Continuous and bimonthly publication
ISSN (on-line): 1806-3756

Licença Creative Commons
5665
Views
Back to summary
Open Access Peer-Reviewed
Artigo Original

Effects of positive expiratory pressure on pulmonary clearance of aerosolized technetium-99m-labeled diethylenetriaminepentaacetic acid in healthy individuals

Efeitos da pressão expiratória positiva na depuração pulmonar do ácido dietilenotriaminopentacético marcado com tecnécio-99m em aerossol em indivíduos saudáveis

Isabella Martins de Albuquerque1, Dannuey Machado Cardoso2, Paulo Ricardo Masiero3, Dulciane Nunes Paiva4, Vanessa Regiane Resqueti5, Guilherme Augusto de Freitas Fregonezi5, Sérgio Saldanha Menna-Barreto6

DOI: http://dx.doi.org/10.1590/S1806-37562015000000320

ABSTRACT

Objective: To evaluate the effects of positive expiratory pressure (PEP) on pulmonary epithelial membrane permeability in healthy subjects. Methods: We evaluated a cohort of 30 healthy subjects (15 males and 15 females) with a mean age of 28.3 ± 5.4 years, a mean FEV1/FVC ratio of 0.89 ± 0.14, and a mean FEV1 of 98.5 ± 13.1% of predicted. Subjects underwent technetium-99m-labeled diethylenetriaminepentaacetic acid (99mTc-DTPA) radioaerosol inhalation lung scintigraphy in two stages: during spontaneous breathing; and while breathing through a PEP mask at one of three PEP levels-10 cmH2O (n = 10), 15 cmH2O (n = 10), and 20 cmH2O (n = 10). The 99mTc-DTPA was nebulized for 3 min, and its clearance was recorded by scintigraphy over a 30-min period during spontaneous breathing and over a 30-min period during breathing through a PEP mask. Results: The pulmonary clearance of 99mTc-DTPA was significantly shorter when PEP was applied-at 10 cmH2O (p = 0.044), 15 cmH2O (p = 0.044), and 20 cmH2O (p = 0.004)-in comparison with that observed during spontaneous breathing. Conclusions: Our findings indicate that PEP, at the levels tested, is able to induce an increase in pulmonary epithelial membrane permeability and lung volume in healthy subjects.

Keywords: Lung/metabolism; Technetium Tc 99m pentetate/pharmacokinetics; Radiopharmaceuticals; Positive-pressure respiration.

RESUMO

Objetivo: Avaliar os efeitos da pressão expiratória positiva (PEP) na permeabilidade da membrana epitelial pulmonar em indivíduos saudáveis. Métodos: Foi avaliada uma coorte de 30 indivíduos saudáveis (15 homens e 15 mulheres), com média de idade de 28,3 ± 5,4 anos, média da relação VEF1/CVF de 0,89 ± 0,14 e média de VEF1 de 98,5 ± 13,1% do previsto. Os indivíduos foram submetidos a cintilografia pulmonar por inalação de radioaerossol de ácido dietilenotriaminopentacético marcado com tecnécio-99m (99mTc-DTPA em inglês) em dois estágios: durante respiração espontânea e durante respiração com uma máscara de PEP de 10 cmH2O (n = 10), 15 cmH2O (n = 10) ou 20 cmH2O (n = 10). O 99mTc-DTPA foi nebulizado por 3 min, e sua depuração foi registrada por cintilografia por um período de 30 min durante respiração espontânea e por um período de 30 min durante a respiração com uma máscara de PEP. Resultados: A depuração pulmonar do 99mTc-DTPA foi significativamente menor quando PEP foi aplicada a 10 cmH2O (p = 0,044), 15 cmH2O (p = 0,044) e 20 cmH2O (p = 0,004), em comparação com a observada durante a respiração espontânea. Conclusões: Nossos achados indicam que o uso de PEP nos níveis testados pode induzir um aumento na permeabilidade da membrana epitelial pulmonar e no volume pulmonar em indivíduos saudáveis.

