(Esi Scheme) Laxminagar, Ajmer Road, Jaipur-302006

Total Page:16

File Type:pdf, Size:1020Kb

(Esi Scheme) Laxminagar, Ajmer Road, Jaipur-302006 DIRECTORATE, MEDICAL & HEALTH SERVICES, (E.S.I. SCHEME) LAXMINAGAR, AJMER ROAD, JAIPUR-302006 Tel/Fax 0141-2223572,www.health.rajasthan.gov.in/esi E-Mail [email protected],[email protected] Ref. No. F434/ESI/Store/LabEmp/2017/5540 Dated:01/11/2017 E- Tender Document For “E- Tender forAnalysis of Drugs, Cotton, Gauzes, Bandage & Other items” For The Office of the Director cum Ex-officio Dy. Secretary, Medical & Health Services ESI Scheme Rajasthan, Laxmi Nagar, Ajmer Road, Jaipur & attached ESIS Institutions in Rajasthan ( for the period of two years from the date of award. ) ( Non-transferable ) Price of Tender Document Rs. 2000/- Last date & time of submission of Technical & Financial Bids is 11.12.17 at 1:30 pm Date & time of online opening of Technical Bid is 11.12.17 at 3:00 pm Visit Us At http://sppp.raj.nic.in, www.dipronline.org, http://eproc.rajasthan.gov.in, www.health.rajasthan.gov.in/esi Our Address: DIRECTORATE, MEDICAL & HEALTH SERVICES, (E.S.I. SCHEME) LAXMINAGAR, AJMER ROAD, JAIPUR-302006 1/71 DIRECTORATE, MEDICAL & HEALTH SERVICES, (E.S.I. SCHEME) LAXMINAGAR, AJMER ROAD, JAIPUR-302006 Tel/Fax 0141-2223572,www.health.rajasthan.gov.in/esi E-Mail [email protected],[email protected] Ref.No.F434/ESI/Store/LabEmp/2017/ 5540 Dated:01/11/2017 E-bids in two separate bids (Technical & Financial) for the Empanelment of Analytic Testing Laboratories For The Test and Analysis of drugs, cotton, bandage, gauze & other items. Brief Details of E-Tender Estimated Cost : Rs 50 lacs EMD (Bid Security)Rs 100000/- RISL processing fees Rs 1000/- Cost of the Tender Document Rs 2000/- Performance Security 5% of contract value Services Required:- The service of analysis of drugs, cotton, gauze, bandages & other items are required in the office of the Director cum Ex- officio Dy. Secretary, Medical & Health Services, ESI Scheme, Laxmi Nagar, Ajmer Road, Jaipur abbreviated as DMHS ESIS in this Document & attached ESIS Institutions in Rajasthan. Period of services will be for 2 years from the date of award. Schedule of Tender Description of Tender Process Date & Time Pre-bid conference(ESI Directorate Meeting 16.11.2017 at 1.30 p.m. Hall) Date & time for downloading Tender 07.11.2017 at 6.00 p.m. Document Last date & time for submission of online 11.12.2017 at 1.30 p.m. bids Last date of physical submission of EMD, 11.12.2017 at 1.30 p.m. Tender Document fees, Processing fees Date & time for on-line opening of 11.12.2017at 3.00 p.m. Technical Bid Date & time for opening of Financial Bid(For Will be intimated later on technically qualified bidders ) Bid validity period/validity of bid offer for 70 days from the date of opening of the acceptance by DM&HS ESI Technical Bid 2/71 Eligibility Criteria for Empanelment (1) Drugs Testing Laboratories should have valid approval for carrying out test on drugs under the Drugs and Cosmetics Act, 1940 and rules there under, with three years standing in drugs, cotton, gauzes, bandages & other item. The Laboratory shall be entitled for empanelment for the categories of items for which Laboratory is having approval. Tender is invited from approved Drugs Testing Laboratories situated in India. (2) The Laboratory should be GLP compliant under the provision of Drugs and Cosmetics Act, 1940 and rules there under and should hold schedule L-1 certificate or should have NABL accreditation with proper scope of accreditation to undertake testing of drugs, cotton, gauzes, bandages & other items. (3) The Laboratory should have an average annual turnover of not less than Rs. 50 Lacs for past preceding three years (2013-14, 2014-15, 2015-16 OR 2014-15, 2015-16, 2016-17).Relaxation will be given to Government undertaking/PSU on producing the certificate issued by the competent authority. The certificate should be scanned & uploaded online at the time of submission of tender documents in Technical Bid. (4) The Laboratory should have undertaken test and analysis of drugs, cotton, gauzes, bandages & other items and supplies of similar nature of at least three government institutions/corporation/ reputed manufacturers of drugs, cotton, gauzes, bandages & other items. (5) The Laboratory should not stand banned / debarred