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The Program for the Prevention of Childhood Asthma: a specialized care program for children with wheezing or asthma in Brazil

Programa Infantil de Prevenção de Asma: um programa de atenção especializada a crianças com sibilância/asma

Marilyn Urrutia-Pereira1, Jennifer Avila1, Dirceu Solé2

DOI: http://dx.doi.org/10.1590/S1806-37562016000004480

ABSTRACT

Objective: To present the Programa Infantil de Prevenção de Asma (PIPA, Program for the Prevention of Childhood Asthma) and the characteristics of the patients followed in this program. Methods: Implemented in the city of Uruguaiana, Brazil, PIPA has as its target population children and adolescents (< 18 years of age) with asthma or suspected asthma. Patients either enroll in PIPA spontaneously or are referred by pediatricians or primary care physicians. In this retrospective study, we use a standardized protocol to assess PIPA patients. Results: By the end of the study period, 646 patients were being followed. Of those, 298 (46.1%) were ≤ 3 years of age. In this group of patients, recurrent wheezing was identified in 60.7%, and the first episode of wheezing occurred in the first six months of life in 86.0%. Severe wheezing was identified in 29.5% and 45.4% in the children ≤ 3 and > 3 years of age, respectively. Physician-diagnosed asthma was reported in 26.5% and 82.2%, respectively. In the sample as a whole, the prevalence of passive smoking was high (> 36%), occurring during pregnancy in > 15%; > 40% of the patients had been born by cesarean section; and 30% had a mother who had had < 8 years of schooling. Conclusions: A prevention program for children with asthma is an effective strategy for controlling the disease. Knowledge of local epidemiological and environmental characteristics is essential to reducing the prevalence of the severe forms of asthma, to improving the use of health resources, and to preventing pulmonary changes that could lead to COPD in adulthood.

Keywords: Asthma/prevention and control; Asthma/epidemiology; Patient care.

RESUMO

Objetivo: Apresentar o Programa Infantil de Prevenção de Asma (PIPA), assim como as características dos pacientes nele acompanhados. Métodos: O PIPA, implantado em Uruguaiana (RS), tem como população alvo crianças e adolescentes com asma ou suspeita de asma, menores de 18 anos, referidos por pediatras, médicos de atenção primária ou por procura espontânea. Neste estudo retrospectivo, os participantes foram avaliados segundo um protocolo padronizado de atendimento. Resultados: Ao final do período do estudo, estavam em seguimento 646 pacientes. Desses, 298 (46,1%) tinham idade ≤ 3 anos. Nesse grupo de pacientes, houve sibilância recorrente em 60,7% e o primeiro episódio de sibilância ocorreu nos primeiros seis meses de vida em 86,0%. Sibilância grave foi apontada em 29,5% e 45,4% nas crianças com ≤ 3 anos e com > 3 anos, respectivamente. Houve diagnóstico médico de asma em 26,5% e 82,2%, respectivamente. Na amostra total, a prevalência de exposição passiva ao fumo foi elevada (> 36%), ocorrendo durante a gestação em > 15%; o número de nascimentos por cesariana foi > 40%, e o nível educacional materno foi inferior a 8 anos em 30%. Conclusões: Um programa de prevenção para atendimento de crianças com asma é uma estratégia eficaz para o controle da doença. O conhecimento das características epidemiológicas e ambientais da população local é primordial para que haja a redução das formas graves da asma, melhor utilização dos recursos de saúde e possível prevenção de alterações pulmonares que possam levar a DPOC no adulto.

Palavras-chave: Asma/prevenção e controle; Asma/epidemiologia; Assistência ao paciente.