Palavras-chave: Pulmão/metabolismo; Pentetato de tecnécio Tc 99m/farmacocinética; Compostos radiofarmacêuticos; Respiração com pressão positiva.

INTRODUCTION

The alveolar-capillary barrier, also known as the blood-gas barrier, is excellent at maintaining the separation be-tween alveolar air and pulmonary capillary blood, allowing rapid, efficient exchange of respiratory gases while pre-venting the diffusion of water-soluble particles suspended in alveolar air.(1,2) The integrity of the blood-gas barrier is extremely important to the maintenance of pulmonary homeostasis. In 1953, Frank Low published the first high-resolution electron micrographs of the human pulmonary blood-gas barrier, showing that a structure only 0.3 µm thick separates capillary blood from alveolar gas, which suggested that the barrier might be vulnerable to mechanical failure if the capillary pressure increased(3) or in states of high lung inflation, in which the capillary wall is under tension because of longitudinal stress in the alveolar walls.(4)

Technetium-99m-labeled diethylenetriaminepentaacetic acid (99mTc-DTPA) radioaerosol inhalation lung scintigraphy is a rapid, easily performed, extremely sensitive, noninvasive technique for assessing lung epithelial permeabil-ity.(5,6) When inhaled, 99mTc-DTPA particles arrive at the alveolar epithelial surface and then diffuse from the air space into the vascular space. The clearance rate of 99mTc-DTPA is a reliable index of alveolar epithelial permeability. Therefore, 99mTc-DTPA aerosol-inhaled scintigraphy has been used in numerous experiments and clinical investiga-tions designed to assess the integrity of the respiratory epithelium.(7,8)

Positive expiratory pressure (PEP) therapy involves breathing with slightly active expiration against mild expiratory resistance (typically 10-20 cmH2O).(9) Its application via a PEP mask represents a reliable, safe, low-cost intervention that can increase lung volumes and intrathoracic pressure.(10,11) It has been shown to improve lung volume, promote dilation of the airways, and decrease pulmonary resistance. The purpose of PEP therapy is to increase the transpul-monary pressure gradient and improve pulmonary expansion, which consequently improves oxygenation and the response to inhaled bronchodilators.(12,13)

The effects of different intensities of PEP on the pulmonary clearance of 99mTc-DTPA in healthy subjects have been largely unexplored in the literature and require further elucidation. Therefore, the aim of the present study was to evaluate the effects of PEP on pulmonary epithelial membrane permeability in healthy subjects.

METHODS

We studied 30 healthy subjects (15 men and 15 women). The mean age was 28.3 ± 5.4 years. Subjects with cardi-ovascular or neuromuscular disease were excluded, as were those with a history of smoking or respiratory disease, as well as those who were pregnant. All participants were recruited from a tertiary care hospital in the city of Porto Alegre, Brazil, and were evaluated between January and July of 2012. The study was approved by the Research Ethics Committee of the Porto Alegre Hospital de Clínicas (Protocol no. 04-418), which is accredited by the Brazilian National Commission on Research Ethics, and all subjects gave written informed consent.

Pulmonary scintigraphy with 99mTc-DTPA radioaerosol was conducted over two 30-min periods: during spontaneous breathing; and while subjects were breathing via a PEP mask (Vital Signs/GE Healthcare, Totowa, NJ, USA), which we adapted to fit each subject by using headgear, coupled to a PEP therapy device (Resistex®; Mercury Medical, Clear-water, FL, USA). Using computer-generated randomization codes, we divided the subjects into three groups: those receiving PEP at 10 cmH2O (PEP10); those receiving PEP at 15 cmH2O (PEP15); and those receiving PEP at 20 cmH2O (PEP20). During data acquisition, the subjects were in a sitting position with their hands on their thighs and their arms held away from their body. For each subject, the spontaneous breathing period served as the control.

