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Pulmonary Embolism Secondary to Partially Thrombosed Aneurysm of the Left Innominate Vein: A Complication of a Narrow Aortosternal Space? 左无名静脉部分栓塞性动脉瘤继发肺栓塞:胸主动脉间隙狭窄的并发症?
IF 9.2 3区 医学 Q1 RESPIRATORY SYSTEM Pub Date : 2026-01-15 DOI: 10.1016/j.arbres.2026.01.003
Luis Gorospe, Ana Villanueva-Campos, Luis Carlos Lomanto-Navarro
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引用次数: 0
Reply to "Saddle Pulmonary Embolism in Hemodynamically Stable Patients: Clinical Implications and Unresolved Questions". 答复“鞍状肺栓塞在血流动力学稳定的患者:临床意义和未解决的问题”。
IF 9.2 3区 医学 Q1 RESPIRATORY SYSTEM Pub Date : 2026-01-15 DOI: 10.1016/j.arbres.2026.01.004
Winnifer Briceño, David Jiménez
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引用次数: 0
Recommendations on the Diagnosis and Treatment of Tuberculosis Infection: SEPAR/SEIMC/Spanish Ministry of Health Consensus Statement. 关于结核病感染诊断和治疗的建议:SEPAR/SEIMC/西班牙卫生部共识声明
IF 9.2 3区 医学 Q1 RESPIRATORY SYSTEM Pub Date : 2026-01-15 DOI: 10.1016/j.arbres.2025.10.021
José Antonio Caminero, Luís Anibarro, Eva Tabernero, Fernando Alcaide, Guillermo Pérez-Mendoza, Joan-Pau Millet, Remedio Guna, Maria-Luiza de Souza-Galvão, Paula López-Roa, Adrián Sánchez-Montalvá, José A Gullón-Blanco, Verónica González-Galán

All strategies on the pathway to tuberculosis (TB) elimination prioritise, among other measures, addressing tuberculosis infection (TBI), particularly the identification of individuals and population groups who should be candidates for tuberculosis preventive treatment (TPT). In Spain, a TBI test is required before recommending TPT. An interferon-gamma release assay (IGRA) is preferred over the tuberculin skin test (TST), although the latter may be used in settings where IGRAs are not available or when deemed necessary to increase diagnostic sensitivity. On the other hand, new skin tests employing specific antigens (TBST) may play a key role. As a general principle, screening for TBI should include all individuals at high risk for progressing from TBI to TB, as described in this guideline, prioritising pulmonary TB contacts, people living with HIV, immunocompromised individuals and those in other situations associated with an elevated risk of developing TB. Once TBI has been diagnosed in these high-risk groups, the algorithm set out in this guideline should be applied to rule out TB disease. Once TB has been excluded, TPT should be recommended. The preferred regimen is daily isoniazid (H) plus rifampicin (R) for 3 months (3HR). However, once rifapentine becomes available in Spain, both the 1-month daily (1HP) and the 3-month weekly (3HP) regimens combining H and rifapentine (P) may also be used. Finally, measures must be taken to ensure adherence to TPT and to monitor and manage potential drug-related adverse effects.

