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RAJIV GANDHI UNIVERSITY OF HEALTH SCIENCES BANGALORE,KARNATAKA ANNEXURE II PROFORMA FOR REGISTRATION OF SUBJECTS FOR DISSERTATION Dr.DEBASISH BARIK 1. Name of the candidate and address POST GRADUATE IN GENERAL MEDICINE BANGALORE MEDICAL COLLEGE AND RESEARCH INSTITUTE,BANGALORE-560002 2 Name of the institution BANGALORE MEDICAL COLLEGE AND RESEARCH INSTITUTE,BANGALORE-560002 3 Course of study and subject M.D. IN GENERAL MEDICINE 4 Date of admission to the course 17TH AUGUST,2013 5 Title of the topic “LEVEL OF SERUM CREATINE KINASE AND MAGNESIUM AS PROGNOSTIC INDICATORS IN ACUTE ORGANOPHOSPHORUS POISONING.” 6.Brief resume of intended work: 6.1 Need for study: Organophosphorus(OP)insecticides are arguably one of the commonest causes of morbidity and mortality due to poisoning worldwide especially in developing countries like India.The morbidity and mortality depends on the time lag between the exposure and the onset of management.With increase use of compounds for agricultural and industrial purposes and due to easy access and low cost,they are becoming a major source of health hazard.So it is cardinal to recognize the entire spectrum of symptoms.Identification,risk stratification,early diagnosis and prompt treatment of OP poisoning victims are equally vital.These compounds act by inhibiting the enzyme acetylcholinesterase which result in accumulation of acetylcholine in nervous tissue and effector organs, principal site being the peripheral nervous system.[1,2] Patients with acute Organophosphorus(OP) poisoning are usually monitored by using serum acetylcholinesterase level which are expected to fall.It is not specific and does not correlate with the severity of poisoning and cannot be used as a prognostic indicator.[3]Estimation of creatine Kinase is easy and levels are increased both in acute phase as well as in intermediate syndrome due to muscle fibre necrosis.[2] Magnesium levels are usually reduced in Organophosphorus poisoning due to gastrointestinal loss,vomiting,diarrohia ,prolonged gastric aspiration. Many manifestation of hypomagnesemia overlap with features of Organophosphorus poisoning.So it may be a contributory factor in severity and outcome.[4] Considering all these factors this study is being undertaken. 6.2.Review of Literature: A study conducted at Kolkata medical College by Kuntal Bhattacharya et al found the correlation between initial increase in serum creatine kinase level and increased risk of complications like respiratory paralysis,arrythmia and increased atropine requirement in patients with acute organophosphorus poisoning.[2] A Study conducted by abdolkarim pajoumond at poison control centre,loghmanhakim hospital,school of medicine,saheed behesti university of medical sciences,tehran, Iran concluded that giving MgSO4 in a dose of 4g per day alongwith conventional therapy reduced the stay in the hospital and rate of mortality.[5] A reveiw article published by paudyal BP,department of medicine,patan hospital,Lalitpur has mentioned regarding Magnesium sulphate as the newer mode of therapy in acute organophosphorus poisoning.Also other modes like fresh frozen plasma,anti oxidants,organophosphorus hydrolases,sodium bicarbonate and gacyclidine(NMDA receptor antagonist) are coming up as latest therapeutic advances.[6] A study conducted by M John et al at department of medicine in CMC vellore showed correlation between the development of muscle injury producing a raised CK level and intermediate syndrome[7]. A study conducted by Singh G,Avasthi G,Khurana D, Whig J, Mahajan R at the department of medicine ,Dayanand Medical college ,Ludhiana,India showed the administration of MgSO4.7H2O at 4 g I.V resulted in a decrease in compound muscle action potential amplitude,loss of repetitive response and conversion of the decrement increment response at higher rate repetitive nerve stimulation to an increment response[8]. 6.3.Objective of study: 1.To assess and categorise the severity of organophosphorus poisoning cases clinically ,on admission by Peradeniya Organophosphorus Poisoning scale. 