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<!--
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||
UID=1662563
|
||
ConceptID=C4721509
|
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Usual interstitial pneumonia<span class="h1sub">(UIP)</span></div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1662563</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C4721509</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonyms:</td>
|
||
<td>Interstitial Pneumonia, Usual; Interstitial Pneumonitis, Usual; Pneumonitides, Usual Interstitial; Pneumonitis, Usual Interstitial; Usual Interstitial Pneumonia; Usual Interstitial Pneumonias; Usual Interstitial Pneumonitides; Usual Interstitial Pneumonitis</td></tr>
|
||
<tr><td><span class="bold">SNOMED CT: </span></td>
|
||
<td>UIP - Usual interstitial pneumonitis (237121003); Usual interstitial pneumonitis (237121003)</td></tr>
|
||
<tr><td colspan="2" class="small"> </td></tr><tr><td>HPO:</td>
|
||
<td><a target="_blank" title="Human Phenotype Ontology" href="https://hpo.jax.org/app/browse/term/HP:0031950">HP:0031950</a></td></tr>
|
||
<tr><td>OMIM<span class="superscript">®</span>:</td>
|
||
<td><a href="https://omim.org/entry/178500" target="_blank">178500</a></td></tr>
|
||
</tbody></table></div><div class="rprt-body jig-ncbiinpagenav" data-jigconfig="smoothScroll: false, gotoTopLink: true, gotoTopLinkText: '', gotoTopLinkAttrs: {'title': 'Go to the top of the page'},allHeadingLevels: ['h1'], topOfPageTOC: true, tocId: 'my-toc'"><div id="rprt-tabs-1" class="rprt-tab"><div id="tb-termsProp-1"><div class="leftCol mgCol"><div>
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<div class="portlet mgSection" id="ID_100">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Definition">Definition</h1><a sid="100" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln">Temporal and spatial heterogeneity in lungs based on presence of fibrosis and honeycombing. [from <a title="Human Phenotype Ontology" href="http://www.human-phenotype-ontology.org" class="defSource" target="_blank">HPO</a>]</div>
|
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Term_Hierarchy">Term Hierarchy</h1><a sid="118" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
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<div class="portlet_content ln HierarchyGTR"><div class="jig-ncbitabs"><ul><li><a href="#tabGTR">GTR</a></li><li><a href="#tabMGEN">MeSH</a></li></ul><div id="tabGTR"><div class="search_result"><div class="rprts"><div class="chiclet_legend"><span class="chiclet_list" style="position:static;"><span title="Clinical test" class="chiclet Ccolor round">C</span><span>Clinical test, </span><span title="Research test" class="chiclet Rcolor round">R</span><span>Research test, </span><span title="OMIM" class="chiclet Ocolor ">O</span><span>OMIM, </span><span title="GeneReview" class="chiclet Gcolor">G</span><span><em>GeneReviews</em>, </span><span title="ClinVar" class="chiclet Vcolor">V</span><span>ClinVar </span></span></div><div id="hierarchy" class="margin_t1"><div class="ds_tree"><ul><li class="matched_ds"><span class="chiclet_list"><span class="chiclet unavailable round" title="Clinical test">C</span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=1662563" target="_blank" href="/omim/178500">O</a></span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet unavailable" title="ClinVar">V</span></span><span class="TLline">Usual interstitial pneumonia</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/867443" ref="tree=MeSH" title="MedGen record for Phenotypic abnormality">Phenotypic abnormality</a></span><ul><li><span class="TLline"><a href="/medgen/866322" ref="tree=MeSH" title="MedGen record for Abnormality of the respiratory system">Abnormality of the respiratory system</a></span><ul><li><span class="TLline"><a href="/medgen/220360" ref="tree=MeSH" title="MedGen record for Abnormal respiratory system physiology">Abnormal respiratory system physiology</a></span><ul><li><span class="TLline"><a href="/medgen/868593" ref="tree=MeSH" title="MedGen record for Abnormal respiratory system morphology">Abnormal respiratory system morphology</a></span><ul><li><span class="TLline"><a href="/medgen/892303" ref="tree=MeSH" title="MedGen record for Abnormality of the lung">Abnormality of the lung</a></span><ul><li><span class="TLline"><a href="/medgen/1788738" ref="tree=MeSH" title="MedGen record for Abnormal pulmonary interstitial morphology">Abnormal pulmonary interstitial morphology</a></span><ul><li><span class="matched_ds">Usual interstitial pneumonia</span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_112">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Conditions_with_this_feature">Conditions with this feature</h1><a sid="112" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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||
<div class="portlet_content ln clinfeat">
|
||
