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  1. Article ; Online: Tuberculosis (HIV-negative people).

    Ziganshina, Lilia E / Eisenhut, Michael

    BMJ clinical evidence

    2011  Volume 2011

    Abstract: Introduction: About one third of the world's population has latent tuberculosis. In 2004, more than 14 million people had active tuberculosis. About 1.7 million people died from the infection in 2006. More than 80% of new cases diagnosed in 2004 were in ...

    Abstract Introduction: About one third of the world's population has latent tuberculosis. In 2004, more than 14 million people had active tuberculosis. About 1.7 million people died from the infection in 2006. More than 80% of new cases diagnosed in 2004 were in people in Africa, South-East Asia, and Western Pacific regions.
    Methods and outcomes: We conducted a systematic review and aimed to answer the following clinical questions: What are the effects of interventions to prevent tuberculosis in people without HIV infection at high risk of developing tuberculosis? What are the effects of interventions to prevent tuberculosis in people without HIV infection at high risk of developing multidrug-resistant tuberculosis? What are the effects of different drug regimens in people with newly diagnosed pulmonary tuberculosis without HIV infection? What are the effects of different drug regimens in people with multidrug-resistant tuberculosis without HIV infection? What are the effects of low-level laser therapy in people with tuberculosis without HIV infection? Which interventions improve adherence to treatment in people with tuberculosis without HIV infection? We searched: Medline, Embase, The Cochrane Library, and other important databases up to June 2010 (Clinical Evidence reviews are updated periodically; please check our website for the most up-to-date version of this review). We included harms alerts from relevant organisations such as the US Food and Drug Administration (FDA) and the UK Medicines and Healthcare products Regulatory Agency (MHRA).
    Results: We found 32 systematic reviews, RCTs, or observational studies that met our inclusion criteria. We performed a GRADE evaluation of the quality of evidence for interventions.
    Conclusions: In this systematic review, we present information relating to the effectiveness and safety of the following interventions: adding pyrazinamide in chemotherapy regimens lasting up to 6 months, adding rifampicin to isoniazid regimens, benefits of different regimens, chemotherapy for <6 months, daily chemotherapy, direct observation treatment, intermittent chemotherapy for 6 months or longer, isoniazid, low-level laser therapy for pulmonary tuberculosis, regimens containing quinolones, rifampicin plus isoniazid, substituting rifampicin with ethambutol in the continuous phase, and support mechanisms for directly observed treatment.
    MeSH term(s) Antitubercular Agents/administration & dosage ; HIV Infections/drug therapy ; Humans ; Isoniazid/administration & dosage ; Low-Level Light Therapy ; Tuberculosis/drug therapy ; Tuberculosis, Multidrug-Resistant/drug therapy ; Tuberculosis, Pulmonary/drug therapy
    Chemical Substances Antitubercular Agents ; Isoniazid (V83O1VOZ8L)
    Language English
    Publishing date 2011-03-11
    Publishing country England
    Document type Journal Article ; Review ; Systematic Review
    ZDB-ID 2393858-4
    ISSN 1752-8526 ; 1757-0816 ; 1475-9225
    ISSN (online) 1752-8526
    ISSN 1757-0816 ; 1475-9225
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Predicting and managing adverse reactions of psychotropic drugs.

    Ilyina, Rosa Yu / Pasynkova, Olga O / Ziganshina, Lilia E

    The International journal of risk & safety in medicine

    2013  Volume 25, Issue 2, Page(s) 95–103

    Abstract: Background: Neuroleptic induced extrapyramidal disorders are often presented in a form of orofacial hyperkinesias and dystonia. Rational use of neuroleptic drugs requires individualised approach to a patient, however simple criteria for determining ... ...