INTRODUCTION

Asthma is a public health problem worldwide and is one of the most common chronic diseases in childhood. It is highly prevalent, impairs the quality of life of patients and their families, and incurs high costs to the health care system and society.(1)

The current level of asthma control in Latin American countries falls far short of the goals set forth by current inter-national guidelines. (2) Asthma is one of the twenty most common reasons for primary care visits in Brazil, being the third leading cause of hospitalization within the Brazilian Unified Health Care System.(3,4)

The mean prevalence of asthma among children and adolescents in Brazil is estimated to be 20%.(5) In the state of Rio Grande do Sul, Brazil, respiratory diseases are the leading cause of hospitalization in those aged under 19 years, and asthma ranks second among these diseases.(4)

There is as yet no curative treatment for asthma; the primary goal of treatment is disease control. However, despite advances in asthma treatment and in the implementation of guidelines for asthma management, the disease remains poorly controlled.(6)

Possible explanations for this failure include lack of patient access to health care, lack of diagnosis of asthma, inap-propriate treatment, and not taking the prescribed medication properly, whether because of lack of understanding or lack of adherence, despite instruction.(7)

Adherence to treatment is one of the most important factors in ensuring treatment success. Many factors, such as knowledge of the disease, cultural standards, socioeconomic factors, lack of perception of asthma symptoms, adverse events, and ability to use inhalers, can influence adherence to treatment and asthma control.(8)

Poor adherence is a serious problem among patients with chronic respiratory disease in developing countries, a problem that is often due to limited access to health care; therefore, in addition to prescription and provision of phar-macological treatment that is appropriate to the level of disease severity, education on self-management is an aspect that must be addressed.(8)

Asthma education for patients so that they know all they need about their disease is not only a right but also an ef-fective strategy of asthma control in the short, medium and long term.(9) Thus, the need to tailor knowledge of asthma education to clinical practice and make it accessible at a public outpatient clinic specializing in asthma motivated the development of the Programa Infantil de Prevenção de Asma (PIPA, Program for the Prevention of Childhood Asthma) in the city of Uruguaiana, Brazil, in order to decrease the morbidity and mortality of childhood asthma in that city.

The objective of the present study was to present PIPA and the characteristics of the patients followed in this pro-gram.

METHODS

This was a retrospective study of children (< 18 years of age) with asthma or suspected asthma who enrolled in PIPA spontaneously or were referred by pediatricians or primary care physicians. PIPA was established in April of 2012 in the city of Uruguaiana, which has a population of approximately 120,000 inhabitants, in southern Brazil.

After being admitted to PIPA, patients underwent the following treatment protocol: a) a medical visit; b) ancillary tests; c) clinical diagnosis; d) functional diagnosis; e) treatment planning; f) follow-up and monitoring of asthma control; and g) a nursing visit and nursing instruction.

At the medical visit, the parents or legal guardians of the patients completed standardized questionnaires, the use of which depended on patient age and the characteristics of the cross-cultural validation of the questionnaire for use in Brazil. For the youngest patients (those aged up to 3 years, 11 months, and 29 days), we used the International Study of Wheezing in Infants (EISL) written questionnaire,(10) whereas for those aged over 4 years, we used the International Study of Asthma and Allergy in Childhood (ISAAC) questionnaire(11) together with the ISAAC phase II questionnaire on risk factors,(11,12) in addition to the Children's Sleep Habits Questionnaire,(13) which began to be used in January of 2014, for those aged between 2 and 12 years. Following the initial interview, patients underwent a detailed physical examination, including assessment of nutritional status (weight and height)), physical examination of the upper airways, cardiopulmonary auscultation, etc.

Ancillary tests included blood workup; quantitative determination of total serum IgE (ImmunoCAP® RAST; Thermo Fisher Scientific Inc., Waltham, MA, USA); determination of 25-hydroxyvitamin D by chemiluminescent microparticle immunoassay; skin prick tests to airborne allergens (Dermatophagoides pteronyssinus, D. farinae, Blomia tropicalis, cockroach mix, Alternaria sp., dog dander, and cat dander),(14) and parasitological examination (direct method).(15)

Depending on age and clinical history, patients underwent imaging assessment, which included a chest and/or si-nus X-ray.

