Differentiation therapy for non-acidic gastroesophageal reflux disease
Aim. To investigate the clinical and pathogenetic features of the non-acidic types of gastroesophageal reflux disease (GERD) and to evaluate the impact of combined therapy versus monotherapy on the course of this disease. Subjects and methods. The investigation enrolled 62 patients with non-acidic G...
Ausführliche Beschreibung
Autor*in: |
N B Lishchuk [verfasserIn] V I Simanenkov [verfasserIn] S V Tikhonov [verfasserIn] |
---|
Format: |
E-Artikel |
---|---|
Sprache: |
Russisch |
Erschienen: |
2017 |
---|
Schlagwörter: |
gastroesophageal reflux disease weakly alkaline) gastroesophageal reflux |
---|
Übergeordnetes Werk: |
In: Терапевтический архив - "Consilium Medicum" Publishing house, 2018, 89(2017), 4, Seite 57-63 |
---|---|
Übergeordnetes Werk: |
volume:89 ; year:2017 ; number:4 ; pages:57-63 |
Links: |
Link aufrufen |
---|
DOI / URN: |
10.17116/terarkh201789457-63 |
---|
Katalog-ID: |
DOAJ012672424 |
---|
LEADER | 01000caa a22002652 4500 | ||
---|---|---|---|
001 | DOAJ012672424 | ||
003 | DE-627 | ||
005 | 20230310045837.0 | ||
007 | cr uuu---uuuuu | ||
008 | 230225s2017 xx |||||o 00| ||rus c | ||
024 | 7 | |a 10.17116/terarkh201789457-63 |2 doi | |
035 | |a (DE-627)DOAJ012672424 | ||
035 | |a (DE-599)DOAJ38407acd26e44211bc7434f81b60f45f | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a rus | ||
100 | 0 | |a N B Lishchuk |e verfasserin |4 aut | |
245 | 1 | 0 | |a Differentiation therapy for non-acidic gastroesophageal reflux disease |
264 | 1 | |c 2017 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a Computermedien |b c |2 rdamedia | ||
338 | |a Online-Ressource |b cr |2 rdacarrier | ||
520 | |a Aim. To investigate the clinical and pathogenetic features of the non-acidic types of gastroesophageal reflux disease (GERD) and to evaluate the impact of combined therapy versus monotherapy on the course of this disease. Subjects and methods. The investigation enrolled 62 patients with non-acidic GERD. The follow-up period was 6 weeks. The patients were divided into 2 groups: 1) weakly acidic gastroesophageal refluxes (GER); 2) weakly alkaline GER. Then each group was distributed, thus making up 4 groups: 1) 19 patients with weakly acidic GER who received monotherapy with rabeprazole 20 mg/day; 2) 21 patients with weakly acidic GER had combined therapy with rabeprazole 20 mg and itopride; 3) 8 patients with weakly alkaline GER who received ursodeoxycholic acid (UDCA) monotherapy; and 4) 14 patients with weakly alkaline GER who had combined therapy with UDCA and itopride, The clinical symptoms of the disease, the endoscopic pattern of the upper gastrointestinal tract (GIT) mucosa, histological changes in the esophageal and gastric mucosa, and the results of 24-hour impedance pH monitoring were assessed over time. Results. During differentiation therapy, the majority of patients reported positive clinical changes and an improved or unchanged endoscopic pattern. Assessment of impedance pH monitoring results revealed decreases in the overall number of GERs, the presence of a bolus in the esophagus, and the number of proximal refluxes. These changes were noted not only in patients taking proton pump inhibitors (PPIs), but also in those treated with UDCA monotherapy or combined PPI and prokinetic therapy. Conclusion. A differentiated approach to non-acidic GER treatment contributes to its efficiency. Adding the prokinetic itomed (itopride hydrochloride) to PPI therapy in a patient with weakly acidic GER enhances the efficiency of treatment, by positively affecting upper GIT motility. The mainstay of therapy for GERD with a predominance of weakly alkaline refluxes is UDCA, the combination of the latter and the prokinetic can exert a more pronounced effect on the clinical and endoscopic pattern and upper GIT motility. | ||
650 | 4 | |a gastroesophageal reflux disease | |
650 | 4 | |a non-acidic (weakly acidic | |
650 | 4 | |a weakly alkaline) gastroesophageal reflux | |
650 | 4 | |a duodenogastroesophageal reflux | |
650 | 4 | |a antisecretory therapy | |
650 | 4 | |a rabeprazole | |
650 | 4 | |a itopride | |
650 | 4 | |a ursodeoxycholic acid | |
653 | 0 | |a Medicine | |
653 | 0 | |a R | |
700 | 0 | |a V I Simanenkov |e verfasserin |4 aut | |
700 | 0 | |a S V Tikhonov |e verfasserin |4 aut | |
773 | 0 | 8 | |i In |t Терапевтический архив |d "Consilium Medicum" Publishing house, 2018 |g 89(2017), 4, Seite 57-63 |w (DE-627)1760620270 |x 23095342 |7 nnns |
773 | 1 | 8 | |g volume:89 |g year:2017 |g number:4 |g pages:57-63 |
856 | 4 | 0 | |u https://doi.org/10.17116/terarkh201789457-63 |z kostenfrei |
856 | 4 | 0 | |u https://doaj.org/article/38407acd26e44211bc7434f81b60f45f |z kostenfrei |
856 | 4 | 0 | |u https://ter-arkhiv.ru/0040-3660/article/viewFile/32209/pdf |z kostenfrei |
856 | 4 | 2 | |u https://doaj.org/toc/0040-3660 |y Journal toc |z kostenfrei |
856 | 4 | 2 | |u https://doaj.org/toc/2309-5342 |y Journal toc |z kostenfrei |
912 | |a GBV_USEFLAG_A | ||
912 | |a SYSFLAG_A | ||
912 | |a GBV_DOAJ | ||
951 | |a AR | ||
952 | |d 89 |j 2017 |e 4 |h 57-63 |
author_variant |
n b l nbl v i s vis s v t svt |
---|---|
matchkey_str |
article:23095342:2017----::ifrnitoteayonncdcatosp |
hierarchy_sort_str |
2017 |
publishDate |
2017 |
allfields |
