Search Journal-type in search term and press enter
Southwest Pulmonary and Critical Care Fellowships

Pulmonary Journal Club

(Click on title to be directed to posting, most recent listed first)

May 2017 Phoenix Pulmonary/Critical Care Journal Club
October 2015 Phoenix Pulmonary Journal Club: Lung Volume Reduction
September 2015 Tucson Pulmonary Journal Club: Genomic Classifier
   for Lung Cancer
April 2015 Phoenix Pulmonary Journal Club: Endo-Bronchial Ultrasound in
   Diagnosing Tuberculosis
February 2015 Tucson Pulmonary Journal Club: Fibrinolysis for PE
January 2015 Tucson Pulmonary Journal Club: Withdrawal of Inhaled
    Glucocorticoids in COPD
January 2015 Phoenix Pulmonary Journal Club: Noninvasive Ventilation In 
   Acute Respiratory Failure
September 2014 Tucson Pulmonary Journal Club: PANTHEON Study
June 2014 Tucson Pulmonary Journal Club: Pirfenidone in Idiopathic
   Pulmonary Fibrosis
September 2014 Phoenix Pulmonary Journal Club: Inhaled Antibiotics
August 2014 Phoenix Pulmonary Journal Club: The Use of Macrolide
   Antibiotics in Chronic Respiratory Disease
June 2014 Phoenix Pulmonary Journal Club: New Therapies for IPF
   and EBUS in Sarcoidosis
March 2014 Phoenix Pulmonary Journal Club: Palliative Care
February 2014 Phoenix Pulmonary Journal Club: Smoking Cessation
January 2014 Pulmonary Journal Club: Interventional Guidelines
December 2013 Tucson Pulmonary Journal Club: Hypothermia
December 2013 Phoenix Pulmonary Journal Club: Lung Cancer
   Screening
November 2013 Tucson Pulmonary Journal Club: Macitentan
November 2013 Phoenix Pulmonary Journal Club: Pleural Catheter
   Infection
October 2013 Tucson Pulmonary Journal Club: Tiotropium Respimat 
October 2013 Pulmonary Journal Club: Pulmonary Artery
   Hypertension
September 2013 Pulmonary Journal Club: Riociguat; Pay the Doctor
August 2013 Pulmonary Journal Club: Pneumococcal Vaccine
   Déjà Vu
July 2013 Pulmonary Journal Club
June 2013 Pulmonary Journal Club
May 2013 Pulmonary Journal Club
March 2013 Pulmonary Journal Club
February 2013 Pulmonary Journal Club
January 2013 Pulmonary Journal Club
December 2012 Pulmonary Journal Club
November 2012 Pulmonary Journal Club
October 2012 Pulmonary Journal Club
September 2012 Pulmonary Journal Club
August 2012 Pulmonary Journal Club
June 2012 Pulmonary Journal Club
June 2012 Pulmonary Journal Club
May 2012 Pulmonary Journal Club
April 2012 Pulmonary Journal Club
March 2012 Pulmonary Journal Club
February 2012 Pulmonary Journal Club
January 2012 Pulmonary Journal Club
December 2011 Pulmonary/Sleep Journal Club
October, 2011 Pulmonary Journal Club
September, 2011 Pulmonary Journal Club
August, 2011 Pulmonary Journal Club
July 2011 Pulmonary Journal Club
May, 2011 Pulmonary Journal Club
April, 2011 Pulmonary Journal Club
February 2011 Pulmonary Journal Club 
January 2011 Pulmonary Journal Club 
December 2010 Pulmonary Journal Club

 

Both the Phoenix Good Samaritan/VA and the Tucson University of Arizona fellows previously had a periodic pulmonary journal club in which current or classic pulmonary articles were reviewed and discussed. A brief summary was written of each discussion describing thearticle and the strengths and weaknesses of each article.