or blacklisted by any State or Central Government Organizations or its central procurement agencies on the due date of bid submission. (6) The Laboratory and its responsible persons should not have been convicted under the provisions of applicable laws with regard to the activities and conduct of the Laboratory. (7) The Laboratory should have all necessary instruments/ equipments/ machines for testing of drugs, cotton, gauzes, bandages & other items. as per standards laid down in Drugs & Cosmetics Act/Pharmacopoeia/ Bureau of Indian Standards and other standards as applicable/ desired. (8) The Bidder should submit test parameters for individual item given in Annexure-IX as per per standards laid down in Drugs & Cosmetics 3/71 Act/Pharmacopoeia/ Bureau of Indian Standards and other standards as applicable/ desired and should have facilities of testing for the same. General Conditions (1) The details of the drugs, cotton, gauzes, bandages & other items to be analyzed has been given in Annexure-IX. (2) The Bidder should fill the names of test and the procedure to be performed for each item given in annexure-IX as per standards laid down in Drugs & Cosmetic Act/ Pharmacopoeia /Bureau of Indian Standards and other standards as applicable/ desired when submitting Technical Bid. However, the rates for the complete analysis of each item should be submitted in BoQ in Financial Bid. Wherever tests are prescribed and their names and methodology for testing are not stated, such Laboratory will not be considered responsive for testing for such item. (3) The rates quoted should be exclusive of taxes. The rates quoted should not be higher than quoted elsewhere in any other government institution or rate prevalent in market, otherwise necessary action will be taken to recover the difference amount. (4) The rates quoted and accepted will be binding on the Bidder for the stipulated period and on no account any revision will be entertained till the completion of the bid period. (5) Analytical Laboratory, which also has its manufacturing activity, if empanelled by Director cum Ex-officio Dy. Secretary, Medical & Health Services E.S.I. Scheme, Rajasthan, Jaipur [DMHS(ESIS)] then samples of its own manufacturing unit shall not be sent to its Empanelled Laboratory for testing. (6) The Laboratory will not be permitted to outsource any test from other Laboratory. (7) DMHS(ESIS) shall have the right to cause the Laboratory to be inspected by the members of its Technical Committee before opening of Financial Bid and subsequently as and when considered appropriate and based on the findings, the Bidder may be disqualified or de-empanelled, as the case may be. 4/71 (8)The successful Bidder will have to collect the samples from Office of the Director cum Ex-officio Dy. Secretary, Medical & Health Services ESI Scheme Rajasthan, Laxmi Nagar, Ajmer Road, Jaipur & attached ESIS Institutions in Rajasthan at his/her own cost & the cost of transport of items will not be paid separately. At present there are 78 ESIS Instiutions under this office in Rajasthan. The number of ESIS Institutions may be increased or decreased at any time. (9)The department reserves the right to amend or withdraw any of the terms and conditions contained in the Tender Document or to reject all tenders without assigning any reason. The decision of the Director cum Ex-officio Dy. Secretary, Medical & Health Services, ESI Scheme Rajasthan, Laxmi Nagar, Ajmer Road, Jaipur in this regard shall be final & binding on all. Special Instruction Before Participating in Tender (1)Read Tender Document carefully :The Bidder should go through the detail mentioned in Tender Document completely before submitting the bids. (2)Compliance with code of integrity: Any person participating in empanelment process shall:- (a) not offer any bribe, reward or gift or any material benefit either directly or indirectly in exchange for an unfair advantage in procurement process or to otherwise influence the procurement process; (b) not misrepresent, omit, mislead or attempt to mislead so as to obtain a financial or other benefit or avoid an obligation; © not indulge in any collusion, bid rigging or any-competitive behavior to impair the transparency, fairness and progress of the procurement process; (d) not misuse any information shared between the