10.17116/terarkh201789457-63 doi (DE-627)DOAJ012672424 (DE-599)DOAJ38407acd26e44211bc7434f81b60f45f DE-627 ger DE-627 rakwb rus N B Lishchuk verfasserin aut Differentiation therapy for non-acidic gastroesophageal reflux disease 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Aim. To investigate the clinical and pathogenetic features of the non-acidic types of gastroesophageal reflux disease (GERD) and to evaluate the impact of combined therapy versus monotherapy on the course of this disease. Subjects and methods. The investigation enrolled 62 patients with non-acidic GERD. The follow-up period was 6 weeks. The patients were divided into 2 groups: 1) weakly acidic gastroesophageal refluxes (GER); 2) weakly alkaline GER. Then each group was distributed, thus making up 4 groups: 1) 19 patients with weakly acidic GER who received monotherapy with rabeprazole 20 mg/day; 2) 21 patients with weakly acidic GER had combined therapy with rabeprazole 20 mg and itopride; 3) 8 patients with weakly alkaline GER who received ursodeoxycholic acid (UDCA) monotherapy; and 4) 14 patients with weakly alkaline GER who had combined therapy with UDCA and itopride, The clinical symptoms of the disease, the endoscopic pattern of the upper gastrointestinal tract (GIT) mucosa, histological changes in the esophageal and gastric mucosa, and the results of 24-hour impedance pH monitoring were assessed over time. Results. During differentiation therapy, the majority of patients reported positive clinical changes and an improved or unchanged endoscopic pattern. Assessment of impedance pH monitoring results revealed decreases in the overall number of GERs, the presence of a bolus in the esophagus, and the number of proximal refluxes. These changes were noted not only in patients taking proton pump inhibitors (PPIs), but also in those treated with UDCA monotherapy or combined PPI and prokinetic therapy. Conclusion. A differentiated approach to non-acidic GER treatment contributes to its efficiency. Adding the prokinetic itomed (itopride hydrochloride) to PPI therapy in a patient with weakly acidic GER enhances the efficiency of treatment, by positively affecting upper GIT motility. The mainstay of therapy for GERD with a predominance of weakly alkaline refluxes is UDCA, the combination of the latter and the prokinetic can exert a more pronounced effect on the clinical and endoscopic pattern and upper GIT motility. gastroesophageal reflux disease non-acidic (weakly acidic weakly alkaline) gastroesophageal reflux duodenogastroesophageal reflux antisecretory therapy rabeprazole itopride ursodeoxycholic acid Medicine R V I Simanenkov verfasserin aut S V Tikhonov verfasserin aut In Терапевтический архив "Consilium Medicum" Publishing house, 2018 89(2017), 4, Seite 57-63 (DE-627)1760620270 23095342 nnns volume:89 year:2017 number:4 pages:57-63 https://doi.org/10.17116/terarkh201789457-63 kostenfrei https://doaj.org/article/38407acd26e44211bc7434f81b60f45f kostenfrei https://ter-arkhiv.ru/0040-3660/article/viewFile/32209/pdf kostenfrei https://doaj.org/toc/0040-3660 Journal toc kostenfrei https://doaj.org/toc/2309-5342 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ AR 89 2017 4 57-63 |
spelling |
10.17116/terarkh201789457-63 doi (DE-627)DOAJ012672424 (DE-599)DOAJ38407acd26e44211bc7434f81b60f45f DE-627 ger DE-627 rakwb rus N B Lishchuk verfasserin aut Differentiation therapy for non-acidic gastroesophageal reflux disease 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Aim. To investigate the clinical and pathogenetic features of the non-acidic types of gastroesophageal reflux disease (GERD) and to evaluate the impact of combined therapy versus monotherapy on the course of this disease. Subjects and methods. The investigation enrolled 62 patients with non-acidic GERD. The follow-up period was 6 weeks. The patients were divided into 2 groups: 1) weakly acidic gastroesophageal refluxes (GER); 2) weakly alkaline GER. Then each group was distributed, thus making up 4 groups: 1) 19 patients with weakly acidic GER who received monotherapy with rabeprazole 20 mg/day; 2) 21 patients with weakly acidic GER had combined therapy with rabeprazole 20 mg and itopride; 3) 8 patients with weakly alkaline GER who received ursodeoxycholic acid (UDCA) monotherapy; and 4) 14 patients with weakly alkaline GER who had combined therapy with UDCA and itopride, The clinical symptoms of the disease, the endoscopic pattern of the upper gastrointestinal tract (GIT) mucosa, histological changes in the esophageal and gastric mucosa, and the results of 24-hour impedance pH monitoring were assessed over time. Results. During differentiation therapy, the majority of patients reported positive clinical changes and an improved or unchanged endoscopic pattern. Assessment of impedance pH monitoring results revealed decreases in the overall number of GERs, the presence of a bolus in the esophagus, and the number of proximal refluxes. These changes were noted not only in patients taking proton pump inhibitors (PPIs), but also in those treated with UDCA monotherapy or combined PPI and prokinetic therapy. Conclusion. A differentiated approach to non-acidic GER treatment contributes to its efficiency. Adding the prokinetic itomed (itopride hydrochloride) to PPI therapy in a patient with weakly acidic GER enhances the efficiency of treatment, by positively affecting upper GIT motility. The mainstay of therapy for GERD with a predominance of weakly alkaline refluxes is UDCA, the combination of the latter and the prokinetic can exert a more pronounced effect on the clinical and endoscopic pattern and upper GIT motility. gastroesophageal reflux disease non-acidic (weakly acidic weakly alkaline) gastroesophageal reflux duodenogastroesophageal reflux antisecretory therapy rabeprazole itopride ursodeoxycholic acid Medicine R V I Simanenkov verfasserin aut S V Tikhonov verfasserin aut In Терапевтический архив "Consilium Medicum" Publishing house, 2018 89(2017), 4, Seite 57-63 (DE-627)1760620270 23095342 nnns volume:89 year:2017 number:4 pages:57-63 https://doi.org/10.17116/terarkh201789457-63 kostenfrei https://doaj.org/article/38407acd26e44211bc7434f81b60f45f kostenfrei https://ter-arkhiv.ru/0040-3660/article/viewFile/32209/pdf kostenfrei https://doaj.org/toc/0040-3660 Journal toc kostenfrei https://doaj.org/toc/2309-5342 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ AR 89 2017 4 57-63 |