A spirometer (MasterScreen v4.31; Jaeger, Würzburg, Germany) was used in order to measure FEV1 and FVC. The technical procedures, acceptability criteria, and reproducibility criteria, as well as standardization of measures, were in accordance with the guidelines established by the Brazilian Thoracic Association.(14) Subjects received instruction regarding the procedures to be performed during the spirometry assessment. The spirometer was routinely calibrated (on a daily basis) with a 3-L syringe in order to compensate for ambient temperature conditions. A minimum of three and a maximum of eight tests were conducted with a 1-min interval between them. Three reproducible maneuvers were performed, and the best curve was considered for the study. Results are expressed as absolute and percent-of-predicted values.(15)

The 99mTc-DTPA was chelated by adding 99mTc-pertechnetate (99mTc-O4−, IPEN-TEC; Institute for Energy Research and Nuclear Science, São Paulo, Brazil) to 740 MBq (20 mCi) of DTPA (Institute for Energy Research and Nuclear Sci-ence) in 5 mL of normal saline. Using instant thin layer chromatography, we determined the labeling efficiency to be above 98%. The solution was placed in the reservoir of the nebulizer (Aerogama Medical, Porto Alegre, Brazil) and was inhaled by the volunteer during 3 min of normal tidal breathing, with an oxygen flow rate of 9 L/min. During nebulization, the subjects remained under supervision, which allowed us to verify the appropriate performance of the inhalation maneuvers, as well as to correct any errors in inhalation techniques. The subjects were placed in a sitting position in front of a gamma camera (Starcam 4000i; GE Medical Systems, Milwaukee, WI, USA), and images were obtained every 20 s over a 30-min period. Two regions of interest were defined-the left lung and the right lung-and were drawn manually, a time-activity curve being constructed by the same investigator. For each lung, we employed the negative slope of the curve to define clearance, using the minimum and maximum clearance values. The 99mTc-DTPA clearance rate was expressed as its half-time (T1/2)-i.e., the time for its activity to decrease to 50% of the peak value.

All statistical analyses were performed with the SPSS Statistics software package, version 20.0 (IBM Corp., Ar-monk, NY, USA). The normality of the variables was assessed with the Shapiro-Wilk test. Categorical data are pre-sented as absolute and relative frequencies. Continuous data with normal distribution are expressed as means and standard deviations. Anthropometric variables and lung function parameters were compared among groups by one-way ANOVA (with the exception of gender, which was compared by the chi-square test). The difference in T1/2 among groups was determined with one-way analysis of covariance, with body weight, height, and body mass index (BMI) as the dependent variables. The influence of the pressure levels on T1/2 was compared among the groups by two-way ANOVA. The level of statistical significance was set at 5% (p<0.05).

RESULTS

We evaluated 30 healthy subjects (15 males and 15 females), with a mean age of 28.26 ± 5.40 years, a mean FEV1/FVC ratio of 0.89 ± 0.14, and a mean FEV1 of 98.5 ± 13.1% of the predicted value. The anthropometric and lung function parameters are presented in Table 1. The spirometric parameters were similar among the three study groups. Body weight, height, and BMI were higher in the PEP20 group than in the PEP15 group (p = 0.038, p = 0.027, and p = 0.015, respectively). The 99mTc-DTPA pulmonary clearance rate was not found to correlate significantly with age (r = −0.120; p = 0.951), body weight (r = 0.115; p = 0.545), height (r = 0.085; p = 0.655), or BMI (r = 0.120; p = 0.528). In the analysis of the results related to the 99mTc-DTPA pulmonary clearance rate, we considered the mean values for the left and right lungs together, given that the difference between the two lungs was not found to be statis-tically significant in the PEP10 group (p = 0.258), the PEP15 group (p = 0.908), or the PEP20 group (p = 0.570).
 



