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Dive into the research topics where Alessia Stanzi is active.

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Featured researches published by Alessia Stanzi.


Transplant International | 2015

A decade of extended-criteria lung donors in a single center: was it justified?

Jana Somers; David Ruttens; Stijn Verleden; Bianca Cox; Alessia Stanzi; Elly Vandermeulen; Robin Vos; Bart Vanaudenaerde; Geert Verleden; Hans Van Veer; Willy Coosemans; Herbert Decaluwé; Philippe Nafteux; Paul De Leyn; Dirk Van Raemdonck

Despite a worldwide need to expand the lung donor pool, approximately 75% of lung offers are not accepted for transplantation. We investigated the impact of liberalizing lung donor acceptance criteria during the last decade on the number of effective transplants and early and late outcomes in our center. All 514 consecutive lung transplants (LTx) performed between Jan 2000 and Oct 2011 were included. Donors were classified as matching standard criteria (SCD; n = 159) or extended criteria (ECD; n = 272) in case they fulfilled at least one of the following criteria: age >55 years, PaO2/FiO2 at PEEP 5 cmH2O < 300 mmHg at time of offer, presence of abnormalities on chest X‐ray, smoking history, presence of aspiration, presence of chest trauma, or donation after circulatory death. Outcome parameters were primary graft dysfunction (PGD) grade at 0, 12, 24, and 48 h after LTx, time to extubation, stay in intensive care unit (ICU), early and late infection, acute rejection and bronchiolitis obliterans syndrome (BOS), and survival. Two hundred and seventy‐two recipients (63.1%) received ECD lungs. PGD grade at T0 was similar between groups, while at T12 (<0.01), T24 (<0.01), and T48 (<0.05), PGD3 was observed more often in ECDs. ICU stay (P < 0.05) was longer in ECDs compared with SCDs. Time to extubation, respiratory infections, acute rejection, lymphocytic bronchiolitis, BOS, and survival were not different between groups. Accepting ECDs contributed in increasing the number of lung transplants performed in our center. Although this lung donor strategy has an impact on early postoperative outcome, liberalizing criteria did not influence long‐term outcome after LTx.


European Journal of Cardio-Thoracic Surgery | 2016

Central tumour location should be considered when comparing N1 upstaging between thoracoscopic and open surgery for clinical stage I non-small-cell lung cancer

Herbert Decaluwé; Alessia Stanzi; Christophe Dooms; Steffen Fieuws; Willy Coosemans; Lieven Depypere; Christophe Deroose; Walter Dewever; Philippe Nafteux; Stéphanie Peeters; Hans Van Veer; Eric Verbeken; Dirk Van Raemdonck; Johnny Moons; Paul De Leyn

OBJECTIVES Nodal upstaging is a quality indicator for oncological thoracic surgery and is found in up to 25% of patients with clinical stage I (cStage-I) non-small-cell lung cancer (NSCLC). In large retrospective series, lower N1 upstaging was reported after video-assisted thoracic surgery (VATS) resections. We studied the impact of central primary tumour location on nodal upstaging in cStage-I NSCLC. METHODS Consecutive patients operated for cStage-I NSCLC were selected from a prospectively managed surgical database. Tumour location was classified as central if the lesion was visible during standard video bronchoscopy. A nodal station mapping was drawn for each patient based on final pathological examination. Univariable and additive multivariable binary logistic regression analyses were performed. RESULTS Between 2007-2014, 334 patients underwent anatomical resection for cStage-I NSCLC, either by open thoracotomy (n = 158) or by VATS (n = 176; conversion rate 1.7%). All patients underwent imaging with [(18)F]-fluorodeoxyglucose positron emission tomography and computer tomography. Invasive mediastinal staging was performed in 24.6% of patients. There were more central tumours in the open group (24.1%, n = 38) compared with the VATS group (4.5%, n = 8). There was no significant difference between the number (mean ± standard deviation) of nodal stations examined (open 5 ± 1.9 vs VATS 5 ± 1.7, P = 0.99). Pathological nodal upstaging was found in 15.9% (n = 53) of cStage-I patients. Nodal pN1 and pN2 upstaging were 13.3 and 8.2%, respectively, for the open group, and 6.3 and 4.5%, respectively, for the VATS group. In 32.6% (n = 15/46) of patients with a central cStage-I tumour pN1, upstaging was found. A binary logistic regression model (including tumour location, technique, tumour size, gender and histology) showed that only tumour location had a significant impact on pN1 upstaging [peripheral versus central; odds ratio (OR) 5.07 (confidence interval, CI: 1.89-13.60), P = 0.001], while surgical technique had no significant impact [VATS versus open; OR 0.74 (CI: 0.31-1.78), P = 0.50]. CONCLUSIONS The number of lymph node stations examined during VATS resections is similar to open resections for cStage-I NSCLC. Almost one-third of the patients with a central cStage-I NSCLC were upstaged to pN1. Tumour location was the only independent variable for pN1 upstaging in logistic regression analysis. It is a potential bias in retrospective studies and should therefore be accounted for when comparing different surgical resection techniques for cStage-I NSCLC.


