Therapeutic Management of Paraquat Poisoning at Colonial War
Transcription
Therapeutic Management of Paraquat Poisoning at Colonial War
Final Technical Report for Research Project Therapeutic Management of Paraquat Poisoning at Colonial War Memorial Hospital. Principal Investigator: Shayna Khan (Fiji National University: College of Medicine, Nursing and Health Sciences) 2014.26.FNRERC.20.SU July 2015 Final Technical Report Disclaimer The access to the Final Technical Report is provided by the Fiji Ministry of Health (MOH) in line with stated objectives of national guidelines on responsible conduct of health research on timely access and dissemination of research findings. This is expected to maximize impact and use of research findings to inform policies and programs in a timely manner. The Final Technical Report is the report as submitted by the principal investigator or his representative on completion of a research project previously approved by an accredited health research ethics review committee for implementation in Fiji. The research report is submitted to Health Research Office in Division of Health Information, Research and Analysis in MOH compliance with National Guidelines on Responsible Conduct of Health Research, which requires all researchers to submit the Final Technical Report to MOH within a defined timeframe. However, the Final Technical Report as submitted may include only preliminary and unpolished results and may differ from the other publications submitted by the investigators in scientific peer review journals or other forums. The Reports have not been edited, proof-read or peer reviewed. These have been published largely as submitted by investigator (s). The cover page of this Report is automatically generated. The name of the principal investigator and co-investigators that appear on the cover page are based on names of principal and other co-investigators provided to health research ethics review committee at the time of proposal submission. The findings, interpretations, and conclusions expressed in the Final Technical Report are entirely those of the author(s)/Investigator (s) and should not be attributed in any manner to the MOH, Health Research Office, or to its affiliated institutes. Citation and the use of material presented in the Final Technical Report should take into account this provisional nature of the publication. The readers may contact the principal investigators or co-investigators for any further questions or enquiries. Powered by TCPDF (www.tcpdf.org) THERAPEUTIC MANAGEMENT OF PARAQUAT POISONING AT COLONIAL WAR MEMORIAL HOSPITAL. PHM 700: MAJOR RESEARCH PROJECT FOR BACHELORS IN PHARMACY PROGRAM DEPARTMENT OF HEALTH SCIENCES Compiled By Shayna Khan S110351 Supervisor Mr Arnold Ram TOWARDS PHARMACY PROGRAM COLLEGE OF MEDICINE, NURSING AND HEALTH SCIENCES FIJI NATIONAL UNIVERSITY SUVA, FIJI. NOVEMBER 2014 2| P a g e DECLARATION This research project titled “Therapeutic Management of Paraquat Poisoning at Colonial War Memorial Hospital” was carried out in partial fulfilment of Bachelors in Pharmacy Program. I declare that this project does not contain any information or materials that have already been published in order to graduate in another university or institution. To my knowledge, no information or opinion that has already been published or written by other writers, were used in the compilation of this project. All information and materials used are owned by the writer. Materials taken from other sources are quoted as such and noted in the reference list. 3rd November 2014 Suva …………………………… Shayna Khan. 3| P a g e ACKNOWLEDGEMENT The compilation of this Major Research Project entitled “Therapeutic Management of Paraquat Poisoning” would not have been accomplished without the help of the following people: 1. Mr Arnold Ram, my research supervisor, for his profoundly valued and constructive suggestions towards the planning and completion of this research work. 2. The doctors, pharmacists and nurses for their participation in this study. 3. Health Information Unit (Ministry of Health) for providing data, to enable completion of this study. 4. Mrs Eve De Silva, who enabled liaison with Mental Health Alliance of Fiji. 3rd November 2014, Suva, Shayna Khan 4| P a g e TABLE OF CONTENTS Topic Page Declaration……………………………………………………………………………….2 Acknowledgement………………………………………………………………………..3 Table of contents…………………………………………………………………………4 Abstract…………………………………………………………………………………..5 CHAPTER 1: INTRODUCTION 1.1. Background Information…………………………………………………………….6-7 1.2. Statement of Problem……………………………………………………………….7-9 1.3. Aim …………………………………………………………………………………10 1.4. Objectives…………………………………………………………………………...10 1.5. Advantages …………………………………………................................................10 CHAPTER 2: LITERATURE REVIEW………………………………………………...11-16 CHAPTER 3: RESEARCH METHODOLOGY 3.1 Study type and variables………………………………………………………….