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	<id>https://wikimd.org/index.php?action=history&amp;feed=atom&amp;title=IPF</id>
	<title>IPF - Revision history</title>
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	<updated>2026-04-25T13:15:36Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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	<entry>
		<id>https://wikimd.org/index.php?title=IPF&amp;diff=6509403&amp;oldid=prev</id>
		<title>Prab: CSV import</title>
		<link rel="alternate" type="text/html" href="https://wikimd.org/index.php?title=IPF&amp;diff=6509403&amp;oldid=prev"/>
		<updated>2025-03-17T14:24:50Z</updated>

		<summary type="html">&lt;p&gt;CSV import&lt;/p&gt;
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				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;← Older revision&lt;/td&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;Revision as of 14:24, 17 March 2025&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot; id=&quot;mw-diff-left-l54&quot;&gt;Line 54:&lt;/td&gt;
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&lt;/table&gt;</summary>
		<author><name>Prab</name></author>
	</entry>
	<entry>
		<id>https://wikimd.org/index.php?title=IPF&amp;diff=6269783&amp;oldid=prev</id>
		<title>Prab: CSV import</title>
		<link rel="alternate" type="text/html" href="https://wikimd.org/index.php?title=IPF&amp;diff=6269783&amp;oldid=prev"/>
		<updated>2025-02-11T02:01:09Z</updated>

		<summary type="html">&lt;p&gt;CSV import&lt;/p&gt;
&lt;table style=&quot;background-color: #fff; color: #202122;&quot; data-mw=&quot;interface&quot;&gt;
				&lt;col class=&quot;diff-marker&quot; /&gt;
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				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;← Older revision&lt;/td&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;Revision as of 02:01, 11 February 2025&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot; id=&quot;mw-diff-left-l53&quot;&gt;Line 53:&lt;/td&gt;
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&lt;/table&gt;</summary>
		<author><name>Prab</name></author>
	</entry>
	<entry>
		<id>https://wikimd.org/index.php?title=IPF&amp;diff=5879602&amp;oldid=prev</id>
		<title>Prab: CSV import</title>
		<link rel="alternate" type="text/html" href="https://wikimd.org/index.php?title=IPF&amp;diff=5879602&amp;oldid=prev"/>
		<updated>2024-06-01T21:49:39Z</updated>

		<summary type="html">&lt;p&gt;CSV import&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;&amp;#039;&amp;#039;&amp;#039;Idiopathic Pulmonary Fibrosis (IPF)&amp;#039;&amp;#039;&amp;#039;&lt;br /&gt;
&lt;br /&gt;
&amp;#039;&amp;#039;&amp;#039;Idiopathic Pulmonary Fibrosis&amp;#039;&amp;#039;&amp;#039; (&amp;#039;&amp;#039;&amp;#039;IPF&amp;#039;&amp;#039;&amp;#039;) is a chronic, progressive lung disease characterized by the thickening and scarring (fibrosis) of lung tissue. This condition leads to a gradual decline in lung function and is classified under the broader category of [[interstitial lung disease]] (ILD).&lt;br /&gt;
&lt;br /&gt;
== Pathophysiology ==&lt;br /&gt;
The exact cause of IPF is unknown, which is why it is termed &amp;quot;idiopathic.&amp;quot; The disease involves the abnormal and excessive deposition of [[extracellular matrix]] proteins, leading to the stiffening of the lung tissue. This fibrosis impairs the ability of the lungs to transfer oxygen into the bloodstream, resulting in symptoms such as [[dyspnea]] (shortness of breath) and a persistent, dry [[cough]].&lt;br /&gt;
&lt;br /&gt;
== Symptoms ==&lt;br /&gt;
Common symptoms of IPF include:&lt;br /&gt;
* Shortness of breath, especially during or after physical activity&lt;br /&gt;
* A dry, persistent cough&lt;br /&gt;
* Fatigue and weakness&lt;br /&gt;
* Unexplained weight loss&lt;br /&gt;
* Clubbing of the fingers or toes&lt;br /&gt;
&lt;br /&gt;
== Diagnosis ==&lt;br /&gt;
Diagnosing IPF typically involves a combination of clinical evaluation, imaging studies, and sometimes lung biopsy. Key diagnostic tools include:&lt;br /&gt;
* [[High-resolution computed tomography]] (HRCT) scans&lt;br /&gt;
* Pulmonary function tests (PFTs)&lt;br /&gt;
* [[Bronchoscopy]] with bronchoalveolar lavage (BAL)&lt;br /&gt;
* Surgical lung biopsy&lt;br /&gt;
&lt;br /&gt;
== Treatment ==&lt;br /&gt;
There is no cure for IPF, but treatments aim to manage symptoms and slow disease progression. Treatment options include:&lt;br /&gt;
* [[Antifibrotic]] medications such as [[pirfenidone]] and [[nintedanib]]&lt;br /&gt;
* [[Oxygen therapy]]&lt;br /&gt;
* Pulmonary rehabilitation&lt;br /&gt;
* Lung transplantation in severe cases&lt;br /&gt;
&lt;br /&gt;
== Prognosis ==&lt;br /&gt;
The prognosis for IPF varies, but the disease is generally progressive and can lead to respiratory failure. The median survival time after diagnosis is approximately 3-5 years.&lt;br /&gt;
&lt;br /&gt;
== Research ==&lt;br /&gt;
Ongoing research is focused on understanding the underlying mechanisms of IPF and developing new treatments. Clinical trials are continually being conducted to explore potential therapies.&lt;br /&gt;
&lt;br /&gt;
== Related Pages ==&lt;br /&gt;
* [[Interstitial lung disease]]&lt;br /&gt;
* [[Pulmonary fibrosis]]&lt;br /&gt;
* [[Dyspnea]]&lt;br /&gt;
* [[Pirfenidone]]&lt;br /&gt;
* [[Nintedanib]]&lt;br /&gt;
* [[Lung transplantation]]&lt;br /&gt;
&lt;br /&gt;
== See Also ==&lt;br /&gt;
* [[Respiratory failure]]&lt;br /&gt;
* [[Pulmonary rehabilitation]]&lt;br /&gt;
* [[Oxygen therapy]]&lt;br /&gt;
&lt;br /&gt;
[[Category:Pulmonology]]&lt;br /&gt;
[[Category:Respiratory diseases]]&lt;br /&gt;
[[Category:Interstitial lung diseases]]&lt;br /&gt;
[[Category:Medical conditions]]&lt;br /&gt;
&lt;br /&gt;
{{medicine-stub}}&lt;/div&gt;</summary>
		<author><name>Prab</name></author>
	</entry>
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