-------------------------------------------------------------------------------------

Entries in pulmonary artery hypertension (3)

Monday
Dec162013

November 2013 Tucson Pulmonary Journal Club: Macitentan

Pulido T, Adzerikho I, Channick RN, Delcroix M, Galiè N, Ghofrani HA, Jansa P, Jing ZC, Le Brun FO, Mehta S, Mittelholzer CM, Perchenet L, Sastry BK, Sitbon O, Souza R, Torbicki A, Zeng X, Rubin LJ, Simonneau G; SERAPHIN Investigators. Macitentan and morbidity and mortality in pulmonary arterial hypertension. N Engl J Med. 2013;369(9):809-18. [CrossRef] [PubMed]

Treatment of pulmonary arterial hypertension (PAH) with endothelin receptor antagonists (ERA) has been shown to improve exercise capacity and functional status, but not mortality. A recent systematic review found uncertainty regarding ERAs’ effects on mortality (1). Macitentan, a new molecule structurally similar to bosentan, targets endothelin-A and endothelin-B receptors, offers greater tissue penetration, and has more sustained receptor binding.

SERAPHIN was an industry-sponsored, double-blinded, randomized controlled trial which examined the effect of long-term macitentan use on PAH morbidity and mortality. Between May 2008 and December 2009, 742 patients in 39 countries were randomized to placebo, macitentan 3 mg daily, or macitentan 10 mg daily. Participants had to be ≥12 years of age with Group 1 PAH confirmed by right heart catheterization and have WHO functional class II, III, or IV heart failure. Participants taking intravenous or subcutaneous prostanoids were excluded, but other concomitant treatments were allowed. The composite endpoint of worsening of PAH (initiation of intravenous or subcutaneous prostanoids, lung transplantation, or atrial septostomy) or death from any cause was the primary endpoint. Secondary outcomes included the composite outcome of hospitalization or death due to PAH, change in 6-minute walk (6MW), improvement in WHO functional class, and adverse events.

As compared to placebo, both the 3 mg and 10 mg daily dose of macitentan were found to reduce the composite endpoint of worsening PAH or death with hazard ratios of 0.70 (CI 95% 0.52-0.96) and 0.55 (CI 95% 0.32-0.76), respectively. Both also improved the composite endpoint of hospitalization or death due to PAH, 6MW and WHO functional class. The proportions of participants with elevated liver enzymes were comparable across the 3 groups (1-5%); however, participants in the 3 mg and 10 mg macitentan groups were more likely to experience anemia, 8.8% and 13.2%, respectively, than the 3.2% of participants in the placebo group.

Treatment with macitentan significantly decreased the composite endpoint of worsening PAH or death. The major driver of this reduction was fewer instances of worsening of PAH rather than fewer deaths. Similar to previous trials, SERAPHIN fails to clearly demonstrate that ERA use reduces all cause or PAH-specific mortality. While macitentan use did appear to result in meaningful reductions in symptom burden and hospitalization, the effect on 6MW is smaller than that previously reported for other ERAs (1). Macitentan use does appear to be safe with a slightly higher risk of anemia being observed. The incremental benefit of macitentan over existing treatments is unknown.

Candy Wong, MD; Cristine Berry, MD; Joe Gerald, PhD

University of Arizona

Tucson, AZ

Reference

  1. Liu C, Chen J, Gao Y, Deng B, Liu K. Endothelin receptor antagonists for pulmonary arterial hypertension. Cochrane Database of Systematic Reviews 2013, Issue 2. Art. No.: CD004434. DOI: 10.1002/14651858.CD004434.pub5. [CrossRef] [PubMed]

Reference as: Wong C, Berry C, Gerald J. November 2013 Tucson pulmonary journal club: macitentan. Southwest J Pulm Crit Care. 2013;7(6):349-50. doi: http://dx.doi.org/10.13175/swjpcc174-13 PDF

Wednesday
Oct302013

October 2013 Pulmonary Journal Club: Pulmonary Artery Hypertension

Pulido T, Adzerikho I, Channick RN, Delcroix M, Galiè N, Ghofrani HA, Jansa P, Jing ZC, Le Brun FO, Mehta S, Mittelholzer CM, Perchenet L, Sastry BK, Sitbon O, Souza R, Torbicki A, Zeng X, Rubin LJ, Simonneau G; SERAPHIN Investigators. Macitentan and morbidity and mortality in pulmonary arterial hypertension. N Engl J Med. 2013;369(9):809-18. [CrossRef] [PubMed]

The October pulmonary journal club was focused on pulmonary hypertension. We reviewed a total of 5 articles on pulmonary hypertension. The 2 articles on riociguat that appeared in the New England Journal of Medicine have been reviewed and summarized in the September Pulmonary Journal Club (1-3).

