INTERSTITIAL LASER PHOTOCOAGULATION OF NORMAL LUNG PARENCHYMA IN RATS

Citation
Di. Fielding et al., INTERSTITIAL LASER PHOTOCOAGULATION OF NORMAL LUNG PARENCHYMA IN RATS, Thorax, 53(8), 1998, pp. 692-697
Citations number
19
Categorie Soggetti
Respiratory System
Journal title
ThoraxACNP
ISSN journal
00406376
Volume
53
Issue
8
Year of publication
1998
Pages
692 - 697
Database
ISI
SICI code
0040-6376(1998)53:8<692:ILPONL>2.0.ZU;2-Y
Abstract
Background-Management of peripheral lung tumours may be risky in patie nts with poor lung function or in the elderly. A new possibility is in terstitial laser photocoagulation (ILP) in which tumours are gently co agulated using thin laser fibres placed percutaneously under radiologi cal guidance. This could have a useful palliative role in selected pat ients, but to be safe the effects on normal lung parenchyma must first be understood. This paper describes the creation and healing of ILP l esions in the normal rat lung. Methods-ILP was performed using single laser fibres placed percutaneously in the left lung of normal rats und er general anaesthetic with radiological guidance (laser power 1-3 W a t 805 nm, treatment time 250-1000 s). The lesion size and healing were studied in rats killed at times from three days to six months after t reatment, the bursting pressure was measured, and any complications no ted. Results-Zones of necrosis up to 12 mm in diameter were produced, the size depending on the laser power and treatment time. Histological examination showed typical thermal effects with complete healing with fibrosis by two months. The effect was very localised with remarkably little effect on the structure and function of the rest of the lung. Adverse effects in the lung parenchyma only occurred if the ILP lesion involved the hilar vessels or the oesophagus, causing pulmonary conge stion and perforation, respectively. Pneumothorax was seen in 6% of ca ses. Conclusions-ILP with a single fibre can produce a localised zone of necrosis in normal lung parenchyma which heals safely and which has Little effect on the rest of the lung. Further study of this techniqu e using multiple fibres in a larger animal model is warranted to see i f it is feasible and safe to produce a large enough volume of necrosis to be of value in the treatment of small peripheral lung tumours in p atients who are unsuitable for surgery or palliative radiotherapy.