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Opioids and adverse outcomes in elderly chronic obstructive pulmonary disease patients

We thank D. Viglino and M. Maignan for their interest in our manuscript [1] and for their insightful comments. They raise a valid point that our mortality results may have been influenced by the potentially confounding effects of palliative care receipt on or following the index date. While we excluded individuals receiving palliative care in the year prior to the index date, we did not do so on or after the index date for practical methodological reasons. However, several points should be considered. First, Viglino and Maignan write that the decision to palliate in chronic obstructive pulmonary disease (COPD) often arises in the context of an acute respiratory exacerbation. Our propensity score model included whether or not a recent acute respiratory exacerbation occurred in the 30 days prior to the index date, and opioid users and nonusers were well balanced on that variable after propensity score weighting [1]. Second, increased respiratory-related and all-cause mortality were found not only among users of opioid-only agents but also among users of combination opioid/nonopioid formulations [1]. Opioids combined with paracetamol or aspirin are unlikely to be used for purposes of palliation and such agents represent ~90% of incident opioid use among older adults with COPD [2]. Third, while the possible residual inclusion of individuals receiving palliative care among opioid users may potentially explain the finding of increased mortality, this would be unlikely to explain why risks of outpatient respiratory exacerbations and emergency visits for COPD or pneumonia were also greater among opioid users. If there was residual inclusion of individuals with recent end-of-life decisions among opioid users in our study, this would have been likely to bias the intensive care admission outcome towards being significantly decreased among opioid users, and not rendered a nonsignificant association, as Viglino and Maignan propose.

DNA damage and repair capacity in lymphocyte of chronic obstructive pulmonary diseases patients during physical exercise with oxygen supplementation

ConclusionCOPD patients who performed physical exercise associated with oxygen supplementation had a better response to DNA damage induced by MMS and a better DNA repair when compared to the condition of physical exercise without oxygen supplementation.Trial registrationUNISC N374.298. Registered 04 JUN 2013 (retrospectively registered). (Source: Multidisciplinary Respiratory Medicine)

National Institutes of Health (NIH) Stroke Scale

Medical professionals and even the public have been trained to recognize basic signs of stroke. These include three features of stroke: slurred speech, drooping of one outstretched arm, and drooping of one side of the face when attempting to smile. When one of these signs is present it’s a fairly sensitive indicator of stroke. When all three are present, sensitivity for stroke is approximately 90%. However, when evaluating patients for inclusion in stroke protocols and prior to fibrinolytic stroke treatments, medical professionals use a slightly more sophisticated series of questions. They often use the NIH stroke scale.

The NIH offers training and certification in the administration and scoring of the stroke scale. An overview of the scale is listed here

Indacaterol/glycopyrronium in symptomatic patients with COPD (GOLD B and GOLD D) versus salmeterol/fluticasone: ILLUMINATE/LANTERN pooled analysis.

Related Articles

Indacaterol/glycopyrronium in symptomatic patients with COPD (GOLD B and GOLD D) versus salmeterol/fluticasone: ILLUMINATE/LANTERN pooled analysis.

Int J Chron Obstruct Pulmon Dis. 2016;11:3189-3197

Authors: Vogelmeier C, Zhong N, Humphries MJ, Mezzi K, Fogel R, Bader G, Patalano F, Banerji D

Abstract
BACKGROUND: Indacaterol/glycopyrronium (IND/GLY) is approved for maintenance treatment of adult patients with COPD. This post hoc analysis explored the efficacy and safety of IND/GLY versus salmeterol/fluticasone (SFC) in symptomatic (Global Initiative for Chronic Obstructive Lung Disease [GOLD] B and GOLD D) patients with moderate-to-severe COPD.
PATIENTS AND METHODS: Data from LANTERN and ILLUMINATE studies were pooled and analyzed. In both studies, symptomatic COPD patients were randomized to once-daily IND/GLY 110 μg/50 μg or twice-daily SFC 50 μg/500 μg. End points were pre-dose trough forced expiratory volume in one second (FEV1), standardized area under the curve for FEV1 from 0 to 12 hours (FEV1 AUC0-12 hours), peak FEV1, peak forced vital capacity (FVC), pre-dose trough FVC, Transition Dyspnea Index (TDI) total score, St George's Respiratory Questionnaire total score, rescue medication use and safety.
RESULTS: A total of 1,263 patients were classified as either GOLD B (n=809) or GOLD D (n=454). At week 26, IND/GLY demonstrated statistically significant improvement in all lung function parameters versus SFC in patients in both the GOLD B and GOLD D subgroups. TDI total score and rescue medication use were significantly improved with IND/GLY versus SFC in the overall population and in the GOLD B (TDI total score only) and GOLD D (rescue medication only) subgroups. IND/GLY also reduced the rate of exacerbations in the pooled population. Overall safety profile was comparable with a higher incidence of pneumonia in the SFC-treated group.
CONCLUSION: In this pooled analysis, IND/GLY demonstrated superior efficacy compared with SFC in patients in the GOLD B and GOLD D subgroups and supported its use in symptomatic COPD patients.

PMID: 28008244 [PubMed - in process]

Lung tumors, COPD and immune response: is epigenetics the bottom line?

Related Articles

Lung tumors, COPD and immune response: is epigenetics the bottom line?

Minerva Med. 2016 Dec;107(6 Suppl 1):1-8

Authors: Balestro E, Baraldo S, Piloni D, Stella GM

Abstract
NSCLC is a heterogeneous disorder consisting of distinct molecular subtypes which can be treated by using specific drugs targeted to distinct genetic lesions. It is well known that NSCLS incidence is higher in chronic obstructive pulmonary disease (COPD) patients because they share a common risk factor (cigarette smoking) and it is believed that the typical inflammatory microenvironment observed in COPD may influence the molecular mechanisms responsible of carcinogenesis. In the last years, the role of epigenetic processes in cell biology and tissue pathology has been extensively studied both in COPD and NSCLC. The recent paper by Wauters et al. showed a specific pattern of driver mutations and molecular features in NSCLC raising in the context of COPD. All these findings have shown for the first time that lung tumors found in COPD patients differ from those observed in patient without COPD due to the presence of a specific tumor microenvironment which is characterized by reduced CD4+ Treg cells. On this basis, the present work aims at discussing and analyzing the context-specific mechanisms of clonal selection and evolution mainly focusing on the epigenetic alterations and at pointing out the potential therapeutic implications.

PMID: 28009152 [PubMed - in process]

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