In comparison with the value obtained during spontaneous breathing, the mean T1/2 was significantly lower in the PEP10 group-90.3 ± 25.4 min versus 73.3 ± 30.6 min (p = 0.044), as can be seen in Figure 1. That difference was also significant in the PEP15 group-89.8 ± 28.9 min versus 63.1 ± 22.1 min (p = 0.044)-and in the PEP20 group-99.3 ± 49.6 min versus 64.5 ± 29.6 min (p = 0.004). Regarding the delta variation in T1/2 values, no statistically significant difference was found among the groups (p = 0.322).
 



DISCUSSION

To our knowledge, this was the first study to investigate the effects that different levels of PEP (10, 15, and 20 cmH2O) have on the rate of pulmonary clearance of 99mTc-DTPA. We demonstrated that PEP was able to induce in-creases in epithelial permeability, at all of the levels tested. Another important finding is that no significant variation in pulmonary clearance rate was observed among the three groups under the effects of any of the three PEP levels.

The effect of positive end-expiratory pressure (PEEP) on solute clearance has been described as a sigmoidal dose-response relationship dependent on the pressure level applied (5-15 cmH2O); in other words, the rate of pulmonary clearance of 99mTc-DTPA accelerates exponentially due to the increase in lung volume caused by the administration of different PEEP levels.(16) Contrary to our hypothesis, we did not find any differences among the three levels of PEP. In accordance with our results, the study conducted by Bishai et al.(17) showed an increase in the pulmonary epithelial permeability in mice at a PEEP level of 10 cmH2O. This difference in pulmonary clearance might be because mice have smaller alveoli and are probably more sensitive to the distension of inter-epithelial junctions of the alveolar epithelium induced by the application of lower pressure levels.

Our findings differ from those reported by Paiva et al.,(18) who assessed the permeability of the alveolar epithelial membrane in 36 healthy individuals submitted to 10 cmH2O and 20 cmH2O under continuous positive airway pressure (CPAP). The authors showed that 20 cmH2O of CPAP induced an increase in epithelial permeability, whereas 10 cmH2O of CPAP did not.

Previous studies in humans,(19) sheep,(20,21) and dogs(22,23) showed that the application of PEEP increases lung vol-ume and accelerates the rate of pulmonary clearance of 99mTc-DTPA. Therefore, the increased end-expiratory lung volume produced by PEP reduces airway resistance and promotes an increase in functional residual capacity.(24) However, other factors, such as airway/alveolar distension, prevention of alveolar collapse during expiration, and recruitment of collapsed alveoli, can also increase functional residual capacity.(25)

In keeping with the findings of the present study, Suzuki et al.(26) observed that, during the application of 20 cmH2O of PEEP, pulmonary clearance of 99mTc-DTPA increased but returned to baseline values when PEEP was discontinued. That suggests that the increase in the 99mTc-DTPA pulmonary clearance rate achieved through the application of PEEP is reversible after breathing returns to atmospheric pressure levels.

The mechanisms by which pulmonary insufflation accelerates the pulmonary clearance of 99mTc-DTPA remain un-clear. Some authors attribute this effect to an increase in the alveolar surface area available for diffusion,(22) due to either the increase in epithelial permeability,(27) functional alterations in the surfactant layer,(28) or distension of the intercellular junctions of the alveolar epithelium.(29)

The present study has some limitations. First, we evaluated subjects with healthy lungs. Therefore, any conclusions drawn from this study cannot be applied to patients with lung disease. This needs to be investigated in different, clearly specified disease groups, especially because PEP is not usually applied in patients with healthy lungs. Sec-ond, the upper airway critical closing pressure was not measured. Nevertheless, our findings offer new perspectives on the role of noninvasive ventilation, particularly in relation to PEP and its influence on the alveolar epithelium.

On the basis of the findings of the present study, we conclude that the application of 10, 15, or 20 cmH2O of PEP for 30 min can induce an increase in epithelial permeability and lung volume in healthy subjects. Given that the applica-tion of PEP represents a reliable, safe, and low-cost intervention in a variety of clinical situations, future investiga-tions should be conducted with a focus on expanding upon these findings.