In this phase, the clinical diagnosis of asthma was made in accordance with the Global Initiative for Asthma (GINA) criteria.(1) For the children aged under 2 years who were referred with suspected asthma, we employed the Asthma Predictive Index (API),(16) and for those aged over 2 years, we employed the modified API, which includes sensitiza-tion to airborne allergens as a prognostic factor of disease progression.(17)


The diagnosis of allergic rhinitis was made in accordance with the criteria established by the Third Brazilian Con-sensus on Rhinitis(18) and by the Allergic Rhinitis and its Impact on Asthma initiative.(19)

The children aged over 6 years who were able to perform the expiratory maneuvers required for functional as-sessment underwent objective measurements of pulmonary function, whether by spirometry or by determination of maximum peak expiratory flow, with the use of a Spirolab III® spirometer (Medical International Research, Rome, Italy). American Thoracic Society acceptability criteria-values from at least the three best maneuvers were select-ed-and reproducibility criteria were used.(20) Following the initial spirometric assessment, patients underwent bron-chodilator testing with albuterol aerosol (400 g) administered with a valve spacer, and the spirometric parameters were measured again 15 minutes later.(21)

Maximum peak expiratory flow was determined with a Mini-Wright® Peak Flow Meter (Clement Clarke Internation-al, Essex, UK), especially in patient follow-up and monitoring of the response to the treatment regimen.(21)

After completion of the clinical and functional assessment and before establishment of a treatment plan, patients were classified with respect to level of asthma control, as well as to the presence of acute exacerbation, as recom-mended by GINA.(1)

On that basis, patients received a written treatment plan for maintenance control and possible exacerbations, as recommended by GINA(1) and by the Brazilian Thoracic Association Guidelines for Asthma Management.(3) The medi-cations available through PIPA are as follows: albuterol (metered dose inhaler; 100 g/puff); and beclomethasone (metered dose inhaler; 250 g/puff); both of which are distributed free of charge at all "aqui tem farmácia popular" facilities of the Brazilian Popular Pharmacy program.(22)

For patients with moderate or severe asthma, montelukast (tablets of 5 and 10 mg) and the combination of albuterol (25 g/puff) and fluticasone dipropionate (125 g or 250 g/puff) metered dose inhaler or dry powder inhaler (Diskus® 50 g/250 g) are available free of charge through the Uruguaiana City Hall.

After being admitted to PIPA, patients were followed and reassessed over 1-3 months, as determined by asthma severity and control.(1)

In addition to medical follow-up, patients were followed by nurses who are specialists in asthma care and who are part of the team of professionals involved in PIPA, as recommended by other groups and by international consensus guidelines.(23,24) The responsibilities of these nurses included the following: a) administer quality-of-life question-naires at the first nursing visit and 6 months later to assess patient's response to treatment(25); b) emphasize, to fami-ly members, the importance of identifying symptoms of uncontrolled disease early; c) always review the (written) action plan(26) with the following aims-1) recognition of asthma-related symptoms; 2) treatment adjustment based on the medical prescription; and 3) identification of when and where to seek medical attention, for patients with poor disease control with the initial treatment(25)-d) check proper use of inhaled medication at all visits; e) encourage adherence to maintenance treatment and provide instruction regarding the difference between treatment of asthma attacks and maintenance treatment; f) address aspects of environmental control, habits such as smoking, and other triggers; and g) encourage regular visits (every 3 months) even if the patient is asymptomatic.(1)

The study was approved by the Research Ethics Committee of the Uruguaiana Municipal Department of Health, Bra-zil.

RESULTS

Since the creation of PIPA, 646 patients have been enrolled, all of whom were being followed at this writing. Of those, 46.1% were aged 3 years or younger (Table 1). Most of the patients aged up to 3 years (> 80%) had a history of recurrent wheezing (three or more episodes), which had started early, before 6 months of age. Episodes of severe wheezing were identified in nearly 30% of these patients, more than half of whom had been hospitalized for wheez-ing. Of all patients aged up to 3 years, 26.5% had physician-diagnosed asthma, 53.0% had been born by cesarean section, and only 29.0% had been exclusively breastfed for at least 6 months (Table 1). Passive exposure to tobacco smoke was reported by 39.5% of the parents/legal guardians of these patients, with exposure occurring during preg-nancy in 15.4% of the cases and the smoker being the mother in 18.7% (Table 1). Attending day care was identified in 38.2% of the cases, presence of household mold was identified in 44.6%, and presence of pets in the household was identified in 73.0% (mainly dogs). A maternal education level of less than 8 years was identified in 35.6% of the cases (Table 1).
 



