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<ArticleSet>
<Article>
<Journal>
				<PublisherName>National Research Institute of Tuberculosis and Lung Disease (NRITLD), Shahid Beheshti University of Medical Sciences, Tehran, Iran</PublisherName>
				<JournalTitle>TANAFFOS (Respiration)</JournalTitle>
				<Issn>1735-0344</Issn>
				<Volume>24</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>2025</Year>
					<Month>10</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Shelter Challenges for Asthma Patients during Disasters: Experiences and Solutions</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>309</FirstPage>
			<LastPage>311</LastPage>
			<ELocationID EIdType="pii">741059</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Ameneh</FirstName>
					<LastName>Marzban</LastName>
<Affiliation>Department of Health in Disasters and Emergencies, School of Health Management and Information Sciences, Iran University of Medical Sciences, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0000-0002-8111-3319</Identifier>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2025</Year>
					<Month>02</Month>
					<Day>25</Day>
				</PubDate>
			</History>
		<Abstract>&lt;strong&gt;&lt;em&gt;&lt;span lang=&quot;EN-US&quot;&gt;Dear Editor, &lt;/span&gt;&lt;/em&gt;&lt;/strong&gt;
&lt;span lang=&quot;EN-US&quot;&gt;Natural disasters such as hurricanes, earthquakes, and floods can have devastating effects on entire communities (1). While the immediate focus often lies on providing shelter, food, and emergency medical care, the unique challenges faced by individuals with chronic conditions, such as asthma, often remain underappreciated (2). It is vital to address these challenges to ensure comprehensive disaster response and mitigate adverse health outcomes for asthma patients (3). Additionally, establishing clear guidelines for managing chronic respiratory conditions in disaster situations is essential. In the absence of existing guidelines, developing one should be advised. In this letter, I aim to highlight the specific challenges faced by asthma patients in emergency shelters during disasters, share experiences from past events, and propose practical solutions to improve care for this vulnerable population.&lt;/span&gt;
&lt;span lang=&quot;EN-US&quot;&gt; &lt;/span&gt;
&lt;strong&gt;&lt;em&gt;&lt;span lang=&quot;EN-US&quot;&gt;Challenges Faced by Asthma Patients in Emergency Shelters&lt;/span&gt;&lt;/em&gt;&lt;/strong&gt;
&lt;em&gt;&lt;span lang=&quot;EN-US&quot;&gt;1. Exposure to Triggers&lt;/span&gt;&lt;/em&gt;
&lt;span lang=&quot;EN-US&quot;&gt;Emergency shelters, often hastily set up, may not be equipped to maintain indoor air quality (4). The presence of dust, mold, and other allergens can exacerbate asthma symptoms. Moreover, continuous exposure to polluted air worsens symptoms, making it necessary to establish designated safe areas with improved air quality and access to medical care. Overcrowding and limited ventilation further increase the risk of exposure to respiratory infections, compromising the health of asthma patients (5). &lt;/span&gt;
&lt;em&gt;&lt;span lang=&quot;EN-US&quot;&gt;2. Limited Access to Medications &lt;/span&gt;&lt;/em&gt;
&lt;span lang=&quot;EN-US&quot;&gt;During disasters, access to asthma medications such as inhalers and nebulizers can be severely disrupted. Supply chain interruptions, loss of personal belongings, and the prioritization of immediate life-saving interventions often result in a shortage of essential medications for asthma patients (6). Efforts should be made to improve communication channels for timely medication delivery and ensure emergency shelters maintain a sufficient stockpile of respiratory medications. &lt;/span&gt;
&lt;em&gt;&lt;span lang=&quot;EN-US&quot;&gt;3. Stress and Anxiety&lt;/span&gt;&lt;/em&gt;
&lt;span lang=&quot;EN-US&quot;&gt;The psychological impact of disasters can significantly affect asthma patients. High levels of stress and anxiety can trigger or worsen asthma symptoms. Providing psychological support, including mental health counseling and stress management programs, can help mitigate this issue. The unfamiliar environment of shelters, separation from loved ones, and uncertainty about the future contribute to heightened stress levels, making asthma management even more challenging (7). &lt;/span&gt;
&lt;em&gt;&lt;span lang=&quot;EN-US&quot;&gt;4. Inadequate Medical Support &lt;/span&gt;&lt;/em&gt;
&lt;span lang=&quot;EN-US&quot;&gt;Emergency shelters may lack adequate medical personnel trained in asthma management. The focus on acute medical care often means that chronic conditions like asthma do not receive the attention they need. Integrating healthcare professionals who specialize in chronic respiratory diseases into disaster response teams can significantly improve patient outcomes. Without proper intervention, patients may suffer from poorly managed symptoms and an increased risk of severe asthma attacks (8). &lt;/span&gt;
&lt;span lang=&quot;EN-US&quot;&gt; &lt;/span&gt;
&lt;strong&gt;&lt;em&gt;&lt;span lang=&quot;EN-US&quot;&gt;Experiences from Past Disasters &lt;/span&gt;&lt;/em&gt;&lt;/strong&gt;
&lt;span lang=&quot;EN-US&quot;&gt;1. Hurricane Katrina (2005): The aftermath of Hurricane Katrina saw thousands of people displaced and living in emergency shelters. Asthma patients reported increased symptoms due to poor air quality and lack of access to medications. Many patients had to rely on the limited medical supplies available in shelters, often receiving suboptimal care for their condition (6).&lt;/span&gt;
&lt;span lang=&quot;EN-US&quot;&gt;2. California Wildfires (2018): During the California wildfires, emergency shelters were set up to accommodate evacuees. The smoke from the fires significantly impacted air quality, both outdoors and within shelters. Asthma patients experienced severe symptoms due to the smoke and had limited access to their medications. Portable air filtration units were eventually introduced to improve indoor air quality, underscoring the importance of proactive air quality measures (3). &lt;/span&gt;
&lt;span lang=&quot;EN-US&quot;&gt;3. Puerto Rico Earthquake (2020): The earthquake in Puerto Rico resulted in many people seeking refuge in emergency shelters. Reports indicated that asthma patients struggled with limited availability of medical support and essential medications. Special arrangements should be made to quickly triage and transport patients with severe asthma attacks to safer environments with better air quality (9). &lt;/span&gt;
&lt;span lang=&quot;EN-US&quot;&gt; &lt;/span&gt;
&lt;strong&gt;&lt;em&gt;&lt;span lang=&quot;EN-US&quot;&gt;Proposed Solutions &lt;/span&gt;&lt;/em&gt;&lt;/strong&gt;
&lt;em&gt;&lt;span lang=&quot;EN-US&quot;&gt;1. Enhanced Preparedness and Planning &lt;/span&gt;&lt;/em&gt;
&lt;span lang=&quot;EN-US&quot;&gt;Disaster preparedness plans must include provisions for managing chronic conditions like asthma (9). This involves pre-positioning asthma medications and medical supplies in emergency shelters, creating stockpiles to meet patient needs, and ensuring collaboration with local pharmacies and healthcare providers to maintain an uninterrupted supply chain for essential medications (5, 8). &lt;/span&gt;
&lt;em&gt;&lt;span lang=&quot;EN-US&quot;&gt;2. Improving Shelter Air Quality &lt;/span&gt;&lt;/em&gt;
&lt;span lang=&quot;EN-US&quot;&gt;Measures should ensure emergency shelters maintain high-quality indoor air to reduce asthma triggers (6). This includes regular cleaning to minimize dust and mold, ensuring adequate ventilation, using portable air filtration units when needed, and establishing designated areas for asthma patients with enhanced air-quality control (3, 6, 9). &lt;/span&gt;
&lt;em&gt;&lt;span lang=&quot;EN-US&quot;&gt;3. Training and Education &lt;/span&gt;&lt;/em&gt;
&lt;span lang=&quot;EN-US&quot;&gt;Shelter staff and volunteers should be trained in early detection of asthma exacerbations, triage protocols for severe cases, and proper medication administration. Additionally, educating asthma patients on self-management techniques during disasters, including recognizing triggers, using inhalers correctly, and maintaining medication schedules, is crucial (2, 5).  &lt;/span&gt;
&lt;em&gt;&lt;span lang=&quot;EN-US&quot;&gt;4. Psychological Support &lt;/span&gt;&lt;/em&gt;
&lt;span lang=&quot;EN-US&quot;&gt;Addressing the psychological impact of disasters is essential for asthma patients (7). Providing access to mental health support, such as counseling, stress management programs, and community support networks, can help reduce anxiety and improve overall asthma control (9). Integrating psychological support into disaster response plans will enhance the well-being of asthma patients during crises (6). &lt;/span&gt;
&lt;em&gt;&lt;span lang=&quot;EN-US&quot;&gt;5. Telemedicine and Remote Monitoring &lt;/span&gt;&lt;/em&gt;
&lt;span lang=&quot;EN-US&quot;&gt;Leveraging technology, such as telemedicine and remote monitoring, can significantly enhance asthma management during disasters (9). Telemedicine consultations with healthcare providers ensure timely medical advice and enable adjustments to treatment plans. Remote monitoring devices track asthma symptoms in real-time, providing healthcare teams with crucial data to intervene proactively (5). &lt;/span&gt;
&lt;span lang=&quot;EN-US&quot;&gt; &lt;/span&gt;
&lt;strong&gt;&lt;span&gt;CONCLUSION&lt;/span&gt;&lt;/strong&gt;
&lt;span lang=&quot;EN-US&quot;&gt;The challenges faced by asthma patients in emergency shelters during disasters are significant but manageable with proactive planning. By incorporating guidelines for asthma management into disaster preparedness, improving shelter air quality, providing training and education, offering psychological support, and utilizing technology, we can ensure better care for this vulnerable population. Establishing a dedicated system for triage and early transportation of asthma patients to safer environments is also critical. Prioritizing asthma care in disaster response efforts will ultimately enhance the health and well-being of affected individuals.&lt;/span&gt;</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Asthma Management</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Emergency Shelters</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Disaster Response</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Air Quality Control</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Chronic Disease Care</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://www.tanaffosjournal.ir/article_741059_142bdbde818c1f3a120e014baf6bd8ac.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>National Research Institute of Tuberculosis and Lung Disease (NRITLD), Shahid Beheshti University of Medical Sciences, Tehran, Iran</PublisherName>
				<JournalTitle>TANAFFOS (Respiration)</JournalTitle>
				<Issn>1735-0344</Issn>
				<Volume>24</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>2025</Year>
					<Month>10</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>COPD and Bronchiectasis Overlap: Coincidence or Phenotype?</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>312</FirstPage>
			<LastPage>320</LastPage>
			<ELocationID EIdType="pii">741060</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Elissavet</FirstName>
					<LastName>Kosti</LastName>
<Affiliation>Laboratory of Human Pathophysiology, Department of Nursing, University of Thessaly, Larissa. Greece</Affiliation>