REFERENCES

1. West JB. Comparative physiology of the pulmonary blood-gas barrier: the unique avian solution. Am J Physiol Regul Integr Comp Physiol. 2009;297(6):R1625-34. http://dx.doi.org/10.1152/ajpregu.00459.2009
2. Maina JN, West JB. Thin and strong! The bioengineering dilemma in the structural and functional design of the blood-gas barrier. Physiol Rev. 2005;85(3):811-44. http://dx.doi.org/10.1152/physrev.00022.2004
3. West JB. Role of the fragility of the pulmonary blood-gas barrier in the evolution of the pulmonary circulation. Am J Physiol Regul Integr Comp Physiol. 2013;304(3):R171-6. http://dx.doi.org/10.1152/ajpregu.00444.2012
4. Budinger GR, Sznajder JI. The alveolar-epithelial barrier: a target for potential therapy. Clin Chest Med. 2006;27(4):655-69; abstract ix. http://dx.doi.org/10.1016/j.ccm.2006.06.007
5. O'Doherty MJ, Peters AM. Pulmonary technetium-99m diethylene triamine penta-acetic acid aerosol clearance as an index of lung injury. Eur J Nucl Med. 1997;24(1):81-7. http://dx.doi.org/10.1007/BF01728316
6. Cayir D, Demirel K, Korkmaz M, Koca G. Evaluation of lung epithelial permeability in volatile substance abuse using Tc-99m DTPA aerosol scintigraphy. Ann Nucl Med. 2011;25(8):554-9. http://dx.doi.org/10.1007/s12149-011-0498-7
7. Ogi S, Gotoh E, Uchiyama M, Fukuda K, Urashima M, Fukumitsu N. Influence of hilar deposition in the evaluation of the alveolar epithelial permeability on 99mTc-DTPA aerosol inhaled scintigraphy. Jpn J Radiol. 2009;27(1):20-4. http://dx.doi.org/10.1007/s11604-008-0288-x
8. Gumuser G, Vural K, Varol T, Parlak Y, Tuglu I, Topal G, et al. Assessment of lung toxicity caused by bleomycin and amiodarone by Tc-99m HMPAO lung scintigraphy in rats. Ann Nucl Med. 2013;27(7):592-9. http://dx.doi.org/10.1007/s12149-013-0722-8
9. Osadnik C, Stuart-Andrews C, Ellis S, Thompson B, McDonald CF, Holland AE. Positive expiratory pressure via mask does not improve ventilation inhomogeneity more than huffing and coughing in individuals with stable chronic obstructive pulmonary disease and chronic sputum expectoration. Respiration. 2014;87(1):38-44. http://dx.doi.org/10.1159/000348546
10. Ricksten SE, Bengtsson A, Soderberg C, Thorden M, Kvist H. Effects of periodic positive airway pressure by mask on postoperative pulmonary function. Chest. 1986;89(6):774-81. http://dx.doi.org/10.1378/chest.89.6.774
11. Myers TR. Positive expiratory pressure and oscillatory positive expiratory pressure therapies. Respir Care. 2007;52(10):1308-26; discussion 1327.
12. Fink JB. Positive pressure techniques for airway clearance. Respir Care. 2002;47(7):786-96.
13. Alcoforado L, Brandão S, Rattes C, Brandão D, Lima V, Ferreira Lima G, et al. Evaluation of lung function and deposition of aerosolized bronchodilators carried by heliox associated with positive expiratory pressure in stable asthmatics: a randomized clinical trial. Respir Med. 2013;107(8):1178-85. http://dx.doi.org/10.1016/j.rmed.2013.03.020
14. Sociedade Brasileira de Pneumologia e Tisiologia. Diretrizes para testes de função pulmonar. J Pneumol. 2002;28(Suppl 3):S1-238.
