<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.3 20210610//EN" "JATS-journalpublishing1-3.dtd">
<article article-type="research-article" dtd-version="1.3" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">medsovet</journal-id><journal-title-group><journal-title xml:lang="ru">Медицинский Совет</journal-title><trans-title-group xml:lang="en"><trans-title>Meditsinskiy sovet = Medical Council</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2079-701X</issn><issn pub-type="epub">2658-5790</issn><publisher><publisher-name>REMEDIUM GROUP Ltd.</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.21518/2079-701X-2017-18-124-128</article-id><article-id custom-type="elpub" pub-id-type="custom">medsovet-2044</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>МУКОВИСЦИДОЗ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>CYSTIC FIBROSIS</subject></subj-group></article-categories><title-group><article-title>ВЛИЯНИЕ НЕОНАТАЛЬНОГО СКРИНИНГА НА ТЕЧЕНИЕ МУКОВИСЦИДОЗА НА ПРИМЕРЕ ГРУППЫ ПАЦИЕНТОВ МОСКОВСКОГО РЕГИОНА</article-title><trans-title-group xml:lang="en"><trans-title>INFLUENCE OF NEONATAL SCREENING FOR CYSTIC FIBROSIS BY THE EXAMPLE OF PATIENTS OF THE MOSCOW REGION</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Шерман</surname><given-names>В. Д.</given-names></name><name name-style="western" xml:lang="en"><surname>Sherman</surname><given-names>V. D.</given-names></name></name-alternatives><bio xml:lang="ru"><p>к.м.н.</p></bio><bio xml:lang="en"><p>PhD in medicine</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Кондратьева</surname><given-names>Е. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Kondratieva</surname><given-names>E. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>д.м.н., профессор</p></bio><bio xml:lang="en"><p>MD, Prof.</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Воронкова</surname><given-names>А. Ю.</given-names></name><name name-style="western" xml:lang="en"><surname>Voronkova</surname><given-names>A. Y.</given-names></name></name-alternatives><bio xml:lang="ru"><p>к.м.н.</p></bio><bio xml:lang="en"><p>PhD in medicine</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Каширская</surname><given-names>Н. Ю.</given-names></name><name name-style="western" xml:lang="en"><surname>Kashirskaya</surname><given-names>N. Y.</given-names></name></name-alternatives><bio xml:lang="ru"><p>д.м.н., профессор</p></bio><bio xml:lang="en"><p>MD, Prof.</p></bio><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Шабалова</surname><given-names>Л. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Shabalova</surname><given-names>L. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>к.м.н</p></bio><bio xml:lang="en"><p>PhD in medicine</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Никонова</surname><given-names>В. С.</given-names></name><name name-style="western" xml:lang="en"><surname>Nikonova</surname><given-names>V. S.</given-names></name></name-alternatives><bio xml:lang="ru"><p>к.м.н.</p></bio><bio xml:lang="en"><p>PhD in medicine</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Жекайте</surname><given-names>Е. К.</given-names></name><name name-style="western" xml:lang="en"><surname>Zhekaite</surname><given-names>E. K.</given-names></name></name-alternatives><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Куцев</surname><given-names>С. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Kutsev</surname><given-names>S. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>д.м.н., профессор, чл.-корр. РАН</p></bio><bio xml:lang="en"><p>MD, Prof., Corresponding Member of RAS</p></bio><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Медико-генетический научный центр, Москва;&#13;
Московский областной консультативно-диагностический научный центр для детей, Москва</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Medico-Genetic Scientific Center, Moscow;&#13;