除其他措施外,关于消除结核病途径的所有战略都将处理结核病感染列为优先事项,特别是确定应该接受结核病预防性治疗的个人和人群。在西班牙,在推荐TPT之前需要进行TBI测试。干扰素- γ释放试验(IGRA)优于结核菌素皮肤试验(TST),尽管后者可用于无法获得IGRA或认为有必要提高诊断敏感性的情况。另一方面,采用特异性抗原(TBST)的新型皮肤试验可能发挥关键作用。如本指南所述,作为一般原则,TBI筛查应包括所有有从TBI发展为结核病高风险的个体,优先考虑肺结核接触者、艾滋病毒感染者、免疫功能低下者和其他与发展为结核病风险升高相关的人群。一旦在这些高危人群中诊断出TBI,应应用本指南中列出的算法来排除结核病。一旦结核病被排除在外,就应该推荐破伤风三联疗法。首选方案是每日异烟肼(H)加利福平(R),持续3个月(3HR)。然而,一旦利福喷丁在西班牙上市,1个月每日(1HP)和3个月每周(3HP)联合H和利福喷丁(P)的方案也可以使用。最后,必须采取措施确保遵守TPT,并监测和管理与药物有关的潜在不利影响。
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引用次数: 0
A 73-Year-Old Woman With a 7-Year History of a Slowly Growing Lung Mass and Hemoptysis Mimicking Malignancy. 一位73岁女性,有7年缓慢生长的肺肿块和类似恶性肿瘤的咯血病史。
IF 9.2 3区 医学 Q1 RESPIRATORY SYSTEM Pub Date : 2026-01-15 DOI: 10.1016/j.arbres.2026.01.002
Lei Qi, Paul R Allyn Iii, Gregory A Fishbein
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引用次数: 0
Routine Blood Biomarkers in Patients With the PI*SZ Genotype of Alpha-1 Antitrypsin Deficiency: Data From the EARCO Registry. α -1抗胰蛋白酶缺乏症PI*SZ基因型患者的常规血液生物标志物:来自EARCO注册的数据
IF 9.2 3区 医学 Q1 RESPIRATORY SYSTEM Pub Date : 2026-01-09 DOI: 10.1016/j.arbres.2025.12.013
Ane Lopez-Gonzalez, Robson Aparecido Prudente, Cristina Aljama, Cristina Esquinas, Maria Torres-Duran, Alice M Turner, Hanan Tanash, Carlota Rodríguez-García, Angelo Corsico, Eva Bartošovská, Catarina Guimarães, José Luis López-Campos, Jens-Ulrik Stæhr Jensen, José María Hernández-Pérez, Christian F Clarenbach, Kenneth R Chapman, Juan Luis Rodríguez-Hermosa, Maria Sucena, Marc Miravitlles, Miriam Barrecheguren
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引用次数: 0
The Future of Lung Cancer Screening. 肺癌筛查的未来。
IF 9.2 3区 医学 Q1 RESPIRATORY SYSTEM Pub Date : 2026-01-09 DOI: 10.1016/j.arbres.2025.12.009
Peter J Mazzone
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引用次数: 0
Long-term Outcomes of Pediatric CFSPID: A 15-Year Clinical and Genomic Study Across Newborn Screening Cystic Fibrosis Units. 儿童CFSPID的长期结果:一项针对新生儿囊性纤维化筛查单位的15年临床和基因组研究
IF 9.2 3区 医学 Q1 RESPIRATORY SYSTEM Pub Date : 2026-01-09 DOI: 10.1016/j.arbres.2025.12.010
Ana Morales-Tirado, Enrique Blitz-Castro, Ana Tabares-González, Celia Gascón-Galindo, Saioa Vicente-Santamaría, Carmen Luna-Paredes, Enrique Salcedo-Lobato, Simon Boutry, Adelaida Lamas-Ferreiro

Background: Newborn blood spot screening (NBS) for cystic fibrosis (CF) increasingly identifies infants with inconclusive results, classified as CF screen-positive inconclusive diagnosis (CFSPID). However, long-term outcome data remain limited.

Objective: To analyze the clinical and biochemical course of children with CFSPID.

Methods: We conducted a bi-center observational cohort study including all children designated as CFSPID through the Madrid NBS program from July 2009 to June 2024. Follow-up assessments included serial sweat chloride (SC) testing, respiratory and gastrointestinal (GI) evaluations, spirometry from age 5 or older, nasopharyngeal cultures, and fecal elastase measurements.