    Abstract Background: Neuroleptic induced extrapyramidal disorders are often presented in a form of orofacial hyperkinesias and dystonia. Rational use of neuroleptic drugs requires individualised approach to a patient, however simple criteria for determining individual, "personalised" dosage regimen have not been fully developed for routine practice in resource-limited hospital settings.
    Objective: To study the tonus of tongue muscles as a measure of orofacial dystonia and the total hepatic oxidative capacity as a potential predictor of excessive vulnerability to neuroleptic-induced dystonia in psychiatric patients.
    Methods: We measured the maximal force of the tongue manoeuvre (F, g/cm2), the total (integral) hepatic oxidative capacity by the antipyrine-test and used chlorpromazine equivalent to calculate the total daily neuroleptic load in 283 psychiatric patients and 30 healthy volunteers.
    Results: The tonus of tongue muscles depends on the total daily neuroleptic dose and the length of antipsychotic treatment. The higher the total daily neuroleptic dose and the longer the treatment history, the greater the tongue muscles' tonus is. The tongue muscles' tonus was greater in patients with low rate of oxidative antipyrine metabolism. Antidepressants contributed to the increased tonus of the tongue muscles in "slow metabolisers" of antipyrine.
    Conclusions: The simple and cheap measurements of total hepatic oxidative capacity and of muscle tonus of the tongue could be used to predict and manage neuroleptic-induced adverse reactions.
    MeSH term(s) Adolescent ; Adult ; Aged ; Aged, 80 and over ; Antidepressive Agents/adverse effects ; Case-Control Studies ; Disease Susceptibility ; Dose-Response Relationship, Drug ; Dyskinesia, Drug-Induced/physiopathology ; Dyskinesia, Drug-Induced/prevention & control ; Female ; Humans ; Liver/metabolism ; Male ; Metabolic Clearance Rate ; Metabolic Detoxication, Phase I ; Middle Aged ; Muscle Tonus ; Psychotropic Drugs/administration & dosage ; Psychotropic Drugs/adverse effects ; Psychotropic Drugs/pharmacokinetics ; Tongue/physiopathology
    Chemical Substances Antidepressive Agents ; Psychotropic Drugs
    Language English
    Publishing date 2013
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 1055458-0
    ISSN 1878-6847 ; 0924-6479
    ISSN (online) 1878-6847
    ISSN 0924-6479
    DOI 10.3233/JRS-130584
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Fluoroquinolones for treating tuberculosis (presumed drug-sensitive).

    Ziganshina, Lilia E / Titarenko, Albina F / Davies, Geraint R

    The Cochrane database of systematic reviews

    2013  , Issue 6, Page(s) CD004795

    Abstract: Background: Currently the World Health Organization only recommend fluoroquinolones for people with presumed drug-sensitive tuberculosis (TB) who cannot take standard first-line drugs. However, use of fluoroquinolones could shorten the length of ... ...

