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Pulmonary Lymphoid Neogenesis in Idiopathic Pulmonary Arterial Hypertension.

CONCLUSIONS: We highlight the main features of lymphoid neogenesis specifically in the lungs of patients with IPAH providing new evidence of immunological mechanisms in this severe condition. PMID: 22108206 [PubMed - as supplied by publisher] (Source: American Journal of Respiratory and Critical Care Medicine)

Update on methicillin-resistant Staphylococcus aureus in cystic fibrosis

Purpose of review: Respiratory infection is a major contributor to morbidity and mortality in cystic fibrosis (CF). One infection the CF community is particularly concerned about is methicillin-resistant Staphylococcus aureus (MRSA). Worldwide, the prevalence of MRSA has been rising and the impact on clinical outcomes and optimal prevention and treatment strategies are unclear. Recent findings: Studies have demonstrated MRSA is independently associated with poor clinical outcomes, even after taking into account severity of illness. Additionally, characteristics of MRSA strains, such as small colony variants and borderline oxacillin-resistant S. aureus, may be important in predicting the subsequent clinical course. The treatment of MRSA has had variable results and emergence of resistance to commonly prescribed antibiotics is a concern. Summary: The evidence to date supports MRSA infection is independently associated with worse outcomes. The next step is to build upon the current research to expand the knowledge about the impact different strains of MRSA have on infection control strategies and MRSA treatment protocols. Interventions should balance patient safety, efficacy, and treatment burden to improve the quality and length of life in patients with CF.

Update in pediatric sleep medicine

Purpose of review: To summarize the most important recent scientific developments in the field of clinical pediatric sleep medicine, specifically as relates to sleep disorders and sleep in special pediatric populations. Recent findings: The major themes covered in this review include sleep-disordered breathing; narcolepsy; restless legs syndrome/periodic limb movement disorder; insomnia; sleep in children with medical conditions; and sleep in children with neurodevelopmental and psychiatric disorders. Summary: An expanded understanding of the pathophysiology, epidemiology, clinical evaluation methods, sequelae, and empirically supported treatment options of common pediatric sleep disorders, especially in high-risk populations, is key to a rational approach to diagnosis and management of these children in clinical settings.

Treating obstructive sleep apnea with hypoglossal nerve stimulation

Purpose of review: Obstructive sleep apnea (OSA) is a common disorder characterized by recurrent pharyngeal collapse secondary to sleep-induced hypotonia of peri-pharyngeal structures. Therapy for OSA is sometimes poorly tolerated and not always effective. The current study reviews a new treatment modality, hypoglossus stimulation, recently evaluated by multiple physiological studies and currently assessed by several clinical studies. Recent findings: A phase-I, implantable hypoglossus nerve stimulation multicenter study was published in 2001. Significant reduction in apnea–hypopnea index (AHI) was reported in seven of the eight implanted OSA patients, but technical faults precluded prolonged follow-up. Over the past 2 years, three new hypoglossus nerve stimulation systems have been evaluated in more than 60 OSA patients. In adequately selected patients, a more than 50% reduction in AHI was observed. Usually, a decrease in OSA severity from moderate–severe to mild–minimal can be achieved. Summary: Ongoing research, including recent initiation of a large multicenter phase-III study, suggests that hypoglossus nerve stimulators are likely to be available as a new treatment modality within a few years. Additional data are needed to define which OSA patients are most likely to benefit from hypoglossus nerve stimulation. Continuous refinement of electrodes design is likely to improve stimulation efficacy in coming years.

Pulmonary exacerbations in cystic fibrosis

Purpose of review: The chronic infection and inflammation of cystic fibrosis (CF) lung disease causes a progressive decline of lung function resulting in daily symptoms such as cough and sputum production. There are intermittent episodes of acute worsening of symptoms, more commonly referred to as pulmonary exacerbations. Despite this being a common event, there is still no standardized definition of an exacerbation. A recent set of guidelines from the CF Foundation Pulmonary Therapies Committee on the treatment of exacerbations noted the paucity of data supporting commonly used therapies. This review describes our current understanding of pulmonary exacerbations and the therapies used to treat them. Recent findings: The treatment of an exacerbation is intended to resolve the worsened symptoms and to restore the lung function that is commonly lost in the acute presentation. A most striking finding is the observation that for many patients there is no restoration of lung function, suggesting we either need better therapies to prevent exacerbations or better treatment of exacerbations. Summary: We have established recommendations on specific treatment of a pulmonary exacerbation and have outlined the areas where we need better information on appropriate therapies. Once we have a standardized definition of an exacerbation, we can proceed with clinical trials of therapies specific for its treatment.

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