Absence of recognition of low alkaline phosphatase level in a tertiary care hospital
Summary Low serum total alkaline phosphatase level (ALP), the hallmark for hypophosphatasia (HPP), must be recognized to provide appropriate care of the patients and to avoid antiresorptive treatment. The prevalence of persistent low ALP in a clinical setting is 0.13 % and the recognition is very lo...
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Veröffentlicht in: | Osteoporosis international 2016-03, Vol.27 (3), p.1251-1254 |
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description | Summary
Low serum total alkaline phosphatase level (ALP), the hallmark for hypophosphatasia (HPP), must be recognized to provide appropriate care of the patients and to avoid antiresorptive treatment. The prevalence of persistent low ALP in a clinical setting is 0.13 % and the recognition is very low (3 %).
Introduction
A low serum total alkaline phosphatase level is the hallmark for the diagnosis of hypophosphatasia. Although very rare, HPP must be recognized to provide appropriate treatment of non-union fractures and to avoid potentially harmful drugs, such as antiresorptive treatments. The aim of this study was to assess the recognition of persistent low ALP in a tertiary care hospital.
Methods
Between the 1st of January and the 31st of December 2013, 48,755 patients had ALP assessment in the Biochemistry Department of our hospital. Sixty-eight patients had all serum ALP values persistently below 40 IU/l. Among them, six had potential causes of secondary hypophosphatasia. We consulted the summary discharges of the 62 patients in order to check for the notation of low ALP. Patients from the departments of rheumatology and internal medicine were contacted to fulfill a questionnaire about clinical manifestations potentially related to HPP.
Results
0.13 % of hospitalized patients had persistently low value. They were 46.5 ± 17.7 years old, and 73 % were females. The low ALP value was notified in the discharge summary for two patients (3 %), without any comment. Twenty-four patients (46 + /-16 years old) were contacted. Eight patients had fractures; two had a diagnosis of rickets in the childhood; two had symptomatic chondrocalcinosis. Nine had dental abnormalities. Three were receiving a bisphosphonate; two of them had a fracture while being treated with bisphosphonate.
Conclusion
Our study shows that low ALP is not recognized in a clinical setting in adults hospitalized in a tertiary care hospital. |
doi_str_mv | 10.1007/s00198-015-3346-0 |
format | Article |
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Low serum total alkaline phosphatase level (ALP), the hallmark for hypophosphatasia (HPP), must be recognized to provide appropriate care of the patients and to avoid antiresorptive treatment. The prevalence of persistent low ALP in a clinical setting is 0.13 % and the recognition is very low (3 %).
Introduction
A low serum total alkaline phosphatase level is the hallmark for the diagnosis of hypophosphatasia. Although very rare, HPP must be recognized to provide appropriate treatment of non-union fractures and to avoid potentially harmful drugs, such as antiresorptive treatments. The aim of this study was to assess the recognition of persistent low ALP in a tertiary care hospital.
Methods
Between the 1st of January and the 31st of December 2013, 48,755 patients had ALP assessment in the Biochemistry Department of our hospital. Sixty-eight patients had all serum ALP values persistently below 40 IU/l. Among them, six had potential causes of secondary hypophosphatasia. We consulted the summary discharges of the 62 patients in order to check for the notation of low ALP. Patients from the departments of rheumatology and internal medicine were contacted to fulfill a questionnaire about clinical manifestations potentially related to HPP.
Results
0.13 % of hospitalized patients had persistently low value. They were 46.5 ± 17.7 years old, and 73 % were females. The low ALP value was notified in the discharge summary for two patients (3 %), without any comment. Twenty-four patients (46 + /-16 years old) were contacted. Eight patients had fractures; two had a diagnosis of rickets in the childhood; two had symptomatic chondrocalcinosis. Nine had dental abnormalities. Three were receiving a bisphosphonate; two of them had a fracture while being treated with bisphosphonate.