2.To estimate the serum levels of creatine kinase and magnesium in acute Organophosphorus poisoning and to correlate the same with clinical severity scoring at admission and serially till discharge. 7.MATERIALS AND METHODS 7.1.Source of data: This consists of patients admitted in the department of medicine of Victoria Hospital and Bowring and Lady Curzon Hospital attached to Bangalore Medical College and Research Institute 7.2.Method of collection of data: A.Study design: cross sectional prospective study design. B.Study period:November 2013 to October 2015 C.Place of study: The study is planned to be conducted in Victoria hospital and Bowring and Lady Curzon hospital. D.Sample size:150 patients. E.Inclusion criteria:All cases of acute organophosphorus poisoning admitted to our hospital within 12 hours of consumption of the poison irrespective of age and sex whose caregivers are willing to give written informed consent. F.Exclusion criteria: 1.Other pesticide poisoning. 2. Mixed poisoning. 3. Consumption of poison with alcohol . 4. Known medical illness like chronic liver disease, myopathy, malignancy, renal failure, autoimmune disorder, coronary artery disease . . 5. Patients on chronic drugs like statins, steroids. G. Methodology: After obtaining clearance and approval from the institutional ethics committee and written informed consent of the caregiver,patients admitted to the emergency with organophosphorus compound consumption will be selected after fulfillment of inclusion and exclusion criteria and enrolled in the study(Annexure I). The eligible patients will be initially subjected to peradeniya Organophosphorus poisoning scale and will be categorised according to severity.(Annexure IV) All routine investigations like CBP,RFT,SE,LFT,ECG,RBS,URINE(R/E),will be performed. Apart from these investigations the other investigations to be done: 1.Serum Cholinesterase level 2.Serum Creatine kinase level 3.Serum magnesium level. The serum creatine kinase and magnesium level will be correlated with the initial peradeniya clinical scoring and subsequently on day 2,3 and on discharge.(Annexure V) H.Statistical analysis: The data obtained will be analysed using 1.Chi square test 2.Analysis of variance 3.Unpaired Student t test 7.3.Does the study require any investigation or interventions to be conducted in patients or animals?if so describe briefly. Animals: NO Patients:patient’s caregiver’s written informed consent will be taken. The following investigations are needed for the study Complete blood count Liver function test Renal function test Serum electrolytes Random blood sugar Urine Routine ECG Serum cholinesterase Serum creatine kinase Serum magnesium 7.4.Has the ethical clearance been obtained from ethics committee of your institution in case of 7.3? “YES”,ethical clearance has been obtained from the ethics committee of our institution. 8.LIST OF REFERENCES: 1.Ernest Hodgson.Organophosphorus insecticides:Ernest Hodgson,Department of Environmental and Biochemical Toxicology,North Carolina State University,editor.A text book of modern toxicology.3rd ed.USA:Wiley-interscience;2004.p.58-60. 2. Kuntal Bhattacharya,Sibaji Phaujdar ,Rathindranath Sarkar and Omar S.Mullick .Serum creatine phosphokinase: A probable marker of severity in organophosphorus poisoning.Toxicol Int 2011 jul-dec;18(2):117-123. 3.Semir Nouira,Fekri Abroug,Souhil Elatrous,Ratik Boujdaria,Slah Bouchoucha.Prognostic value of serum cholinesterase in organophosphate poisoning.Chest 1994;106(6):1811-1814 4.CS Limaye,VA Londhey,MY Nadkar,NE Borges.Hypomagnesemia in critically ill medical patients.Journal of the Associations of Physicians of India 2011;59:19-22. 5.Abdolkarim Pajoumand,Shahin Shadina,Ali Rezaie,Mehboobeh Abdi,Mohammad Abdollahi.Benifits of magnesium sulphate in the management of acute human poisoning by organophosphorus insecticide.Hum Exp Toxicol.2004 dec;23(12):565569. 6.Paudayal BP .Organophosphorus Poisoning.J Nepal Med Assoc.2008;47(172):251258. 