</Author>
<Author>
					<FirstName>Ourania S.</FirstName>
					<LastName>Kotsiou</LastName>
<Affiliation>Laboratory of Human Pathophysiology, Department of Nursing, University of Thessaly, Larissa. Greece</Affiliation>
<Identifier Source="ORCID">0000-0001-5219-6971</Identifier>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2024</Year>
					<Month>11</Month>
					<Day>27</Day>
				</PubDate>
			</History>
		<Abstract>&lt;span lang=&quot;EN-US&quot;&gt;The coexistence of chronic obstructive pulmonary disease (COPD) and bronchiectasis is increasingly recognized as a distinct clinical phenotype that presents unique diagnostic and therapeutic challenges. This overlap syndrome is characterized by heightened airway inflammation, frequent bacterial colonization, and a greater burden of respiratory symptoms, leading to poorer clinical outcomes. In this review, we explore the pathophysiological mechanisms underlying COPD-bronchiectasis overlap, emphasizing the role of chronic infection, impaired mucociliary clearance, and structural lung damage in driving disease progression. Bronchiectasis in COPD patients is associated with increased airflow obstruction, higher exacerbation rates, and greater disease severity compared to COPD alone. The shared pathophysiology includes chronic inflammation, often initiated by cigarette smoke or other environmental pollutants, and recurrent infections, especially with pathogens like Pseudomonas aeruginosa. These infections create a vicious cycle of inflammation and bronchial wall damage, resulting in airway dilation and impaired lung function. Diagnosing bronchiectasis in COPD patients remains challenging due to overlapping symptoms. High-resolution computed tomography (HRCT) is essential for identifying bronchial abnormalities, while spirometry confirms obstructive patterns. This review also highlights the need for tailored therapeutic strategies, including aggressive management of infections, use of long-acting bronchodilators, and cautious application of inhaled corticosteroids, which may exacerbate inflammation in patients with bronchiectasis. By recognizing COPD-bronchiectasis overlap as a distinct phenotype, we aim to improve clinical outcomes through a more personalized and comprehensive approach to diagnosis and treatment, ultimately enhancing patient quality of life.&lt;/span&gt;</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Bronchiectasis</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">COPD</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Overlap Syndrome</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Phenotype</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://www.tanaffosjournal.ir/article_741060_8265ed3ee751f874cc5319ac2444a53a.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>National Research Institute of Tuberculosis and Lung Disease (NRITLD), Shahid Beheshti University of Medical Sciences, Tehran, Iran</PublisherName>
				<JournalTitle>TANAFFOS (Respiration)</JournalTitle>
				<Issn>1735-0344</Issn>
				<Volume>24</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>2025</Year>
					<Month>10</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Galactooligosaccharides Suppress the Development of Biofilm in the Presence of Blood Polymorphonuclear Cells of Non-Small Cell Lung Cancer (NSCLC) Patients: A Pilot Study</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>321</FirstPage>
			<LastPage>329</LastPage>
			<ELocationID EIdType="pii">741061</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Masoumeh</FirstName>
					<LastName>Nomani</LastName>
<Affiliation>Clinical Tuberculosis and Epidemiology Research Center, National Research Institute of Tuberculosis and Lung Diseases(NRITLD), Shahid Beheshti University of Medical Sciences, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Babak</FirstName>
					<LastName>Salimi</LastName>
<Affiliation>Clinical Tuberculosis and Epidemiology Research Center, National Research Institute of Tuberculosis and Lung Diseases(NRITLD), Shahid Beheshti University of Medical Sciences, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0000-0002-5541-8434</Identifier>

</Author>
<Author>
					<FirstName>Mohammad</FirstName>
					<LastName>Varahtam</LastName>
<Affiliation>Mycobacteriology Research Center, NRITLD, Shahid Beheshti University of Medical Sciences, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0000-0002-8033-1867</Identifier>

</Author>
<Author>
					<FirstName>Hamidreza</FirstName>
					<LastName>Jamaati</LastName>
<Affiliation>Chronic Respiratory Diseases Research Center, NRITLD, Shahid Beheshti University of Medical Sciences, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0000-0002-5402-1531</Identifier>

</Author>
<Author>
					<FirstName>Esmaeil</FirstName>
					<LastName>Mortaz</LastName>

						<AffiliationInfo>
						<Affiliation>Clinical Tuberculosis and Epidemiology Research Center, National Research Institute of Tuberculosis and Lung Diseases(NRITLD), Shahid Beheshti University of Medical Sciences, Tehran, Iran</Affiliation>
						</AffiliationInfo>

						<AffiliationInfo>
						<Affiliation>Chronic Respiratory Diseases Research Center, NRITLD, Shahid Beheshti University of Medical Sciences, Tehran, Iran</Affiliation>
						</AffiliationInfo>

						<AffiliationInfo>
						<Affiliation>Department of Immunology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran</Affiliation>
						</AffiliationInfo>