Procuring Entity and the bidders with an intent to gain unfair advantage in the procurement process; (e) not indulge in any coercion including impairing or harming or threatening to do the same, directly or indirectly, to any part or to its property to influence the procurement process; (f) not obstruct any investigation or audit of a procurement process; (g) disclose Conflict of Interest, if any; and 5/71 (h) disclose any previous transgressions with any entity in India or any other country during the last three years or any debarment by any other Procuring Entity. (3)No Conflict of Interest: The Bidder participating in a bidding process must not have a Conflict of Interest. A Conflict of Interest is considered to be a situation in which a party has interests that could improperly influence that party’s performance of official duties or responsibilities, contractual obligations, or compliance with applicable laws and regulations. A Bidder may be considered to be in Conflict of Interest with one or more parties in bidding process if including but not limited to : (a) have controlling partners/shareholders in common; or (b) receive or have received any direct or indirect subsidy from any of them; or (c) have the same legal representative for purposes of the bid; or (d) have a relationship with each other, directly or through common third parties, that puts them in a position to have access to information about or influence on the bid of another Bidder, or influence the decisions of the Procuring Entity regarding the bidding process; or (e) the Bidder participates in more than one bid in a bidding process, participation by a Bidder in more than one bid will result in the disqualification of all bids in which the Bidder is involved.
Recommended publications
  • Specifications of Approved Drug Compound Library
    Annexure-I : Specifications of Approved drug compound library The compounds should be structurally diverse, medicinally active, and cell permeable Compounds should have rich documentation with structure, Target, Activity and IC50 should be known Compounds which are supplied should have been validated by NMR and HPLC to ensure high purity Each compound should be supplied as 10mM solution in DMSO and at least 100µl of each compound should be supplied. Compounds should be supplied in screw capped vial arranged as 96 well plate format.
    [Show full text]
  • Pharmacological Treatment Options for Alcohol Use Disorder*
    Dusunen Adam The Journal of Psychiatry and Neurological Sciences 2015;28:283-300 Editorial / Editoryal DOI: 10.5350/DAJPN20152804001 Pharmacological Treatment Cuneyt Evren1, Muge Bozkurt2 1Assoc. Prof. Dr., 2Psychiatrist, Bakirkoy Training and Options for Alcohol Use Research Hospital for Psychiatry, Neurology and Neurosurgery, Alcohol and Drug Research, Treatment and Training Center (AMATEM), Disorder* Istanbul - Turkey Address reprint requests to / Yazışma adresi: Assoc. Prof. Dr. Cuneyt Evren, Bakirkoy Training and Research Hospital for Psychiatry, Neurology and Neurosurgery, Alcohol and Drug Research, Treatment and Training Center (AMATEM), Istanbul, Turkey Phone / Telefon: +90-212-409-1515/2111, Fax / Faks: +90-212-409-1590, E-mail address / Elektronik posta adresi: [email protected] *Abridged version of the “Therapeutic Guideline for Alcohol Use Disorder” prepared by the Working Group Therapeutic Guideline for Alcohol Use Disorder. PHARMACOLOGICAL TREATMENT assess information obtained from studies regarding OPTIONS FOR ALCOHOL USE DISORDER drug treatments used in clinical practice today, which are summarized in Table 1. However, when examining Alcohol Use Disorder (AUD) and other alcohol- study results for pharmacological treatments, we related health problems are a significant public health immediately have to remember that all of those issue all over the world. The World Health Organization (WHO) reports that each year 3.3 million people lose Table 1: Drugs used for the therapy of alcohol use their lives due to harmful alcohol use, with 5.9% of all disorder (AUD) deaths being related to alcohol consumption (1). It has Drugs for AUD approved in Turkey been estimated that in 2010, the economic burden of Disulfiram Naltrexone alcohol-related costs was 155.8 billion Euro, of which Acamprosate 60% were connected to alcohol addiction (2).