<div class="divPopper rprt" id="rdis_410074"><div><strong>Interstitial lung disease due to ABCA3 deficiency</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>410074</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C1970456</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">For a general phenotypic description and a discussion of genetic heterogeneity of pulmonary surfactant metabolism dysfunction, see SMDP1 (265120).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/410074">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_766531"><div><strong>Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>766531</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C3553617</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Dyskeratosis congenita and related telomere biology disorders (DC/TBD) are caused by impaired telomere maintenance resulting in short or very short telomeres. The phenotypic spectrum of telomere biology disorders is broad and includes individuals with classic dyskeratosis congenita (DC) as well as those with very short telomeres and an isolated physical finding. Classic DC is characterized by a triad of dysplastic nails, lacy reticular pigmentation of the upper chest and/or neck, and oral leukoplakia, although this may not be present in all individuals. People with DC/TBD are at increased risk for progressive bone marrow failure (BMF), myelodysplastic syndrome or acute myelogenous leukemia, solid tumors (usually squamous cell carcinoma of the head/neck or anogenital cancer), and pulmonary fibrosis. Other findings can include eye abnormalities (epiphora, blepharitis, sparse eyelashes, ectropion, entropion, trichiasis), taurodontism, liver disease, gastrointestinal telangiectasias, and avascular necrosis of the hips or shoulders. Although most persons with DC/TBD have normal psychomotor development and normal neurologic function, significant developmental delay is present in both forms; additional findings include cerebellar hypoplasia (Hoyeraal Hreidarsson syndrome) and bilateral exudative retinopathy and intracranial calcifications (Revesz syndrome and Coats plus syndrome). Onset and progression of manifestations of DC/TBD vary: at the mild end of the spectrum are those who have only minimal physical findings with normal bone marrow function, and at the severe end are those who have the diagnostic triad and early-onset BMF.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/766531">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_901644"><div><strong>Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 3</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>901644</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C4225346</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Dyskeratosis congenita and related telomere biology disorders (DC/TBD) are caused by impaired telomere maintenance resulting in short or very short telomeres. The phenotypic spectrum of telomere biology disorders is broad and includes individuals with classic dyskeratosis congenita (DC) as well as those with very short telomeres and an isolated physical finding. Classic DC is characterized by a triad of dysplastic nails, lacy reticular pigmentation of the upper chest and/or neck, and oral leukoplakia, although this may not be present in all individuals. People with DC/TBD are at increased risk for progressive bone marrow failure (BMF), myelodysplastic syndrome or acute myelogenous leukemia, solid tumors (usually squamous cell carcinoma of the head/neck or anogenital cancer), and pulmonary fibrosis. Other findings can include eye abnormalities (epiphora, blepharitis, sparse eyelashes, ectropion, entropion, trichiasis), taurodontism, liver disease, gastrointestinal telangiectasias, and avascular necrosis of the hips or shoulders. Although most persons with DC/TBD have normal psychomotor development and normal neurologic function, significant developmental delay is present in both forms; additional findings include cerebellar hypoplasia (Hoyeraal Hreidarsson syndrome) and bilateral exudative retinopathy and intracranial calcifications (Revesz syndrome and Coats plus syndrome). Onset and progression of manifestations of DC/TBD vary: at the mild end of the spectrum are those who have only minimal physical findings with normal bone marrow function, and at the severe end are those who have the diagnostic triad and early-onset BMF.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/901644">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1794136"><div><strong>Interstitial lung disease 2</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1794136</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C5561926</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Interstitial lung disease (ILD) comprises a heterogeneous group of rare diseases affecting the distal part of the lung and characterized by a progressive remodeling of the alveolar interstitium. The manifestations form a spectrum ranging from idiopathic interstitial pneumonia (IIP) or pneumonitis to the more severe idiopathic pulmonary fibrosis (IPF). IPF is associated with an increased risk of developing lung cancer, which occurs in a subset of patients with ILD. Clinical features of ILD include dyspnea, clubbing of the fingers, and restrictive lung capacity. Imaging typically shows ground glass opacities and inter- and intraseptal thickening, while histologic studies usually show a pattern consistent with 'usual interstitial pneumonia' (UIP) (review by Gross and Hunninghake, 2001; summary by Legendre et al., 2020). Idiopathic pulmonary fibrosis is one of a family of idiopathic pneumonias sharing clinical features of shortness of breath, radiographically evident diffuse pulmonary infiltrates, and varying degrees in inflammation, fibrosis, or both on lung biopsy. In some cases, the disorder can be rapidly progressive and characterized by sequential acute lung injury with subsequent scarring and end-stage lung disease. Although older studies included several forms of interstitial pneumonia under the term 'idiopathic pulmonary fibrosis,' the clinical label of 'idiopathic pulmonary fibrosis' should be reserved for patients with a specific form of fibrosing interstitial pneumonia referred to as usual interstitial pneumonia (Gross and Hunninghake, 2001). It is estimated that 0.5 to 2.2% of cases of idiopathic pulmonary fibrosis are familial (Marshall et al., 2000). Gross and Hunninghake (2001) reviewed idiopathic pulmonary fibrosis, emphasizing definition, pathogenesis, diagnosis, natural history, and therapy. Antoniou et al. (2004) provided a 'top ten list' of references pertaining to etiopathogenesis, prognosis, diagnosis, therapy, and other aspects of idiopathic pulmonary fibrosis. For a discussion of genetic heterogeneity of ILD, see ILD1 (619611). Pulmonary fibrosis can also be a feature in patients with mutations in the TERT (187270) or the TERC (602322) gene; see PFBMFT1 (614742) and PFBMFT2 (614743). Some patients with surfactant protein C deficiency (610913) who survive to adulthood manifest features of pulmonary fibrosis.