Conclusion
Our study shows that low ALP is not recognized in a clinical setting in adults hospitalized in a tertiary care hospital.</description><identifier>ISSN: 0937-941X</identifier><identifier>EISSN: 1433-2965</identifier><identifier>DOI: 10.1007/s00198-015-3346-0</identifier><identifier>PMID: 26446772</identifier><language>eng</language><publisher>London: Springer London</publisher><subject>Adult ; Aged ; Alkaline Phosphatase - blood ; Endocrinology ; Female ; Fractures, Spontaneous - etiology ; Hospitalization ; Humans ; Hypophosphatasia - complications ; Hypophosphatasia - diagnosis ; Male ; Medical diagnosis ; Medicine ; Medicine & Public Health ; Middle Aged ; Orthopedics ; Osteomalacia - etiology ; Phosphates ; Rheumatology ; Short Communication ; Tertiary Healthcare - standards ; Young Adult</subject><ispartof>Osteoporosis international, 2016-03, Vol.27 (3), p.1251-1254</ispartof><rights>International Osteoporosis Foundation and National Osteoporosis Foundation 2015</rights><rights>International Osteoporosis Foundation and National Osteoporosis Foundation 2016</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c508t-c5a0b0c62bf95dcbce7c98738cffa2ba2f5fda61996fc898b470223f05c7abfa3</citedby><cites>FETCH-LOGICAL-c508t-c5a0b0c62bf95dcbce7c98738cffa2ba2f5fda61996fc898b470223f05c7abfa3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00198-015-3346-0$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00198-015-3346-0$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26446772$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Maman, E.</creatorcontrib><creatorcontrib>Borderie, D.</creatorcontrib><creatorcontrib>Roux, C.</creatorcontrib><creatorcontrib>Briot, K.</creatorcontrib><title>Absence of recognition of low alkaline phosphatase level in a tertiary care hospital</title><title>Osteoporosis international</title><addtitle>Osteoporos Int</addtitle><addtitle>Osteoporos Int</addtitle><description>Summary
Low serum total alkaline phosphatase level (ALP), the hallmark for hypophosphatasia (HPP), must be recognized to provide appropriate care of the patients and to avoid antiresorptive treatment. The prevalence of persistent low ALP in a clinical setting is 0.13 % and the recognition is very low (3 %).
Introduction
A low serum total alkaline phosphatase level is the hallmark for the diagnosis of hypophosphatasia. Although very rare, HPP must be recognized to provide appropriate treatment of non-union fractures and to avoid potentially harmful drugs, such as antiresorptive treatments. The aim of this study was to assess the recognition of persistent low ALP in a tertiary care hospital.
Methods
Between the 1st of January and the 31st of December 2013, 48,755 patients had ALP assessment in the Biochemistry Department of our hospital. Sixty-eight patients had all serum ALP values persistently below 40 IU/l. Among them, six had potential causes of secondary hypophosphatasia. We consulted the summary discharges of the 62 patients in order to check for the notation of low ALP. Patients from the departments of rheumatology and internal medicine were contacted to fulfill a questionnaire about clinical manifestations potentially related to HPP.
Results
0.13 % of hospitalized patients had persistently low value. They were 46.5 ± 17.7 years old, and 73 % were females. The low ALP value was notified in the discharge summary for two patients (3 %), without any comment. Twenty-four patients (46 + /-16 years old) were contacted. Eight patients had fractures; two had a diagnosis of rickets in the childhood; two had symptomatic chondrocalcinosis. Nine had dental abnormalities. Three were receiving a bisphosphonate; two of them had a fracture while being treated with bisphosphonate.
Conclusion
Our study shows that low ALP is not recognized in a clinical setting in adults hospitalized in a tertiary care hospital.</description><subject>Adult</subject><subject>Aged</subject><subject>Alkaline Phosphatase - blood</subject><subject>Endocrinology</subject><subject>Female</subject><subject>Fractures, Spontaneous - etiology</subject><subject>Hospitalization</subject><subject>Humans</subject><subject>Hypophosphatasia - complications</subject><subject>Hypophosphatasia - diagnosis</subject><subject>Male</subject><subject>Medical diagnosis</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Middle Aged</subject><subject>Orthopedics</subject><subject>Osteomalacia - etiology</subject><subject>Phosphates</subject><subject>Rheumatology</subject><subject>Short Communication</subject><subject>Tertiary Healthcare - standards</subject><subject>Young Adult</subject><issn>0937-941X</issn><issn>1433-2965</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp1kE9LBCEYhyWK2rY-QJcQunSZUmfU8RhL_2ChywbdxHFfazZ33HSm6NvnsltE0EURn9_v1QehE0ouKCHyMhFCVV0QyouyrERBdtCIVmVZMCX4LhoRVcpCVfTpAB2mtCA5o5TcRwdMVJWQko3Q7KpJ0FnAweEINjx3bd-Gbn304QMb_2p82wFevYS0ejG9SYA9vIPHbYcN7iH2rYmf2JoIeM20vfFHaM8Zn-B4u4_R4831bHJXTB9u7ydX08JyUvd5NaQhVrDGKT63jQVpVS3L2jpnWGOY425uBFVKOFuruqkkYax0hFtpGmfKMTrf9K5ieBsg9XrZJgvemw7CkDSVouaiokpm9OwPughD7PLrNK2Z4oIzRjNFN5SNIaUITq9iu8z_05TotXK9Ua6zcr1WrknOnG6bh2YJ85_Et-MMsA2Q8lX3DPHX6H9bvwDhLoyl</recordid><startdate>20160301</startdate><enddate>20160301</enddate><creator>Maman, E.