    [Show full text]
  • Patent Application Publication ( 10 ) Pub . No . : US 2019 / 0192440 A1
    US 20190192440A1 (19 ) United States (12 ) Patent Application Publication ( 10) Pub . No. : US 2019 /0192440 A1 LI (43 ) Pub . Date : Jun . 27 , 2019 ( 54 ) ORAL DRUG DOSAGE FORM COMPRISING Publication Classification DRUG IN THE FORM OF NANOPARTICLES (51 ) Int . CI. A61K 9 / 20 (2006 .01 ) ( 71 ) Applicant: Triastek , Inc. , Nanjing ( CN ) A61K 9 /00 ( 2006 . 01) A61K 31/ 192 ( 2006 .01 ) (72 ) Inventor : Xiaoling LI , Dublin , CA (US ) A61K 9 / 24 ( 2006 .01 ) ( 52 ) U . S . CI. ( 21 ) Appl. No. : 16 /289 ,499 CPC . .. .. A61K 9 /2031 (2013 . 01 ) ; A61K 9 /0065 ( 22 ) Filed : Feb . 28 , 2019 (2013 .01 ) ; A61K 9 / 209 ( 2013 .01 ) ; A61K 9 /2027 ( 2013 .01 ) ; A61K 31/ 192 ( 2013. 01 ) ; Related U . S . Application Data A61K 9 /2072 ( 2013 .01 ) (63 ) Continuation of application No. 16 /028 ,305 , filed on Jul. 5 , 2018 , now Pat . No . 10 , 258 ,575 , which is a (57 ) ABSTRACT continuation of application No . 15 / 173 ,596 , filed on The present disclosure provides a stable solid pharmaceuti Jun . 3 , 2016 . cal dosage form for oral administration . The dosage form (60 ) Provisional application No . 62 /313 ,092 , filed on Mar. includes a substrate that forms at least one compartment and 24 , 2016 , provisional application No . 62 / 296 , 087 , a drug content loaded into the compartment. The dosage filed on Feb . 17 , 2016 , provisional application No . form is so designed that the active pharmaceutical ingredient 62 / 170, 645 , filed on Jun . 3 , 2015 . of the drug content is released in a controlled manner. Patent Application Publication Jun . 27 , 2019 Sheet 1 of 20 US 2019 /0192440 A1 FIG .
    [Show full text]
  • Toxicological Profile for Carbon Tetrachloride
    CARBON TETRACHLORIDE 27 3. HEALTH EFFECTS 3.1 INTRODUCTION The primary purpose of this chapter is to provide public health officials, physicians, toxicologists, and other interested individuals and groups with an overall perspective on the toxicology of carbon tetrachloride. It contains descriptions and evaluations of toxicological studies and epidemiological investigations and provides conclusions, where possible, on the relevance of toxicity and toxicokinetic data to public health. A glossary and list of acronyms, abbreviations, and symbols can be found at the end of this profile. 3.2 DISCUSSION OF HEALTH EFFECTS BY ROUTE OF EXPOSURE To help public health professionals and others address the needs of persons living or working near hazardous waste sites, the information in this section is organized first by route of exposure (inhalation, oral, and dermal) and then by health effect (death, systemic, immunological, neurological, reproductive, developmental, genotoxic, and carcinogenic effects). These data are discussed in terms of three exposure periods: acute (14 days or less), intermediate (15–364 days), and chronic (365 days or more). Levels of significant exposure for each route and duration are presented in tables and illustrated in figures. The points in the figures showing no-observed-adverse-effect levels (NOAELs) or lowest­ observed-adverse-effect levels (LOAELs) reflect the actual doses (levels of exposure) used in the studies. LOAELs have been classified into "less serious" or "serious" effects. "Serious" effects are those that evoke failure in a biological system and can lead to morbidity or mortality (e.g., acute respiratory distress or death). "Less serious" effects are those that are not expected to cause significant dysfunction or death, or those whose significance to the organism is not entirely clear.