Moscow Regional Consultative Diagnostic Scientific Center for Children, Moscow</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Медико-генетический научный центр, Москва;</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Medico-Genetic Scientific Center, Moscow</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2017</year></pub-date><pub-date pub-type="epub"><day>03</day><month>11</month><year>2017</year></pub-date><volume>0</volume><issue>18</issue><fpage>124</fpage><lpage>128</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Шерман В.Д., Кондратьева Е.И., Воронкова А.Ю., Каширская Н.Ю., Шабалова Л.А., Никонова В.С., Жекайте Е.К., Куцев С.И., 2017</copyright-statement><copyright-year>2017</copyright-year><copyright-holder xml:lang="ru">Шерман В.Д., Кондратьева Е.И., Воронкова А.Ю., Каширская Н.Ю., Шабалова Л.А., Никонова В.С., Жекайте Е.К., Куцев С.И.</copyright-holder><copyright-holder xml:lang="en">Sherman V.D., Kondratieva E.I., Voronkova A.Y., Kashirskaya N.Y., Shabalova L.A., Nikonova V.S., Zhekaite E.K., Kutsev S.I.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://www.med-sovet.pro/jour/article/view/2044">https://www.med-sovet.pro/jour/article/view/2044</self-uri><abstract><sec><title>Цель исследования</title><p>Цель исследования: сравнительная оценка клинического статуса пациентов с муковисцидозом (МВ) 6–9 лет, диагноз которым был установлен до начала неонатального скрининга (НС) на МВ в Московском регионе и в аналогичной возрастной группе с момента начала НС по данным регистра 2012 и 2015 гг. Пациенты и методы. Пациенты были разделены на 2 группы: I – 45 детей 6–9 лет, диагностированных до начала НС, II – 86 детей 6–9 лет, выявленных после начала НС. Результаты. При сравнительной оценке возраста установки диагноза получено достоверное различие между I и II группами. Средний возраст установления диагноза в группе I составил 2,29 (±2,29) года, в группе II средний возраст установления диагноза – 0,66 (± 1,13) года (p = 0,0000). По данным микробиологического статуса группа пациентов, диагностированных по программе НС (группа II), достоверно реже имела хроническое инфицирование дыхательных путей Ps. aeruginosa (37,78% пациентов в группе I против 14,10% в группе II) (р = 0,0026). В группе больных, выявленных по программе скрининга новорожденных (группа II), отмечено статистически значимое уменьшение объема проводимой внутривенной (р = 0,0000) и ингаляционной антибактериальной терапии (р = 0,0139) и снижение по сравнению с группой I числа пациентов, принимающих бронхолитики (р = 0,0322). Заключение. Продемонстрировано положительное влияние неонатального скрининга на МВ на возраст установки диагноза и ряд важных показателей течения заболевания.</p></sec><sec><title> </title><p> </p></sec></abstract><trans-abstract xml:lang="en"><sec><title>Study objective</title><p>Study objective: comparative evaluation of clinical status of patients with cystic fibrosis (CF) 6–9 years, the diagnosis of which was established before the start of neonatal screening (NS) for MV in the Moscow region and in same age group since the start of the NS according to the register 2012 and 2015. Patients and methods. The patients were divided into 2 groups: I – 45 children aged 6–9 years, diagnosed before the beginning of the NS, II – 86 children aged 6–9 years, identified after the start of the NS. Results. A comparative assessment of the age of diagnosis had a significant difference between groups I and II. The average age of diagnosis in group I was 2.29 (±2.29) years, in group II the average age of diagnosis – 0.66 (± 1.13) years (p = 0.0000). According to the microbiological status diagnosed according to the NS program (group II), chronic infection of the respiratory tract by Ps. aeruginosa was less frequent in this group (37.78% of patients in group I vs. 14,10 % in group II) (p = 0.0026). In the group of patients identified by the newborns screening program directed at newborns (group II) a statistically significant decrease of the ongoing intravenous (p = 0.0000) and inhaled antibiotic therapy (p = 0.0139) and reduced compared with group I patients receiving bronchodilators (p = 0.0322). Conclusion. A positive impact of neonatal screening for MV at the age of diagnosis and a number of important indicators of the disease was demonstrated.</p></sec><sec><title> </title><p> </p></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>муковисцидоз</kwd><kwd>неонатальный скрининг</kwd><kwd>потовая проба</kwd></kwd-group><kwd-group xml:lang="en"><kwd>cystic fibrosis</kwd><kwd>neonatal screening</kwd><kwd>sweat test</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Муковисцидоз. Монография. Под ред. Н.И. Капранова, Н.Ю. Каширской. М., 2014.</mixed-citation><mixed-citation xml:lang="en">Муковисцидоз. Монография. Под ред. Н.