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1794136">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1794231"><div><strong>Interstitial lung disease 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1794231</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C5562021</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Interstitial lung disease (ILD) comprises a heterogeneous group of rare diseases affecting the distal part of the lung and characterized by a progressive remodeling of the alveolar interstitium. The manifestations form a spectrum ranging from idiopathic interstitial pneumonia (IIP) or pneumonitis to the more severe idiopathic pulmonary fibrosis (IPF). IPF is associated with an increased risk of developing lung cancer, which occurs in a subset of patients with ILD. Clinical features of ILD include dyspnea, clubbing of the fingers, and restrictive lung capacity. Imaging typically shows ground glass opacities and inter- and intraseptal thickening, while histologic studies usually show a pattern consistent with 'usual interstitial pneumonia' (UIP) (summary by Nathan et al., 2016, Doubkova et al., 2019). Genetic Heterogeneity of Interstitial Lung Disease See also ILD2 (178500), caused by mutation in the SFTPA2 gene (178642) on chromosome 10q22.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1794231">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1841132"><div><strong>Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 8</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1841132</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C5830496</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Telomere-related pulmonary fibrosis and/or bone marrow failure syndrome-8 (PFBMFT8) is an autosomal dominant disorder characterized by the onset of progressive pulmonary fibrosis in adulthood. Some affected individuals have signs of bone marrow failure, such as thrombocytopenia, or liver dysfunction, including hepatopulmonary syndrome. Other features of dyskeratosis congenita, including premature graying of the hair, may be observed. Telomeres are shortened compared to controls (Kelich et al., 2022). For a discussion of genetic heterogeneity of telomere-related pulmonary fibrosis and/or bone marrow failure, see PFBMFT1 (614742).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1841132">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1794231" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Interstitial lung disease 1</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1794136" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Interstitial lung disease 2</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_410074" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Interstitial lung disease due to ABCA3 deficiency</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1841132" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 8</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_766531" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 1</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_901644" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 3</a></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_105">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Professional_guidelines">Professional guidelines</h1><a sid="105" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><h3 class="subhead">PubMed<a class="help jig-ncbi-popper" data-jig="ncbipopper" href="#guidelinesHelpPM"><img class="pulldown" src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a></h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/34437662">Diagnosis and Management of Idiopathic Pulmonary Fibrosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Munchel JK,
|
||
Shea BS</span><br />
|
||
<span class="medgenPMjournal">R I Med J (2013)</span>
|
||
2021 Sep 1;104(7):26-29.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34437662" target="_blank">34437662</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30168753">Diagnosis of Idiopathic Pulmonary Fibrosis. An Official ATS/ERS/JRS/ALAT Clinical Practice Guideline.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Raghu G,
|
||
Remy-Jardin M,
|
||
Myers JL,
|
||
Richeldi L,
|
||
Ryerson CJ,
|
||
Lederer DJ,
|
||
Behr J,
|
||
Cottin V,
|
||
Danoff SK,
|
||
Morell F,
|
||
Flaherty KR,
|
||
Wells A,
|
||
Martinez FJ,
|
||
Azuma A,
|
||
Bice TJ,
|
||
Bouros D,
|
||
Brown KK,
|
||
Collard HR,
|
||
Duggal A,
|
||
Galvin L,
|
||
Inoue Y,
|
||
Jenkins RG,
|
||
Johkoh T,
|
||
Kazerooni EA,
|
||
Kitaichi M,
|
||
Knight SL,
|
||
Mansour G,
|
||
Nicholson AG,
|
||
Pipavath SNJ,
|
||
Buendía-Roldán I,
|
||
Selman M,
|
||
Travis WD,
|
||
Walsh S,
|
||
Wilson KC;
|
||
American Thoracic Society, European Respiratory Society, Japanese Respiratory Society, and Latin American Thoracic Society</span><br />