						<AffiliationInfo>
						<Affiliation>Respiratory Immunology Research Center, NRITLD, Shahid Beheshti University of Medical Sciences, Tehran, Iran</Affiliation>
						</AffiliationInfo>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2025</Year>
					<Month>05</Month>
					<Day>10</Day>
				</PubDate>
			</History>
		<Abstract>&lt;strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;Background:&lt;/span&gt;&lt;/strong&gt;&lt;span lang=&quot;EN-US&quot;&gt; Bacterial biofilms pose a significant healthcare challenge due to their robust resistance to antibiotics and their involvement in various diseases, including cancer and infectious conditions. Biofilms hinder the antimicrobial activity of polymorphonuclear leukocytes (PMNs) by restricting their penetration through the extracellular matrix. With the rise of antimicrobial resistance, non-antibiotic strategies are gaining attention. Galacto-oligosaccharides (GOS) have been investigated for their potential to inhibit bacterial growth. This study investigates the impact of GOS on the biofilm development of GFP-labelled &lt;em&gt;Staphylococcus aureus&lt;/em&gt; (GFP-SA) and &lt;em&gt;Pseudomonas aeruginosa&lt;/em&gt; (GFP-PA) in the presence of blood PMNs from patients with non-small-cell lung cancer (NSCLC) and healthy controls.&lt;/span&gt;&lt;br&gt;&lt;strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;Materials and Methods: &lt;/span&gt;&lt;/strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;Bacterial biofilms were investigated in the presence or absence of PMNs isolated from the blood of 12 NSCLC patients and 3 healthy controls (HC), with the inclusion of GOS. These PMNs were incubated with GFP-SA or GFP-PA biofilms and exposed to various concentrations of GOS (2.5%, 5%, 10%, 15%, and 20%) for 24 hours in a microplate setting. The progress of bacterial biofilm was quantified using the crystal violet assay.&lt;/span&gt;&lt;br&gt;&lt;strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;Results: &lt;/span&gt;&lt;/strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;GOS itself, with bacteria at high concentrations (10%, 15%, and 20%), suppressed biofilm formation. PMNs of NSCLC patients show higher biofilm formation than in the absence of PMNs. &lt;/span&gt;&lt;br&gt;&lt;strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;Conclusion: &lt;/span&gt;&lt;/strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;Based on our findings, PMNs in NSCLC patients may disrupt the natural balance of bacteria in the lungs, potentially leading to an overgrowth of biofilm-forming bacteria. GOS are known to influence immune function and may improve the ability of PMNs to fight infections. Consequently, it is proposed that GOS could enhance the ability of PMNs to phagocytose bacterial biofilms and counteract the negative effects of cancerous PMNs on biofilm formation. However, further research is needed to confirm whether GOS can effectively manage bacterial biofilms in lung cancer patients.&lt;/span&gt;</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Polymorphonuclear leukocytes (PMNs)</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">biofilm</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Galacto-oligosaccharides (GOS)</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Staphylococcus aureus</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Pseudomonas aeruginosa</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">NSCLC patients</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Phagocytosis</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://www.tanaffosjournal.ir/article_741061_99e3cb9535ac9160cf23d4a6490dbeab.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>National Research Institute of Tuberculosis and Lung Disease (NRITLD), Shahid Beheshti University of Medical Sciences, Tehran, Iran</PublisherName>
				<JournalTitle>TANAFFOS (Respiration)</JournalTitle>
				<Issn>1735-0344</Issn>
				<Volume>24</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>2025</Year>
					<Month>10</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Predicting COPD Severity by Red Cell Distribution Width as a Potential Marker</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>330</FirstPage>
			<LastPage>337</LastPage>
			<ELocationID EIdType="pii">741062</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Fateme</FirstName>
					<LastName>Mohammadzade</LastName>
<Affiliation>Department Of Internal Medicine, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Mohammad</FirstName>
					<LastName>Yousefi</LastName>
<Affiliation>Student Research Committee, Birjand University of Medical Sciences, Birjand, Iran</Affiliation>

</Author>
<Author>
					<FirstName>AmirAli</FirstName>
					<LastName>Moodi Ghalibaf</LastName>
<Affiliation>Student Research Committee, Birjand University of Medical Sciences, Birjand, Iran</Affiliation>
<Identifier Source="ORCID">0000-0002-3892-5047</Identifier>

</Author>
<Author>
					<FirstName>Mostafa</FirstName>
					<LastName>Kamandi</LastName>
<Affiliation>Department Of Internal Medicine, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Farid</FirstName>
					<LastName>Poursadegh</LastName>
<Affiliation>Lung Diseases Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.</Affiliation>
<Identifier Source="ORCID">0009-0000-7238-5542</Identifier>

</Author>
<Author>
					<FirstName>Fariba</FirstName>
					<LastName>Rezaeetalab</LastName>
<Affiliation>Lung Diseases Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.</Affiliation>
<Identifier Source="ORCID">0000-0003-3836-0944</Identifier>

</Author>
<Author>
					<FirstName>Sepideh</FirstName>
					<LastName>Hejazi</LastName>
<Affiliation>Lung Diseases Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.</Affiliation>
<Identifier Source="ORCID">0000-0002-2723-1699</Identifier>

</Author>
<Author>
					<FirstName>Mahnaz</FirstName>
					<LastName>Mozdourian</LastName>
<Affiliation>Lung Diseases Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.</Affiliation>
<Identifier Source="ORCID">0000-0002-1692-4510</Identifier>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2024</Year>
					<Month>05</Month>
					<Day>20</Day>
				</PubDate>
			</History>
		<Abstract>&lt;strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;Background: &lt;/span&gt;&lt;/strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;Chronic obstructive pulmonary disease (COPD) is a condition of the lower airways and lungs with stable inflammation and alterations in the structure of small airways. There are some biomarkers linked to acute exacerbations of COPD (AECOPD). Red cell distribution width (RDW) is one of these biomarkers. To investigate the correlation between RDW and the severity of COPD, and to assess its relationship with the stage of airway obstruction in spirometry among COPD patients.&lt;/span&gt;
&lt;strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;Materials and Methods: &lt;/span&gt;&lt;/strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;In an 18-month retrospective study, a total of 255 participants were enrolled, including 170 patients with COPD (85 with stable COPD and 85 with acute exacerbations of COPD) and 85 age- and sex-matched healthy individuals. Demographic factors and blood laboratory tests were conducted for each group. The COPD groups had their COPD severity, spirometry parameters, and inflammation indices recorded and then compared.&lt;/span&gt;
&lt;strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;Results: &lt;/span&gt;&lt;/strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;RDW levels are increased in COPD patients (p&lt;/span&gt;&lt;span lang=&quot;EN-US&quot;&gt;˂&lt;/span&gt;&lt;span lang=&quot;EN-US&quot;&gt;0.001). However&lt;span&gt;, no statistically significant relationships between RDW values and CAT scores or mMRC grades were observed. Our analysis revealed that spirometry parameters and RDW levels are negatively correlated (&lt;/span&gt;p&lt;/span&gt;&lt;span lang=&quot;EN-US&quot;&gt;˂&lt;/span&gt;&lt;span lang=&quot;EN-US&quot;&gt;0.05&lt;span&gt;). Additionally, the RDW parameter has a positive and significant correlation with PCO&lt;sub&gt;2&lt;/sub&gt; and a negative and significant relationship with pH (&lt;/span&gt;p&lt;/span&gt;&lt;span lang=&quot;EN-US&quot;&gt;˂&lt;/span&gt;&lt;span lang=&quot;EN-US&quot;&gt;0.05&lt;span&gt;), while no significant correlation exists between the RDW parameter and PHCO&lt;sub&gt;3&lt;/sub&gt;&lt;/span&gt;&lt;/span&gt;&lt;span lang=&quot;EN-US&quot;&gt;.&lt;/span&gt;
&lt;strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;Conclusion: &lt;/span&gt;&lt;/strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;Our findings indicate that RDW could serve as a potential predictor of COPD conditions, especially in spirometry parameters&lt;/span&gt;</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Chronic Obstructive Pulmonary Disease (COPD)</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Red cell distribution width (RDW)</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Acute Exacerbation</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">biomarker</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://www.tanaffosjournal.ir/article_741062_e5627ef8e22cff75ec7735394a4dceaa.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>National Research Institute of Tuberculosis and Lung Disease (NRITLD), Shahid Beheshti University of Medical Sciences, Tehran, Iran</PublisherName>
				<JournalTitle>TANAFFOS (Respiration)</JournalTitle>
				<Issn>1735-0344</Issn>
				<Volume>24</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>2025</Year>
					<Month>10</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Oxidative Stress Mediates Cross-Talk between the Thioredoxin System and NLRP3 Inflammasome in Patients with COVID-19</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>338</FirstPage>
			<LastPage>352</LastPage>
			<ELocationID EIdType="pii">741063</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Rajab</FirstName>
					<LastName>Mardani</LastName>
<Affiliation>Department of Clinical Biochemistry, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran</Affiliation>
<Identifier Source="ORCID">0000-0001-7730-3040</Identifier>