Current therapies in the treatment of pulmonary hypertension have been based on their efficacy in improving exercise tolerance and 6 minute walk time. Macitentan is a new endothelin receptor antagonist that has now been approved by the FDA for the treatment of Class I pulmonary hypertension. The trial was a multicenter double-blind, placebo-controlled study. A total of 742 patients were included and divided into 3 arms (placebo, 3mg, and 10mg). Inclusion criteria were Class I pulmonary hypertension, World Health Organization (WHO) class 2-4, and confirmation of pulmonary hypertension by right heart catheterization.  Patients were excluded if they were receiving subcutaneous or IV prostacyclin therapy. Composite primary endpoints were monitored for morbidity (decrease in 6 minute walk, increase in symptoms, need for additional therapy, septoplasty, lung transplantation) and mortality. The results showed that there was a reduction in composite endpoint for morbidity but this was largely due to an improvement in 6 minute walk time. There was no significant reduction in mortality. The studying initially looks exciting in that it was a large study and the first to look at morbidity and mortality. The problem however lies in using composite endpoints in defining morbidity. By using multiple variables as 1 composite endpoint it’s easier to report a significant effect when there really is not much of one. The study is promising and the medication does show an improved exercise tolerance.  A longer term study would be more fruitful in further evaluating mortality.  Our review yielded that we would consider using this medication, but were unsure as to what tier it would fall in. Cost will likely be a prohibitive factor especially since other less expensive endothelin receptor antagonists have similar efficacy.

Minai OA, Yared JP, Kaw R, Subramaniam K, Hill NS.Perioperative risk and management in patients with pulmonary hypertension. Chest. 2013;144(1):329-40. [CrossRef] [PubMed]

Kosarek L, Fox C, Baluch AR, Kaye AD. Pulmonary hypertension and current anesthetic implications. Middle East J Anesthesiol. 2009;20(3):337-46

The perioperative care of patients with pulmonary hypertension remains a challenge with no formal guidelines on management. The above 2 articles were a review on the physiology of pulmonary hypertension, and the rationale for use of certain medications. Our review of the articles led to the consensus that our current model of practice follows that of expert opinion. We often start a PDE5 inhibitor as first line therapy preoperatively and will delay surgery in high risk patients until pulmonary hypertension management has been optimized. The main differences we encountered were in the use of pulmonary artery catheters over continuous TEE probes and whether to initiate IV prostacyclin therapy based on echo findings alone. Our practice style has been to place pulmonary artery catheters preoperatively and leave them in during the post operative period for the first 24-48hrs while medications such as inhaled nitric oxide or IV prostacyclin infusions are in use.  Echocardiograms are often misleading in identifying the severity of pulmonary hypertension, but once you identified that that a severe pulmonary hypertension scenario is present, we advocate having an experienced cardiac anesthetist and/or pulmonologist experienced with inhaled nitric oxide, IV prostacyclin therapy on standby while undergoing moderate sedation or anesthesia, and this even includes the initial right heart catheterization. Much of the perioperative management is recognizing the potential needs of the patient and having the appropriate meds and personnel available. I think it goes without saying that these patients should be managed in specialized centers.