7.M John,A Oommen,A Zachariah .Muscle injury in organophosphorus poisoning and its role in the development of intermediate syndrome .Neurotoxicology.2003 jan;24(1):43-53 8.Singh G,Avasthi G,Khurana D,Whig J,Mahaian R.Neurophysiological Monitoring of Pharmacological manipulation in acute organophosphorus poisoning .the effect of pralidoxime,magnesium sulphate and pancuronium.Electroencephalog.Clin Neurophysiol.1998 Aug;107(2):140-148. 9.MgSO4 Treatment against Sarin Poisoning :Dissociation between overt convulsion and recorded cortical seizure activity.Archives Of Toxicology.February 2013;87(2):347-360. 10.Balali Mood M,Saber H.Recent advances in the treatment of organophosphorus poisoning.Iranian Journal of Medical science 2012;37(2):74-91. 11.Dursun Aygun,Ali Kemal Erenler ,Ayedin Deniz Karatas,Ahmet Baydin.Intermediate syndrome following Acute Organophosphate poisoning:Correlation with initial Serum levels of Muscle Enzymes.Basic Clin Pharmacol Toxicol 2007;100(3):201-204. 9. Signature of the candidate 10. Remarks of the Guide Acute organophosphorus compound poisoning is very common among patients admitted to casualty in our hospitals.Methods to diagnose,monitor and prognosticate are non specific.There is a need to develope the parameters other than clinical in these patients for the better outcome.Creatine kinase and magnesium levels appear to be good options in this aspect. 11. Name and Designation of DR. NAGARAJA B.S, MD 11.1 Guide Professor,Department of General Medicine BMC&RI,Bangalore 11.2 Signature DR.PRABHAKAR.B, MD 11.3 Head of the Department 11.6 Signature 12. 12.1 Remarks of Chairman and principal 12.2 signature Professor&HOD,Department of General Medicine,BMC&RI,Bangalore. ANNEXURE III STUDY PROFORMA DATE: I.P. NO. PATIENT IDENTIFICATION NO. I.PATIENT INFORMATION: NAME AGE SEX I.P. NO. ADDRESS PHONE No. OCCUPATION II.POISONING COMPOUND AMOUNT TIME OF CONSUMPTION III.SYMPTOMS: VOMITING LOOSE STOOLS SALIVATION/LACRIMATION/SWEATING DYSPNOEA BLURRING OF VISION SEIZURES LOSS OF CONSCIOUSNESS IV.PAST HISTORY: DIABETES MELLITUS HYPERTENSION BRONCHIAL ASTHMA/COPD TUBERCULOSIS V.PERSONAL HISTORY: SMOKING ALCOHOLISM VI.SYSTEMIC EXAMINATION: CVS RS ABDOMEN CNS VII.INVESTIGATIONS: CBP LFT RFT SE RBS URINE(R/E) ECG AchE(DAY 1) ANNEXURE IV PERADENIYA ORGANOPHOSPHORUS SCALE PARAMETERS 0 1 2 PUPIL SIZE ≥2 mm <2mm PINPOINT RESPIRATORY RATE <20/min ≥20/min HEART RATE >60/min 41-60/min FASCICULATION None Conscious and LEVEL OF CONSCIOUSNESS rationale SEIZURE Absent GRADE Mild(0-3) Present Generalised/continuous Impaired response to verbal commands Present Moderate(4-7) ≥20/min with central cyanosis <40/min Both generalised and continuous No response to verbal commands Severe(8-11) SCORE ANNEXURE V SERIAL ESTIMATION OF SERUM CREATINE KINASE AND MAGNESIUM DAY 1 DAY 2 DAY 3 ON DISCHARGE SERUM CK SERUM MAGNESIUM CLINICAL SCORING ATROPINE REQUIREMENT COMPLICATIONS IF ANY DURATION OF HOSPITAL STAY - ANNEXURE I PROFORMA FOR WRITTEN INFORMED CONSENT Date: Place: I,Mr/MS/Mrs , son/daughter/wife of Mr. ,aged about years, have been explained in a language understood by me about the study entitled “LEVEL OF SERUM CREATINE KINASE AND MAGNESIUM AS PROGNOSTIC INDICATORS IN ACUTE ORGANOPHOSPHORUS POISONING”.at the department of general medicine of Victoria hospital and Bowring and Lady Curzon hospital,Bangalore. I have been explained about the procedures and investigations that will be done during this study. I have no objections in sharing my patient’s medical information and details in case records with the investigators of this study.I have been informed that I will not be sharing any incentives.Personal identity will not be revealed and data may be used for publication/dissertation purpose. I understand that my patient’s participation in this study is entirely voluntary and I willfully give consent regarding participation of my patient in this study for the specified duration. Signature of the caregiver Relation with the patient Signature of the doctor