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<article 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" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="other" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Terapevticheskii arkhiv</journal-id><journal-title-group><journal-title xml:lang="en">Terapevticheskii arkhiv</journal-title><trans-title-group xml:lang="ru"><trans-title>Терапевтический архив</trans-title></trans-title-group></journal-title-group><issn publication-format="print">0040-3660</issn><issn publication-format="electronic">2309-5342</issn><publisher><publisher-name xml:lang="en">LLC Obyedinennaya Redaktsiya</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">29789</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>Editorial article</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>Передовая статья</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">Pulmonary hypertension in patients with systemic sclerosis with CREST-syndrome and without it</article-title><trans-title-group xml:lang="ru"><trans-title>Легочная гипертония у больных системной склеродермией с CREST-синдромом и без такового</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Karoli</surname><given-names>N A</given-names></name><name xml:lang="ru"><surname>Кароли</surname><given-names>Н А</given-names></name></name-alternatives><bio xml:lang="ru"><p>Саратовский государственный медицинский университет</p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Rebrov</surname><given-names>A P</given-names></name><name xml:lang="ru"><surname>Ребров</surname><given-names>А П</given-names></name></name-alternatives><bio xml:lang="ru"><p>Саратовский государственный медицинский университет</p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Orlova</surname><given-names>E E</given-names></name><name xml:lang="ru"><surname>Орлова</surname><given-names>Е Е</given-names></name></name-alternatives><bio xml:lang="ru"><p>Саратовский государственный медицинский университет</p></bio><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en"></institution></aff><aff><institution xml:lang="ru">Саратовский государственный медицинский университет</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2004-05-15" publication-format="electronic"><day>15</day><month>05</month><year>2004</year></pub-date><volume>79</volume><issue>5</issue><issue-title xml:lang="en">NO5 (2004)</issue-title><issue-title xml:lang="ru">ТОМ 79, №5 (2004)</issue-title><fpage>15</fpage><lpage>18</lpage><history><date date-type="received" iso-8601-date="2020-04-09"><day>09</day><month>04</month><year>2020</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2004, Consilium Medicum</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2004, ООО "Консилиум Медикум"</copyright-statement><copyright-year>2004</copyright-year><copyright-holder xml:lang="en">Consilium Medicum</copyright-holder><copyright-holder xml:lang="ru">ООО "Консилиум Медикум"</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://creativecommons.org/licenses/by-nc-sa/4.0</ali:license_ref></license></permissions><self-uri xlink:href="https://ter-arkhiv.ru/0040-3660/article/view/29789">https://ter-arkhiv.ru/0040-3660/article/view/29789</self-uri><abstract xml:lang="en"><p>Aim. To study incidence rate and characteristics of pulmonary hypertension development in patients with systemic sclerosis (SS).
Material and methods. The study included 31 SS patients (30 females, 1 male, age 33-75 years mean age 47.7+1.7 years).
Results. Pulmonary hypertension occurred more frequently in SS patients with CREST-syndrome than in SS patients free of this syndrome. SS patients with CREST-syndrome had also more severe ventricular hypertrophy than ventricular dilation.
Conclusion. Echocardiography proved to be a highly informative method for detection of pulmonary hypertension in patients with SS. The necessity of hemodynamical study in SS patients is emphasized.</p></abstract><trans-abstract xml:lang="ru"><p>Цель исследования. Изучение частоты встречаемости и особенностей развития легочной гипертензии у пациентов с системной склеродермией.
Материалы и методы. Обследован 31 пациент с системной склеродермией (30 женщин и 1 мужчина). Возраст пациентов составлял от 33 до 75 лет (в среднем 47,7 ± 1,7 года). Результаты. Легочная гипертония при ССД чаще встречается у больных с CREST-синдромом, чем без такового, у них также более выражены явления гипертрофии желудочков, чем их дилатационные изменения.