</creator><creator>Borderie, D.</creator><creator>Roux, C.</creator><creator>Briot, K.</creator><general>Springer London</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QP</scope><scope>7RV</scope><scope>7TS</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20160301</creationdate><title>Absence of recognition of low alkaline phosphatase level in a tertiary care hospital</title><author>Maman, E. ; Borderie, D. ; Roux, C. ; Briot, K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c508t-c5a0b0c62bf95dcbce7c98738cffa2ba2f5fda61996fc898b470223f05c7abfa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Alkaline Phosphatase - blood</topic><topic>Endocrinology</topic><topic>Female</topic><topic>Fractures, Spontaneous - etiology</topic><topic>Hospitalization</topic><topic>Humans</topic><topic>Hypophosphatasia - complications</topic><topic>Hypophosphatasia - diagnosis</topic><topic>Male</topic><topic>Medical diagnosis</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Middle Aged</topic><topic>Orthopedics</topic><topic>Osteomalacia - etiology</topic><topic>Phosphates</topic><topic>Rheumatology</topic><topic>Short Communication</topic><topic>Tertiary Healthcare - standards</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Maman, E.</creatorcontrib><creatorcontrib>Borderie, D.</creatorcontrib><creatorcontrib>Roux, C.</creatorcontrib><creatorcontrib>Briot, K.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Physical Education Index</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Osteoporosis international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Maman, E.</au><au>Borderie, D.</au><au>Roux, C.</au><au>Briot, K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Absence of recognition of low alkaline phosphatase level in a tertiary care hospital</atitle><jtitle>Osteoporosis international</jtitle><stitle>Osteoporos Int</stitle><addtitle>Osteoporos Int</addtitle><date>2016-03-01</date><risdate>2016</risdate><volume>27</volume><issue>3</issue><spage>1251</spage><epage>1254</epage><pages>1251-1254</pages><issn>0937-941X</issn><eissn>1433-2965</eissn><abstract>Summary
Low serum total alkaline phosphatase level (ALP), the hallmark for hypophosphatasia (HPP), must be recognized to provide appropriate care of the patients and to avoid antiresorptive treatment. The prevalence of persistent low ALP in a clinical setting is 0.13 % and the recognition is very low (3 %).
Introduction
A low serum total alkaline phosphatase level is the hallmark for the diagnosis of hypophosphatasia. Although very rare, HPP must be recognized to provide appropriate treatment of non-union fractures and to avoid potentially harmful drugs, such as antiresorptive treatments. The aim of this study was to assess the recognition of persistent low ALP in a tertiary care hospital.
Methods
Between the 1st of January and the 31st of December 2013, 48,755 patients had ALP assessment in the Biochemistry Department of our hospital. Sixty-eight patients had all serum ALP values persistently below 40 IU/l. Among them, six had potential causes of secondary hypophosphatasia. We consulted the summary discharges of the 62 patients in order to check for the notation of low ALP. Patients from the departments of rheumatology and internal medicine were contacted to fulfill a questionnaire about clinical manifestations potentially related to HPP.
Results
0.13 % of hospitalized patients had persistently low value. They were 46.5 ± 17.7 years old, and 73 % were females. The low ALP value was notified in the discharge summary for two patients (3 %), without any comment. Twenty-four patients (46 + /-16 years old) were contacted. Eight patients had fractures; two had a diagnosis of rickets in the childhood; two had symptomatic chondrocalcinosis. Nine had dental abnormalities. Three were receiving a bisphosphonate; two of them had a fracture while being treated with bisphosphonate.
Conclusion
Our study shows that low ALP is not recognized in a clinical setting in adults hospitalized in a tertiary care hospital.</abstract><cop>London</cop><pub>Springer London</pub><pmid>26446772</pmid><doi>10.1007/s00198-015-3346-0</doi><tpages>4</tpages></addata></record> |
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subjects | Adult Aged Alkaline Phosphatase - blood Endocrinology Female Fractures, Spontaneous - etiology Hospitalization Humans Hypophosphatasia - complications Hypophosphatasia - diagnosis Male Medical diagnosis Medicine Medicine & Public Health Middle Aged Orthopedics Osteomalacia - etiology Phosphates Rheumatology Short Communication Tertiary Healthcare - standards Young Adult |
title | Absence of recognition of low alkaline phosphatase level in a tertiary care hospital |
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