</Author>
<Author>
					<FirstName>Seyed Davood</FirstName>
					<LastName>Mosavinasab</LastName>
<Affiliation>National Reference Laboratory, Department of Arboviruses and Viral Hemorrhagic Fevers, Pasteur Institute of Iran, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Heidar</FirstName>
					<LastName>Tavilani</LastName>
<Affiliation>Department of Clinical Biochemistry, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Jamshid</FirstName>
					<LastName>Karimi</LastName>
<Affiliation>Department of Clinical Biochemistry, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Jalal</FirstName>
					<LastName>Poorolajal</LastName>
<Affiliation>Department of Epidemiology, School of Health, Hamadan University of Medical Sciences, Hamadan, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Iraj</FirstName>
					<LastName>Khodadadi</LastName>

						<AffiliationInfo>
						<Affiliation>Department of Clinical Biochemistry, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran</Affiliation>
						</AffiliationInfo>

						<AffiliationInfo>
						<Affiliation>Nutrition Health Research Centre, Hamadan University of Medical Sciences, Hamadan-Iran</Affiliation>
						</AffiliationInfo>
<Identifier Source="ORCID">0000-0001-9048-4528</Identifier>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2024</Year>
					<Month>10</Month>
					<Day>08</Day>
				</PubDate>
			</History>
		<Abstract>&lt;strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;Background:&lt;/span&gt;&lt;/strong&gt;&lt;span lang=&quot;EN-US&quot;&gt; &lt;span&gt;COVID-19 is known as a fatal respiratory disease with an inflammatory basis. Imbalance of the thioredoxin system in peripheral blood mononuclear cells (PBMCs) may cause NLRP3 inflammasome activation and interleukin-1β production.&lt;/span&gt;&lt;/span&gt;
&lt;strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;Materials and Methods: &lt;/span&gt;&lt;/strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;Forty patients with COVID-19 and forty healthy individuals were included in this case-control study.&lt;span&gt;  &lt;/span&gt;All participants had previously received two doses of the coronavirus vaccine.&lt;span&gt;  &lt;/span&gt;PBMCs were isolated, and the expression of thioredoxin-interacting protein (TXNIP), thioredoxin-1 (TRX-1), NLRP3, caspase-1, and IL-1β genes was determined.&lt;span&gt;  &lt;/span&gt;Protein levels of TXNIP, NLRP3, and IL-1β were measured.&lt;span&gt;  &lt;/span&gt;Moreover, to confirm the involvement of oxidative stress in evoking inflammation in COVID-19, PBMCs were isolated from three independent healthy subjects, cultured &lt;em&gt;in vitro&lt;/em&gt;, and infected with the SARS-CoV-2 virus in the presence or absence of vitamin C.&lt;span&gt;  &lt;/span&gt;Reactive oxygen species (ROS) and IL-1β levels were determined in cultured PBMCs.&lt;/span&gt;
&lt;strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;Results: &lt;/span&gt;&lt;/strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;Oxidative stress was higher in COVID-19 patients.&lt;span&gt;  &lt;/span&gt;The mRNA expression and protein levels of TXNIP, NLRP3, and IL-1β were significantly higher in PBMCs of COVID-19 patients compared with the control group, whereas the expression of TRX-1 was found to be lower in patients. The enhancement in ROS, TXNIP protein, and NLRP3 gene expression levels was positively associated with increased IL-1β.&lt;/span&gt;
&lt;strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;Conclusion: &lt;/span&gt;&lt;/strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;The concurrent elevation of ROS, TXNIP, NLRP3, and IL-1β suggests the potential role of the thioredoxin system in activating the NLRP3 inflammasome and generating inflammatory IL-1β in patients with COVID-19.&lt;span&gt;  &lt;/span&gt;In addition, vitamin C, as an adjunct therapeutic agent, beneficially suppressed oxidative stress and inflammation in infected PBMCs.&lt;/span&gt;</Abstract>
		<ObjectList>
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			<Param Name="value">COVID-19</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Inflammasomes</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Interleukin-1beta</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Oxidative stress</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Thioredoxins</Param>
			</Object>
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<ArchiveCopySource DocType="pdf">https://www.tanaffosjournal.ir/article_741063_3cf3c09a0fc1df641c8fb4e6b2dfbf40.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>National Research Institute of Tuberculosis and Lung Disease (NRITLD), Shahid Beheshti University of Medical Sciences, Tehran, Iran</PublisherName>
				<JournalTitle>TANAFFOS (Respiration)</JournalTitle>
				<Issn>1735-0344</Issn>
				<Volume>24</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>2025</Year>
					<Month>10</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Can the Eosinophil-to-Platelet Ratio Predict Chronic Obstructive Pulmonary Disease Exacerbations and Length of Hospital Stay?</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>353</FirstPage>
			<LastPage>363</LastPage>
			<ELocationID EIdType="pii">741065</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Sina</FirstName>
					<LastName>Homaee</LastName>
<Affiliation>Department of Internal Medicine, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0000-0002-4389-3705</Identifier>

</Author>
<Author>
					<FirstName>Reyhaneh</FirstName>
					<LastName>Toluei</LastName>
<Affiliation>Department of Internal Medicine, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0009-0007-0798-8380</Identifier>

</Author>
<Author>
					<FirstName>Atefeh</FirstName>
					<LastName>Abedini</LastName>
<Affiliation>Chronic Respiratory Diseases Research Center, National Research Institute of Tuberculosis and 
Lung Diseases (NRITLD), Shahid Beheshti University of Medical Sciences, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0000-0002-4262-9873</Identifier>

</Author>
<Author>
					<FirstName>Azadeh</FirstName>
					<LastName>Moradkhani</LastName>
<Affiliation>Chronic Respiratory Diseases Research Center, National Research Institute of Tuberculosis and 
Lung Diseases (NRITLD), Shahid Beheshti University of Medical Sciences, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0000-0002-6872-3577</Identifier>

</Author>
<Author>
					<FirstName>Niloufar</FirstName>
					<LastName>Taherpour</LastName>
<Affiliation>Department of Epidemiology, School of Public Health &amp; Safety, Shahid Beheshti University of Medical Sciences, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0000-0002-8336-0671</Identifier>