Заключение. Исследования показали высокую информативность эхокардиографии для выявления легочной гипертонии у больных системной склеродермией и необходимость тщательного изучения гемодинамики у этих пациентов.</p></trans-abstract><kwd-group xml:lang="en"><kwd>systemic sclerosis</kwd><kwd>pulmonary hypertension</kwd><kwd>echocardiography</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>системная склеродермия</kwd><kwd>легочная гипертензия</kwd><kwd>эхокардиография</kwd></kwd-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Гусева Н. Г. Системная склеродермия и псевдосклеродер мические синдромы. М.: Медицина; 1993.</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Fagan К. A., Collier D. H., Badesch D. В. Scleroderma-associ ated pulmonary hypertension who's at rick and why. Advance in pulmonary hypertension. www.Phassociation.org/medical, Advances_in_PH/.../Scleroderma-Associated_PH.as</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>Rockall A. G., Rickards D., Shaw P. J. Imaging of the pulmonary manifestation of systemic disease. Postgrad. Med. J. 2001 77:621-638.</mixed-citation></ref><ref id="B4"><label>4.</label><mixed-citation>Lee P., Langevilz P., Alderdice С. et al. Mortality in systemic sclerosis (scleroderma). Quart. J. Med. 1992; 82: 139-148.</mixed-citation></ref><ref id="B5"><label>5.</label><mixed-citation>Steen V., Owens G., Fino G. et al. Pulmonary involvement ir systemic sclerosis (scleroderma). Arthr. and Rheum. 1985; 28 759-767.</mixed-citation></ref><ref id="B6"><label>6.</label><mixed-citation>Minai O. A., Dweik R. A., Arroliga A. C. Manifestations of scleroderma pulmonary disease. Clin. Chest Med. 1998; 19: 713- 731.</mixed-citation></ref><ref id="B7"><label>7.</label><mixed-citation>MacGregor A. J, Canavan R., Knight С. et al. Pulmonary hypertension in systemic sclerosis: risk factor for progression and consequences for survival. Rheumatology 2001; 40: 453-459.</mixed-citation></ref><ref id="B8"><label>8.</label><mixed-citation>Murata I., Kihara H., Shinohara S. et al. Echocardiography evaluation of pulmonary arterial hypertension in patients with progressive systemic sclerosis and related syndomes. Jpn. Cire J. 1992; 56: 983-991.</mixed-citation></ref><ref id="B9"><label>9.</label><mixed-citation>Stupi A. M., Steen V. D., Owens G. R. et al. Pulmonary hypertension in the CREST syndrome variant of systemic sclerosis. Arthr. and Rheum. 1986; 29: 515-524.</mixed-citation></ref><ref id="B10"><label>10.</label><mixed-citation>Yousem S. A. The pulmonary pathologic manifestations of the CREST syndrome. Hum. Pathol. 1990; 21: 467-474.</mixed-citation></ref><ref id="B11"><label>11.</label><mixed-citation>Battle R. W., Davitt M. A., Cooper S. M. et al. Prevalence of pulmonary hypertension in limited and diffuse scleroderma. Chest 1996; 110: 1515-1519.</mixed-citation></ref><ref id="B12"><label>12.</label><mixed-citation>Hoeper M. M. Pulmonary hypertension in collagen vascular disease. Eur. Respir. J. 2002; 19: 571-576.</mixed-citation></ref><ref id="B13"><label>13.</label><mixed-citation>Yamane K., Ihn H., Asano Y. et al. Clinical and laboratory features of scleroderma patients with pulmonary hypertension. Rheumatology 2000; 39: 1269-1271.</mixed-citation></ref><ref id="B14"><label>14.</label><mixed-citation>Шиллер Н., Осипов М. А. Клиническая эхокардиография. M.; 1993.</mixed-citation></ref><ref id="B15"><label>15.</label><mixed-citation>Ungerer R. G., Tashkin D. P., Furst D. et al. Prevalence and clinical correlates of pulmonary arterial hypertension in progression systemic sclerosis. Am. J. Med. 1983; 75: 65-74.</mixed-citation></ref><ref id="B16"><label>16.</label><mixed-citation>D'Angelo W., Fries J., Masi A. et al. Pathologic observations in systemic sclerosis (scleroderma). Am. J. Med. 1969; 46: 428- 440.</mixed-citation></ref><ref id="B17"><label>17.</label><mixed-citation>Koh E. Т., Lee P., Gladman D. D., Abu-Shakra M. Pulmonary hypertension in systemic sclerosis an analysis of 17 patients. Br. J. Rheumatol. 1996; 35: 989-993.</mixed-citation></ref><ref id="B18"><label>18.</label><mixed-citation>Насонова В. А., Астапенко М. Г. Клиническая ревматология: Руководство для врачей. М.: Медицина; 1989. 175- 197.</mixed-citation></ref></ref-list></back></article>