allfields_unstemmed |
10.17116/terarkh201789457-63 doi (DE-627)DOAJ012672424 (DE-599)DOAJ38407acd26e44211bc7434f81b60f45f DE-627 ger DE-627 rakwb rus N B Lishchuk verfasserin aut Differentiation therapy for non-acidic gastroesophageal reflux disease 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Aim. To investigate the clinical and pathogenetic features of the non-acidic types of gastroesophageal reflux disease (GERD) and to evaluate the impact of combined therapy versus monotherapy on the course of this disease. Subjects and methods. The investigation enrolled 62 patients with non-acidic GERD. The follow-up period was 6 weeks. The patients were divided into 2 groups: 1) weakly acidic gastroesophageal refluxes (GER); 2) weakly alkaline GER. Then each group was distributed, thus making up 4 groups: 1) 19 patients with weakly acidic GER who received monotherapy with rabeprazole 20 mg/day; 2) 21 patients with weakly acidic GER had combined therapy with rabeprazole 20 mg and itopride; 3) 8 patients with weakly alkaline GER who received ursodeoxycholic acid (UDCA) monotherapy; and 4) 14 patients with weakly alkaline GER who had combined therapy with UDCA and itopride, The clinical symptoms of the disease, the endoscopic pattern of the upper gastrointestinal tract (GIT) mucosa, histological changes in the esophageal and gastric mucosa, and the results of 24-hour impedance pH monitoring were assessed over time. Results. During differentiation therapy, the majority of patients reported positive clinical changes and an improved or unchanged endoscopic pattern. Assessment of impedance pH monitoring results revealed decreases in the overall number of GERs, the presence of a bolus in the esophagus, and the number of proximal refluxes. These changes were noted not only in patients taking proton pump inhibitors (PPIs), but also in those treated with UDCA monotherapy or combined PPI and prokinetic therapy. Conclusion. A differentiated approach to non-acidic GER treatment contributes to its efficiency. Adding the prokinetic itomed (itopride hydrochloride) to PPI therapy in a patient with weakly acidic GER enhances the efficiency of treatment, by positively affecting upper GIT motility. The mainstay of therapy for GERD with a predominance of weakly alkaline refluxes is UDCA, the combination of the latter and the prokinetic can exert a more pronounced effect on the clinical and endoscopic pattern and upper GIT motility. gastroesophageal reflux disease non-acidic (weakly acidic weakly alkaline) gastroesophageal reflux duodenogastroesophageal reflux antisecretory therapy rabeprazole itopride ursodeoxycholic acid Medicine R V I Simanenkov verfasserin aut S V Tikhonov verfasserin aut In Терапевтический архив "Consilium Medicum" Publishing house, 2018 89(2017), 4, Seite 57-63 (DE-627)1760620270 23095342 nnns volume:89 year:2017 number:4 pages:57-63 https://doi.org/10.17116/terarkh201789457-63 kostenfrei https://doaj.org/article/38407acd26e44211bc7434f81b60f45f kostenfrei https://ter-arkhiv.ru/0040-3660/article/viewFile/32209/pdf kostenfrei https://doaj.org/toc/0040-3660 Journal toc kostenfrei https://doaj.org/toc/2309-5342 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ AR 89 2017 4 57-63 |
allfieldsGer |
10.17116/terarkh201789457-63 doi (DE-627)DOAJ012672424 (DE-599)DOAJ38407acd26e44211bc7434f81b60f45f DE-627 ger DE-627 rakwb rus N B Lishchuk verfasserin aut Differentiation therapy for non-acidic gastroesophageal reflux disease 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Aim. To investigate the clinical and pathogenetic features of the non-acidic types of gastroesophageal reflux disease (GERD) and to evaluate the impact of combined therapy versus monotherapy on the course of this disease. Subjects and methods. The investigation enrolled 62 patients with non-acidic GERD. The follow-up period was 6 weeks. The patients were divided into 2 groups: 1) weakly acidic gastroesophageal refluxes (GER); 2) weakly alkaline GER. Then each group was distributed, thus making up 4 groups: 1) 19 patients with weakly acidic GER who received monotherapy with rabeprazole 20 mg/day; 2) 21 patients with weakly acidic GER had combined therapy with rabeprazole 20 mg and itopride; 3) 8 patients with weakly alkaline GER who received ursodeoxycholic acid (UDCA) monotherapy; and 4) 14 patients with weakly alkaline GER who had combined therapy with UDCA and itopride, The clinical symptoms of the disease, the endoscopic pattern of the upper gastrointestinal tract (GIT) mucosa, histological changes in the esophageal and gastric mucosa, and the results of 24-hour impedance pH monitoring were assessed over time. Results. During differentiation therapy, the majority of patients reported positive clinical changes and an improved or unchanged endoscopic pattern. Assessment of impedance pH monitoring results revealed decreases in the