    [Show full text]
  • Alcool Expertise Collective Alcool Effets Sur La Santé Effets Sur La Santé
    Expertise collective Alcool Expertise collective Alcool Effets sur la santé Effets sur la santé Les effets de l’alcool sur la santé font aujour- d’hui encore l’objet d’une importante recherche. Les travaux nous apprennent que ces effets dépendent non seulement des niveaux de consommation, mais également de la suscepti- bilité du consommateur et de ses modalités de consommation. Effets cardiovasculaires délé- tères ou bénéfiques, cancers, hépatopathies, atteintes des systèmes nerveux central ou péri- phérique, toutes les conséquences d’une consommation d’alcool ont été passées au crible dans le cadre de cette expertise collective de l’Inserm effectuée à la demande de la Cnamts, du CFES et de la Mildt. Comment traduire les données récentes en Effets sur la santé termes d’information et de messages de préven- tion ? Les conclusions de cette expertise invitent à adapter ces messages aux différentes popula- tions (jeunes, adultes, personnes âgées) et aux situations particulières (femmes enceintes, Alcool conduite automobile, professions à risque, situations sanitaires à risque…). Prix 180 FF € 27,44 Expertise collective ISBN 2-85598-797-0 ISSN 1264-1782 www.inserm.fr Cet ouvrage présente les travaux du groupe d’experts réunis par l’Inserm dans le cadre de la procédure d’expertise collective, pour répondre aux questions posées par le Comité français d’éducation pour la santé (CFES), la Caisse nationale d’assurance maladie des travailleurs salariés (Cnamts) et la Mission interministérielle de lutte contre la drogue et la toxicomanie (Mildt) concer- nant les effets de la consommation d’alcool sur la santé. Il s’appuie sur les données scientifiques disponibles en date du premier semes- tre 2001.
    [Show full text]
  • Drug Delivery System for Use in the Treatment Or Diagnosis of Neurological Disorders
    (19) TZZ __T (11) EP 2 774 991 A1 (12) EUROPEAN PATENT APPLICATION (43) Date of publication: (51) Int Cl.: 10.09.2014 Bulletin 2014/37 C12N 15/86 (2006.01) A61K 48/00 (2006.01) (21) Application number: 13001491.3 (22) Date of filing: 22.03.2013 (84) Designated Contracting States: • Manninga, Heiko AL AT BE BG CH CY CZ DE DK EE ES FI FR GB 37073 Göttingen (DE) GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO •Götzke,Armin PL PT RO RS SE SI SK SM TR 97070 Würzburg (DE) Designated Extension States: • Glassmann, Alexander BA ME 50999 Köln (DE) (30) Priority: 06.03.2013 PCT/EP2013/000656 (74) Representative: von Renesse, Dorothea et al König-Szynka-Tilmann-von Renesse (71) Applicant: Life Science Inkubator Betriebs GmbH Patentanwälte Partnerschaft mbB & Co. KG Postfach 11 09 46 53175 Bonn (DE) 40509 Düsseldorf (DE) (72) Inventors: • Demina, Victoria 53175 Bonn (DE) (54) Drug delivery system for use in the treatment or diagnosis of neurological disorders (57) The invention relates to VLP derived from poly- ment or diagnosis of a neurological disease, in particular oma virus loaded with a drug (cargo) as a drug delivery multiple sclerosis, Parkinsons’s disease or Alzheimer’s system for transporting said drug into the CNS for treat- disease. EP 2 774 991 A1 Printed by Jouve, 75001 PARIS (FR) EP 2 774 991 A1 Description FIELD OF THE INVENTION 5 [0001] The invention relates to the use of virus like particles (VLP) of the type of human polyoma virus for use as drug delivery system for the treatment or diagnosis of neurological disorders.