</Author>
<Author>
					<FirstName>Farnaz</FirstName>
					<LastName>Saberian</LastName>
<Affiliation>Department of Internal Medicine, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0000-0002-6019-7197</Identifier>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2025</Year>
					<Month>07</Month>
					<Day>12</Day>
				</PubDate>
			</History>
		<Abstract>&lt;strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;Background: &lt;/span&gt;&lt;/strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;An acute exacerbation of chronic obstructive pulmonary disease is a severe condition that escalates the burden on patients and the healthcare system. This study aimed to evaluate the prognostic value of the eosinophil-to-platelet ratio (EPR) in predicting COPD exacerbations and hospital admissions, with these outcomes also assessed as secondary endpoints.&lt;/span&gt;&lt;br&gt;&lt;strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;Materials and Methods: &lt;/span&gt;&lt;/strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;This cohort study was conducted from 2023 to 2025 at Masih Daneshvari Educational Hospital in Tehran, Iran, among patients with confirmed COPD exacerbation. Participants were assessed during the recovery phase after management of the acute exacerbation. Collected clinical data included the history and frequency of exacerbations in the preceding 12 months; blood test results at discharge; 90-day mortality; hospital readmission; ICU admission; and corticosteroid use within 12 months post-discharge. Data were analyzed using STATA version 17.&lt;/span&gt;&lt;br&gt;&lt;strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;Results: &lt;/span&gt;&lt;/strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;This study evaluated 249 individuals with COPD exacerbation, with a mean age of 65.66±9.17 years. In individuals with EPR≤1, the risk of experiencing more COPD exacerbations was 17% higher than in those with EPR&gt;1 (adjusted RR=1.17, 95% CI=0.92 –1.49, P=0.195). These results were not statistically significant. In addition, in patients with EPR≤1, the risk of having a higher number of hospitalization days was 16% lower compared to those with EPR&gt;1 (adjusted RR=0.84, 95% CI=0.72–0.98, P=0.036). EPR was not associated with ICU admission and the need for systemic corticosteroids&lt;strong&gt;.&lt;/strong&gt;&lt;/span&gt;&lt;br&gt;&lt;strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;Conclusion: &lt;/span&gt;&lt;/strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;The association between lower EPR values and a higher number of exacerbations, as well as shorter hospital stays, suggests that EPR could reflect distinct exacerbation phenotypes or patterns of disease activity.&lt;/span&gt;</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Chronic Obstructive Pulmonary Disease</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Eosinophil</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Platelet</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Prognosis</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://www.tanaffosjournal.ir/article_741065_88b1b23c3df1b569527e154e46da4914.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>National Research Institute of Tuberculosis and Lung Disease (NRITLD), Shahid Beheshti University of Medical Sciences, Tehran, Iran</PublisherName>
				<JournalTitle>TANAFFOS (Respiration)</JournalTitle>
				<Issn>1735-0344</Issn>
				<Volume>24</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>2025</Year>
					<Month>10</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Characteristics of Bacterial Isolates from Patients with Ventilator-Associated Pneumonia and the Hospital Environment in Urmia, Iran</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>364</FirstPage>
			<LastPage>374</LastPage>
			<ELocationID EIdType="pii">741066</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Mahdieh</FirstName>
					<LastName>Delfi</LastName>

						<AffiliationInfo>
						<Affiliation>Cellular and Molecular Medicine Research Institute, Urmia University of Medical Sciences, Urmia, Iran</Affiliation>
						</AffiliationInfo>

						<AffiliationInfo>
						<Affiliation>Department of Microbiology and Virology, Faculty of Medicine, Urmia University of Medical Sciences, Urmia, Iran</Affiliation>
						</AffiliationInfo>
<Identifier Source="ORCID">0000-0002-1554-8808</Identifier>

</Author>
<Author>
					<FirstName>Masome</FirstName>
					<LastName>Rabieepour</LastName>
<Affiliation>School of Medicine, Urmia University of Medical Sciences, Urmia, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Vajihe Sadat</FirstName>
					<LastName>Nikbin</LastName>
<Affiliation>Department of Bacteriology, Pasteur Institute of Iran, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Saber</FirstName>
					<LastName>Yousefi</LastName>

						<AffiliationInfo>
						<Affiliation>Cellular and Molecular Medicine Research Institute, Urmia University of Medical Sciences, Urmia, Iran</Affiliation>
						</AffiliationInfo>

						<AffiliationInfo>
						<Affiliation>Department of Microbiology and Virology, Faculty of Medicine, Urmia University of Medical Sciences, Urmia, Iran</Affiliation>
						</AffiliationInfo>
<Identifier Source="ORCID">0000-0002-5314-3860</Identifier>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2024</Year>
					<Month>08</Month>
					<Day>05</Day>
				</PubDate>
			</History>
		<Abstract>&lt;strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;Background:&lt;/span&gt;&lt;/strong&gt;&lt;span lang=&quot;EN-US&quot;&gt; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot;&gt;Ventilator-associated pneumonia is a nosocomial infection involving hospitalized patients using mechanical ventilation. The endotracheal tube&lt;/span&gt;&lt;span lang=&quot;EN-US&quot;&gt; is a place for colonizing microbial populations and subsequent biofilm formation, leading to relative drug resistance. Also, the hospital environment may worsen the infection. This study aims to identify the microbial cause of the infection and evaluate its characteristics.&lt;/span&gt;
&lt;span lang=&quot;FA&quot;&gt;&lt;span&gt; &lt;/span&gt;&lt;/span&gt;&lt;strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;Materials and Methods: &lt;/span&gt;&lt;/strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;Sampling was done using endotracheal tube suction among hospitalized patients and from different places in intensive care units in selected hospitals in Urmia, Iran. All specimens were identified by microbial and biochemical tests. Then, the antibiotic susceptibility tests were performed using disk diffusion and minimum inhibitory and bacteriocidal concentrations for selected antibiotics. Finally, the biofilm formation rates of all isolates were evaluated. &lt;/span&gt;
&lt;strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;Results: &lt;/span&gt;&lt;/strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;The majority of clinical bacterial isolates were Gram-negative bacilli, including &lt;em&gt;A. baumannii&lt;/em&gt;. &lt;em&gt;Bacillus spp. &lt;/em&gt;and&lt;em&gt; Staphylococcus aureus &lt;/em&gt;were the most isolated bacteria from environmental samples. The antibiotic susceptibility testing results showed that most Gram-negative bacilli were resistant to common antibiotics and were extensively-drug resistant. The intermediate rate was higher than resistance to colistin, but evidence showed the efficiency of colistin against Gram-negative bacilli. Most of the isolates were strong biofilm producers, and this was correlated with the extensively drug-resistant pattern of bacteria. &lt;/span&gt;
&lt;strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;Conclusion:&lt;/span&gt;&lt;/strong&gt;&lt;span lang=&quot;EN-US&quot;&gt; The evidence shows that &lt;/span&gt;&lt;span lang=&quot;EN-US&quot;&gt;Ventilator-associated pneumonia is a critical infection. According to the findings, there is a high rate of biofilm formation and consequent drug resistance among bacterial causes of Ventilator-associated pneumonia, which needs new insights for preventing and controlling this healthcare problem.&lt;/span&gt;</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Biofilms</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Intensive Care Units</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Antimicrobial sensitivity tests</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Nosocomial infections</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">ventilator-associated pneumonia</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://www.tanaffosjournal.ir/article_741066_595a737e62b5e0413f9fd4021a5dd348.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>National Research Institute of Tuberculosis and Lung Disease (NRITLD), Shahid Beheshti University of Medical Sciences, Tehran, Iran</PublisherName>
				<JournalTitle>TANAFFOS (Respiration)</JournalTitle>
				<Issn>1735-0344</Issn>
				<Volume>24</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>2025</Year>
					<Month>10</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Genetic Variants in Inflammatory Response Genes and Lung Cancer Risk: A Case-Control Study</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>375</FirstPage>
			<LastPage>383</LastPage>
			<ELocationID EIdType="pii">741067</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Adnan</FirstName>
					<LastName>Khosravi</LastName>
<Affiliation>Research Center of Thoracic Oncology (RCTO), National Research Institute of Tuberculosis and Lung Diseases (NRITLD), Shahid Beheshti University of Medical Sciences, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0000-0001-6813-4847</Identifier>

</Author>
<Author>
					<FirstName>Sharareh</FirstName>
					<LastName>Seifi</LastName>
<Affiliation>Research Center of Thoracic Oncology (RCTO), National Research Institute of Tuberculosis and Lung Diseases (NRITLD), Shahid Beheshti University of Medical Sciences, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0000-0002-1340-0949</Identifier>

</Author>
<Author>
					<FirstName>Babak D</FirstName>
					<LastName>Salimi</LastName>
<Affiliation>Research Center of Thoracic Oncology (RCTO), National Research Institute of Tuberculosis and Lung Diseases (NRITLD), Shahid Beheshti University of Medical Sciences, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0000-0002-5541-8434</Identifier>