….17 3.2 Sampling …………………………………………………………………………….17 3.3 Data collection……………………………………………………………………….18 3.4 Data Processing and analysis……………………………………………….………..18 3.5 Ethical Issues………………………………………………………………..……….19 CHAPTER 4: RESULTS 4.1 Results……………………………………………………………….……………….20 – 27 4.2 Discussion…………………………………………………………….………….......28 – 29 4.3 Conclusion…………………………………………………………….……………...30 4.4 Recommendation and Limitations………………………………….…………….…..31 APPENDIX 1. Annex 1 – References…………………………………………………………………..32-34 2. Annex 2 – Information Sheet…………………………………………………………...35-36 3. Annex 3 – Consent Form……………………………………………………………….37 4. Annex 4 – Data Collection Tool (Questionnaires, Table Form)………………………..38-39 5. Annex 5 – Approval Letter……………………………………………………………...40-42 5| P a g e ABSTRACT BACKGROUND: Paraquat is a very effective herbicide that has been marketed since 1962 by a company called Syngenta. In Fiji paraquat is available as a concentrated solution and is sold under the brand names Gramoxone®, Royal®, Gramoxone Extra® and Agazone®. These preparations are then diluted and sprayed in plantations. AIM: To determine the therapeutic management of paraquat poisoning at Colonial War Memorial Hospital. OBJECTIVES: To determine the gender, ethnicity and age groups of the patients diagnosed with paraquat poisoning in Fiji from the year 2009-2013. To determine how paraquat poisoning is diagnosed. To determine the treatment options available for paraquat poisoning patients reporting to Colonial War Memorial Hospital. METHODS: A non-experimental descriptive cross-sectional study was conducted where convenient sampling was done of doctors, nurses and pharmacist. A total of 20 self administered questionnaires were distributed and 14 were received. Data regarding gender, ethnicity and age groups of paraquat poisoning patients in Divisional hospitals from the year 2009-2013 was sourced from Health Information Unit of Ministry of Health. Additional data was sourced from Mental Health Alliance of Fiji. RESULTS: It was found that the gender, ethnicity and age groups most susceptible to paraquat poisoning were males, Indo-Fijians and in age group of 26 years and over respectively. Paraquat poisoning patients at Colonial War Memorial Hospital are diagnosed by clinical symptoms and information provided by relatives. These patients are treated using fullers Earth, activated charcoal and mannitol. CONCLUSION: The fact that paraquat poisoning does not have an antidote, coupled with the toxicity of paraquat, pose a challenge in the management of paraquat poisoning patients. There is a need for more reliable diagnostic tests and further research is needed to determine the possibility of banning paraquat use. 6| P a g e CHAPTER 1: INTRODUCTION 1.1 BACKGROUND INFORMATION Paraquat is a very effective herbicide that has been marketed since 1962 by a company called Syngenta. In Fiji paraquat is available as a concentrated solution and is sold under the brand name Gramoxone® which contains 20% w/v paraquat dichloride(1). Other brands of paraquat used in Fiji include Royal® brand paraquat, Gramoxone Extra® (contains 27.6%w/v of paraquat dichloride) and Agazone®. These preparations are then diluted and sprayed in plantations. Other brands of paraquat include Crisquat®, Dextrone®, Herba-xone®, Ortho Weed®, and Spotkiller®[23]. Paraquat and its salts are listed as poisons under part II of the poisons list in the third schedule of the Pharmacy and Poisons Act. Initially death from paraquat resulted from accidental ingestion. However, as the toxicity of paraquat became known, deaths due to intentional paraquat poisoning began to arise(2). In order to hinder ingestion, some preparations of paraquat contain an emetic, or a laxative and some contain a malodorous agent. In developed countries, paraquat poisoning is not widely utilised as a method of inflicting self harm however, in developing countries like Fiji intentional paraquat poisoning is relatively common. This is because paraquat is a widely used herbicide in Fiji. It is easily accessible to people; it may be bought from most hardware stores (only licensed storekeepers are allowed to sell specific poisons such as paraquat) or from the various agriculture departments representing the Ministry of Agriculture. A dose of 10 to 15mL of the concentrate (20%w/v) is considered to be lethal (3) . Clinical manifestations of paraquat poisoning include convulsions (CNS involvement), jaundice (liver toxicity), gastro-intestinal ulceration and bleeding, respiratory distress (due to pulmonary oedema), hypovolaemic shock, hypotension and cardiac failure which eventually lead to death(2). 