    [Show full text]
  • Metadoxine in the Treatment of Acute and Chronic Alcoholism: a Review
    INTERNATIONAL JOURNAL OF IMMUNOI'ATIIOLOGY AND I'IIARMACOLOGY Vol. 16, no. 3, 207·214 (2003) REVIEWARTICLE METADOXINE IN THE TREATMENT OF ACUTE AND CHRONIC ALCOHOLISM: A REVIEW G. ADDOLORATO, C. ANCONA, E. CAPRISTO and G. GASBARRINI Institute ofInternal Medicine, Catholic University ofRome, Italy Received February 27, 2003 - Accepted August 5, 2003 Alcohol abuse and alcoholism are responsible for a wide variety of medical problems. The pharmaco­ therapeutic aspect of alcoholism includes the use of drugs, with different actions and objectives. Among them, metadoxine seems to be of interest. Metadoxine is able to accelerate the elimination of alcohol from the blood and tissues, to help restore the functional structure of the liver and to relieve neuro-psychological disorders associated with alcohol intoxication. Metadoxine also seems to be safe; in more than 15 years of post-marketing surveillance only minor aspecific and reversible events were monitored in patients exposed to the treatment. In this review the preclinical and clinical results obtained using metadoxine in acute and chronic alcohol intoxication are reported. Alcoholism is a multifactorial disorder in which major contributing factors to road accidents, suicide biologic and genetic factor interact along withcultural and violent death in young adults (11). and social factors (1,2). Alcohol addiction represents The pharmaco-therapeutic aspect of alcoholism a social problem and a relatively common disease of includes the use of drugs, with different actions and western countries like Europe and the USA. From 20 objectives (12). Among them, metadoxine seems to to 40% of subjects admitted to hospitals have alcohol­ be of interest. The present review evaluates the related problems (3) and in elderly people alcohol­ pharmacology and the therapeutic use ofmetadoxine related disorders represent as frequent a reason for (figure I), a drug promoted for the treatment of acute hospitalization as myocardial infarction (4).
    [Show full text]
  • Orphan Drug Dummy File
    Orphan Drug Designations and Approvals List as of 09‐01‐2016 Governs October 1, 2016 ‐ December 31, 2016 Row Contact Generic Name Trade Name Designation Date Designation Num Company/Sponsor 1 1. Prevention of secondary carnitine deficiency in valproic acid toxicity 2. Treatment of secondary carnitine deficiency in Sigma-Tau levocarnitine Carnitor 11/15/1989 valproic acid toxicity Pharmaceuticals, Inc. 2 1. Treatment of graft versus host disease in patients receiving bone marrow transplantation 2. Prevention of graft versus host disease in patients receiving Pediatric thalidomide n/a 9/19/1988 bone marrow transplantation Pharmaceuticals, Inc. 3 A Diagnostic for the management Advanced Imaging Theranost 68 Ga RGD n/a 10/1/2014 of Moyamoya disease (MMD) Projects, LLC (AIP) 4 Cadila heat killed Mycobacterium w Pharmaceuticals immunomodulator Cadi Mw 9/3/2004 Active tuberculosis Limited, Inc. 5 Adjunct to cytokine therapy in the treatment of acute myeloid Histamine Ceplene 12/15/1999 leukemia. EpiCept Corporation 6 Adjunct to surgery in cases of rh-microplasmin, ocriplasmin Jetrea 3/16/2004 pediatric vitrectomy ThromboGenics Inc. 7 Adjunct to the non-operative management of secreting cutaneous fistulas of the stomach, duodenum, small intestine (jejunum and ileum), or Ferring Laboratories, Somatostatin Zecnil 6/20/1988 pancreas. Inc. Page 1 of 377 Orphan Drug Designations and Approvals List as of 09‐01‐2016 Governs October 1, 2016 ‐ December 31, 2016 Row Contact Generic Name Trade Name Designation Date Designation Num Company/Sponsor 8 Adjunct to whole brain radiation therapy for the treatment of brain metastases in patients with Allos Therapeutics, efaproxiral n/a 7/28/2004 breast cancer Inc.