Transplantation Proceedings | 2014

Lobar Lung Transplantation From Deceased Donors: A Valid Option for Small-Sized Patients With Cystic Fibrosis

Alessia Stanzi; Herbert Decaluwé; Willy Coosemans; P. De Leyn; Philippe Nafteux; H. Van Veer; Lieven Dupont; Geert Verleden; D. Van Raemdonck

BACKGROUND Small-sized patients with cystic fibrosis usually face long waiting times for a suitable lung donor. Reduced-size lung transplantation (LTx) was promoted to shorten waiting times. We compared donor and recipient characteristics and outcome in lobar ([L]) versus full-size ([FS]) lung recipients. METHODS Between July 1, 1991, and February 28, 2011, 535 isolated LTx were performed, including 74 in cystic fibrosis patients (8 L, 66 FS). Patients were followed up until September 2012. RESULTS [L] recipients were younger, smaller, and lighter. Sex, waiting times, and donor data (age, sex, height, weight, PaO2/FiO2, and ventilation time) were comparable. Cardiopulmonary bypass was used more often in [L]; cold ischemia was comparable for first lung but longer in [L] for second lung; implantation times were comparable. In-hospital mortality rate was 0% in [L] versus 3% in [FS]. Both intensive care unit and hospital stay were longer in [L]. Grade 3 primary graft dysfunction was more pronounced in [L] at T0 and at T48. FEV1 increased significantly in both groups from preoperative value. Bronchiolitis obliterans syndrome was absent in [L] and diagnosed in 18 patients in [FS], accounting for 6 of 15 late deaths. All [L] are still alive. No differences in survival were found between the groups. CONCLUSIONS Although hindered by a higher incidence of primary graft dysfunction, L-LTx is a viable option with excellent survival and pulmonary function comparable to FS-LTx.


European Journal of Cardio-Thoracic Surgery | 2018

Is central lung tumour location really predictive for occult mediastinal nodal disease in (suspected) non-small-cell lung cancer staged cN0 on 18F-fluorodeoxyglucose positron emission tomography–computed tomography?

Herbert Decaluwé; Johnny Moons; Steffen Fieuws; Walter De Wever; Christophe Deroose; Alessia Stanzi; Lieven Depypere; Kristiaan Nackaerts; Johan Coolen; Maarten Lambrecht; Eric Verbeken; Dirk De Ruysscher; Johan Vansteenkiste; Dirk Van Raemdonck; Paul De Leyn; Christophe Dooms

OBJECTIVES Current guidelines recommend preoperative invasive mediastinal staging in centrally located tumours with negative mediastinum on positron emission tomography-computed tomography, based on a 20-30% prevalence of occult mediastinal disease (pN2-3). However, a uniform definition of central tumour location is lacking. Our objective was to determine the best definition in predicting occult pN2-3. METHODS A single-institution database was queried for patients with (suspected) non-small-cell lung cancer staged cN0 after positron emission tomography-computed tomography and referred to invasive staging and/or primary surgery. We evaluated 5 definitions: inner 1/3, inner 2/3, contact with bronchovascular structures, ≤2 cm from bronchus or endobronchial visualization. RESULTS Between 2005 and 2015, 813 patients were eligible (cT1: 42%, cT2: 28%, cT3: 17% and cT4: 11%). Invasive mediastinal staging and resection were performed in 30% and 97% of patients, respectively. Any nodal upstaging (pN+) was found in 21% of patients, of whom pN2-3 was found in 8%. Central tumour location demonstrated 4 times higher odds for any pN+ [for inner 1/3 vs outer 2/3, odds ratio 3.90 (95% confidence interval 2.24-6.77), P < 0.001], whereas no significantly different odds was observed for pN2-3. The discriminative ability for pN+ was not significantly different between the several definitions. CONCLUSIONS The prevalence of occult pN2-3 was only 8% when modern fusion positron emission tomography-computed tomography imaging pointed at clinical N0 non-small-cell lung cancer. None of the 5 verified definitions of centrality was predictive for occult pN2-3. However, each definition of centrality was related to any pN+ at a prevalence of 21%, without significant differences in discriminative ability between definitions. These data question whether indication for preoperative invasive mediastinal staging should be based on centrality alone.