7| P a g e In addition to being highly toxic when ingested, prolonged exposure of skin to concentrated solution of paraquat while spraying the herbicide can also be fatal. Paraquat becomes safe when it comes into contact with soil thus fullers’ earth is one of the treatment options administered to paraquat poisoning patients. 1.2 STATEMENT OF THE PROBLEM 1.2.1 The Research Problem The number of attempted suicide and suicide fatalities are increasing every year in Fiji. With each suicide attempt individuals are stigmatised, families are devastated, economies lose productive workers, and the health sector incurs extra costs for providing care. Extensive research has been conducted regarding suicide in Fiji generally; however, there is a lack of research that explores the individual methods of self-harm separately. This research will explore paraquat as a method of self-harm as seen from the health care perspective. The research is based on intentional paraquat poisoning in Fiji focusing in particular on the therapeutic management of paraquat poisoning patients reporting to the Colonial War Memorial Hospital. 1.2.2 The Solutions One solution that had been tried internationally for preventing paraquat use and sale was the launch of the pesticide action networks (PAN) Dirty Dozen Campaign in 1985(4). PAN international is a company based in the United Kingdom and it had come up with a list of extremely hazardous pesticides. Paraquat was among this list and the company was advocating that all pesticides contained within the list should be banned, or its sale restricted and safer pesticides be used as alternatives. 8| P a g e Furthermore, non-governmental organisations of Asia, America and Europe had launched the ‘Stop Paraquat’ campaign in 2002(5). The campaign targeted Syngenta a company based in Switzerland that supplies pesticides to many countries. The stop paraquat campaign was aimed at preventing production of harmful pesticides by Syngenta. As a result of this campaign, Malaysia became the first Asian country to ban paraquat use and sale. According to Watts (6) “in 2006 Malaysia reversed the ban and allowed its use in oil palm plantations. In 2007 the Malaysian government announced that the ban was postponed until further notice”. The situation in Malaysia teaches us that banning paraquat might seem to be the best solution; however, it failed to eradicate the problem. This is because trade in paraquat is still rife even in countries that have banned paraquat. One solution that had been tried locally was increasing public awareness. However, the publicity of paraquat as a suicide agent seemed to exacerbate the problem. The addition of an emetic and stenching agent to paraquat to make it less palatable failed to decrease paraquat induced suicides in Fiji (7) . Efforts to use an alternative to paraquat proved futile as the alternative was more expensive than paraquat. In addition to this banning the import of paraquat has not received much approval as paraquat is the major pesticide utilised in the sugar industry in Fiji. According to a fact sheet prepared by the Pesticide Action Network Asia and the Pacific(8), as of February 2012 paraquat is banned in a total of 36 countries. Unfortunately Fiji is not part of these 36 countries; however, Fiji has been listed among the countries that have restricted paraquat use. 9| P a g e 1.2.3 Relevance of the Problem to National/Local Activities Paraquat ingestion can become fatal very quickly as it is extremely toxic to humans. Finding out about the therapeutic management of paraquat poisoning will help ascertain the different types of treatment available and the expertise required by health care staff when providing treatment. 10 | P a g e 1.3. AIM OF THE RESEARCH: To determine the therapeutic management of paraquat poisoning at Colonial War Memorial Hospital. 1.4. OBJECTIVES: 1. To determine the demographic details (such as gender, ethnicity and age groups) of the patients diagnosed with paraquat poisoning in Fiji from 2009-2013. 2. To determine how paraquat poisoning is diagnosed. 3. To determine the treatment options available for paraquat poisoning patients reporting to Colonial War Memorial Hospital. 