|
||
<span class="medgenPMjournal">Am J Respir Crit Care Med</span>
|
||
2018 Sep 1;198(5):e44-e68.
|
||
doi: 10.1164/rccm.201807-1255ST.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30168753" target="_blank">30168753</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29154106">Diagnostic criteria for idiopathic pulmonary fibrosis: a Fleischner Society White Paper.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lynch DA,
|
||
Sverzellati N,
|
||
Travis WD,
|
||
Brown KK,
|
||
Colby TV,
|
||
Galvin JR,
|
||
Goldin JG,
|
||
Hansell DM,
|
||
Inoue Y,
|
||
Johkoh T,
|
||
Nicholson AG,
|
||
Knight SL,
|
||
Raoof S,
|
||
Richeldi L,
|
||
Ryerson CJ,
|
||
Ryu JH,
|
||
Wells AU</span><br />
|
||
<span class="medgenPMjournal">Lancet Respir Med</span>
|
||
2018 Feb;6(2):138-153.
|
||
Epub 2017 Nov 15
|
||
doi: 10.1016/S2213-2600(17)30433-2.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29154106" target="_blank">29154106</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22usual%20interstitial%20pneumonia%22%5Btiab%3A~0%5D)%20AND%20(%22english%20and%20humans%22%5BFilter%5D)%20AND%20(%20(%22practice%20guideline%22%5BFilter%5D)%20OR%20(practice*%5Btitl%5D%20AND%20(guideline%5Btitl%5D%20OR%20parameter%5Btitl%5D%20OR%20resource%5Btitl%5D%20OR%20bulletin%5Btitl%5D%20OR%20best%5Btitl%5D))%20OR%20(genetic*%5Btitl%5D%20AND%20(evaluation%5Btitl%5D%20OR%20counseling%5Btitl%5D%20OR%20screening%5Btitl%5D%20OR%20test*%5Btitl%5D))%20OR%20(clinical%5Btitl%5D%20AND%20((expert%5Btitl%5D%20AND%20consensus%5Btitl%5D)%20OR%20utility%5Btitl%5D%20OR%20guideline*%5Btitl%5D))%20OR%20(management%5Btitl%5D%20AND%20(clinical%5Btitl%5D%20OR%20diagnos*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20pain%5Btitl%5D%20OR%20surveillance%5Btitl%5D%20OR%20emergency%5Btitl%5D%20OR%20guideline*%5Btitl%5D%20OR%20therap*))%20OR%20(treatment%5Btitl%5D%20AND%20((evaluation%5Btitl%5D%20AND%20diagnosis%5Btitl%5D)%20OR%20(assessment%5Btitl%5D%20AND%20prevention%5Btitl%5D)%20OR%20therap*))%20OR%20(Diagnos*%5Btitl%5D%20AND%20(prenatal%5Btitl%5D%20OR%20treatment%5Btitl%5D%20OR%20follow-up%5Btitl%5D%20OR%20statement%5Btitl%5D%20OR%20criteria%5Btitl%5D%20OR%20newborn%5Btitl%5D%20OR%20differential%5Btitl%5D%20OR%20neonatal%5Btitl%5D%20OR%20neonate%5Btitl%5D))%20OR%20(guideline*%5Btitl%5D%20AND%20(pharmacogenetic*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20evidence-based%5Btitl%5D%20OR%20consensus%5Btitl%5D%20OR%20(technical%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20(molecular%5Btitl%5D%20AND%20testing%5Btitl%5D)))%20OR%20(risk%5Btitl%5D%20AND%20assessment%5Btitl%5D)%20OR%20(recommendation*%5Btitl%5D%20AND%20(statement%5Btitl%5D%20OR%20Evidence-based%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(care%20AND%20((Patient%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20primary%5Btitl%5D%20OR%20psychosocial%5Btitl%5D))%20OR%20(Health%5Btitl%5D%20AND%20supervision%5Btitl%5D)%20OR%20(statement%5Btitl%5D%20AND%20(policy%5Btitl%5D%20OR%20position%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(pharmacogenetics%5Btitl%5D%20AND%20(Dosing%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20genotype*%5Btitl%5D%20OR%20drug*%5Btitl%5D))%20OR%20(Chemotherapy%5Btitl%5D%20AND%20decision*%5Btitl%5D)%20OR%20(screening%5Btitl%5D%20AND%20(newborn%5Btitl%5D%20OR%20neonat*%5Btitl%5D%20OR%20detection%5Btitl%5D%20OR%20diagnos*%5Btitl%5D))%20OR%20(criteria%5Btitl%5D%20OR%20genotype*%5Btitl%5D)%20)%20NOT%20(%22Case%20reports%22%5BPublication%20type%5D%20OR%20%22clinical%20study%22%5BPublication%20Type%5D%20OR%20%22randomized%20controlled%20trial%22%5BPublication%20Type%5D)" title="PubMed search">See all (100)</a></div></div>
|
||
</div>
|
||
<div class="display-none help-popup" id="guidelinesHelpPM">These guidelines are articles in PubMed that match specific search criteria developed by MedGen to capture the most relevant practice guidelines. This list may not be comprehensive and may include broader topics as well. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div><div class="display-none help-popup" id="guidelinesHelpCurated">These guidelines are manually curated by the MedGen team
|
||
to supplement articles available in PubMed. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div>
|
||
<div class="portlet mgSection" id="ID_103">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Recent_clinical_studies">Recent clinical studies</h1><a sid="103" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><h3 class="subhead">Etiology</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/36640788">Usual interstitial pneumonia as a stand-alone diagnostic entity: the case for a paradigm shift?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Selman M,