    Abstract Background: Currently the World Health Organization only recommend fluoroquinolones for people with presumed drug-sensitive tuberculosis (TB) who cannot take standard first-line drugs. However, use of fluoroquinolones could shorten the length of treatment and improve other outcomes in these people. This review summarises the effects of fluoroquinolones in first-line regimens in people with presumed drug-sensitive TB.
    Objectives: To assess fluoroquinolones as substitute or additional components in antituberculous drug regimens for drug-sensitive TB.
    Search methods: We searched the Cochrane Infectious Diseases Group Specialized Register; CENTRAL (The Cochrane Library 2013, Issue 1); MEDLINE; EMBASE; LILACS; Science Citation Index; Databases of Russian Publications; and metaRegister of Controlled Trials up to 6 March 2013.
    Selection criteria: Randomized controlled trials (RCTs) of antituberculous regimens based on rifampicin and pyrazinamide and containing fluoroquinolones in people with presumed drug-sensitive pulmonary TB.
    Data collection and analysis: Two authors independently applied inclusion criteria, assessed the risk of bias in the trials, and extracted data. We used the risk ratio (RR) for dichotomous data and the fixed-effect model when it was appropriate to combine data and no heterogeneity was present. We assessed the quality of evidence using the GRADE approach.
    Main results: We identified five RCTs (1330 participants) that met the inclusion criteria. None of the included trials examined regimens of less than six months duration. Fluoroquinolones added to standard regimensA single trial (174 participants) added levofloxacin to the standard first-line regimen. Relapse and treatment failure were not reported. For death, sputum conversion, and adverse events we are uncertain if there is an effect (one trial, 174 participants, very low quality evidence for all three outcomes). Fluoroquinolones substituted for ethambutol in standard regimens Three trials (723 participants) substituted ethambutol with moxifloxacin, gatifloxacin, and ofloxacin into the standard first-line regimen. For relapse, we are uncertain if there is an effect (one trial, 170 participants, very low quality evidence). No trials reported on treatment failure. For death, sputum culture conversion at eight weeks, or serious adverse events we do not know if there was an effect (three trials, 723 participants, very low quality evidence for all three outcomes). Fluoroquinolones substituted for isoniazid in standard regimens A single trial (433 participants) substituted moxifloxacin for isoniazid. Treatment failure and relapse were not reported. For death, sputum culture conversion, or serious adverse events the substitution may have little or no difference (one trial, 433 participants, low quality evidence for all three outcomes). Fluoroquinolines in four month regimensSix trials are currently in progress testing shorter regimens with fluoroquinolones.
    Authors' conclusions: Ofloxacin, levofloxacin, moxifloxacin, and gatifloxacin have been tested in RCTs of standard first-line regimens based on rifampicin and pyrazinamide for treating drug-sensitive TB. There is insufficient evidence to be clear whether addition or substitution of fluoroquinolones for ethambutol or isoniazid in the first-line regimen reduces death or relapse, or increases culture conversion at eight weeks. Much larger trials with fluoroquinolones in short course regimens of four months are currently in progress.
    MeSH term(s) Antitubercular Agents/therapeutic use ; Ciprofloxacin/therapeutic use ; Drug Substitution ; Fluoroquinolones/therapeutic use ; Humans ; Levofloxacin ; Ofloxacin/therapeutic use ; Randomized Controlled Trials as Topic ; Tuberculosis, Multidrug-Resistant/drug therapy ; Tuberculosis, Pulmonary/drug therapy
    Chemical Substances Antitubercular Agents ; Fluoroquinolones ; Ciprofloxacin (5E8K9I0O4U) ; Levofloxacin (6GNT3Y5LMF) ; Ofloxacin (A4P49JAZ9H)
    Language English
    Publishing date 2013-06-06
    Publishing country England
    Document type Journal Article ; Meta-Analysis ; Research Support, Non-U.S. Gov't ; Review ; Systematic Review
    ISSN 1469-493X
    ISSN (online) 1469-493X
    DOI 10.1002/14651858.CD004795.pub4
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Tuberculosis (HIV-negative people).

    Ziganshina, Lilia E / Garner, Paul

    BMJ clinical evidence

    2009  Volume 2009

    Abstract: Introduction: About a third of the world's population has latent tuberculosis. In 2004, over 14 million people had active tuberculosis. Approximately 1.7 million people died from the infection. Over 80% of new cases diagnosed in 2004 were in people in ... ...