Clinical Respiratory Journal | 2018

Tailored intraoperative localization of non-palpable pulmonary lesions for thoracoscopic wedge resection using hybrid room technology

Alessia Stanzi; Federico Mazza; Francesco Lucio; Donatella Ghirardo; Maurizio Grosso; Alessandro Locatelli; Giulio Melloni

VATS wedge resection can require conversion to thoracotomy when pulmonary lesions cannot be identified. Hybrid operating rooms (HORs) provide real‐time image acquisition capabilities allowing the intraoperative placement of markers to facilitate the removal of non‐palpable nodules during VATS.


Interactive Cardiovascular and Thoracic Surgery | 2015

Thoracoscopic tunnel technique for anatomical lung resections: a ‘fissure first, hilum last’ approach with staplers in the fissureless patient

Herbert Decaluwé; Youri Sokolow; Frederic F. Deryck; Alessia Stanzi; Lieven Depypere; Johnny Moons; Dirk Van Raemdonck; Paul De Leyn


Journal of Surgical Research | 2014

Do we need to cool the lung graft after ex vivo lung perfusion? A preliminary study

Alessia Stanzi; Arne Neyrinck; Jana Somers; Hans Cauwenberghs; Eric Verbeken; Luigi Santambrogio; Dirk Van Raemdonck


Interactive Cardiovascular and Thoracic Surgery | 2015

V-065IDENTIFICATION OF THE INTER-SEGMENTAL PLANE BY PUNCTURE AND INSUFFLATION OF THE TRANSECTED BRONCHUS DURING VIDEO-ASSISTED THORACOSCOPIC ANATOMICAL SEGMENTECTOMIES

Herbert Decaluwé; Lieven Depypere; Alessia Stanzi; Lc Silva Corten; Willy Coosemans; Philippe Nafteux; J Moons; Hans Van Veer; Dirk Van Raemdonck; Paul De Leyn


Transplant International | 2011

CADAVERIC LOBAR LUNG TRANSPLANT: A VALID OPTION FOR SMALL-SIZED CF PATIENTS

Alessia Stanzi; Joyce Tiek; Shana Wauters; Herbert Decaluwé; Willy Coosemans; Paul De Leyn; Philippe Nafteux; Lieven Dupont; Geert Verleden; Dirk Van Raemdonck


Journal of the American College of Cardiology | 2018

TCT-643 Antiplatelet therapy with cangrelor in patients undergoing surgery after coronary stent implantation: a real-world bridging protocol experience

Roberta Rossini; Giulia Masiero; Fabrizio Rolfo; Federico Pappalardo; Claudia Fruttero; Enrico Passamonti; Elba Calvaruso; Moreno Cecconi; Cesare Carlucci; Elisa Bertone; Nicoletta Barzaghi; Giulio Melloni; Alessia Stanzi; Alessandro Locatelli; Giorgio Baralis; Dominick J. Angiolillo; Giuseppe Musumeci

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Herbert Decaluwé

Katholieke Universiteit Leuven

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Dirk Van Raemdonck

Katholieke Universiteit Leuven

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Philippe Nafteux

Katholieke Universiteit Leuven

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Paul De Leyn

The Catholic University of America

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Willy Coosemans

Free University of Brussels

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Lieven Depypere

Katholieke Universiteit Leuven

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Hans Van Veer

Katholieke Universiteit Leuven

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Geert Verleden

Katholieke Universiteit Leuven

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Arne Neyrinck

Katholieke Universiteit Leuven

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Christophe Dooms

Katholieke Universiteit Leuven

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