overall number of GERs, the presence of a bolus in the esophagus, and the number of proximal refluxes. These changes were noted not only in patients taking proton pump inhibitors (PPIs), but also in those treated with UDCA monotherapy or combined PPI and prokinetic therapy. Conclusion. A differentiated approach to non-acidic GER treatment contributes to its efficiency. Adding the prokinetic itomed (itopride hydrochloride) to PPI therapy in a patient with weakly acidic GER enhances the efficiency of treatment, by positively affecting upper GIT motility. The mainstay of therapy for GERD with a predominance of weakly alkaline refluxes is UDCA, the combination of the latter and the prokinetic can exert a more pronounced effect on the clinical and endoscopic pattern and upper GIT motility. gastroesophageal reflux disease non-acidic (weakly acidic weakly alkaline) gastroesophageal reflux duodenogastroesophageal reflux antisecretory therapy rabeprazole itopride ursodeoxycholic acid Medicine R V I Simanenkov verfasserin aut S V Tikhonov verfasserin aut In Терапевтический архив "Consilium Medicum" Publishing house, 2018 89(2017), 4, Seite 57-63 (DE-627)1760620270 23095342 nnns volume:89 year:2017 number:4 pages:57-63 https://doi.org/10.17116/terarkh201789457-63 kostenfrei https://doaj.org/article/38407acd26e44211bc7434f81b60f45f kostenfrei https://ter-arkhiv.ru/0040-3660/article/viewFile/32209/pdf kostenfrei https://doaj.org/toc/0040-3660 Journal toc kostenfrei https://doaj.org/toc/2309-5342 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ AR 89 2017 4 57-63 |
allfieldsSound |
10.17116/terarkh201789457-63 doi (DE-627)DOAJ012672424 (DE-599)DOAJ38407acd26e44211bc7434f81b60f45f DE-627 ger DE-627 rakwb rus N B Lishchuk verfasserin aut Differentiation therapy for non-acidic gastroesophageal reflux disease 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Aim. To investigate the clinical and pathogenetic features of the non-acidic types of gastroesophageal reflux disease (GERD) and to evaluate the impact of combined therapy versus monotherapy on the course of this disease. Subjects and methods. The investigation enrolled 62 patients with non-acidic GERD. The follow-up period was 6 weeks. The patients were divided into 2 groups: 1) weakly acidic gastroesophageal refluxes (GER); 2) weakly alkaline GER. Then each group was distributed, thus making up 4 groups: 1) 19 patients with weakly acidic GER who received monotherapy with rabeprazole 20 mg/day; 2) 21 patients with weakly acidic GER had combined therapy with rabeprazole 20 mg and itopride; 3) 8 patients with weakly alkaline GER who received ursodeoxycholic acid (UDCA) monotherapy; and 4) 14 patients with weakly alkaline GER who had combined therapy with UDCA and itopride, The clinical symptoms of the disease, the endoscopic pattern of the upper gastrointestinal tract (GIT) mucosa, histological changes in the esophageal and gastric mucosa, and the results of 24-hour impedance pH monitoring were assessed over time. Results. During differentiation therapy, the majority of patients reported positive clinical changes and an improved or unchanged endoscopic pattern. Assessment of impedance pH monitoring results revealed decreases in the overall number of GERs, the presence of a bolus in the esophagus, and the number of proximal refluxes. These changes were noted not only in patients taking proton pump inhibitors (PPIs), but also in those treated with UDCA monotherapy or combined PPI and prokinetic therapy. Conclusion. A differentiated approach to non-acidic GER treatment contributes to its efficiency. Adding the prokinetic itomed (itopride hydrochloride) to PPI therapy in a patient with weakly acidic GER enhances the efficiency of treatment, by positively affecting upper GIT motility. The mainstay of therapy for GERD with a predominance of weakly alkaline refluxes is UDCA, the combination of the latter and the prokinetic can exert a more pronounced effect on the clinical and endoscopic pattern and upper GIT motility. gastroesophageal reflux disease non-acidic (weakly acidic weakly alkaline) gastroesophageal reflux duodenogastroesophageal reflux antisecretory therapy rabeprazole itopride ursodeoxycholic acid Medicine R V I Simanenkov verfasserin aut S V Tikhonov verfasserin aut In Терапевтический архив "Consilium Medicum" Publishing house, 2018 89(2017), 4, Seite 57-63 (DE-627)1760620270 23095342 nnns volume:89 year:2017 number:4 pages:57-63 https://doi.org/10.17116/terarkh201789457-63 kostenfrei https://doaj.org/article/38407acd26e44211bc7434f81b60f45f kostenfrei https://ter-arkhiv.ru/0040-3660/article/viewFile/32209/pdf kostenfrei https://doaj.org/toc/0040-3660 Journal toc kostenfrei https://doaj.org/toc/2309-5342 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ AR 89 2017 4 57-63 |
language |
Russian |
source |
In Терапевтический архив 89(2017), 4, Seite 57-63 volume:89 year:2017 number:4 pages:57-63 |
sourceStr |
In Терапевтический архив 89(2017), 4, Seite 57-63 volume:89 year:2017 number:4 pages:57-63 |
format_phy_str_mv |
Article |
institution |
findex.gbv.de |
topic_facet |
gastroesophageal reflux disease non-acidic (weakly acidic weakly alkaline) gastroesophageal reflux duodenogastroesophageal reflux antisecretory therapy rabeprazole itopride ursodeoxycholic acid Medicine R |
isfreeaccess_bool |
true |
container_title |
Терапевтический архив |
authorswithroles_txt_mv |
N B Lishchuk @@aut@@ V I Simanenkov @@aut@@ S V Tikhonov @@aut@@ |
publishDateDaySort_date |
2017-01-01T00:00:00Z |
hierarchy_top_id |
