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Applicability of (99m)Tc‐Labeled Human Serum Albumin Scintigraphy in Dogs With Protein‐Losing Enteropathy
BACKGROUND: Diagnosis of protein loss into the gastrointestinal tract using noninvasive techniques is challenging. In people, scintigraphy not only is a sensitive tool to confirm protein‐losing enteropathy (PLE), but it also allows for localization of protein loss. HYPOTHESIS/OBJECTIVES: To investig...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5354035/ https://www.ncbi.nlm.nih.gov/pubmed/28220598 http://dx.doi.org/10.1111/jvim.14673 |
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author | Engelmann, N. Ondreka, N. von Pückler, K. Mohrs, S. Sicken, J. Neiger, R. |
author_facet | Engelmann, N. Ondreka, N. von Pückler, K. Mohrs, S. Sicken, J. Neiger, R. |
author_sort | Engelmann, N. |
collection | PubMed |
description | BACKGROUND: Diagnosis of protein loss into the gastrointestinal tract using noninvasive techniques is challenging. In people, scintigraphy not only is a sensitive tool to confirm protein‐losing enteropathy (PLE), but it also allows for localization of protein loss. HYPOTHESIS/OBJECTIVES: To investigate the feasibility of (99m)Tc‐labeled human serum albumin (HSA) scintigraphy in dogs with PLE in comparison with control dogs. ANIMALS: A total of 8 clinically healthy control research dogs and 7 client‐owned dogs with gastrointestinal clinical signs and hypoalbuminemia (serum albumin concentration <2.0 g/dL). METHODS: Prospective case–control study. After IV injection of 400 MBq freshly prepared (99m)Tc HSA (30 mg/dog), images of the abdomen were obtained 10, 60, 120, and 240 minutes postinjection. Additional images of the salivary and thyroid glands were obtained to rule out free (99m)Tc. A scan was considered positive for PLE when radiopharmaceutical exudation was detectable in the intestinal tract. RESULTS: Only 1 control dog showed exudation of the radiopharmaceutical into the intestinal tract. No free (99m)Tc was detected in any dog. In dogs with PLE, focal small intestinal and diffuse small intestinal radiopharmaceutical exudation into the bowel was detected in 2 and 3 dogs, respectively, whereas in 2 dogs, there was disagreement about whether radiopharmaceutical exudation was focal or diffuse. CONCLUSION AND CLINICAL IMPORTANCE: (99m)Tc‐labeled HSA scintigraphy was feasible to diagnose PLE in dogs. |
format | Online Article Text |
id | pubmed-5354035 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-53540352017-03-22 Applicability of (99m)Tc‐Labeled Human Serum Albumin Scintigraphy in Dogs With Protein‐Losing Enteropathy Engelmann, N. Ondreka, N. von Pückler, K. Mohrs, S. Sicken, J. Neiger, R. J Vet Intern Med SMALL ANIMAL BACKGROUND: Diagnosis of protein loss into the gastrointestinal tract using noninvasive techniques is challenging. In people, scintigraphy not only is a sensitive tool to confirm protein‐losing enteropathy (PLE), but it also allows for localization of protein loss. HYPOTHESIS/OBJECTIVES: To investigate the feasibility of (99m)Tc‐labeled human serum albumin (HSA) scintigraphy in dogs with PLE in comparison with control dogs. ANIMALS: A total of 8 clinically healthy control research dogs and 7 client‐owned dogs with gastrointestinal clinical signs and hypoalbuminemia (serum albumin concentration <2.0 g/dL). METHODS: Prospective case–control study. After IV injection of 400 MBq freshly prepared (99m)Tc HSA (30 mg/dog), images of the abdomen were obtained 10, 60, 120, and 240 minutes postinjection. Additional images of the salivary and thyroid glands were obtained to rule out free (99m)Tc. A scan was considered positive for PLE when radiopharmaceutical exudation was detectable in the intestinal tract. RESULTS: Only 1 control dog showed exudation of the radiopharmaceutical into the intestinal tract. No free (99m)Tc was detected in any dog. In dogs with PLE, focal small intestinal and diffuse small intestinal radiopharmaceutical exudation into the bowel was detected in 2 and 3 dogs, respectively, whereas in 2 dogs, there was disagreement about whether radiopharmaceutical exudation was focal or diffuse. CONCLUSION AND CLINICAL IMPORTANCE: (99m)Tc‐labeled HSA scintigraphy was feasible to diagnose PLE in dogs. John Wiley and Sons Inc. 2017-02-21 2017 /pmc/articles/PMC5354035/ /pubmed/28220598 http://dx.doi.org/10.1111/jvim.14673 Text en Copyright © 2017 The Authors. Journal of Veterinary Internal Medicine published by Wiley Periodicals, Inc. on behalf of the American College of Veterinary Internal Medicine. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | SMALL ANIMAL Engelmann, N. Ondreka, N. von Pückler, K. Mohrs, S. Sicken, J. Neiger, R. Applicability of (99m)Tc‐Labeled Human Serum Albumin Scintigraphy in Dogs With Protein‐Losing Enteropathy |
title | Applicability of (99m)Tc‐Labeled Human Serum Albumin Scintigraphy in Dogs With Protein‐Losing Enteropathy |
title_full | Applicability of (99m)Tc‐Labeled Human Serum Albumin Scintigraphy in Dogs With Protein‐Losing Enteropathy |
title_fullStr | Applicability of (99m)Tc‐Labeled Human Serum Albumin Scintigraphy in Dogs With Protein‐Losing Enteropathy |
title_full_unstemmed | Applicability of (99m)Tc‐Labeled Human Serum Albumin Scintigraphy in Dogs With Protein‐Losing Enteropathy |
title_short | Applicability of (99m)Tc‐Labeled Human Serum Albumin Scintigraphy in Dogs With Protein‐Losing Enteropathy |
title_sort | applicability of (99m)tc‐labeled human serum albumin scintigraphy in dogs with protein‐losing enteropathy |
topic | SMALL ANIMAL |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5354035/ https://www.ncbi.nlm.nih.gov/pubmed/28220598 http://dx.doi.org/10.1111/jvim.14673 |
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