Among the older patients (those aged over 3 years), it is of note that wheezing in the previous year was reported in 88.7% of the cases, wheezing was severe in 45.4%, and hospitalization for wheezing was required in 8.0% (Table 1). Physician-diagnosed asthma was identified in 82.2% of the cases, and, in most of them, asthma had been classified as uncontrolled. In addition, concomitant rhinoconjunctivitis was reported in 74.4% of the cases. Exclusive breast-feeding for at least 6 months was reported in 62.6% of the cases; however, passive exposure to tobacco smoke and maternal smoking during pregnancy were reported in 36.4% and 17.5% of the cases, respectively (Table 1). Nearly 60.0% of the patients attended day care in the first year of life, and presence of pets in the household was reported in 79.0% of the cases (most often dogs). A maternal education level of less than 8 years was reported by 48.4% of the respondents (Table 1).

DISCUSSION

The high prevalence rates of asthma in children (9 to 11 years of age) and recurrent wheezing in infants (12 to 15 months of age) identified in Uruguaiana by the ISAAC(12) and by the International Study of Wheezing in Infants(27) prompted the local managers to establish PIPA.

As can be seen in Table 1, most of the children aged up to 3 years followed in the program experienced symptom onset in the first year of life, and the first episode of wheezing occurred before 6 months of age, as reported by other researchers.(28) In addition, a significant number of children in the two groups studied had severe wheezing.

Recent studies have increasingly shown that COPD has its origins in severe childhood asthma; therefore, identify-ing these children and the risk factors leading to more severe asthma is of the utmost importance for public health.(29)

Pre- and postnatal exposure to cigarette smoke has been identified as one of the most important risk factors for the development of wheezing in infants and asthma in older children. (30) Among the patients enrolled in PIPA, the preva-lence of passive smoking was significant, since, in approximately 40% of the cases, there was at least one smoker in the household, and, in approximately 15%, the smoker was the mother. To this we must add prenatal exposure to tobacco smoke, which was identified in more than 15% of the cases. Knowledge of these factors and of their magni-tude is very important, because exposure so early in life can cause epigenetic changes in lung development that may extend to future generations.(31) A recent study also pointed out that exposure to tobacco smoke during pregnancy increases the risk of asthma and wheezing in adolescence, and that pulmonary function changes in these children would be related to potential epigenetic effects of tobacco smoke rather than to immune function changes or atopy.(32)

Another finding worthy of note in this population was the large number of children who had been born by cesarean section, which is identified as a risk factor for developing asthma later in life, especially if associated with a family history of asthma.(33)

Maternal education level, especially in populations in developing countries, has been associated with the develop-ment of asthma. A significant proportion of the patients evaluated here had a mother who had had less than 8 years of schooling. Previous studies conducted in Brazil have related a low level of education to an increased risk of asth-ma or wheezing in children aged under 5 years.(34) This is possibly due to poor understanding of the disease by mothers, unawareness of the possibility of obtaining free controller medications, poor adherence to the asthma action plan, and, in particular, the lack of a bond between mothers and a specific facility where they can feel supported and welcomed if their children experience an acute asthma exacerbation.

For greater success in establishing an asthma program, the following should be taken into consideration: a) get to know the local situation, through a local or regional epidemiological survey, so as to properly adjust the health poli-cies needed for optimal care of the target population; b) build the foundations of the program upon the major consen-sus guidelines on the different aspects to be addressed in an asthma program(1,3,24,28,35); c) get different categories of professionals, such as primary care physicians, nurses, physical therapists, social workers, physical education teach-ers, and community health agents, involved in the program,(36) thus preventing the program from being focused on a single person(9); d) pharmaceutical care should be seen as a set of tasks performed by the pharmacist and other health professionals, in which medications are the essential material and which involve selecting, scheduling, pur-chasing, distributing, and dispensing medications, as well as ensuring the quality of the products and services and the follow-up and assessment of their use, with a view to achieving concrete results and improving the quality of life of the population(37)-understanding this concept is of paramount importance, since, often times, medications are dis-tributed regardless of the fulfillment of the necessary criteria for the rational and safe use of these products(38); e) get the population involved through the use of advisory boards, associations, and the media; f) get managers(9,36) in-volved and keep them permanently informed about the results of the program; and g) make the asthma program known through the media, television, or new communication tools (such as the Internet), which offer innovations in physician-patient communication and in knowledge and recommendations about the disease.(38) PIPA has a page on Facebook through which it has achieved greater communication and integration with patients and their families, as well as allowing the general public to get acquainted with the activities of the program.