1760620270 |
id |
DOAJ012672424 |
language_de |
russisch |
fullrecord |
<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">DOAJ012672424</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230310045837.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">230225s2017 xx |||||o 00| ||rus c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.17116/terarkh201789457-63</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)DOAJ012672424</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-599)DOAJ38407acd26e44211bc7434f81b60f45f</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">rus</subfield></datafield><datafield tag="100" ind1="0" ind2=" "><subfield code="a">N B Lishchuk</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Differentiation therapy for non-acidic gastroesophageal reflux disease</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2017</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">Text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">Computermedien</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Online-Ressource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Aim. To investigate the clinical and pathogenetic features of the non-acidic types of gastroesophageal reflux disease (GERD) and to evaluate the impact of combined therapy versus monotherapy on the course of this disease. Subjects and methods. The investigation enrolled 62 patients with non-acidic GERD. The follow-up period was 6 weeks. The patients were divided into 2 groups: 1) weakly acidic gastroesophageal refluxes (GER); 2) weakly alkaline GER. Then each group was distributed, thus making up 4 groups: 1) 19 patients with weakly acidic GER who received monotherapy with rabeprazole 20 mg/day; 2) 21 patients with weakly acidic GER had combined therapy with rabeprazole 20 mg and itopride; 3) 8 patients with weakly alkaline GER who received ursodeoxycholic acid (UDCA) monotherapy; and 4) 14 patients with weakly alkaline GER who had combined therapy with UDCA and itopride, The clinical symptoms of the disease, the endoscopic pattern of the upper gastrointestinal tract (GIT) mucosa, histological changes in the esophageal and gastric mucosa, and the results of 24-hour impedance pH monitoring were assessed over time. Results. During differentiation therapy, the majority of patients reported positive clinical changes and an improved or unchanged endoscopic pattern. Assessment of impedance pH monitoring results revealed decreases in the overall number of GERs, the presence of a bolus in the esophagus, and the number of proximal refluxes. These changes were noted not only in patients taking proton pump inhibitors (PPIs), but also in those treated with UDCA monotherapy or combined PPI and prokinetic therapy. Conclusion. A differentiated approach to non-acidic GER treatment contributes to its efficiency. Adding the prokinetic itomed (itopride hydrochloride) to PPI therapy in a patient with weakly acidic GER enhances the efficiency of treatment, by positively affecting upper GIT motility. The mainstay of therapy for GERD with a predominance of weakly alkaline refluxes is UDCA, the combination of the latter and the prokinetic can exert a more pronounced effect on the clinical and endoscopic pattern and upper GIT motility.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">gastroesophageal reflux disease</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">non-acidic (weakly acidic</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">weakly alkaline) gastroesophageal reflux</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">duodenogastroesophageal reflux</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">antisecretory therapy</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">rabeprazole</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">itopride</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">ursodeoxycholic acid</subfield></datafield><datafield tag="653" ind1=" " ind2="0"><subfield code="a">Medicine</subfield></datafield><datafield tag="653" ind1=" " ind2="0"><subfield code="a">R</subfield></datafield><datafield tag="700" ind1="0" ind2=" "><subfield code="a">V I Simanenkov</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="0" ind2=" "><subfield code="a">S V Tikhonov</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">In</subfield><subfield code="t">Терапевтический архив</subfield><subfield code="d">"Consilium Medicum" Publishing house, 2018</subfield><subfield code="g">89(2017), 4, Seite 57-63</subfield><subfield code="w">(DE-627)1760620270</subfield><subfield code="x">23095342</subfield><subfield code="7">nnns</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:89</subfield><subfield code="g">year:2017</subfield><subfield code="g">number:4</subfield><subfield code="g">pages:57-63</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://doi.org/10.17116/terarkh201789457-63</subfield><subfield code="z">kostenfrei</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://doaj.org/article/38407acd26e44211bc7434f81b60f45f</subfield><subfield code="z">kostenfrei</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://ter-arkhiv.ru/0040-3660/article/viewFile/32209/pdf</subfield><subfield code="z">kostenfrei</subfield></datafield><datafield tag="856" ind1="4" ind2="2"><subfield code="u">https://doaj.org/toc/0040-3660</subfield><subfield code="y">Journal toc</subfield><subfield code="z">kostenfrei</subfield></datafield><datafield tag="856" ind1="4" ind2="2"><subfield code="u">https://doaj.org/toc/2309-5342</subfield><subfield code="y">Journal toc</subfield><subfield code="z">kostenfrei</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_A</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SYSFLAG_A</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_DOAJ</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">89</subfield><subfield code="j">2017</subfield><subfield code="e">4</subfield><subfield code="h">57-63</subfield></datafield></record></collection>
