George Alex Eapen

Dr. George Alex Eapen


Research Focus & Metrics

Academic Career Length

21Years (2006-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 May 2019 in Medical Clinics of North America
Verified
Journal Article
Closed access
FNFaria Nasim
Faria Nasim
BSBruce F. Sabath
Bruce F. Sabath
GEGeorge Alex Eapen
George Alex Eapen

1 April 2013 in Chest
Verified
Journal Article
Closed access
GEGeorge Alex Eapen
George Alex Eapen
ASArchan M. Shah
Archan M. Shah
XLXiudong Lei
Xiudong Lei
CJCarlos A. Jimenez
Carlos A. Jimenez
RMRodolfo C. Morice
Rodolfo C. Morice
DODavid Ost
David Ost

1 April 2008 in Thorax
Verified
Journal Article
Open access
PDF file
MKM P Kennedy
M P Kennedy
CJC A Jimenez
C A Jimenez
JBJ F Bruzzi
J F Bruzzi
AMA D Mhatre
A D Mhatre
XLX Lei
X Lei
GEGeorge Alex Eapen
George Alex Eapen
Background: The diagnostic accuracy of endobronchial ultrasound-guided transbronchial needle aspiration (EBUS-TBNA) for the diagnosis of lymphoma in patients with mediastinal lymphadenopathy is not well defined. Methods: A retrospective review was performed of all patients with mediastinal lymphadenopathy referred for EBUS-TBNA between August 2005 and December 2006 in whom lymphoma was suspected based on prior history or clinical presentation. Mediastinal biopsy specimens were taken using a linear array ultrasonic bronchoscope (Olympus XBF-UC 160F) and a 22-gauge cytology needle (NA-202C Olympus) with on-site cytopathological support. The EBUS-TBNA result was compared with a reference standard of pathological tissue diagnosis or a composite of ⩾6 months of clinical follow-up with radiographic imaging. Results: Of 236 patients who underwent EBUS-TBNA, 25 were eligible for inclusion. Indications for EBUS-TBNA were suspected mediastinal recurrence of lymphoma (n = 13) and mediastinal lymphadenopathy of unknown cause (n = 12). Adequate lymph node sampling was accomplished in 24/25 patients (96%); there were no complications. EBUS-TBNA identified lymphoma in 10 patients and benign disease in 14 patients. There was one false negative EBUS-TBNA for lymphoma (lymphoma prevalence 11/25 (44%)). Follow-up over a median of 10.5 months (range 1–19) confirmed stable or regressive lymphadenopathy in all 14 patients without a lymphoma diagnosis, consistent with a benign diagnosis. Overall, EBUS-TBNA had a sensitivity of 90.9%, specificity of 100%, positive predictive value of 100% and negative predictive value of 92.9% for the diagnosis of lymphoma. Conclusions: EBUS-TBNA is an accurate, safe and useful tool in the investigation of suspected lymphoma with isolated mediastinal adenopathy, and may diminish the need for more invasive procedures such as mediastinoscopy.

1 September 2017 in Journal of Thoracic Disease
Verified
Journal Article
Closed access
PDF file
LMLakshmi Mudambi
Lakshmi Mudambi
RMRussell Miller
Russell Miller
GEGeorge Alex Eapen
George Alex Eapen
This review comprehensively describes recent advances in the management of malignant central airway obstruction (CAO). Malignant CAO can be a dramatic and devastating manifestation of primary lung cancer or metastatic disease. A variety of diagnostic modalities are available to provide valuable information to plan a therapeutic intervention. Clinical heterogeneity in the presentation of malignant CAO provides opportunities to adapt and utilize endoscopic technology and tools in many ways. Mechanical debulking, thermal tools, cryotherapy and airway stents are methods and instruments used to rapidly restore airway patency. Delayed bronchoscopic methods, such as photodynamic therapy (PDT) and brachytherapy can also be utilized in specific non-emergent situations to establish airway patency. Although data regarding the success and complications of therapeutic interventions are retrospective and characterized by clinical and outcome measure variability, the symptoms of malignant CAO can often be successfully palliated. Assessment of risks and benefits of interventions in each individual patient during the decision-making process forms the critical foundation of the management of malignant CAO.

1 March 2018 in Clinics in Chest Medicine
Verified
Journal Article
Closed access
RMRussell J. Miller
Russell J. Miller
RCRoberto F. Casal
Roberto F. Casal
DLDonald R. Lazarus
Donald R. Lazarus
DODavid E. Ost
David E. Ost
GEGeorge Alex Eapen
George Alex Eapen

30 August 2017 in Respirology
Verified
Journal Article
Open access
PDF file
MVMacarena R. Vial
Macarena R. Vial
OOOisin J. O'Connell
Oisin J. O'Connell
HGHoriana B. Grosu
Horiana B. Grosu
MHMike Hernandez
Mike Hernandez
LNLaila Noor
Laila Noor
GEGeorge Alex Eapen
George Alex Eapen
Background and objective: Standard nodal staging of lung cancer consists of positron emission tomography/computed tomography (PET/CT), followed by endobronchial ultrasound‐guided transbronchial needle aspiration (EBUS‐TBNA) if PET/CT shows mediastinal lymphadenopathy. Sensitivity of EBUS‐TBNA in patients with N0/N1 disease by PET/CT is unclear and largely based on retrospective studies. We assessed the sensitivity of EBUS‐TBNA in this setting.Methods: We enrolled patients with proven or suspected lung cancer staged as N0/N1 by PET/CT and without metastatic disease (M0), who underwent staging EBUS‐TBNA. Primary outcome was sensitivity of EBUS‐TBNA compared with a composite reference standard of surgical stage or EBUS‐TBNA stage if EBUS demonstrated N2/N3 disease.Results: Seventy‐five patients were included in the analysis. Mean tumour size was 3.52 cm (±1.63). Fifteen of 75 patients (20%) had N2 disease. EBUS‐TBNA identified six while nine were only identified at surgery. Sensitivity of EBUS‐TBNA for N2 disease was 40% (95% CI: 16.3–67.7%).Conclusion: A significant proportion of patients with N0/N1 disease by PET/CT had N2 disease (20%) and EBUS‐TBNA identified a substantial fraction of these patients, thus improving diagnostic accuracy compared with PET/CT alone. Sensitivity of EBUS‐TBNA however appears lower compared with historical data from patients with larger volume mediastinal disease. Therefore, strategies to improve EBUS‐TBNA accuracy in this population should be further explored