    [Show full text]
  • Wo 2008/127291 A2
    (12) INTERNATIONAL APPLICATION PUBLISHED UNDER THE PATENT COOPERATION TREATY (PCT) (19) World Intellectual Property Organization International Bureau (43) International Publication Date PCT (10) International Publication Number 23 October 2008 (23.10.2008) WO 2008/127291 A2 (51) International Patent Classification: Jeffrey, J. [US/US]; 106 Glenview Drive, Los Alamos, GOlN 33/53 (2006.01) GOlN 33/68 (2006.01) NM 87544 (US). HARRIS, Michael, N. [US/US]; 295 GOlN 21/76 (2006.01) GOlN 23/223 (2006.01) Kilby Avenue, Los Alamos, NM 87544 (US). BURRELL, Anthony, K. [NZ/US]; 2431 Canyon Glen, Los Alamos, (21) International Application Number: NM 87544 (US). PCT/US2007/021888 (74) Agents: COTTRELL, Bruce, H. et al.; Los Alamos (22) International Filing Date: 10 October 2007 (10.10.2007) National Laboratory, LGTP, MS A187, Los Alamos, NM 87545 (US). (25) Filing Language: English (81) Designated States (unless otherwise indicated, for every (26) Publication Language: English kind of national protection available): AE, AG, AL, AM, AT,AU, AZ, BA, BB, BG, BH, BR, BW, BY,BZ, CA, CH, (30) Priority Data: CN, CO, CR, CU, CZ, DE, DK, DM, DO, DZ, EC, EE, EG, 60/850,594 10 October 2006 (10.10.2006) US ES, FI, GB, GD, GE, GH, GM, GT, HN, HR, HU, ID, IL, IN, IS, JP, KE, KG, KM, KN, KP, KR, KZ, LA, LC, LK, (71) Applicants (for all designated States except US): LOS LR, LS, LT, LU, LY,MA, MD, ME, MG, MK, MN, MW, ALAMOS NATIONAL SECURITY,LLC [US/US]; Los MX, MY, MZ, NA, NG, NI, NO, NZ, OM, PG, PH, PL, Alamos National Laboratory, Lc/ip, Ms A187, Los Alamos, PT, RO, RS, RU, SC, SD, SE, SG, SK, SL, SM, SV, SY, NM 87545 (US).
    [Show full text]
  • Emergence Agitation After Intraoperative Neurolytic Celiac Plexus Block with Alcohol: a Case Report Huixuan Zhou, Yinbing Pan, Cunming Liu and Xiaodi Sun*
    Zhou et al. BMC Anesthesiol (2021) 21:204 https://doi.org/10.1186/s12871-021-01426-2 CASE REPORT Open Access Emergence agitation after intraoperative neurolytic celiac plexus block with alcohol: a case report Huixuan Zhou, Yinbing Pan, Cunming Liu and Xiaodi Sun* Abstract Background: Emergence agitation after general anesthesia may cause several undesirable events in the clinic during patient anesthesia recovery, and acute alcohol intoxication, while rare in surgery, is one of the risk factors. Case presentation: A 66-year-old male patient was found to have pancreatic tail neoplasm upon computed tomog- raphy (CT) examination. The surgeon planned to resect the pancreatic tail under general anesthesia. However, the surgeon found extensive tumor metastasis in the abdominal cavity, and thus performed a neurolytic celiac plexus block (NCPB) with 40 ml 95% ethyl alcohol and fnished the surgery in approximately 1 h. Twenty minutes later, the patient was extubated and developed signifcant emergence agitation in the postoperative care unit, characterized by restlessness, uncontrollable movements, confusion and disorientation. The patient was fushed and febrile with an alcohol smell in his breath and was unable to follow commands. Patient symptoms were suspected to be due to acute alcohol intoxication. Thus, the patient was given 40 mg of propofol intravenously. Following treatment, the patient recovered with less confusion and disorientation after approximately 10 min. After treatment with propofol twice more, he regained consciousness, was calm and cooperative, had no pain, and could obey instructions approxi- mately 1 h and 40 min following the last treatment. Following this treatment, the patient was transferred to the inpatient ward and felt well.