|
||
Pardo A,
|
||
Wells AU</span><br />
|
||
<span class="medgenPMjournal">Lancet Respir Med</span>
|
||
2023 Feb;11(2):188-196.
|
||
Epub 2023 Jan 11
|
||
doi: 10.1016/S2213-2600(22)00475-1.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36640788" target="_blank">36640788</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35855575">Pleuroparenchymal fibroelastosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Cottin V,
|
||
Si-Mohamed S,
|
||
Diesler R,
|
||
Bonniaud P,
|
||
Valenzuela C</span><br />
|
||
<span class="medgenPMjournal">Curr Opin Pulm Med</span>
|
||
2022 Sep 1;28(5):432-440.
|
||
Epub 2022 Jul 18
|
||
doi: 10.1097/MCP.0000000000000907.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35855575" target="_blank">35855575</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31996266">Progression of fibrosing interstitial lung disease.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Wong AW,
|
||
Ryerson CJ,
|
||
Guler SA</span><br />
|
||
<span class="medgenPMjournal">Respir Res</span>
|
||
2020 Jan 29;21(1):32.
|
||
doi: 10.1186/s12931-020-1296-3.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31996266" target="_blank">31996266</a><a href="/pmc/articles/PMC6988233" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28345383">Pulmonary fibrosis, part I: epidemiology, pathogenesis, and diagnosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Meyer KC</span><br />
|
||
<span class="medgenPMjournal">Expert Rev Respir Med</span>
|
||
2017 May;11(5):343-359.
|
||
Epub 2017 Apr 10
|
||
doi: 10.1080/17476348.2017.1312346.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28345383" target="_blank">28345383</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/24993703">Telomeres in lung diseases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Calado RT</span><br />
|
||
<span class="medgenPMjournal">Prog Mol Biol Transl Sci</span>
|
||
2014;125:173-83.
|
||
doi: 10.1016/B978-0-12-397898-1.00008-6.
|
||
<span class="bold">PMID: </span><a href="/pubmed/24993703" target="_blank">24993703</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Usual%20interstitial%20pneumonia%22%20AND%20Etiology%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (827)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/36737162">Idiopathic pulmonary fibrosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Benegas Urteaga M,
|
||
Ramírez Ruz J,
|
||
Sánchez González M</span><br />
|
||
<span class="medgenPMjournal">Radiologia (Engl Ed)</span>
|
||
2022 Dec;64 Suppl 3:227-239.
|
||
doi: 10.1016/j.rxeng.2022.10.009.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36737162" target="_blank">36737162</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/36034006">Usual interstitial pneumonia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Badjate DM,
|
||
Jain M</span><br />
|
||
<span class="medgenPMjournal">Pan Afr Med J</span>
|
||
2022;42:92.
|
||
Epub 2022 Jun 3
|
||
doi: 10.11604/pamj.2022.42.92.35264.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36034006" target="_blank">36034006</a><a href="/pmc/articles/PMC9379445" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34531525">Hypersensitivity pneumonitis: new concepts and classifications.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Churg A</span><br />
|
||
<span class="medgenPMjournal">Mod Pathol</span>
|
||
2022 Jan;35(Suppl 1):15-27.
|
||
Epub 2021 Sep 16
|
||
doi: 10.1038/s41379-021-00866-y.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34531525" target="_blank">34531525</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29052582">Idiopathic pulmonary fibrosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Martinez FJ,