In conclusion, considering that Brazil is a country with many "types of asthma",(39) the establishment of regional asthma programs, based on epidemiological and environmental differences, would facilitate the implementation of appropriately targeted prevention, early diagnosis, and treatment measures, so as to allow proper allocation of finan-cial resources, as occurs in other successful programs in Brazil for adults.(40)

Therefore, there would be appropriate disease follow-up from symptom onset and a consequent reduction in the number of emergency room visits and hospitalizations, especially in patients with undiagnosed, undertreated, or poorly controlled asthma, thus preventing pulmonary changes that could lead to COPD in adulthood.

REFERENCES

1. Global Initiative for Asthma [homepage on the Internet]. Bethesda: GINA. [cited 2014 Mar 1]. Global strategy for Asthma management and prevention: Revised 2014. Available from http://www.ginasthma.org/local/uploads/files/GINA_Report_2014.pdf
2. Fisher GB, Camargos PA, Mocelin HT. The burden of asthma in children: a Latin American perspective. Paediatr Respir Rev. 2005;6(1):8-13. http://dx.doi.org/10.1016/j.prrv.2004.11.002
3. Sociedade Brasileira de Pneumologia e Tisiologia. Diretrizes da Sociedade Brasileira de Pneumologia e Tisiologia para o Manejo da Asma. J Bras Pneumol. 2012;38(Suppl 1):S1-S46.
4. Portal da Saúde [homepage on the Internet]. Brasília: Ministério de Saúde. [cited 2014 Mar 1]. Indicadores e dados básicos 2008. Available from: http://tabnet.datasus.gov.br
5. Asher MI, Keil U, Anderson HR, Beasley R, Crane J, Martinez F, et al. International Study of Asthma and Allergies in Childhood (ISAAC): rationale and methods. Eur Respir J. 1995;8(3):483-91. http://dx.doi.org/10.1183/09031936.95.08030483
6. Fasciglione MP, Castañeiras CE. The educational component in an integrated approach to bronchial asthma J Bras Pneumol. 2010;36(2):252-9. Erratum in: J Bras Pneumol. 2010;36(5):669.
7. Klok T, Lubbers S, Kaptein AA, Bland PL. Every parent tells a story: why non-adherence may persist in children receiving guideline-based comprehensive asthma care. J Asthma. 2014;51(1):106-12. http://dx.doi.org/10.3109/02770903.2013.841191
8. Souza-Machado A, Santos PM, Cruz AA. Adherence to treatment in severe asthma: predicting factors in a program for asthma control in Brazil. World Allergy Organ J. 2010;3(3):48-52. http://dx.doi.org/10.1097/WOX.0b013e3181d25e8e
9. Stelmach R, Neto AC, Fonseca AC, Ponte EV, Alves G, Araujo-Costa IN, et al. A workshop on asthma management programs and centers in Brazil: reviewing and explaining concepts. J Bras Pneumol. 2015;41(1):3-15. http://dx.doi.org/10.1590/S1806-37132015000100002
10. Bianca AC, Wandalsen GF, Miyagi K, Camargo L, Cezarin D, Mallol J, et al. International Study of Wheezing in Infants (EISL): validation of written questionnaire for children aged below 3 years. J Investig Allergol Clin Immunol. 2009,19(1):35-42.
11. Weiland SK, Björkstén B, Brunekreef B, Cookson WO, von Muttis E, Strachan DP, et al. Phase II of the International Study of Asthma and Allergies in Childhood (ISAAC II): rationale and methods. Eur Respir J. 2004;24(3):406-12. http://dx.doi.org/10.1183/09031936.04.00090303