    [Show full text]
  • Och Beroendevård, 2006-123-21
    Faktaunderlag till Nationella riktlinjer för missbruks- och beroendevård Socialstyrelsen klassificerar sin utgivning i olika dokumenttyper. Detta är ett Underlag från experter. Det innebär att det bygger på vetenskap och/eller be- prövad erfarenhet. Författarna svarar själva för innehåll och slutsatser. Social- styrelsen drar inga egna slutsatser i dokumentet. Experternas sammanställning kan dock bli underlag för myndighetens ställningstaganden. Artikelnr: 006-3- Sättning: Per-Erik Engström Publicerad: www.socialstyrelsen.se, april 2006 Förord Ett förslag till Nationella riktlinjer för missbruks- och beroendevård skick- as ut på remiss till bl.a. kommuner och landsting den 5 april 2006. Doku- mentet kommer även att vara tillgängligt på Socialstyrelsens webbplats. Samtidigt kommer faktaunderlaget till dessa riktlinjer och som här pre- senteras att publiceras på samma sida. I faktaunderlaget har samtliga de kunskapsöversikter som riktlinjerna baseras på samlats. Det omfattande materialet har varit föremål för viss redigering och granskning av Socialstyrelsen, men författarna svarar dock ensamma för innehållet. Översikterna utgör slutresultatet av de beställningar som Socialstyrel- sen gjorde årsskiftet 2002–2003 till de fem expertgrupper som anlitats. Kunskapsöversikterna ska i princip omfatta kunskapsläget fram till och med våren 2004. Kunskapsproduktionen inom missbruksområdet är om- fattande, vilket aktualiserar behovet av återkommande revisioner av fak- taunderlaget. Socialstyrelsen har för avsikt att påbörja ett sådant arbete under 2007. Medverkande i de expertgrupper som deltagit i framtagandet av detta faktaunderlag redovisas på sidan 13 (övriga medverkande i arbetet redo- visas i ovan nämnda riktlinjedokument). Socialstyrelsen vill samtidigt varmt tacka samtliga experter för deras engagerade och viktiga insats. Kjell Asplund Generaldirektör Ola Arvidsson och Ulf Malmström 3 Innehåll Expertgruppernas sammansättning ������������������������������������������������������� 3 1.
    [Show full text]
  • Changes in Glutathione Content in Liver Diseases: an Update
    antioxidants Review Changes in Glutathione Content in Liver Diseases: An Update Mariapia Vairetti , Laura Giuseppina Di Pasqua * , Marta Cagna, Plinio Richelmi, Andrea Ferrigno * and Clarissa Berardo Unit of Cellular and Molecular Pharmacology and Toxicology, Department of Internal Medicine and Therapeutics, University of Pavia, 27100 Pavia, Italy; [email protected] (M.V.); [email protected] (M.C.); [email protected] (P.R.); [email protected] (C.B.) * Correspondence: [email protected] (L.G.D.P.); [email protected] (A.F.); Tel.: +39-0382-98687 (L.G.D.P.); +39-0382-986451 (A.F.) Abstract: Glutathione (GSH), a tripeptide particularly concentrated in the liver, is the most important thiol reducing agent involved in the modulation of redox processes. It has also been demonstrated that GSH cannot be considered only as a mere free radical scavenger but that it takes part in the network governing the choice between survival, necrosis and apoptosis as well as in altering the function of signal transduction and transcription factor molecules. The purpose of the present review is to provide an overview on the molecular biology of the GSH system; therefore, GSH synthesis, metabolism and regulation will be reviewed. The multiple GSH functions will be described, as well as the importance of GSH compartmentalization into distinct subcellular pools and inter-organ transfer. Furthermore, we will highlight the close relationship existing between GSH content and the pathogenesis of liver disease, such as non-alcoholic fatty liver disease (NAFLD), alcoholic liver disease (ALD), chronic cholestatic injury, ischemia/reperfusion damage, hepatitis C virus (HCV), hepatitis B virus (HBV) and hepatocellular carcinoma.
    [Show full text]