|
||
Collard HR,
|
||
Pardo A,
|
||
Raghu G,
|
||
Richeldi L,
|
||
Selman M,
|
||
Swigris JJ,
|
||
Taniguchi H,
|
||
Wells AU</span><br />
|
||
<span class="medgenPMjournal">Nat Rev Dis Primers</span>
|
||
2017 Oct 20;3:17074.
|
||
doi: 10.1038/nrdp.2017.74.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29052582" target="_blank">29052582</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28345383">Pulmonary fibrosis, part I: epidemiology, pathogenesis, and diagnosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Meyer KC</span><br />
|
||
<span class="medgenPMjournal">Expert Rev Respir Med</span>
|
||
2017 May;11(5):343-359.
|
||
Epub 2017 Apr 10
|
||
doi: 10.1080/17476348.2017.1312346.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28345383" target="_blank">28345383</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Usual%20interstitial%20pneumonia%22%20AND%20Diagnosis%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (967)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/36889782">Prevalence, imaging patterns and risk factors of interstitial lung disease in connective tissue disease: a systematic review and meta-analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Joy GM,
|
||
Arbiv OA,
|
||
Wong CK,
|
||
Lok SD,
|
||
Adderley NA,
|
||
Dobosz KM,
|
||
Johannson KA,
|
||
Ryerson CJ</span><br />
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<div class="nl"><a target="_blank" href="/pubmed/33095142">Interstitial lung disease in Sjögren's syndrome: a clinical review.</a></div>
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Sebastiani M,
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<div class="nl"><a target="_blank" href="/pubmed/31996266">Progression of fibrosing interstitial lung disease.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Wong AW,
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<div class="nl"><a target="_blank" href="/pubmed/31566307">Nintedanib in Progressive Fibrosing Interstitial Lung Diseases.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Flament T,
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Bigot A,
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Chaigne B,
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Usual%20interstitial%20pneumonia%22%20AND%20Therapy%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (344)</a></div><h3 class="subhead">Prognosis</h3>
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<div class="nl"><a target="_blank" href="/pubmed/36737162">Idiopathic pulmonary fibrosis.</a></div>
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<span class="bold">PMID: </span><a href="/pubmed/36737162" target="_blank">36737162</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/31996266">Progression of fibrosing interstitial lung disease.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Wong AW,
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Ryerson CJ,
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Guler SA</span><br />
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2020 Jan 29;21(1):32.
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doi: 10.1186/s12931-020-1296-3.
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<span class="bold">PMID: </span><a href="/pubmed/31996266" target="_blank">31996266</a><a href="/pmc/articles/PMC6988233" target="_blank" class="PubMedFree">Free PMC Article</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/31010461">Idiopathic Pulmonary Fibrosis: Epidemiology, Diagnosis andOutcomes.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Wakwaya Y,
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Brown KK</span><br />
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2019 May;357(5):359-369.
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<span class="bold">PMID: </span><a href="/pubmed/31010461" target="_blank">31010461</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/28345383">Pulmonary fibrosis, part I: epidemiology, pathogenesis, and diagnosis.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Meyer KC</span><br />
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<span class="medgenPMjournal">Expert Rev Respir Med</span>
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2017 May;11(5):343-359.
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<span class="bold">PMID: </span><a href="/pubmed/28345383" target="_blank">28345383</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/27246587">Pulmonary manifestations of Sjögren's syndrome.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Flament T,
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Bigot A,
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Chaigne B,
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Henique H,
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Diot E,
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Marchand-Adam S</span><br />
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<span class="medgenPMjournal">Eur Respir Rev</span>
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<span class="bold">PMID: </span><a href="/pubmed/27246587" target="_blank">27246587</a><a href="/pmc/articles/PMC9487244" target="_blank" class="PubMedFree">Free PMC Article</a></div>
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Usual%20interstitial%20pneumonia%22%20AND%20Prognosis%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (728)</a></div><h3 class="subhead">Clinical prediction guides</h3>
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<div class="nl"><a target="_blank" href="/pubmed/37095673">Imaging of Pulmonary Fibrosis: An Update, From the AJR Special Series on Imaging of Fibrosis.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Lee KS,
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Han J,
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Wada N,
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Hata A,
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Lee HY,
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Yi C,
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Hino T,
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Doyle TJ,
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Hatabu H</span><br />
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2024 Feb;222(2):e2329119.
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<span class="bold">PMID: </span><a href="/pubmed/37095673" target="_blank">37095673</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/33095142">Interstitial lung disease in Sjögren's syndrome: a clinical review.</a></div>
|
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<div class="portlet_content ln"><span class="medgenPMauthor">Luppi F,
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Sebastiani M,
|
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Silva M,
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Sverzellati N,
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Cavazza A,
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Salvarani C,
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Manfredi A</span><br />
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<span class="medgenPMjournal">Clin Exp Rheumatol</span>
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2020 Jul-Aug;38 Suppl 126(4):291-300.