И. Капранова, Н.Ю. Каширской. М., 2014.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Шерман В.Д., Каширская Н.Ю., Кондратьева Е.И., Воронкова А.Ю., Капранов Н.И., Амелина Е.Л. и др. Национальный консенсус. Муковисцидоз: определение, диагностические критерии, терапия, раздел «диагностика муковисцидоза». Педиатрия, 2017, 2: 90-98.</mixed-citation><mixed-citation xml:lang="en">Шерман В.Д., Каширская Н.Ю., Кондратьева Е.И., Воронкова А.Ю., Капранов Н.И., Амелина Е.Л. и др. Национальный консенсус. Муковисцидоз: определение, диагностические критерии, терапия, раздел «диагностика муковисцидоза». Педиатрия, 2017, 2: 90-98.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Castellani C, Southern KW, Brownlee K, Dankert Roelse J, Duff A, Farrell M, et al. European best practice guidelines for cystic fibrosis neonatal screening. J Cyst Fibros, 2009, 8: 153–73.</mixed-citation><mixed-citation xml:lang="en">Castellani C, Southern KW, Brownlee K, Dankert Roelse J, Duff A, Farrell M, et al. European best practice guidelines for cystic fibrosis neonatal screening. J Cyst Fibros, 2009, 8: 153–73.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Кондратьева Е.И., Каширская Н.Ю., Капранов Н.И. Национальный консенсус «Муковисцидоз: определение, диагностические критерии, терапия». М.: «Компания Боргес», 205 с.</mixed-citation><mixed-citation xml:lang="en">Кондратьева Е.И., Каширская Н.Ю., Капранов Н.И. Национальный консенсус «Муковисцидоз: определение, диагностические критерии, терапия». М.: «Компания Боргес», 205 с.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Sezer RG, Aydemir G, Akcan AB et al. Nanoduct sweat conductivity measurements in 2664 patients: relationship to age, arterial blood gas, serum electrolyte profiles and clinical diagnosis. J Clin Med Res, 2013 Feb, 5(1): 34-41</mixed-citation><mixed-citation xml:lang="en">Sezer RG, Aydemir G, Akcan AB et al. Nanoduct sweat conductivity measurements in 2664 patients: relationship to age, arterial blood gas, serum electrolyte profiles and clinical diagnosis. J Clin Med Res, 2013 Feb, 5(1): 34-41</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Langen AV, Dompeling E, Yntema JB et al. Clinical evaluation of the Nanoduct sweat test system in the diagnosis of cystic fibrosis after newborn screening. Eur J Pediatr, 2015 Aug, 174(8): 1025-34.</mixed-citation><mixed-citation xml:lang="en">Langen AV, Dompeling E, Yntema JB et al. Clinical evaluation of the Nanoduct sweat test system in the diagnosis of cystic fibrosis after newborn screening. Eur J Pediatr, 2015 Aug, 174(8): 1025-34.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Barben J, Ammann RA, Metlagel A, Schöni MH. Conductivity determined by a new sweat analyzer compared with chloride concentrations for the diagnosis of cystic fibrosis. J Pediatr, 2005, 146: 183–8.</mixed-citation><mixed-citation xml:lang="en">Barben J, Ammann RA, Metlagel A, Schöni MH. Conductivity determined by a new sweat analyzer compared with chloride concentrations for the diagnosis of cystic fibrosis. J Pediatr, 2005, 146: 183–8.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Регистр больных муковисцидозом в Российской Федерации. 2015 год. Под ред. Е.И. Кондратьевой, С.А. Красовского, А.Ю. Воронковой, Е.Л. Амелиной, А.В. Черняка, Н.Ю. Каширской. М.: ИД «Медпрактика-М», 2016, 72 с.</mixed-citation><mixed-citation xml:lang="en">Регистр больных муковисцидозом в Российской Федерации. 2015 год. Под ред. Е.И. Кондратьевой, С.А. Красовского, А.Ю. Воронковой, Е.Л. Амелиной, А.В. Черняка, Н.Ю. Каширской. М.: ИД «Медпрактика-М», 2016, 72 с.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Farell PM, Rosenstein BJ, White TB et al. Cystic fibrosis foundation. Guidelines for diagnosis of cystic fibrosis in newborns through older adults: Cystic Fibrosis Foundation consensus report. J Pediatr, 2008, 153(2): S4-S14.</mixed-citation><mixed-citation xml:lang="en">Farell PM, Rosenstein BJ, White TB et al. Cystic fibrosis foundation. Guidelines for diagnosis of cystic fibrosis in newborns through older adults: Cystic Fibrosis Foundation consensus report. J Pediatr, 2008, 153(2): S4-S14.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">European cystic fibrosis society standarts of care working group. Best practice guidelines. В редакции Alan R Smith и Scott Bell (http://www. ecfs.eu/ecfs-standarts-care/introduction), 2014.