15. Pereira CA, Sato T, Rodrigues SC. New reference values for forced spirometry in white adults in Brazil. J Bras Pneumol. 2007;33(4):397-406. http://dx.doi.org/10.1590/S1806-37132007000400008
16. Marks JD, Luce JM, Lazar NM, Wu JN, Lipavsky A, Murray JF. Effect of increases in lung volume on clearance of aerosolized solute from human lungs. J Appl Physiol. 1985;59(4):1242-8.
17. Bishai JM, Mitzner W, Tankersley CG, Wagner EM. PEEP-induced changes in permeability in inbred mouse strains. Respir Physiol Neurobiol. 2007;156(3):340-4. http://dx.doi.org/10.1016/j.resp.2006.10.009
18. Paiva DN, Masiero PR, Spiro BL, Jost RT, Albuquerque IM, Cardoso DM, et al. Continuous positive airway pressure and body position alter lung clearance of the radiopharmaceutical 99mtechnetium-diethylenetriaminepentaacetic acid (99mTc-DTPA). Afr J Biotechnol. 2012;11(99):16519-24. http://dx.doi.org/10.5897/AJB12.2563
19. Rinderknecht J, Shapiro L, Krauthammer M, Taplin G, Wasserman K, Uszler JM, et al. Accelerated clearance of small solutes from the lungs in interstitial lung disease. Am Rev Respir Dis. 1980;121(1):105-17.
20. O'Brodovich H, Coates G, Marrin, M. Effect of inspiratory resistance and PEEP on 99mTc-DTPA clearance. J Appl Physiol (1985). 1986;60(5):1461-5.
21. Cooper JA, van der Zee H, Line BR, Malik AB. Relationship of end-expiratory pressure, lung volume, and 99mTc-DTPA clearance. J Appl Physiol . 1987;63(4):1586-90.
22. Rizk NW, Luce JM, Hoeffel JM, Price DC, Murray JF. Site of deposition and factors affecting clearance of aerosolized solute from canine lungs, J Appl Physiol Respir Environ Exerc Physiol. 1984;56(3):723-9.
23. Oberdörster G, Utell MJ, Weber DA, Ivanovich M, Hyde RW, Morrow PE. Lung clearance of inhaled 99mTc-DTPA in the dog. J Appl Physiol Respir Environ Exerc Physiol. 1984;57(2):589-95.
24. Finucane KE, Panizza JA, Singh B. Efficiency of the normal human diaphragm with hyperinflation. J Appl Physiol (1985). 2005;99(4):1402-11. http://dx.doi.org/10.1152/japplphysiol.01165.2004
25. Villar J. The use of positive end-expiratory pressure in the management of the acute respiratory distress syndrome. Minerva Anestesiol. 2005;71(6):265-72.
26. Suzuki Y, Kanazawa M, Fujishima S, Ishizaka A, Kubo A. Effect of external negative pressure on pulmonary 99mTc-DTPA clearance in humans. Am J Respir Crit Care Med. 1995;152(1):108-12. http://dx.doi.org/10.1164/ajrccm.152.1.7599807
27. Mason GR, Mena I, Maublant, J, Sietsma K, Effros RM. The effect of PEEP and posture on the clearance of inhaled small solutes from the lungs in normal subjects. Am Rev Respir Dis. 1984;129(4 Pt 2):A346.
28. Groth S. Pulmonary clearance of 99mTc-DTPA. An index of alveolar epithelial permeability. Dan Med Bull. 1991;38(3):189-203.
29. Ludwigs U, Philip A. Pulmonary epithelial permeability and gas exchange: a compari-son of inverse ratio ventilation and conventional mechanical ventilation in oleic acid-induced lung injury in rabbits. Chest. 1998;113(2):459-66. http://dx.doi.org/10.1378/chest.113.2.459

Indexes

Development by:

© All rights reserved 2024 - Jornal Brasileiro de Pneumologia