12. Pereira MU, Sly PD, Pitrez PM, Jones MH, Escouto D, Dias AC, et al. Nonatopic asthma is associated with helminth infections and bronchiolitis in poor children. Eur Respir J. 2007(6):1154-60. http://dx.doi.org/10.1183/09031936.00127606
13. Silva FG, Silva CR, Braga LB Neto AS. Portuguese Children's Sleep Habits Questionnaire - validation and cross-cultural comparison. J Pediatr (Rio J) 2014;90(1):78-84. http://dx.doi.org/10.1016/j.jped.2013.06.009
14. Illi S, Garcia-Marcos L, Hernando V, Guillen JJ, Liese A, von Mutius E. Reproducibility of skin prick test results in epidemiologic studies: a comparison of two devices. Allergy. 1998;53(4):353-8. http://dx.doi.org/10.1111/j.1398-9995.1998.tb03905.x
15. Menezes RA, Gomes MS, Barbosa FH, Machado RL, Andrade RF, Couto AA. Sensibilidade de métodos para diagnóstico das enteroparasitoses em Macapá - Amapá, Brasil. Rev Biol Ciênc Terra. 2013;13(2):66-73.
16. Castro-Rodríguez JA, Holberg JC, Wright AL, Martinez FD. A clinical index to define risk of asthma in young children with recurrent wheezing. Am J Respir Crit Care Med. 2000;162(4 Pt 1):1403-6. http://dx.doi.org/10.1164/ajrccm.162.4.9912111
17. Guilbert TW, Morgan WJ, Zeiger RS, Bacharier LB, Boehmer SJ, Krawiec M, et al. Atopic characteristics of children with recurrent wheezing at risk for the development of childhood asthma. J Allergy Clin Immunol. 2004;114(6):1282-7. http://dx.doi.org/10.1016/j.jaci.2004.09.020
18. Solé D, Sakano E. III Consenso Brasileiro sobre Rinites. Braz J Otorhinolaryngol. 2012;75(6S):1-50.
19. Bousquet J, Schünemann HJ, Samolinski B, Demoly P, Baena-Cagnani CE, Bachert J, et al. Allergic Rhinitis and its Impact on Asthma (ARIA): achievements in 10 years and future needs. J Allergy Clin Immunol. 2012;130(5):1049-62. http://dx.doi.org/10.1016/j.jaci.2012.07.053
20. American Thoracic Society; European Respiratory Society. ATS/ERS statement: raised volume forced expirations in infants: guidelines for current practice. Am J Respir Crit Care Med. 2005;172(11):1463-71. http://dx.doi.org/10.1164/rccm.200408-1141ST
21. Rodrigues JC, Cardieri JM, Bussamra MH, Nakaie CM, Almeida MB, Silva Filho LV, et al. Provas de função pulmonar em crianças e adolescentes. In: Pereira CA, Neder JA, editors. Diretrizes para testes de função pulmonar. J Pneumol. 2002;28(Suppl 3):S207-S221.
22. Portal de Saúde [homepage on the Internet]. Brasília: Ministério de Saúde [cited 2010 Apr 20]. Brasil Carinhoso 1: Farmácia Popular terá remédio de graça para asma. Available from: http://portalsaude.saude.gov.br/portalsaude/noticia/5034/162/farmacia-popular-tera-%Cbr%Eremedio-de-graca-para-asma.html.
23. Griffirths C, Foster G, Barnes N, Eldridge S, Tate H, Begum S, et al. Specialist nurse intervention to reduce unscheduled asthma care in a deprived multiethnic area: the east London randomised controlled trial for high risk asthma (ELECTRA). BMJ. 2004;328(7432):144. http://dx.doi.org/10.1136/bmj.37950.784444.EE
24. British Thoracic Society [homepage on the Internet] London: BTS. [cited 2014 Mar 1]. British Guideline on the Management of Asthma. revised 2012. http://www.brit-thoracic.org.uk/
25. Liu AH, Zeiguer R, Sorkness C, Mahr T, Ostrom N, Burgess S, et al. Development and cross-sectional validation of the Childhood Asthma Control Test. J Allergy Clin Immunol. 2007;119(4):817-25. http://dx.doi.org/10.1016/j.jaci.2006.12.662