    Abstract Introduction: About a third of the world's population has latent tuberculosis. In 2004, over 14 million people had active tuberculosis. Approximately 1.7 million people died from the infection. Over 80% of new cases diagnosed in 2004 were in people in Africa, South-East Asia, and Western Pacific regions.
    Methods and outcomes: We conducted a systematic review and aimed to answer the following clinical questions: What are the effects of interventions to prevent tuberculosis in people without HIV infection at high risk of developing tuberculosis? What are the effects of interventions to prevent tuberculosis in people without HIV infection at high risk of developing multidrug-resistant tuberculosis? What are the effects of different drug regimens in people with newly diagnosed pulmonary tuberculosis without HIV infection? What are the effects of different drug regimens in people with multidrug-resistant tuberculosis without HIV infection? What are the effects of low-level laser therapy in people with tuberculosis without HIV infection? Which interventions improve adherence to treatment in people with tuberculosis without HIV infection? We searched: Medline, Embase, The Cochrane Library, and other important databases up to July 2008 (Clinical Evidence reviews are updated periodically, please check our website for the most up-to-date version of this review). We included harms alerts from relevant organisations such as the US Food and Drug Administration (FDA) and the UK Medicines and Healthcare products Regulatory Agency (MHRA).
    Results: We found 31 systematic reviews, RCTs, or observational studies that met our inclusion criteria. We performed a GRADE evaluation of the quality of evidence for interventions.
    Conclusions: In this systematic review we present information relating to the effectiveness and safety of the following interventions: adding pyrazinamide in chemotherapy regimens lasting up to 6 months; adding rifampicin to isoniazid regimens; benefits of different regimens; chemotherapy for less than 6 months; daily chemotherapy; direct observation treatment; intermittent chemotherapy for 6 months or longer; isoniazid; low-level laser therapy for pulmonary tuberculosis; regimens containing quinolones; rifampicin plus isoniazid; substituting rifampicin with ethambutol in the continuous phase; and support mechanisms for directly observed treatment.
    MeSH term(s) Antitubercular Agents/administration & dosage ; HIV Infections/drug therapy ; Humans ; Isoniazid/therapeutic use ; Latent Tuberculosis/drug therapy ; Low-Level Light Therapy ; Rifampin/therapeutic use ; Tuberculosis/drug therapy ; Tuberculosis, Multidrug-Resistant/drug therapy ; Tuberculosis, Pulmonary/drug therapy
    Chemical Substances Antitubercular Agents ; Isoniazid (V83O1VOZ8L) ; Rifampin (VJT6J7R4TR)
    Language English
    Publishing date 2009-04-14
    Publishing country England
    Document type Journal Article ; Review ; Systematic Review
    ZDB-ID 2393858-4
    ISSN 1752-8526 ; 1757-0816 ; 1475-9225
    ISSN (online) 1752-8526
    ISSN 1757-0816 ; 1475-9225
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online ; Conference proceedings: Quality information for quality use of medicines; 2nd International Conference, Kazan, 15-16 October 2010.

    Ziganshina, Lilia E / Menkes, David B / Herxheimer, Andrew

    The International journal of risk & safety in medicine

    2011  Volume 23, Issue 3, Page(s) 187–192

    Abstract: Kazan hosted Russia's first international conference on medicines that was entirely independent of the pharmaceutical industry, attracting 414 participants from 9 countries and 20 regions of the Russian Federation. The meeting was greeted and endorsed by ...

    Abstract Kazan hosted Russia's first international conference on medicines that was entirely independent of the pharmaceutical industry, attracting 414 participants from 9 countries and 20 regions of the Russian Federation. The meeting was greeted and endorsed by world leaders in pharmaceutical information, policy and regulation. Delegates discussed the professional and social problems arising from unethical drug promotion, including compromised evidence from clinical trials and consequent impairments in health service delivery. The Conference adopted a resolution prioritizing policy development and health system needs, notably including the development of clinical pharmacology. A website documents conference materials and provides an interface for future collaboration: http://evidenceupdate-tatarstan.ru/confer.
    MeSH term(s) Advertising as Topic ; Drug Industry ; Drug Information Services ; Education, Medical, Continuing ; Humans ; Marketing ; Pharmaceutical Preparations ; Pharmacology, Clinical ; Quality Assurance, Health Care ; Russia
    Chemical Substances Pharmaceutical Preparations
    Language English
    Publishing date 2011
    Publishing country Netherlands
    Document type Congresses
    ZDB-ID 1055458-0
    ISSN 1878-6847 ; 0924-6479
    ISSN (online) 1878-6847
    ISSN 0924-6479
    DOI 10.3233/JRS-2011-0535
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Cerebrolysin for acute ischaemic stroke.

    Ziganshina, Lilia E / Abakumova, Tatyana / Kuchaeva, Alexandra

    The Cochrane database of systematic reviews

    2010  , Issue 4, Page(s) CD007026

    Abstract: Background: Cerebrolysin is a mixture of low-molecular-weight peptides and amino acids derived from pigs' brain tissue which has proposed neuroprotective and neurotrophic properties. It is widely used in the treatment of acute ischaemic stroke in Russia ...