Manoj Mathew, MD FCCP

Associate Editor

Pulmonary Journal Club

References

  1. Ghofrani HA, D'Armini AM, Grimminger F, Hoeper MM, Jansa P, Kim NH, Mayer E, Simonneau G, Wilkins MR, Fritsch A, Neuser D, Weimann G, Wang C; CHEST-1 Study Group. Riociguat for the treatment of chronic thromboembolic pulmonary hypertension. N Engl J Med. 2013;369(4):319-29. [CrossRef] [PubMed]
  2. Ghofrani HA, Galiè N, Grimminger F, Grünig E, Humbert M, Jing ZC, Keogh AM, Langleben D, Kilama MO, Fritsch A, Neuser D, Rubin LJ; PATENT-1 Study Group. Riociguat for the treatment of pulmonary arterial hypertension. N Engl J Med. 2013;369(4):330-40. [CrossRef] [PubMed] 
  3. Robbins RA. September 2013 pulmonary journal club: riociguat; pay the doctor. Southwest J Pulm Crit Care. 2013;7(3):190-2. [CrossRef]

Reference as: Mathew M. October 2013 pulmonary journal club: pulmonary artery hypertension. Southwest J Pulm Crit Care. 2013;7(4):267-8. doi: http://dx.doi.org/10.13175/swjpcc146-13 PDF

Monday
Jul292013

July 2013 Pulmonary Journal Club

Ghofrani HA, D'Armini AM, Grimminger F, Hoeper MM, Jansa P, Kim NH, Mayer E, Simonneau G, Wilkins MR, Fritsch A, Neuser D, Weimann G, Wang C; CHEST-1 Study Group. Riociguat for the treatment of chronic thromboembolic pulmonary hypertension. N Engl J Med. 2013;369:319-32. [CrossRef] [PubMed]

Chronic Thromboembolic Disease (CTED) leading to pulmonary hypertension has an incidence of 5000 cases per year. It is estimated that up to 3% of all patients with pulmonary embolism develop CTED within 2 years of initial pulmonary embolism event.

The diagnosis of CTED is made through a ventilation perfusion scan detecting chronic thromboembolic disease. Treatment of CTED centers on anticoagulation and surgical thromboendartectomy. Thromboendartectomy is a unique procedure offered only in a few specialized centers throughout the country. Pharmacologic agents in the treatment of CTED have been ineffective except for bosentan. Bosentan, an endothelin receptor antagonist, has been shown to decrease pulmonary vascular resistance but not improve 6 minute walk time. Riociguat is a soluble guanylate cyclase stimulator, which works by increasing levels of cyclic GMP levels, resulting in vasorelaxation.

This study is a randomized double blind placebo controlled 16 week phase 3 trial evaluating the efficacy and safety of riociguat. The study was performed between 2009 – 2012 within 26 countries and 89 centers. A total of 261 patients were included in the study. Patients were excluded if they were pharmacologic agents used in the treatment of pulmonary hypertension. The primary outcome of the study was the improvement in 6 minute walk distance. Secondary outcomes included changes in pulmonary vascular resistance, N terminal BNP levels, WHO functional classification, Dyspnea severity. Medication side effect profiles were also noted.

Patients were divided into 2 groups, 88 subjects in the placebo group and 173 subjects in the treatment group. The discrepancy in sample size was based on needing 173 subjects within the treatment arm to reach a power of 90%. The dose of riociguat was adjusted between 0.5 mg to 2.5mg three times a day based on tolerance to side effects. This dose adjustment was done over the first 8 weeks and then a stable dose maintained for the next 8 weeks. At the end of the 16 weeks outcomes and safety profiles were measured.

The results showed that riociguat improved 6 minute walk distance by a mean of 39 meters as opposed to a decline of 6 meters within placebo. Secondary outcomes were also favorable showing an improvement in cardiac output while decreasing the pulmonary vascular resistance and pulmonary pressures.

The side effects included right ventricular failure in 3% and syncope in 2% of the subjects, both of which were the same in the placebo group. Two percent of patients stopped the drug due to nausea, vomiting and headache and another 2% developed hemoptysis. Two patients died in the treatment arm secondary to drug related heart failure and acute renal failure.

The study demonstrated that riociguat may offer benefit in patients ineligible for thromboendartectomy. Further studies to evaluate longitudinal benefits and safety profiles are needed.

Manoj Mathew, MD FCCP MCCM

Reference as: Mathew M. July 2013 pulmonary journal club. Southwest J Pulm Crit Care. 2013;7(1):51-2. doi: http://dx.doi.org/10.13175/swjpcc097-13 PDF