</Author>
<Author>
					<FirstName>Maryam</FirstName>
					<LastName>Mabani</LastName>
<Affiliation>Research Center of Thoracic Oncology (RCTO), National Research Institute of Tuberculosis and Lung Diseases (NRITLD), Shahid Beheshti University of Medical Sciences, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Patsa</FirstName>
					<LastName>Rostami</LastName>
<Affiliation>Research Center of Thoracic Oncology (RCTO), National Research Institute of Tuberculosis and Lung Diseases (NRITLD), Shahid Beheshti University of Medical Sciences, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Masoumeh</FirstName>
					<LastName>Nomani</LastName>
<Affiliation>Research Center of Thoracic Oncology (RCTO), National Research Institute of Tuberculosis and Lung Diseases (NRITLD), Shahid Beheshti University of Medical Sciences, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Shima</FirstName>
					<LastName>Seif</LastName>
<Affiliation>Mycobacteriology Research Center (MRS), NRITLD, Shahid Beheshti University of Medical Sciences, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Hoda</FirstName>
					<LastName>Dezhkhi</LastName>
<Affiliation>Mycobacteriology Research Center (MRS), NRITLD, Shahid Beheshti University of Medical Sciences, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Seyedeh Faezeh</FirstName>
					<LastName>Sadatkiaei</LastName>
<Affiliation>Research Center of Thoracic Oncology (RCTO), National Research Institute of Tuberculosis and Lung Diseases (NRITLD), Shahid Beheshti University of Medical Sciences, Tehran, Iran</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2024</Year>
					<Month>12</Month>
					<Day>04</Day>
				</PubDate>
			</History>
		<Abstract>&lt;strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;Background:&lt;/span&gt;&lt;/strong&gt;&lt;span lang=&quot;EN-US&quot;&gt; Lung cancer, a leading cause of cancer-related mortality, is influenced by both environmental and genetic factors. Chronic inflammation is recognized as a key driver of tumorigenesis. This study investigates the role of genetic variations in three inflammatory response genes in modulating lung cancer susceptibility. By examining the frequencies of specific polymorphisms in lung cancer patients and healthy controls, we aim to identify potential genetic markers for increased risk.&lt;/span&gt;
&lt;strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;Materials and Methods: &lt;/span&gt;&lt;/strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;We conducted a case-control study comparing the frequencies of 5 inflammatory response gene polymorphisms (TNF-α-308, TNF-α-238, IFN-γ-2109, IL-10-819, and IL-10-1082) in 62 patients with lung cancer and 78 controls. DNA samples were genotyped using PCR-based methods, and statistical analyses were performed to assess the associations between polymorphisms and lung cancer risk.&lt;/span&gt;
&lt;strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;Results: &lt;/span&gt;&lt;/strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;This study is the first to comprehensively analyze five key inflammatory response gene polymorphisms (TNF-α-308, TNF-α-238, IFN-γ-2109, IL-10-819, and IL-10-1082) in lung cancer patients. Our findings reveal significant associations between four of these polymorphisms and lung cancer risk.&lt;/span&gt;
&lt;strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;Conclusion: &lt;/span&gt;&lt;/strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;This study provides novel insights into the genetic basis of lung cancer susceptibility, highlighting the potential role of inflammatory response gene polymorphisms as biomarkers for risk assessment. Future research should develop deeper into the underlying biological mechanisms through which these genetic variants influence lung cancer development. By elucidating these pathways, we may identify novel therapeutic targets and develop personalized prevention and treatment strategies.&lt;/span&gt;</Abstract>
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			<Param Name="value">Lung cancer</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Polymorphisms</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Cancer Risk</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Iran</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://www.tanaffosjournal.ir/article_741067_47ad77a6f2270f49f736b7dbed7dc3f8.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>National Research Institute of Tuberculosis and Lung Disease (NRITLD), Shahid Beheshti University of Medical Sciences, Tehran, Iran</PublisherName>
				<JournalTitle>TANAFFOS (Respiration)</JournalTitle>
				<Issn>1735-0344</Issn>
				<Volume>24</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>2025</Year>
					<Month>10</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Comparative Analysis of Clinical, Laboratory, and Imaging Profiles in Tuberculosis Patients Pre- and Post-COVID-19 Pandemic</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>384</FirstPage>
			<LastPage>389</LastPage>
			<ELocationID EIdType="pii">741069</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Roya</FirstName>
					<LastName>Alavi-Naini</LastName>
<Affiliation>Department of Infectious Disease, School of Medicine, Zahedan University of Medical Sciences, Zahedan, Iran. Infectious Diseases and Tropical Medicine Research Center, Resistant Tuberculosis Institute, Zahedan University of Medical Sciences, Zahedan, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Ilia</FirstName>
					<LastName>Mirzaei</LastName>
<Affiliation>Student Research Committee, Zahedan University of Medical Sciences, Zahedan, Iran</Affiliation>
<Identifier Source="ORCID">0000-0002-0235-3833</Identifier>

</Author>
<Author>
					<FirstName>Mohammad Ali</FirstName>
					<LastName>Zeinali Moghadam</LastName>
<Affiliation>Department of Infectious Disease, School of Medicine, Zahedan University of Medical Sciences, Zahedan, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Abolfazl</FirstName>
					<LastName>Parsi-Moud</LastName>
<Affiliation>Student Research Committee, Zahedan University of Medical Sciences, Zahedan, Iran</Affiliation>
<Identifier Source="ORCID">0000-0001-8156-2379</Identifier>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2024</Year>
					<Month>03</Month>
					<Day>06</Day>
				</PubDate>
			</History>
		<Abstract>&lt;strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;Background:&lt;/span&gt;&lt;/strong&gt;&lt;span lang=&quot;EN-US&quot;&gt; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot;&gt;While the COVID-19 pandemic has understandably dominated global attention, Tuberculosis (TB) remains a persistent and formidable global health threat. Acknowledging the impact of COVID-19 on immune function and the decreased referrals of TB patients to medical clinics during the pandemic, we sought to assess the clinical and paraclinical characteristics of TB patients in two distinct periods: pre-pandemic and pandemic periods.&lt;/span&gt;
&lt;strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;Materials and Methods: &lt;/span&gt;&lt;/strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;We retrospectively identified 105 TB patients from the year preceding the pandemic and, during the pandemic, selected 72 TB patients with a positive history of COVID-19. A comprehensive analysis of various features, including age, gender, fever, cough, hemoptysis, and different imaging and laboratory parameters, was conducted and compared between the two groups.&lt;/span&gt;
&lt;strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;Results: &lt;/span&gt;&lt;/strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;Post-pandemic TB patients exhibited a higher prevalence of hemoptysis, chest pain, and elevated erythrocyte sedimentation rate (ESR) levels, with P-values of 0.014, 0.006, and &lt;0.001, respectively. Furthermore, our findings indicated an increased incidence of bilateral imaging features in COVID-19 TB patients (P= 0.02).&lt;/span&gt;
&lt;strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;Conclusion: &lt;/span&gt;&lt;/strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;Given the potential effects of COVID-19 on immune function and the diagnostic challenges posed by overlapping clinical manifestations, clinicians should maintain a high index of suspicion for tuberculosis (TB) in patients with COVID-19, particularly those presenting with atypical or complex symptoms.&lt;/span&gt;</Abstract>
		<ObjectList>
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			<Param Name="value">tuberculosis</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">COVID-19</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Pandemic</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://www.tanaffosjournal.ir/article_741069_9ea5ce82c2473ee4e05ee1c138b46edb.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>National Research Institute of Tuberculosis and Lung Disease (NRITLD), Shahid Beheshti University of Medical Sciences, Tehran, Iran</PublisherName>
				<JournalTitle>TANAFFOS (Respiration)</JournalTitle>
				<Issn>1735-0344</Issn>
				<Volume>24</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>2025</Year>
					<Month>10</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Association between Telomere Length and Idiopathic Pulmonary Fibrosis: A Case-Control Study</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>390</FirstPage>
			<LastPage>398</LastPage>
			<ELocationID EIdType="pii">741070</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Alireza</FirstName>
					<LastName>Eslaminejad</LastName>
<Affiliation>Chronic Respiratory Diseases Research Center, National Research Institute of Tuberculosis and Lung diseases (NRITLD), Shahid Beheshti University of Medical Sciences, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0000-0002-8788-4544</Identifier>

</Author>
<Author>
					<FirstName>Jalal</FirstName>
					<LastName>Heshmatnia</LastName>
<Affiliation>Chronic Respiratory Diseases Research Center, National Research Institute of Tuberculosis and Lung diseases (NRITLD), Shahid Beheshti University of Medical Sciences, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0000-0003-2966-4380</Identifier>

