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Annual General Meeting of the Irish Thoracic Society - IJMS | Irish ...

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51<br />

1<br />

SESSION FIVE ONE<br />

ANNUAL MEETING OF THE IRISH THORACIC SOCIETY • 11 - 12 November 2005 • WESTWOOD HOUSE HOTEL, GALWAY<br />

Session 5: Smoking / Lung Cancer<br />

ANNUAL MEETING OF THE IRISH THORACIC SOCIETY • 11 - 12 November 2005 • WESTWOOD HOUSE HOTEL, GALWAY<br />

5<br />

SESSION<br />

SESSION FIVE ONE<br />

5.1<br />

A study to compare <strong>the</strong> efficiency <strong>of</strong> sterile talc, tetracycline<br />

and bleomycin as sclerosing agents for medical pluerodesis<br />

in <strong>the</strong> treatment <strong>of</strong> malignant pleural effusions<br />

Background<br />

Malignant pleural effusion is a common<br />

complication <strong>of</strong> metastatic disease.Particularly<br />

lung cancer, that is <strong>of</strong>ten managed by drainage<br />

and medical pleurodesis. Sterile talc, tetracycline,<br />

and bleomycin have all been shown to be effective<br />

sclerosants. No randomized clinical trial has<br />

directly compared all three agents in <strong>the</strong> medical<br />

management <strong>of</strong> malignant pleural effusion.<br />

Methods<br />

A prospective, randomised trial was carried out across<br />

multiple sites between September 2001 and August<br />

2005. After complete drainage with symptom relief,<br />

patients with confirmed malignant pleural effusions,<br />

were allocated to receive intrapleural sterile talc (5g),<br />

tetracycline (1500mg) or bleomycin (60mg). Exclusion<br />

criteria included WHO performance status >2, small<br />

cell cancers and leukaemias. Primary outcome was<br />

response rate evaluated by radiographic improvement<br />

at one month after pleurodesis.<br />

Results<br />

Seventy patients were enrolled in <strong>the</strong> study; six<br />

patients were withdrawn before pleurodesis.<br />

Demographics and pleural fluid characteristics were<br />

comparable across all three groups. One patient<br />

randomised to talc experienced adult respiratory<br />

distress syndrome (ARDS).<br />

There was no significant difference in response rates<br />

between sclerosants. While <strong>the</strong>re was a significantly<br />

higher CRP response to pleurodesis in <strong>the</strong> talc group,<br />

this was not associated with an improved response<br />

rate at one month.<br />

Conclusion<br />

There was no difference in <strong>the</strong> efficacy <strong>of</strong> sterile talc,<br />

tetracycline and bleomycin as sclerosant agents<br />

in <strong>the</strong> medical management <strong>of</strong> malignant pleural<br />

effusions.<br />

TALC TETRACYCLINE BLEOMYCIN P-VALUES<br />

N 23 19 22<br />

CXR response at one month 79% 77% 88% ns<br />

Mean ΔCRP mg/L<br />

(Pre to Day 3 post pleurodesis)<br />

+156 +63 +43<br />

Talc:Tet, 0.023,<br />

Talc:Bleo, 0.004<br />

Tet: Bleo, 0.455<br />

MT Henry, 1 B Ladd, 1<br />

J Tuggey, 1 C Bowker, 1<br />

AG Arnold, 2<br />

1. Dept <strong>of</strong> Respiratory<br />

Medicine, Leeds<br />

<strong>General</strong> Infirmary,<br />

Leeds, UK<br />

2. Castle Hill Hospital,<br />

East Yorkshire, UK<br />

5.3<br />

material in 58.1% <strong>of</strong> all patients (68.8% <strong>of</strong> Group<br />

A and 46.3% <strong>of</strong> Group B). It was <strong>the</strong> only positive<br />

procedure in 11.6% (11.1% <strong>of</strong> Group A and 12.2%<br />

<strong>of</strong> Group B). A cytopathologist attended 51.2% <strong>of</strong><br />

procedures, resulting in a diagnostic TBNA in 63.6%.<br />

In comparison, TBNA was diagnostic in 42.8% when<br />

ROSE was not performed (p=0.053).<br />

Conclusions<br />

The results suggest that central TBNA compliments<br />

o<strong>the</strong>r diagnostic techniques in evaluation <strong>of</strong> <strong>the</strong><br />

visualized portion <strong>of</strong> <strong>the</strong> endobronchial tree, and may<br />

improve diagnostic yield. This appears to be fur<strong>the</strong>r<br />

enhanced by ROSE.<br />

Diagnostic yield <strong>of</strong> fluoroscopic-guided transbronchial<br />

needle aspiration <strong>of</strong> peripheral pulmonary lesions<br />

Introduction<br />

Peripheral pulmonary lesions which are not visible<br />

within <strong>the</strong> endobronchial tree usually require<br />

radiological or surgical techniques to provide tissue<br />

diagnosis. The role <strong>of</strong> transbronchial needle aspirate<br />

(TBNA) in central lesions is well documented.<br />

However it is not routinely utilized as part <strong>of</strong> <strong>the</strong><br />

evaluation <strong>of</strong> peripheral lesions.<br />

Method<br />

We carried out a retrospective analysis <strong>of</strong> all<br />

patients over a two-year period in whom TBNA<br />

was performed as part <strong>of</strong> <strong>the</strong> diagnostic work-up<br />