|
author |
N B Lishchuk |
spellingShingle |
N B Lishchuk misc gastroesophageal reflux disease misc non-acidic (weakly acidic misc weakly alkaline) gastroesophageal reflux misc duodenogastroesophageal reflux misc antisecretory therapy misc rabeprazole misc itopride misc ursodeoxycholic acid misc Medicine misc R Differentiation therapy for non-acidic gastroesophageal reflux disease |
authorStr |
N B Lishchuk |
ppnlink_with_tag_str_mv |
@@773@@(DE-627)1760620270 |
format |
electronic Article |
delete_txt_mv |
keep |
author_role |
aut aut aut |
collection |
DOAJ |
remote_str |
true |
illustrated |
Not Illustrated |
issn |
23095342 |
topic_title |
Differentiation therapy for non-acidic gastroesophageal reflux disease gastroesophageal reflux disease non-acidic (weakly acidic weakly alkaline) gastroesophageal reflux duodenogastroesophageal reflux antisecretory therapy rabeprazole itopride ursodeoxycholic acid |
topic |
misc gastroesophageal reflux disease misc non-acidic (weakly acidic misc weakly alkaline) gastroesophageal reflux misc duodenogastroesophageal reflux misc antisecretory therapy misc rabeprazole misc itopride misc ursodeoxycholic acid misc Medicine misc R |
topic_unstemmed |
misc gastroesophageal reflux disease misc non-acidic (weakly acidic misc weakly alkaline) gastroesophageal reflux misc duodenogastroesophageal reflux misc antisecretory therapy misc rabeprazole misc itopride misc ursodeoxycholic acid misc Medicine misc R |
topic_browse |
misc gastroesophageal reflux disease misc non-acidic (weakly acidic misc weakly alkaline) gastroesophageal reflux misc duodenogastroesophageal reflux misc antisecretory therapy misc rabeprazole misc itopride misc ursodeoxycholic acid misc Medicine misc R |
format_facet |
Elektronische Aufsätze Aufsätze Elektronische Ressource |
format_main_str_mv |
Text Zeitschrift/Artikel |
carriertype_str_mv |
cr |
hierarchy_parent_title |
Терапевтический архив |
hierarchy_parent_id |
1760620270 |
hierarchy_top_title |
Терапевтический архив |
isfreeaccess_txt |
true |
familylinks_str_mv |
(DE-627)1760620270 |
title |
Differentiation therapy for non-acidic gastroesophageal reflux disease |
ctrlnum |
(DE-627)DOAJ012672424 (DE-599)DOAJ38407acd26e44211bc7434f81b60f45f |
title_full |
Differentiation therapy for non-acidic gastroesophageal reflux disease |
author_sort |
N B Lishchuk |
journal |
Терапевтический архив |
journalStr |
Терапевтический архив |
lang_code |
rus |
isOA_bool |
true |
recordtype |
marc |
publishDateSort |
2017 |
contenttype_str_mv |
txt |
container_start_page |
57 |
author_browse |
N B Lishchuk V I Simanenkov S V Tikhonov |
container_volume |
89 |
format_se |
Elektronische Aufsätze |
author-letter |
N B Lishchuk |
doi_str_mv |
10.17116/terarkh201789457-63 |
author2-role |
verfasserin |
title_sort |
differentiation therapy for non-acidic gastroesophageal reflux disease |
title_auth |
Differentiation therapy for non-acidic gastroesophageal reflux disease |
abstract |
Aim. To investigate the clinical and pathogenetic features of the non-acidic types of gastroesophageal reflux disease (GERD) and to evaluate the impact of combined therapy versus monotherapy on the course of this disease. Subjects and methods. The investigation enrolled 62 patients with non-acidic GERD. The follow-up period was 6 weeks. The patients were divided into 2 groups: 1) weakly acidic gastroesophageal refluxes (GER); 2) weakly alkaline GER. Then each group was distributed, thus making up 4 groups: 1) 19 patients with weakly acidic GER who received monotherapy with rabeprazole 20 mg/day; 2) 21 patients with weakly acidic GER had combined therapy with rabeprazole 20 mg and itopride; 3) 8 patients with weakly alkaline GER who received ursodeoxycholic acid (UDCA) monotherapy; and 4) 14 patients with weakly alkaline GER who had combined therapy with UDCA and itopride, The clinical symptoms of the disease, the endoscopic pattern of the upper gastrointestinal tract (GIT) mucosa, histological changes in the esophageal and gastric mucosa, and the results of 24-hour impedance pH monitoring were assessed over time. Results. During differentiation therapy, the majority of patients reported positive clinical changes and an improved or unchanged endoscopic pattern. Assessment of impedance pH monitoring results revealed decreases in the overall number of GERs, the presence of a bolus in the esophagus, and the number of proximal refluxes. These changes were noted not only in patients taking proton pump inhibitors (PPIs), but also in those treated with UDCA monotherapy or combined PPI and prokinetic therapy. Conclusion. A differentiated approach to non-acidic GER treatment contributes to its efficiency. Adding the prokinetic itomed (itopride hydrochloride) to PPI therapy in a patient with weakly acidic GER enhances the efficiency of treatment, by positively affecting upper GIT motility. The mainstay of therapy for GERD with a predominance of weakly alkaline refluxes is UDCA, the combination of the latter and the prokinetic can exert a more pronounced effect on the clinical and endoscopic pattern and upper GIT motility. |