</Author>
<Author>
					<FirstName>Seyed Alireza</FirstName>
					<LastName>Nadji</LastName>
<Affiliation>Virology Research Center, NRITLD, Shahid Beheshti University of Medical Sciences, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Makan</FirstName>
					<LastName>Sadr</LastName>
<Affiliation>Virology Research Center, NRITLD, Shahid Beheshti University of Medical Sciences, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0000-0002-8781-8176</Identifier>

</Author>
<Author>
					<FirstName>Hooman</FirstName>
					<LastName>Sharifi</LastName>
<Affiliation>Tobacco Prevention and Control Research Center, NRITLD, Shahid Beheshti University of Medical Sciences ,Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0000-0001-6448-046X</Identifier>

</Author>
<Author>
					<FirstName>Reyhaneh</FirstName>
					<LastName>Dehghani</LastName>
<Affiliation>School of Medicine, TeMS.C., Islamic Azad University, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Mobina</FirstName>
					<LastName>Zargar</LastName>
<Affiliation>School of Medicine, TeMS.C., Islamic Azad University, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Mohsen</FirstName>
					<LastName>Sadeghi</LastName>

						<AffiliationInfo>
						<Affiliation>Chronic Respiratory Diseases Research Center, National Research Institute of Tuberculosis and Lung diseases (NRITLD), Shahid Beheshti University of Medical Sciences, Tehran, Iran</Affiliation>
						</AffiliationInfo>

						<AffiliationInfo>
						<Affiliation>Inflammatory Lung Disease Research Center, Department of Internal Medicine, Razi Hospital, School  of Medicine, Guilan University of Medical Sciences, Rasht, Iran</Affiliation>
						</AffiliationInfo>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract></Abstract>
<ArchiveCopySource DocType="pdf">https://www.tanaffosjournal.ir/article_741070_e7f7a2fcdb9caec79427ac396caf8c2e.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>National Research Institute of Tuberculosis and Lung Disease (NRITLD), Shahid Beheshti University of Medical Sciences, Tehran, Iran</PublisherName>
				<JournalTitle>TANAFFOS (Respiration)</JournalTitle>
				<Issn>1735-0344</Issn>
				<Volume>24</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>2025</Year>
					<Month>10</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>A Rare Mechanism of Hypoxemia: A Case Report</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>399</FirstPage>
			<LastPage>403</LastPage>
			<ELocationID EIdType="pii">741071</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Maria Laura</FirstName>
					<LastName>Vega Pittao</LastName>

						<AffiliationInfo>
						<Affiliation>Respiratory and Critical Care Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy</Affiliation>
						</AffiliationInfo>

						<AffiliationInfo>
						<Affiliation>Alma Mater Studiorum, Department of Medicine and Surgical Sciences (DIMEC), University of Bologna, Italy</Affiliation>
						</AffiliationInfo>
<Identifier Source="ORCID">0000-0002-8317-6364</Identifier>

</Author>
<Author>
					<FirstName>Davide</FirstName>
					<LastName>Femia</LastName>
<Affiliation>Alma Mater Studiorum, Department of Medicine and Surgical Sciences (DIMEC), University of Bologna, Italy</Affiliation>

</Author>
<Author>
					<FirstName>Marco</FirstName>
					<LastName>Carpano</LastName>

						<AffiliationInfo>
						<Affiliation>Respiratory and Critical Care Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy</Affiliation>
						</AffiliationInfo>

						<AffiliationInfo>
						<Affiliation>Alma Mater Studiorum, Department of Medicine and Surgical Sciences (DIMEC), University of Bologna, Italy</Affiliation>
						</AffiliationInfo>

</Author>
<Author>
					<FirstName>Massimiliano</FirstName>
					<LastName>Polastri</LastName>
<Affiliation>Department of Continuity of Care and Integration, Physical Medicine and Rehabilitation, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy</Affiliation>
<Identifier Source="ORCID">0000-0001-8548-0813</Identifier>

</Author>
<Author>
					<FirstName>Vito</FirstName>
					<LastName>Catalanotti</LastName>
<Affiliation>Respiratory and Critical Care Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy</Affiliation>
<Identifier Source="ORCID">0000-0001-9871-9475</Identifier>

</Author>
<Author>
					<FirstName>Manuel</FirstName>
					<LastName>Lucchin</LastName>
<Affiliation>Alma Mater Studiorum, Department of Medicine and Surgical Sciences (DIMEC), University of Bologna, Italy</Affiliation>

</Author>
<Author>
					<FirstName>Chiara</FirstName>
					<LastName>Folchi Vici D’Arcevia</LastName>
<Affiliation>Alma Mater Studiorum, Department of Medicine and Surgical Sciences (DIMEC), University of Bologna, Italy</Affiliation>

</Author>
<Author>
					<FirstName>Anna Gabriela</FirstName>
					<LastName>Lisowska</LastName>
<Affiliation>Alma Mater Studiorum, Department of Medicine and Surgical Sciences (DIMEC), University of Bologna, Italy</Affiliation>

</Author>
<Author>
					<FirstName>Lara</FirstName>
					<LastName>Pisani</LastName>

						<AffiliationInfo>
						<Affiliation>Respiratory and Critical Care Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy</Affiliation>
						</AffiliationInfo>

						<AffiliationInfo>
						<Affiliation>Alma Mater Studiorum, Department of Medicine and Surgical Sciences (DIMEC), University of Bologna, Italy</Affiliation>
						</AffiliationInfo>
<Identifier Source="ORCID">0000-0001-9224-8158</Identifier>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2024</Year>
					<Month>06</Month>
					<Day>07</Day>
				</PubDate>
			</History>
		<Abstract>&lt;span lang=&quot;EN-US&quot;&gt;The leading causes of hypoxemia and acute respiratory failure commonly observed in the intensive care unit setting are ventilator/perfusion mismatch and intrapulmonary shunt. The main objective of the current report was to describe the treatment and the diagnostic procedures in a patient with methemoglobinemia. &lt;/span&gt;
&lt;span lang=&quot;EN-US&quot;&gt;A 66-year-old woman arrived at the emergency department after suddenly losing coordination while walking and reported having experienced increased cough and sputum in the previous days. The patient, a current smoker with 35 pack–years, had comorbidities and chronic obstructive pulmonary disease, requiring long-term oxygen therapy. Extensive laboratory analyses revealed elevated methemoglobin (MetHb) levels, increasing from 10% upon admission to 25% of total hemoglobin (Hb), and the onset of post-surgical anemia (Hb 9.6 g/dL). &lt;/span&gt;
&lt;span lang=&quot;EN-US&quot;&gt;In the present case, the hypoxemia was caused by an increase in MetHb levels, in addition to anemia due to surgical intervention and overhydration. Antibiotic and diuretic therapy for treating infection and right heart failure was effective, leading to a favorable postoperative course.&lt;/span&gt;</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Acute respiratory failure</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Cough</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Dyspnea</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Intensive care unit</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Methemoglobinemia</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://www.tanaffosjournal.ir/article_741071_6c7e9447a831149971e2188eaf77c52c.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>National Research Institute of Tuberculosis and Lung Disease (NRITLD), Shahid Beheshti University of Medical Sciences, Tehran, Iran</PublisherName>
				<JournalTitle>TANAFFOS (Respiration)</JournalTitle>
				<Issn>1735-0344</Issn>
				<Volume>24</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>2025</Year>
					<Month>10</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Pericardiocentesis in Massive Pericardial Effusion in the Setting of Pulmonary Hypertension: Is It Beneficial?</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>404</FirstPage>
			<LastPage>407</LastPage>
			<ELocationID EIdType="pii">741072</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Ahmad</FirstName>
					<LastName>Mirdamadi</LastName>
<Affiliation>Department of Cardiology, Najafabad Branch, Islamic Azad University, Najafabad, Isfahan, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Mahsa</FirstName>
					<LastName>Hashemirad</LastName>
<Affiliation>Faculty of Medicine, Islamic Azad University, Najafabad Branch, Isfahan, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Shakiba</FirstName>
					<LastName>Seifi</LastName>
<Affiliation>Nosocomial Infection Research Center, Isfahan University of Medical Sciences, Isfahan, Iran</Affiliation>
<Identifier Source="ORCID">0000-0001-8759-5817</Identifier>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2024</Year>
					<Month>12</Month>
					<Day>21</Day>
				</PubDate>
			</History>
		<Abstract>&lt;strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;Background:&lt;/span&gt;&lt;/strong&gt; &lt;span lang=&quot;EN-US&quot;&gt;A serious complication of pulmonary hypertension (PH) is pericardial effusion (PE), which can significantly increase the mortality rate of affected patients. While managing this condition is critical, there is ongoing debate regarding the best therapeutic approaches. Although pericardiocentesis is mostly indicated in patients with cardiac tamponade, it may inadvertently increase mortality in the context of PH.&lt;/span&gt;&lt;br&gt;&lt;strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;Case Presentation&lt;/span&gt;&lt;/strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;: This case series reports on three patients who experienced PE associated with PH. Each patient received a different treatment, resulting in varying outcomes. One patient, unfortunately, died within 24 hours after undergoing pericardiocentesis. In contrast, the other two patients did not receive the procedure; instead, they were treated with medication. One of them has shown significant improvement after receiving more aggressive medical treatment. Both are alive with unremarkable limitations.&lt;/span&gt;&lt;br&gt;&lt;strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;Conclusion: &lt;/span&gt;&lt;/strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;The coexistence of pulmonary hypertension and massive pericardial effusion presents a complex challenge for management decisions. An effective approach requires a multidisciplinary strategy to optimize patient outcomes. While pericardiocentesis is essential in cases of massive pericardial effusion, it should be reconsidered if the underlying cause is pulmonary hypertension.&lt;/span&gt;</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Pericardiocentesis</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Massive Pericardial Effusion</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Pulmonary hypertension</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Cardiac tamponade</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Management Guidelines</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://www.tanaffosjournal.ir/article_741072_6871ffecb5f4660d20b335056c6c45eb.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>National Research Institute of Tuberculosis and Lung Disease (NRITLD), Shahid Beheshti University of Medical Sciences, Tehran, Iran</PublisherName>
				<JournalTitle>TANAFFOS (Respiration)</JournalTitle>
				<Issn>1735-0344</Issn>
				<Volume>24</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>2025</Year>
					<Month>10</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Pulmonary Nodules and Lymphadenopathy in a Patient with Advanced HIV Infection</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>408</FirstPage>
			<LastPage>410</LastPage>
			<ELocationID EIdType="pii">741073</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Alireza</FirstName>
					<LastName>Eskandari</LastName>
<Affiliation>Clinical Tuberculosis and Epidemiology Research Center, National Research Institute of Tuberculosis and Lung Diseases (NRITLD), Shahid Beheshti University of Medical Sciences, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0009-0007-4664-1953</Identifier>