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Epub 2020 Oct 23
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<span class="bold">PMID: </span><a href="/pubmed/33095142" target="_blank">33095142</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/32005430">Connective Tissue Disease Related Interstitial Lung Disease.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Schulte JJ,
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Husain AN</span><br />
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2020 Mar;13(1):165-188.
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<div class="nl"><a target="_blank" href="/pubmed/31841044">Etiology, Risk Factors, and Biomarkers in Systemic Sclerosis with Interstitial Lung Disease.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Khanna D,
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Tashkin DP,
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Denton CP,
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2020 Mar 15;201(6):650-660.
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|
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||
<div class="nl"><a target="_blank" href="/pubmed/27246587">Pulmonary manifestations of Sjögren's syndrome.</a></div>
|
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<div class="portlet_content ln"><span class="medgenPMauthor">Flament T,
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Bigot A,
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Chaigne B,
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Henique H,
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Diot E,
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Marchand-Adam S</span><br />
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<span class="medgenPMjournal">Eur Respir Rev</span>
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2016 Jun;25(140):110-23.
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doi: 10.1183/16000617.0011-2016.
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<span class="bold">PMID: </span><a href="/pubmed/27246587" target="_blank">27246587</a><a href="/pmc/articles/PMC9487244" target="_blank" class="PubMedFree">Free PMC Article</a></div>
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Usual%20interstitial%20pneumonia%22%20AND%20Clinical%20prediction%20guides%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (621)</a></div></div>
|
||
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||
|
||
<div class="portlet mgSection" id="ID_104">
|
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Recent_systematic_reviews">Recent systematic reviews</h1><a sid="104" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln">
|
||
<div class="nl"><a target="_blank" href="/pubmed/37434169">Incidence, risk factors, and prognosis of acute exacerbation of rheumatoid arthritis-associated interstitial lung disease: a systematic review and meta-analysis.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Xie M,
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Zhu C,
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Ye Y</span><br />
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<span class="medgenPMjournal">BMC Pulm Med</span>
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2023 Jul 11;23(1):255.
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doi: 10.1186/s12890-023-02532-2.
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||
<span class="bold">PMID: </span><a href="/pubmed/37434169" target="_blank">37434169</a><a href="/pmc/articles/PMC10337154" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/36889782">Prevalence, imaging patterns and risk factors of interstitial lung disease in connective tissue disease: a systematic review and meta-analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Joy GM,
|
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Arbiv OA,
|
||
Wong CK,
|
||
Lok SD,
|
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Adderley NA,
|
||
Dobosz KM,
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||
Johannson KA,
|
||
Ryerson CJ</span><br />
|
||
<span class="medgenPMjournal">Eur Respir Rev</span>
|
||
2023 Mar 31;32(167)
|
||
Epub 2023 Mar 8
|
||
doi: 10.1183/16000617.0210-2022.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36889782" target="_blank">36889782</a><a href="/pmc/articles/PMC10032591" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35499855">Transbronchial Lung Cryobiopsy in Patients with Interstitial Lung Disease: A Systematic Review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kheir F,
|
||
Uribe Becerra JP,
|
||
Bissell B,
|
||
Ghazipura M,
|
||
Herman D,
|
||
Hon SM,
|
||
Hossain T,
|
||
Khor YH,
|
||
Knight SL,
|
||
Kreuter M,
|
||
Macrea M,
|
||
Mammen MJ,
|
||
Martinez FJ,
|
||
Poletti V,
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||
Troy L,
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Raghu G,
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||
Wilson KC</span><br />
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<span class="medgenPMjournal">Ann Am Thorac Soc</span>
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||
2022 Jul;19(7):1193-1202.
|
||
doi: 10.1513/AnnalsATS.202102-198OC.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35499855" target="_blank">35499855</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35499854">Nintedanib in Progressive Pulmonary Fibrosis: A Systematic Review and Meta-Analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ghazipura M,
|
||
Mammen MJ,
|
||
Herman DD,
|
||
Hon SM,
|
||
Bissell BD,
|
||
Macrea M,
|
||
Kheir F,
|
||
Khor YH,
|
||
Knight SL,
|
||
Raghu G,
|
||
Wilson KC,
|
||
Hossain T</span><br />
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||
<span class="medgenPMjournal">Ann Am Thorac Soc</span>
|
||
2022 Jun;19(6):1040-1049.
|
||
doi: 10.1513/AnnalsATS.202103-343OC.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35499854" target="_blank">35499854</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31831537">Systematic review and meta-analysis of the prognosis and prognostic factors of interstitial pneumonia with autoimmune features.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kamiya H,
|
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Panlaqui OM</span><br />
|
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<span class="medgenPMjournal">BMJ Open</span>
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2019 Dec 11;9(12):e031444.
|
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doi: 10.1136/bmjopen-2019-031444.