abstractGer |
Aim. To investigate the clinical and pathogenetic features of the non-acidic types of gastroesophageal reflux disease (GERD) and to evaluate the impact of combined therapy versus monotherapy on the course of this disease. Subjects and methods. The investigation enrolled 62 patients with non-acidic GERD. The follow-up period was 6 weeks. The patients were divided into 2 groups: 1) weakly acidic gastroesophageal refluxes (GER); 2) weakly alkaline GER. Then each group was distributed, thus making up 4 groups: 1) 19 patients with weakly acidic GER who received monotherapy with rabeprazole 20 mg/day; 2) 21 patients with weakly acidic GER had combined therapy with rabeprazole 20 mg and itopride; 3) 8 patients with weakly alkaline GER who received ursodeoxycholic acid (UDCA) monotherapy; and 4) 14 patients with weakly alkaline GER who had combined therapy with UDCA and itopride, The clinical symptoms of the disease, the endoscopic pattern of the upper gastrointestinal tract (GIT) mucosa, histological changes in the esophageal and gastric mucosa, and the results of 24-hour impedance pH monitoring were assessed over time. Results. During differentiation therapy, the majority of patients reported positive clinical changes and an improved or unchanged endoscopic pattern. Assessment of impedance pH monitoring results revealed decreases in the overall number of GERs, the presence of a bolus in the esophagus, and the number of proximal refluxes. These changes were noted not only in patients taking proton pump inhibitors (PPIs), but also in those treated with UDCA monotherapy or combined PPI and prokinetic therapy. Conclusion. A differentiated approach to non-acidic GER treatment contributes to its efficiency. Adding the prokinetic itomed (itopride hydrochloride) to PPI therapy in a patient with weakly acidic GER enhances the efficiency of treatment, by positively affecting upper GIT motility. The mainstay of therapy for GERD with a predominance of weakly alkaline refluxes is UDCA, the combination of the latter and the prokinetic can exert a more pronounced effect on the clinical and endoscopic pattern and upper GIT motility. |
abstract_unstemmed |
Aim. To investigate the clinical and pathogenetic features of the non-acidic types of gastroesophageal reflux disease (GERD) and to evaluate the impact of combined therapy versus monotherapy on the course of this disease. Subjects and methods. The investigation enrolled 62 patients with non-acidic GERD. The follow-up period was 6 weeks. The patients were divided into 2 groups: 1) weakly acidic gastroesophageal refluxes (GER); 2) weakly alkaline GER. Then each group was distributed, thus making up 4 groups: 1) 19 patients with weakly acidic GER who received monotherapy with rabeprazole 20 mg/day; 2) 21 patients with weakly acidic GER had combined therapy with rabeprazole 20 mg and itopride; 3) 8 patients with weakly alkaline GER who received ursodeoxycholic acid (UDCA) monotherapy; and 4) 14 patients with weakly alkaline GER who had combined therapy with UDCA and itopride, The clinical symptoms of the disease, the endoscopic pattern of the upper gastrointestinal tract (GIT) mucosa, histological changes in the esophageal and gastric mucosa, and the results of 24-hour impedance pH monitoring were assessed over time. Results. During differentiation therapy, the majority of patients reported positive clinical changes and an improved or unchanged endoscopic pattern. Assessment of impedance pH monitoring results revealed decreases in the overall number of GERs, the presence of a bolus in the esophagus, and the number of proximal refluxes. These changes were noted not only in patients taking proton pump inhibitors (PPIs), but also in those treated with UDCA monotherapy or combined PPI and prokinetic therapy. Conclusion. A differentiated approach to non-acidic GER treatment contributes to its efficiency. Adding the prokinetic itomed (itopride hydrochloride) to PPI therapy in a patient with weakly acidic GER enhances the efficiency of treatment, by positively affecting upper GIT motility. The mainstay of therapy for GERD with a predominance of weakly alkaline refluxes is UDCA, the combination of the latter and the prokinetic can exert a more pronounced effect on the clinical and endoscopic pattern and upper GIT motility. |
collection_details |
GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ |
container_issue |
4 |
title_short |
Differentiation therapy for non-acidic gastroesophageal reflux disease |
url |
https://doi.org/10.17116/terarkh201789457-63 https://doaj.org/article/38407acd26e44211bc7434f81b60f45f https://ter-arkhiv.ru/0040-3660/article/viewFile/32209/pdf https://doaj.org/toc/0040-3660 https://doaj.org/toc/2309-5342 |
remote_bool |
true |
author2 |
V I Simanenkov S V Tikhonov |
author2Str |
V I Simanenkov S V Tikhonov |
ppnlink |
1760620270 |
mediatype_str_mv |
c |
isOA_txt |
true |
hochschulschrift_bool |
false |
doi_str |
10.17116/terarkh201789457-63 |
up_date |
2024-07-03T13:24:36.998Z |
_version_ |
1803564432230449152 |
fullrecord_marcxml |