</Author>
<Author>
					<FirstName>Mitra</FirstName>
					<LastName>Rezaei</LastName>
<Affiliation>Clinical Tuberculosis and Epidemiology Research Center, National Research Institute of Tuberculosis and Lung Diseases (NRITLD), Shahid Beheshti University of Medical Sciences, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0000-0002-7242-5839</Identifier>

</Author>
<Author>
					<FirstName>Babak</FirstName>
					<LastName>Salimi</LastName>
<Affiliation>Research Center of Thoracic Oncology (RCTO), NRITLD, Shahid Beheshti University of Medical Sciences, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0000-0002-5541-8434</Identifier>

</Author>
<Author>
					<FirstName>Majid</FirstName>
					<LastName>Marjani</LastName>
<Affiliation>Clinical Tuberculosis and Epidemiology Research Center, National Research Institute of Tuberculosis and Lung Diseases (NRITLD), Shahid Beheshti University of Medical Sciences, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0000-0003-1466-8645</Identifier>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2026</Year>
					<Month>06</Month>
					<Day>03</Day>
				</PubDate>
			</History>
		<Abstract>&lt;strong&gt;&lt;span lang=&quot;EN-US&quot;&gt;WHAT IS YOUR DIAGNOSIS?&lt;/span&gt;&lt;/strong&gt;
&lt;span lang=&quot;EN-US&quot;&gt;A 28-year-old woman was admitted with a two-month history of dysphagia and a two-week history of non-massive hemoptysis. She had been diagnosed with human immunodeficiency virus (HIV) infection five years earlier and was receiving antiretroviral therapy, although adherence was poor&lt;/span&gt;&lt;span dir=&quot;RTL&quot; lang=&quot;AR-SA&quot;&gt;.&lt;/span&gt;
&lt;span lang=&quot;EN-US&quot;&gt;On admission, she was afebrile and hemodynamically stable. Physical examination revealed multiple violaceous cutaneous plaques on the trunk and extremities. Lung examination was unremarkable. Multiple bilateral, non-tender, mobile cervical lymph nodes were palpable. On abdominal examination, the splenic edge was palpable below the left costal margin&lt;/span&gt;&lt;span dir=&quot;RTL&quot; lang=&quot;AR-SA&quot;&gt;.&lt;/span&gt;
&lt;span lang=&quot;EN-US&quot;&gt;Laboratory studies demonstrated pancytopenia, with a white blood cell count of 2.46 × 10&lt;/span&gt;&lt;span lang=&quot;EN-US&quot;&gt;⁹&lt;/span&gt;&lt;span lang=&quot;EN-US&quot;&gt;/L (absolute neutrophil count, 1.96 &lt;/span&gt;&lt;span lang=&quot;EN-US&quot;&gt;×&lt;/span&gt;&lt;span lang=&quot;EN-US&quot;&gt; 10&lt;/span&gt;&lt;span lang=&quot;EN-US&quot;&gt;⁹&lt;/span&gt;&lt;span lang=&quot;EN-US&quot;&gt;/L), hemoglobin of 10.6 g/dL, and platelet count of 44 &lt;/span&gt;&lt;span lang=&quot;EN-US&quot;&gt;×&lt;/span&gt;&lt;span lang=&quot;EN-US&quot;&gt; 10&lt;/span&gt;&lt;span lang=&quot;EN-US&quot;&gt;⁹&lt;/span&gt;&lt;span lang=&quot;EN-US&quot;&gt;/L. The erythrocyte sedimentation rate was 52 mm/h. Her HIV viral load was 1895 copies/mL, and the CD4+ T-lymphocyte count was 7 cells/µL&lt;/span&gt;&lt;span dir=&quot;RTL&quot; lang=&quot;AR-SA&quot;&gt;.&lt;/span&gt;
&lt;span lang=&quot;EN-US&quot;&gt;Contrast-enhanced CT of the neck demonstrated multiple bilateral cervical and supraclavicular lymphadenopathies, the largest measuring approximately 125 × 90 mm, associated with contour deformity and luminal narrowing of the oropharynx. Endoscopic evaluation revealed an erythematous lesion on the mucosal surface of the left nasal cavity; however, further evaluation of the nasopharynx was not feasible because of significant upper airway obstruction&lt;/span&gt;&lt;span dir=&quot;RTL&quot; lang=&quot;AR-SA&quot;&gt;.&lt;/span&gt;
&lt;span lang=&quot;EN-US&quot;&gt;Contrast-enhanced CT of the chest revealed multiple bilateral pulmonary nodules with mediastinal, hilar, and axillary lymphadenopathies (Figure 1). CT of the abdomen demonstrated mild hepatosplenomegaly&lt;/span&gt;&lt;span dir=&quot;RTL&quot; lang=&quot;AR-SA&quot;&gt;.&lt;/span&gt;
&lt;span lang=&quot;EN-US&quot;&gt;Given the presence of pancytopenia and generalized lymphadenopathy, both infectious and hematologic etiologies were considered. Sputum smear examination for acid-fast bacilli and Mycobacterium tuberculosis GeneXpert testing were negative. Bone marrow examination and an excisional biopsy of a cervical lymph node were subsequently performed for diagnostic evaluation. Histopathologic findings from the lymph node biopsy are shown in Figure 2.&lt;/span&gt;</Abstract>
<ArchiveCopySource DocType="pdf">https://www.tanaffosjournal.ir/article_741073_7c997fb615e0a6fb957aed1823079809.pdf</ArchiveCopySource>
</Article>
</ArticleSet>