</mixed-citation><mixed-citation xml:lang="en">European cystic fibrosis society standarts of care working group. Best practice guidelines. В редакции Alan R Smith и Scott Bell (http://www. ecfs.eu/ecfs-standarts-care/introduction), 2014.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Grosse SD, Rosenfeld M, Devine OJ, et al. Potential impact of newborn screening for cystic fibrosis on child survival: a systematic review and analysis. J Pediatr, 2006, 149: 362-366.</mixed-citation><mixed-citation xml:lang="en">Grosse SD, Rosenfeld M, Devine OJ, et al. Potential impact of newborn screening for cystic fibrosis on child survival: a systematic review and analysis. J Pediatr, 2006, 149: 362-366.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Dankert-Roelse JE, Mérelle ME. Newborn screening for CF: published evidence from Europe. J Pediatrics, 2005, 147(3Suppl): S15–20.</mixed-citation><mixed-citation xml:lang="en">Dankert-Roelse JE, Mérelle ME. Newborn screening for CF: published evidence from Europe. J Pediatrics, 2005, 147(3Suppl): S15–20.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Koscik RL, Lai HJ, Laxova A, et al. Preventing early, prolonged vitamin E deﬁciency: an opportunity for better cognitive outcomes via early diagnosis through neonatal screening. J Pediatr, 2005, 147: S51–6.</mixed-citation><mixed-citation xml:lang="en">Koscik RL, Lai HJ, Laxova A, et al. Preventing early, prolonged vitamin E deﬁciency: an opportunity for better cognitive outcomes via early diagnosis through neonatal screening. J Pediatr, 2005, 147: S51–6.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Accurso FJ, Sontag MK, Wagener JS. Complications associated with symptomatic diagnosis in infants with cystic fibrosis. Journal of Pediatrics, 2005, 147(3 suppl.): S37-S41.</mixed-citation><mixed-citation xml:lang="en">Accurso FJ, Sontag MK, Wagener JS. Complications associated with symptomatic diagnosis in infants with cystic fibrosis. Journal of Pediatrics, 2005, 147(3 suppl.): S37-S41.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Farrell PM, Lai HJ, Li Z, Kosorok MR, Laxova A, Green CG, et al. Evidence on improved outcomes with early diagnosis of cystic fibrosis through neonatal screening: Enough is enough! Journal of Pediatrics, 2005, 147(3 suppl.): S30-S6.</mixed-citation><mixed-citation xml:lang="en">Farrell PM, Lai HJ, Li Z, Kosorok MR, Laxova A, Green CG, et al. Evidence on improved outcomes with early diagnosis of cystic fibrosis through neonatal screening: Enough is enough! Journal of Pediatrics, 2005, 147(3 suppl.): S30-S6.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Sims EJ, Clark A, McCormick J, Mehta G, Connett G, Mehta A, et al. Cystic fibrosis diagnosed after 2 months of age leads to worse outcomes and requires more therapy. Pediatrics, 2007, 119(1): 19-28.</mixed-citation><mixed-citation xml:lang="en">Sims EJ, Clark A, McCormick J, Mehta G, Connett G, Mehta A, et al. Cystic fibrosis diagnosed after 2 months of age leads to worse outcomes and requires more therapy. Pediatrics, 2007, 119(1): 19-28.</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Sims EJ, McCormick J, Mehta G, Mehta A. Neonatal screening for cystic fibrosis is beneficial even in the context of modern treatment. Journal of Pediatrics, 2005, 147(3 suppl.): S42-S6.</mixed-citation><mixed-citation xml:lang="en">Sims EJ, McCormick J, Mehta G, Mehta A. Neonatal screening for cystic fibrosis is beneficial even in the context of modern treatment. Journal of Pediatrics, 2005, 147(3 suppl.): S42-S6.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Wang SS, Fitzsimmons SC, O’Leary LA, Rock MJ, Gwinn ML, Khoury MJ. Early diagnosis of cystic fibrosis in the newborn period and risk of Pseudomonas aeruginosa acquisition in the first 10 years of life: A registry-based longitudinal study. Pediatrics, 2001, 107(2): 274-9.</mixed-citation><mixed-citation xml:lang="en">Wang SS, Fitzsimmons SC, O’Leary LA, Rock MJ, Gwinn ML, Khoury MJ. Early diagnosis of cystic fibrosis in the newborn period and risk of Pseudomonas aeruginosa acquisition in the first 10 years of life: A registry-based longitudinal study. Pediatrics, 2001, 107(2): 274-9.