<strong>of</strong> peripheral pulmonary lesions. We compared <strong>the</strong><br />

overall yield <strong>of</strong> TBNA when rapid on-site cytologic<br />

evaluation (ROSE) was available with that when a<br />

cytopathologist was not available. We also compared<br />

<strong>the</strong> diagnostic yield <strong>of</strong> TBNA with that <strong>of</strong> BAL and<br />

transbronchial biopsy (TBBx) in those patients who<br />

had all 3 tests performed and had a final diagnosis <strong>of</strong><br />

malignancy.<br />

Results<br />

Of 146 patients in whom TBNA was perfomed, 143<br />

were available for analysis. Mean age was 66 years.<br />

A cytopathologist attended for 60% <strong>of</strong> all procedures<br />

resulting in a diagnositic TBNA in 50.4%. In<br />

comparison, only 25.9% <strong>of</strong> TBNAs yielded a diagnosis<br />

when ROSE was not performed (p=0.003).<br />

Malignancy was confirmed in 56 patients by a<br />

combination <strong>of</strong> TBNA, TBBx and BAL. TBNA was<br />

positive for malignancy in 43 (76.8%) <strong>of</strong> cases, and<br />

was <strong>the</strong> only positive diagnostic procedure in 12<br />

(21.4%). TBBx was positive in 36 (64.3%) and was <strong>the</strong><br />

only positive procedure in 10 (17.9%). BAL was positive<br />

in 19 (33.9%) but was <strong>the</strong> only positive procedure in<br />

only 2 cases (3.6%).<br />

Conclusions<br />

The addition <strong>of</strong> fluoroscopic-guided TBNA to BAL and<br />

TBBx enhances <strong>the</strong> diagnostic yield <strong>of</strong> bronchoscopy<br />

in peripheral lung cancer. This appears to be fur<strong>the</strong>r<br />

enhanced by ROSE.<br />

D Breen, D O’Callaghan,<br />

B Kent, S Nicholson,<br />

J Keane, F O’Connell<br />

Dept <strong>of</strong> Respiratory<br />

Medicine and<br />

Histopathology,<br />

St James’s Hospital,<br />

Dublin<br />

5.2<br />

Med. Survival (days) 96 102 201 ns<br />

Diagnostic usefulness <strong>of</strong> central transbronchial needle<br />

aspirate<br />

Introduction<br />

Central transbronchial needle aspiration (TBNA) is an<br />

established tool for sampling <strong>the</strong> visualized portion<br />

<strong>of</strong> <strong>the</strong> endobronchial tree. This may compliment<br />

o<strong>the</strong>r conventional diagnostic techniques routinely<br />

used at bronchoscopy, including airway lavage,<br />

brushings and biopsy.<br />

Method<br />

We carried out a review <strong>of</strong> all patients over a twoyear<br />

period in whom central TBNA was performed as<br />

part <strong>of</strong> <strong>the</strong>ir diagnostic work-up. We also compared<br />

<strong>the</strong> overall yield <strong>of</strong> TBNA when rapid on-site cytologic<br />

evaluation (ROSE) was available with that when a<br />

cytopathologist was not available.<br />

Results<br />

Central TBNA was carried out in 86 patients. Average<br />

age was 64.1 years. An endobronchial abnormality<br />

[Group A] was noted in 45 (52.3%) and <strong>the</strong> airways<br />

were entirely normal [Group B] in 41 (47.7%).<br />

Specimens obtained by TBNA contained diagnostic<br />

D O’Callaghan, D Breen,<br />

B Kent, S Nicholson,<br />

J Keane, F O’Connell<br />

Dept <strong>of</strong> Respiratory<br />

Medicine, CResT<br />

Directorate, St James’s<br />

Hospital, Dublin<br />

5.4<br />

The <strong>Irish</strong> workplace smoking ban; an analysis <strong>of</strong> <strong>the</strong><br />

exposure levels in Dublin bars<br />

Introduction<br />

On <strong>the</strong> 29 th March 2004, <strong>the</strong> <strong>Irish</strong> Government<br />

introduced legislation prohibiting <strong>the</strong> consumption<br />

<strong>of</strong> tobacco products in most workplaces.<br />

Controversially, <strong>the</strong> ban applied to <strong>the</strong> hospitality<br />

industry, including licensed premises. The time<br />

prior and subsequent to <strong>the</strong> introduction <strong>of</strong> <strong>the</strong> ban<br />

provided an opportunity to assess <strong>the</strong> exposure<br />

levels <strong>of</strong> particulates and benzene in Dublin pubs,<br />

and <strong>the</strong> effectiveness <strong>of</strong> <strong>the</strong> new legislation at<br />

protecting workers and patrons from unnecessary<br />

exposure to Environmental Tobacco Smoke<br />

Method<br />

Particulate levels (PM2.5 and PM10) were measured<br />

in 43 pubs, prior and subsequent to <strong>the</strong> introduction<br />

<strong>of</strong> <strong>the</strong> smoking ban, using a light scattering optical<br />

based instrument (Aerocet 531). For consistency<br />

purposes, repeat measurements were conducted<br />

on <strong>the</strong> same day <strong>of</strong> <strong>the</strong> week, and <strong>the</strong> same month,<br />

one year later from <strong>the</strong> original measurements.<br />

Simultaneously, benzene levels were monitored<br />

using passive benzene badges incorporating an<br />

activated carbon absorption element. In each public<br />

house, <strong>the</strong> benzene sampler was co-located with<br />

<strong>the</strong> AEROCET monitor, as near as possible to <strong>the</strong><br />

breathing zone.<br />

M McCaffrey, 1<br />

PG Goodman, 2<br />

L Clancy 3<br />

1. Dublin City Council<br />

2. Dublin Institute <strong>of</strong><br />

Technology,<br />

3. Research Institute<br />

for a Tobacco Free<br />

<strong>Society</strong><br />

50 IRISH JOURNAL OF MEDICAL SCIENCE • VOLUME 174 • NUMBER 4 • SUPPLEMENT 3<br />

IRISH JOURNAL OF MEDICAL SCIENCE • VOLUME 174 • NUMBER 4 • SUPPLEMENT 3 51

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