<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">DOAJ012672424</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230310045837.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">230225s2017 xx |||||o 00| ||rus c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.17116/terarkh201789457-63</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)DOAJ012672424</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-599)DOAJ38407acd26e44211bc7434f81b60f45f</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">rus</subfield></datafield><datafield tag="100" ind1="0" ind2=" "><subfield code="a">N B Lishchuk</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Differentiation therapy for non-acidic gastroesophageal reflux disease</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2017</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">Text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">Computermedien</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Online-Ressource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Aim. To investigate the clinical and pathogenetic features of the non-acidic types of gastroesophageal reflux disease (GERD) and to evaluate the impact of combined therapy versus monotherapy on the course of this disease. Subjects and methods. The investigation enrolled 62 patients with non-acidic GERD. The follow-up period was 6 weeks. The patients were divided into 2 groups: 1) weakly acidic gastroesophageal refluxes (GER); 2) weakly alkaline GER. Then each group was distributed, thus making up 4 groups: 1) 19 patients with weakly acidic GER who received monotherapy with rabeprazole 20 mg/day; 2) 21 patients with weakly acidic GER had combined therapy with rabeprazole 20 mg and itopride; 3) 8 patients with weakly alkaline GER who received ursodeoxycholic acid (UDCA) monotherapy; and 4) 14 patients with weakly alkaline GER who had combined therapy with UDCA and itopride, The clinical symptoms of the disease, the endoscopic pattern of the upper gastrointestinal tract (GIT) mucosa, histological changes in the esophageal and gastric mucosa, and the results of 24-hour impedance pH monitoring were assessed over time. Results. During differentiation therapy, the majority of patients reported positive clinical changes and an improved or unchanged endoscopic pattern. Assessment of impedance pH monitoring results revealed decreases in the overall number of GERs, the presence of a bolus in the esophagus, and the number of proximal refluxes. These changes were noted not only in patients taking proton pump inhibitors (PPIs), but also in those treated with UDCA monotherapy or combined PPI and prokinetic therapy. Conclusion. A differentiated approach to non-acidic GER treatment contributes to its efficiency. Adding the prokinetic itomed (itopride hydrochloride) to PPI therapy in a patient with weakly acidic GER enhances the efficiency of treatment, by positively affecting upper GIT motility. The mainstay of therapy for GERD with a predominance of weakly alkaline refluxes is UDCA, the combination of the latter and the prokinetic can exert a more pronounced effect on the clinical and endoscopic pattern and upper GIT motility.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">gastroesophageal reflux disease</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">non-acidic (weakly acidic</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">weakly alkaline) gastroesophageal reflux</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">duodenogastroesophageal reflux</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">antisecretory therapy</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">rabeprazole</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">itopride</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">ursodeoxycholic acid</subfield></datafield><datafield tag="653" ind1=" " ind2="0"><subfield code="a">Medicine</subfield></datafield><datafield tag="653" ind1=" " ind2="0"><subfield code="a">R</subfield></datafield><datafield tag="700" ind1="0" ind2=" "><subfield code="a">V I Simanenkov</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="0" ind2=" "><subfield code="a">S V Tikhonov</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">In</subfield><subfield code="t">Терапевтический архив</subfield><subfield code="d">"Consilium Medicum" Publishing house, 2018</subfield><subfield code="g">89(2017), 4, Seite 57-63</subfield><subfield code="w">(DE-627)1760620270</subfield><subfield code="x">23095342</subfield><subfield code="7">nnns</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:89</subfield><subfield code="g">year:2017</subfield><subfield code="g">number:4</subfield><subfield code="g">pages:57-63</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://doi.org/10.17116/terarkh201789457-63</subfield><subfield code="z">kostenfrei</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://doaj.org/article/38407acd26e44211bc7434f81b60f45f</subfield><subfield code="z">kostenfrei</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://ter-arkhiv.ru/0040-3660/article/viewFile/32209/pdf</subfield><subfield code="z">kostenfrei</subfield></datafield><datafield tag="856" ind1="4" ind2="2"><subfield code="u">https://doaj.org/toc/0040-3660</subfield><subfield code="y">Journal toc</subfield><subfield code="z">kostenfrei</subfield></datafield><datafield tag="856" ind1="4" ind2="2"><subfield code="u">https://doaj.org/toc/2309-5342</subfield><subfield code="y">Journal toc</subfield><subfield code="z">kostenfrei</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_A</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SYSFLAG_A</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_DOAJ</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">89</subfield><subfield code="j">2017</subfield><subfield code="e">4</subfield><subfield code="h">57-63</subfield></datafield></record></collection>
|
score |
7.400923 |