    Abstract Background: Cerebrolysin is a mixture of low-molecular-weight peptides and amino acids derived from pigs' brain tissue which has proposed neuroprotective and neurotrophic properties. It is widely used in the treatment of acute ischaemic stroke in Russia and China.
    Objectives: To assess the benefits and risks of cerebrolysin for treating acute ischaemic stroke.
    Search strategy: We searched the Cochrane Stroke Group Trials Register (February 2009), the Cochrane Central Register of Controlled Trials (CENTRAL) (The Cochrane Library Issue 1, 2009), MEDLINE (1966 to February 2009), EMBASE (1974 to February 2009), LILACS (1982 to February 2009), Science Citation Index (1940 to February 2009), SIGLE Archive (1980 to March 2005), and a number of relevant Russian Databases (1988 to February 2009). We also searched reference lists, ongoing trials registers and conference proceedings.
    Selection criteria: Randomised controlled trials comparing cerebrolysin with placebo or no treatment in patients with acute ischaemic stroke.
    Data collection and analysis: Three review authors independently applied the inclusion criteria, assessed trial quality and extracted the data.
    Main results: We included one trial involving 146 participants. There was no difference in death (6/78 in the cerebrolysin group versus 6/68 in the placebo group; risk ratio (RR) 0.87, 95% confidence interval (CI) 0.29 to 2.58) or in the total number of adverse events (16.4% versus 10.3%; RR 1.62, 95% CI 0.69 to 3.82) between the treatment and control groups.
    Authors' conclusions: There is not enough evidence to evaluate the effect of cerebrolysin on survival and dependency in people with acute ischaemic stroke. High-quality and large-scale randomised controlled trials may help to gain a better understanding of the potential value of cerebrolysin in acute ischaemic stroke.
    MeSH term(s) Amino Acids/therapeutic use ; Humans ; Neuroprotective Agents/therapeutic use ; Stroke/drug therapy
    Chemical Substances Amino Acids ; Neuroprotective Agents ; cerebrolysin (37KZM6S21G)
    Language English
    Publishing date 2010-04-14
    Publishing country England
    Document type Journal Article ; Review ; Systematic Review
    ISSN 1469-493X
    ISSN (online) 1469-493X
    DOI 10.1002/14651858.CD007026.pub2
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: The Russian health care system today: can American-Russian CME programs help?

    Farmer, Richard G / Sirotkin, Alexei Y / Ziganshina, Lilia E / Greenberg, Henry M

    Cleveland Clinic journal of medicine

    2003  Volume 70, Issue 11, Page(s) 937–8, 941–2, 944

    Abstract: The health of the Russian people has deteriorated dramatically since the fall of communism, due particularly to cardiovascular disease. The Eurasian Medical Education Program was developed in response to provide continuing medical education for Russian ... ...

    Abstract The health of the Russian people has deteriorated dramatically since the fall of communism, due particularly to cardiovascular disease. The Eurasian Medical Education Program was developed in response to provide continuing medical education for Russian physicians. Programs are directed mainly toward primary care physicians and focus on outpatient management of diseases that cause high rates of mortality and morbidity. This experience provides an opportunity to assess the structure and functioning of the Russian health care system and emphasizes the importance of general internal medicine training in detection, management, and prevention of disease complications.
    MeSH term(s) Delivery of Health Care/organization & administration ; Education, Medical, Continuing ; Education, Medical, Graduate ; Humans ; International Educational Exchange ; Russia ; United States
    Language English
    Publishing date 2003-10-21
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 639116-3
    ISSN 0891-1150
    ISSN 0891-1150
    DOI 10.3949/ccjm.70.11.937
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article: Effects of chronic specific urogenital infections on contractility of the human isolated pregnant myometrium.

    Zefirova, Julia T / Zefirova, Tatiana P / Ziganshina, Lilia E / Ziganshin, Airat U

    Autonomic neuroscience : basic & clinical

    2002  Volume 99, Issue 1, Page(s) 58–61

    Abstract: The contractile activity of the isolated myometrium of pregnant women with mycoplasma, chlamydia and mixed infections has been studied by pharmacological organ bath method. We found that mycoplasma infection decreased while chlamydia or mixed infection ... ...

