Tom J. G.
Drenth, Joost P. H.
Symptom relief and not cyst reduction determines treatment success in aspiration sclerotherapy of hepatic cysts
title Symptom relief and not cyst reduction determines treatment success in aspiration sclerotherapy of hepatic cysts
title_full Symptom relief and not cyst reduction determines treatment success in aspiration sclerotherapy of hepatic cysts
title_fullStr Symptom relief and not cyst reduction determines treatment success in aspiration sclerotherapy of hepatic cysts
title_full_unstemmed Symptom relief and not cyst reduction determines treatment success in aspiration sclerotherapy of hepatic cysts
title_short Symptom relief and not cyst reduction determines treatment success in aspiration sclerotherapy of hepatic cysts
title_sort symptom relief and not cyst reduction determines treatment success in aspiration sclerotherapy of hepatic cysts
topic Gastrointestinal
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6510865/
https://www.ncbi.nlm.nih.gov/pubmed/30542749
http://dx.doi.org/10.1007/s00330-018-5851-y
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