Results: A total of 100 children were enrolled. After a median follow-up of 3.59 years [IQR, 1.73-5.43], 25% were reclassified as unaffected carriers following CFTR variant reinterpretation. The remaining 75 were categorized into 3 genotype groups: 66 with CF-causing (CFc)/Variant of Varying Clinical Consequence (VVCC), 4 with VVCC/VVCC, and 5 with CFc/Variant of Uncertain Significance (VUS). By the end of follow-up, 42.67% developed at least 1 intermediate or positive SC value. Three children (4%), all carrying the CFc/VVCC genotype, converted to cystic fibrosis (mean age at conversion, 4.23 years), and 1 child (1.3%) developed a CFTR-related disorder. Clinical signs were mild, with normal spirometry and full pancreatic sufficiency. No Pseudomonas aeruginosa isolates were detected.

Conclusions: Conversion from CFSPID to CF was rare (4%), but abnormal SC values were frequent (42.67%), supporting the need for structured, long-term monitoring. Continued follow-up in specialized CF centers is essential for early detection of disease progression.

背景:新生儿血斑筛查(NBS)对囊性纤维化(CF)越来越多地发现结果不确定的婴儿,被归类为CF筛查阳性不确定诊断(CFSPID)。然而,长期结果数据仍然有限。目的:分析儿童CFSPID的临床及生化过程。方法:我们进行了一项双中心观察队列研究,包括2009年7月至2024年6月通过马德里NBS计划指定为CFSPID的所有儿童。随访评估包括连续汗液氯化物(SC)测试、呼吸和胃肠道(GI)评估、5岁及以上儿童的肺活量测定、鼻咽培养和粪便弹性蛋白酶测量。结果:共纳入100名儿童。中位随访3.59年[IQR, 1.73-5.43]后,25%的患者在CFTR变异重新解释后被重新归类为未受影响的携带者。其余75例被分为3个基因型组:66例为cf -病因(CFc)/不同临床后果变异(VVCC), 4例为VVCC/VVCC, 5例为CFc/不确定意义变异(VUS)。随访结束时,42.67%的患者出现至少1个中间或阳性SC值。3名携带CFc/VVCC基因型的儿童(4%)转化为囊性纤维化(转化时平均年龄4.23岁),1名儿童(1.3%)发展为cftr相关疾病。临床症状轻,肺活量测定正常,胰功能充足。未检出铜绿假单胞菌。结论:从CFSPID到CF的转换很少见(4%),但异常SC值很常见(42.67%),支持需要结构化的长期监测。在专门的CF中心持续随访对于早期发现疾病进展至关重要。
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引用次数: 0
Central Sleep Apnea in Multiple Sclerosis: An Underrecognized Comorbidity. 多发性硬化症的中枢性睡眠呼吸暂停:一种未被认识的合并症。
IF 9.2 3区 医学 Q1 RESPIRATORY SYSTEM Pub Date : 2026-01-09 DOI: 10.1016/j.arbres.2025.12.011
Manuela Herrera, Juan Jose Zapata, Mireia Dalmases
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引用次数: 0
Two for One: Percutaneous CT-Guided Drainage of a Lung Abscess and Parapneumonic Effusion in a Single Procedure. 二合一:经皮ct引导下肺脓肿及肺旁积液引流术。
IF 9.2 3区 医学 Q1 RESPIRATORY SYSTEM Pub Date : 2026-01-09 DOI: 10.1016/j.arbres.2025.12.012
María López-Paraja, Ignacio Donate-Velasco, Luis Gorospe
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引用次数: 0
Anomalous Loop Formation of the Left Brachiocephalic Vein: Imaging Findings of an Extremely Rare Congenital Venous Anomaly. 左头臂静脉异常环状形成:一种极为罕见的先天性静脉异常的影像学表现。
IF 9.2 3区 医学 Q1 RESPIRATORY SYSTEM Pub Date : 2026-01-09 DOI: 10.1016/j.arbres.2025.12.014
Ahmet Büber, Fatih Can Yüksel, Gökhan Polat
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引用次数: 0
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Archivos De Bronconeumologia
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