    Abstract The contractile activity of the isolated myometrium of pregnant women with mycoplasma, chlamydia and mixed infections has been studied by pharmacological organ bath method. We found that mycoplasma infection decreased while chlamydia or mixed infection increased myometrium contraction evoked by oxytocin or prostaglandin F2alpha. The results of this study could be important for the prediction of possible complications during pregnancy and labour in women with chronic specific urogenital infections.
    MeSH term(s) Chlamydia Infections/microbiology ; Chlamydia Infections/physiopathology ; Chronic Disease ; Dinoprost/pharmacology ; Down-Regulation/drug effects ; Down-Regulation/physiology ; Female ; Histamine/pharmacology ; Humans ; Mycoplasma Infections/microbiology ; Mycoplasma Infections/physiopathology ; Myometrium/drug effects ; Myometrium/microbiology ; Myometrium/physiopathology ; Organ Culture Techniques ; Oxytocin/pharmacology ; Potassium Chloride/pharmacology ; Pregnancy ; Pregnancy Complications, Infectious/microbiology ; Pregnancy Complications, Infectious/physiopathology ; Up-Regulation/drug effects ; Up-Regulation/physiology ; Uterine Contraction/drug effects ; Uterine Contraction/immunology
    Chemical Substances Oxytocin (50-56-6) ; Potassium Chloride (660YQ98I10) ; Histamine (820484N8I3) ; Dinoprost (B7IN85G1HY)
    Language English
    Publishing date 2002-08-08
    Publishing country Netherlands
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2020105-9
    ISSN 1872-7484 ; 1566-0702
    ISSN (online) 1872-7484
    ISSN 1566-0702
    DOI 10.1016/s1566-0702(02)00058-9
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article: Temperature dependency of P2 receptor-mediated responses.

    Ziganshin, Airat U / Rychkov, Alexey V / Ziganshina, Lilia E / Burnstock, Geoffrey

    European journal of pharmacology

    2002  Volume 456, Issue 1-3, Page(s) 107–114

    Abstract: The P2 receptor-mediated responses of isolated guinea pig urinary bladder and vas deferens (P2X receptors) and taenia caeci (P2Y receptors) were registered at the three temperature conditions of 30, 37 and 42 degrees C. The contractile responses of both ... ...

    Abstract The P2 receptor-mediated responses of isolated guinea pig urinary bladder and vas deferens (P2X receptors) and taenia caeci (P2Y receptors) were registered at the three temperature conditions of 30, 37 and 42 degrees C. The contractile responses of both urinary bladder and vas deferens to a P2X receptor agonist alpha,beta-methylene ATP (alpha,beta-meATP; 0.01-30 microM) and to electrical field stimulation (1-64 Hz, 0.1 ms, supramaximal voltage) in the presence of atropine (0.1 microM) and phentolamine (1 microM) were markedly more prominent at a temperature of 30 degrees C than at 37 or 42 degrees C. Similarly, relaxation of carbachol-precontracted taenia caeci caused by electrical field stimulation (0.5-8 Hz, 0.1 ms, supramaximal voltage) temperature-dependently increased with decrease of temperature, while relaxation of this tissue by exogenous ATP (1-100 microM) was not affected by the temperature. A P2 receptor antagonist pyridoxalphosphate-6-azophenyl-2',4'-disulphonic acid (PPADS, 1-30 microM) at all three temperature conditions concentration-dependently antagonised contractile responses to alpha,beta-methylene ATP and electrical field stimulation in both urinary bladder and vas deferens. PPADS, even at the highest concentration tested (30 microM), had no effect on the relaxant responses of the taenia caeci either to electrical field stimulation or ATP and its action was not affected by the change of temperature. It is concluded from this study that the effectiveness of P2 receptor-mediated responses in guinea pig urinary bladder, vas deferens and taenia caeci increases by decrease of temperature.
    MeSH term(s) Adenosine Triphosphate/analogs & derivatives ; Adenosine Triphosphate/pharmacology ; Animals ; Dose-Response Relationship, Drug ; Electric Stimulation ; Guinea Pigs ; In Vitro Techniques ; Male ; Muscle Contraction/drug effects ; Muscle Contraction/physiology ; Pyridoxal Phosphate/analogs & derivatives ; Pyridoxal Phosphate/pharmacology ; Receptors, Purinergic P2/physiology ; Temperature ; Urinary Bladder/drug effects ; Urinary Bladder/physiology ; Vas Deferens/drug effects ; Vas Deferens/physiology
    Chemical Substances Receptors, Purinergic P2 ; pyridoxal phosphate-6-azophenyl-2',4'-disulfonic acid (149017-66-3) ; Pyridoxal Phosphate (5V5IOJ8338) ; Adenosine Triphosphate (8L70Q75FXE) ; alpha,beta-methyleneadenosine 5'-triphosphate (NYX13NT29D)
    Language English
    Publishing date 2002-12-05
    Publishing country Netherlands
    Document type Comparative Study ; Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 80121-5
    ISSN 1879-0712 ; 0014-2999
    ISSN (online) 1879-0712
    ISSN 0014-2999
    DOI 10.1016/s0014-2999(02)02655-9
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article: Identification and management of patients with hypertension in the polyclinic system of the Russian Federation.