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<span class="bold">PMID: </span><a href="/pubmed/31831537" target="_blank">31831537</a><a href="/pmc/articles/PMC6924795" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Usual%20interstitial%20pneumonia%22%20AND%20systematic%5Bsb%5D%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (20)</a></div></div>
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||
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<div class="portlet_content ln"><ul class="a_poppers"><li><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22usual%20interstitial%20pneumonia%22%5Btiab%3A~0%5D)%20AND%20(%22english%20and%20humans%22%5BFilter%5D)%20AND%20(%20(%22practice%20guideline%22%5BFilter%5D)%20OR%20(practice*%5Btitl%5D%20AND%20(guideline%5Btitl%5D%20OR%20parameter%5Btitl%5D%20OR%20resource%5Btitl%5D%20OR%20bulletin%5Btitl%5D%20OR%20best%5Btitl%5D))%20OR%20(genetic*%5Btitl%5D%20AND%20(evaluation%5Btitl%5D%20OR%20counseling%5Btitl%5D%20OR%20screening%5Btitl%5D%20OR%20test*%5Btitl%5D))%20OR%20(clinical%5Btitl%5D%20AND%20((expert%5Btitl%5D%20AND%20consensus%5Btitl%5D)%20OR%20utility%5Btitl%5D%20OR%20guideline*%5Btitl%5D))%20OR%20(management%5Btitl%5D%20AND%20(clinical%5Btitl%5D%20OR%20diagnos*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20pain%5Btitl%5D%20OR%20surveillance%5Btitl%5D%20OR%20emergency%5Btitl%5D%20OR%20guideline*%5Btitl%5D%20OR%20therap*))%20OR%20(treatment%5Btitl%5D%20AND%20((evaluation%5Btitl%5D%20AND%20diagnosis%5Btitl%5D)%20OR%20(assessment%5Btitl%5D%20AND%20prevention%5Btitl%5D)%20OR%20therap*))%20OR%20(Diagnos*%5Btitl%5D%20AND%20(prenatal%5Btitl%5D%20OR%20treatment%5Btitl%5D%20OR%20follow-up%5Btitl%5D%20OR%20statement%5Btitl%5D%20OR%20criteria%5Btitl%5D%20OR%20newborn%5Btitl%5D%20OR%20differential%5Btitl%5D%20OR%20neonatal%5Btitl%5D%20OR%20neonate%5Btitl%5D))%20OR%20(guideline*%5Btitl%5D%20AND%20(pharmacogenetic*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20evidence-based%5Btitl%5D%20OR%20consensus%5Btitl%5D%20OR%20(technical%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20(molecular%5Btitl%5D%20AND%20testing%5Btitl%5D)))%20OR%20(risk%5Btitl%5D%20AND%20assessment%5Btitl%5D)%20OR%20(recommendation*%5Btitl%5D%20AND%20(statement%5Btitl%5D%20OR%20Evidence-based%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(care%20AND%20((Patient%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20primary%5Btitl%5D%20OR%20psychosocial%5Btitl%5D))%20OR%20(Health%5Btitl%5D%20AND%20supervision%5Btitl%5D)%20OR%20(statement%5Btitl%5D%20AND%20(policy%5Btitl%5D%20OR%20position%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(pharmacogenetics%5Btitl%5D%20AND%20(Dosing%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20genotype*%5Btitl%5D%20OR%20drug*%5Btitl%5D))%20OR%20(Chemotherapy%5Btitl%5D%20AND%20decision*%5Btitl%5D)%20OR%20(screening%5Btitl%5D%20AND%20(newborn%5Btitl%5D%20OR%20neonat*%5Btitl%5D%20OR%20detection%5Btitl%5D%20OR%20diagnos*%5Btitl%5D))%20OR%20(criteria%5Btitl%5D%20OR%20genotype*%5Btitl%5D)%20)%20NOT%20(%22Case%20reports%22%5BPublication%20type%5D%20OR%20%22clinical%20study%22%5BPublication%20Type%5D%20OR%20%22randomized%20controlled%20trial%22%5BPublication%20Type%5D)" title="PubMed search">PubMed</a><div class="help-popup">See practice and clinical guidelines in PubMed. The search results may include broader topics and may not capture all published guidelines. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div></li><li><a target="_blank" href="/books/?term=((%22clinical%20guidelines%22%5BResource%20Type%5D)%20OR%20%22practice%20guideline%22%5BPublication%20Type%5D)%20AND%20(%22Usual%20interstitial%20pneumonia%22)">Bookshelf</a><div class="help-popup">See practice and clinical guidelines in NCBI Bookshelf. The search results may include broader topics and may not capture all published guidelines. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div></li></ul></div>
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