26. Tan NC, Chen Z, Soo WF, Ngoh AS, Tai BC. Effects of a written asthma action plan on caregivers' management of children with asthma: a cross-sectional questionnaire survey. Prim Care Respir J. 2013;22(2):188-94. http://dx.doi.org/10.4104/pcrj.2013.00040
27. Pereira MU, Ivancevich JC, Solé D, Mallol J. Prevalence of recurrent wheezing in infants in a poor urban city in South Brazil. World Allergy Organ J. 2013;6(Suppl 1):43. http://dx.doi.org/10.1186/1939-4551-6-S1-P43
28. Bacharier LB, Boner A, Carlsen KH, Eigenmann PA, Frischer T, Götz M, et al. Diagnosis and treatment of asthma in childhood: a PRACTALL consensus report. Allergy. 2008;63(1):5-34. http://dx.doi.org/10.1111/j.1398-9995.2007.01586.x
29. Mattes J, Gibson PG. The early origins of COPD in severe asthma: the one thing that leads to another or the two things that come together? Thorax. 2014;69(9):789-90. http://dx.doi.org/10.1136/thoraxjnl-2014-205401
30. Burke H, Leonardi-Bee J, Hasmim A, Pine-Abata H, Chen Y, Cook DG, et al. Prenatal and passive smoke exposure and incidence of asthma and wheeze: systematic review and meta-analysis. Pediatrics. 2012;129(4):735-44. http://dx.doi.org/10.1542/peds.2011-2196
31. Leslie FM. Multigenerational epigenetic effects of nicotine on lung function. BMC Med. 2013;11:27. http://dx.doi.org/10.1186/1741-7015-11-27
32. Hollams EM, de Klerk NH, Holt PG, Sly PD. Persistent effects of maternal smoking during pregnancy on lung function and asthma in adolescents. Am J Respir Crit Care Med. 2014;189(4):401-7. http://dx.doi.org/10.1164/rccm.201302-0323OC
33. Weng M, Walker WA. The role of gut microbiota in programming the immune phenotype. J Dev Orig Health Dis. 2013;4(3):203-14. http://dx.doi.org/10.1017/S2040174412000712
34. Lima JA, Fischer GB, Sarria EE, Mattiello R, Solé D. Prevalence of and risk factors for wheezing in the first year of life. J Bras Pneumol. 2010;36(5):525-31.
35. Papadopoulos NG, Arakawa H, Carlsen KH, Custovic A, Gern J, Lemanske R, et al. International consensus on (ICON) pediatric asthma. Allergy. 2012;67(8):976-97. http://dx.doi.org/10.1111/j.1398-9995.2012.02865.x
36. Brasil. Ministério da Saúde [homepage on the Internet]. Brasília: Ministério de Saúde. c2010 [cited 2014 Mar 1]. Série A. Normas e Manuais Técnicos. Cadernos de Atenção Básica 25. Doenças Respiratórias Crônicas. [Adobe Acrobat document, 160p.]. Available from: http://189.28.128.100/dab/docs/publicacoes/cadernos_ab/abcad25.pdf
37. Brasil. Ministério da Saúde. Resolução do Conselho Federal de Farmácia-CFF No. 578, de 26 de julho de .2013. Diário Oficial da União, 19 Ago 2013.
38. Boulet LP, FitzGerald JM, Levy ML, Cruz AA, Pedersen S, Haahtela T, et al. A guide to the translation of the Global Initiative for Asthma (GINA) strategy into improved care. Eur Respir J. 2012;39(5):1220-9. http://dx.doi.org/10.1183/09031936.00184511
39. Solé D, Camelo-Nunes I, Wandalsen GF, Mallozi MC. Asthma in children and adolescents in Brazil: contribution of the International Study of Asthma and Allergies in Childhood (ISAAC). Rev Paul Pediatr. 2014;32(1):114-25. http://dx.doi.org/10.1590/S0103-05822014000100018
a. Cerci Neto A, Ferreira Filho OF, Bueno T. Brazilian examples of programs for the control of asthma. J Bras Pneumol. 2008;34(2):103-6. http://dx.doi.org/10.1590/S1806-37132008000200007

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