    Greenberg, Henry M / Galyavich, Albert S / Ziganshina, Lilia E / Tinchurina, Maria R / Chamidullin, Albert G / Farmer, Richard G

    American journal of hypertension

    2005  Volume 18, Issue 7, Page(s) 943–948

    Abstract: Background: Cardiovascular diseases, including hypertension and type 2 diabetes mellitus, are the major determinants of poor health in the Russian Federation.: Methods: This study assessed the feasibility of establishing a program to identify and ... ...

    Abstract Background: Cardiovascular diseases, including hypertension and type 2 diabetes mellitus, are the major determinants of poor health in the Russian Federation.
    Methods: This study assessed the feasibility of establishing a program to identify and manage hypertension and associated cardiovascular risk factors in an outpatient clinic within the Russian polyclinic system. In urban polyclinic in Kazan, Tatarstan, which is responsible for 77,000 covered lives, we enrolled 192 patients with hypertension of whom 68 had type 2 diabetes mellitus screened from various clinics within the polyclinic. After collection of baseline data, patients were treated for hypertension and those risk factors amenable to pharmaceutic intervention and counseled on those that required behavior modification.
    Results: Baseline blood pressure was 173.9+/-20.7/104.2+/-15.3 mm Hg in those with hypertension only (n=124) and 172.9+/-26.0/97.9+/-16.4 mm Hg in those with both hypertension and type 2 diabetes mellitus. More than 80% of the entire group had a body mass index >25 kg/m2 and left ventricular hypertrophy. Nearly 70% had total cholesterol >5.2 mmol/L. Of the diabetics, more than 50% had glycosylated hemoglobin (HbA1c)>or=8%. Less than 10% of this self-selected population smoked. Blood pressure decreased modestly, but significantly, in both groups of patients. There were no significant changes in obesity, cholesterol, smoking, or HbA1c in the diabetics.
    Conclusions: Identification, recruitment, management, and follow-up of patients with chronic disorders is feasible within the Russian polyclinic system. However, to have a more profound effect on risk factor profiles, a wider effort is needed than one restricted to the clinic itself.
    MeSH term(s) Adult ; Aged ; Antihypertensive Agents/therapeutic use ; Blood Pressure/physiology ; Databases, Factual ; Diabetes Mellitus, Type 2/epidemiology ; Diabetes Mellitus, Type 2/physiopathology ; Female ; Humans ; Hypertension/diagnosis ; Hypertension/drug therapy ; Hypertension/epidemiology ; Male ; Middle Aged ; National Health Programs ; Risk Assessment ; Risk Factors ; Russia/epidemiology ; Sex Factors ; Treatment Refusal
    Chemical Substances Antihypertensive Agents
    Language English
    Publishing date 2005-07
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 639383-4
    ISSN 1879-1905 ; 0895-7061
    ISSN (online) 1879-1905
    ISSN 0895-7061
    DOI 10.1016/j.amjhyper.2005.01.012
    Database MEDical Literature Analysis and Retrieval System OnLINE

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