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Siret D, Bretaudeau G, Branger B, et al. Comparing the clinical evolution of cystic fibrosis screened neonatally to that of cystic fibrosis diagnosed from clinical symptoms: a 10-year retrospective study in a French region (Brittany). Pediatr Pulmonol, 2003, 35: 342-9.</mixed-citation><mixed-citation xml:lang="en">Siret D, Bretaudeau G, Branger B, et al. Comparing the clinical evolution of cystic fibrosis screened neonatally to that of cystic fibrosis diagnosed from clinical symptoms: a 10-year retrospective study in a French region (Brittany). Pediatr Pulmonol, 2003, 35: 342-9.</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Кусова З.А. Эффективность программы массового обследования новорожденных на муковисцидоз. Автореферат дис. ... канд. мед. наук. М., 2011. 23 с.</mixed-citation><mixed-citation xml:lang="en">Кусова З.А. Эффективность программы массового обследования новорожденных на муковисцидоз. Автореферат дис. ... канд. мед. наук. М., 2011. 23 с.</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Merelle ME, Schouten JP, Gerritsen J, Dankert-Roelse JE. Influence of neonatal screening and central-ized treatment on long-term clinical outcome and survival of CF patients. Eur Respir J, 2001, 18: 306-15.</mixed-citation><mixed-citation xml:lang="en">Merelle ME, Schouten JP, Gerritsen J, Dankert-Roelse JE. Influence of neonatal screening and central-ized treatment on long-term clinical outcome and survival of CF patients. Eur Respir J, 2001, 18: 306-15.</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Lai HJ, Cheng Y, Cho H, Kosorok MR, Farrell PM. Association between initial disease presentation, lung disease outcomes, and survival in patients with cystic fibrosis. Am J Epidemiol, 2004, 159: 537-46.</mixed-citation><mixed-citation xml:lang="en">Lai HJ, Cheng Y, Cho H, Kosorok MR, Farrell PM. Association between initial disease presentation, lung disease outcomes, and survival in patients with cystic fibrosis. Am J Epidemiol, 2004, 159: 537-46.</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Carroll A.E, Downs SM. Comprehensive cost-utility analysis of newborn screening strategies. Pediatrics, 2006 May, 117(5 Pt 2): S287-95.</mixed-citation><mixed-citation xml:lang="en">Carroll A.E, Downs SM. Comprehensive cost-utility analysis of newborn screening strategies. Pediatrics, 2006 May, 117(5 Pt 2): S287-95.</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Grosse SD, Thompson JD, Ding Y, Glass M. The Use of Economic Evaluation to Inform Newborn Screening Policy Decisions: The Washington State Experience. Milbank Q, 2016, 94: 366-91.</mixed-citation><mixed-citation xml:lang="en">Grosse SD, Thompson JD, Ding Y, Glass M. The Use of Economic Evaluation to Inform Newborn Screening Policy Decisions: The Washington State Experience. Milbank Q, 2016, 94: 366-91.</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Report of the UK Cystic Fibrosis Trust Bone Mineralisation Working Group. Bone mineralization in cystic fibrosis. Cystic Fibrosis. 2007.</mixed-citation><mixed-citation xml:lang="en">Report of the UK Cystic Fibrosis Trust Bone Mineralisation Working Group. Bone mineralization in cystic fibrosis. Cystic Fibrosis. 2007.</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Sermet-Gaudelus I, Bianchi ML, Garabédian M, Aris RM, Morton A, Hardin DS, Elkin SL et al. European cystic fibrosis bone mineralisation guidelines. Journal of Cystic Fibrosis, 2011, 10(suppl 2): S16–S23.</mixed-citation><mixed-citation xml:lang="en">Sermet-Gaudelus I, Bianchi ML, Garabédian M, Aris RM, Morton A, Hardin DS, Elkin SL et al. European cystic fibrosis bone mineralisation guidelines. Journal of Cystic Fibrosis, 2011, 10(suppl 2): S16–S23.</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Красовский С.А. Остеопороз у взрослых больных муковисцидозом. Автореферат дис. ... канд. мед. наук. М., 2012</mixed-citation><mixed-citation xml:lang="en">Красовский С.А. Остеопороз у взрослых больных муковисцидозом. Автореферат дис. ... канд. мед. наук. М., 2012</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Kelly А, Moran A. Update on cystic fibrosis-related diabetes. Journal of Cystic Fibrosis, 2013, 12: 318–331</mixed-citation><mixed-citation xml:lang="en">Kelly А, Moran A. Update on cystic fibrosis-related diabetes. Journal of Cystic Fibrosis, 2013, 12: 318–331</mixed-citation></citation-alternatives></ref></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