1.5. ADVANTAGES: The results may be used to review the therapeutic management of paraquat poisoning in other hospitals around the country. The results may also be used in future should Fijian policy makers consider banning paraquat imports altogether instead of just restricting its use. 11 | P a g e CHAPTER 2: LITERATURE REVIEW Suicide is defined as death due to intentional self-inflicted injury. Attempted suicide is defined as intentional self-inflicted injury not resulting in death(9). According to the World Health Organisation(10), approximately one million people commit suicide each year worldwide which is about one death every 40 seconds or 3000 per day. ‘Suicide is among the three leading causes of death among those aged 15-44 years in some countries, and the second leading cause of death in the 10-24 years age group’(10). At one point, the suicide rates of Fiji were considered to be the second highest in the world behind rural China (11). Statistics released in the year 2010 reveal that hanging, ingesting poisons and drug overdose are the most common methods of committing suicide in Fiji(12). This fact is reciprocated in a study done by Hanson(13). In this study, cases of hospitalised clients who were referred to the Pacific Counselling and Social Services of Fiji were reviewed. Out of all the cases reviewed, 2.7% represented cases of attempted suicide. Among these cases, the most common method of attempted suicide was intentional self poisoning (78.4%) followed by hanging, strangulation and suffocation (10.5%). Studies conducted by Peiris John(14) and Aghanwa(15) explored the substances used in intentional poisoning. In the study conducted by Peiris-John(14), it was found that substances used for intentional poisoning included chemicals (41.2%), drugs (35.3%) and pesticides (23.5%). One limitation of this study was that the records did not state the specific chemicals, drugs and pesticides used. The study conducted by Aghanwa(15), however, did not have this limitation. In the study conducted by Aghanwa, deliberate self poisoning patients were examined in CWM hospital. 12 | P a g e Thirty one (31) patients with deliberate drug overdose and 27 patients with self poisoning were compared. The study found that Paracetamol (35.5%) and Paraquat (29.7%) were the most commonly used agents in self poisoning. In most cases, paraquat poisoning is ascertained by the containers brought in by relatives of the patient. This is also used to determine the amount of paraquat ingested. At times the containers are not brought in but the doctor is just informed by the relatives and he takes their word for it. Mistakes in identifying the poison have occurred as a result of this. A case report in one study (17), highlighted this fact. ‘A 27 year old woman was sent to a local hospital after ingesting 30mL of herbicide. According to her relatives, she had ingested glyphosate, and she was therefore treated with gastric lavage, atropine and fluid administration. The patient was given oxygen before it was clear that the herbicide was paraquat.’ In paraquat poisoning, administration of oxygen exacerbates the problem. In the above case, the patient had survived, however, misdiagnosis can prove fatal to patients. A test that can be used to diagnose paraquat poisoning is the bicarbonate and sodium dithionate urine test. ‘In alkaline medium, sodium dithionite reduces paraquat to a blue radical. If the urine paraquat concentration is more than 1mg/L, the urine will appear blue and this finding alone indicates a very poor prognosis’(16) . Plasma paraquat concentrations are also measured but these require quantitative analysis using complex machines and techniques such as spectrophotometry and HPLC, which is beyond the scope of local hospital laboratories. The search for an antidote for paraquat poisoning is still on-going. Since there is no antidote, standard treatments are often altered according to the patients’ needs in an effort to obtain a 13 | P a g e better prognosis. It is suggested that part of the lethality of paraquat is due to the lack of effective treatment (10,20). ‘There is no specific treatment for paraquat poisoning and the immediate aim is to remove or inactivate the paraquat’(3). Initially treatment involves removal of contaminated clothing and irrigation of eyes and skin that is exposed. A precaution to be taken is to avoid giving oxygen to the patient initially as it accelerates pulmonary toxicity of paraquat (3). In a study conducted by Winchester(2), four main aims for management were listed: to prevent gastro-intestinal absorption, extract paraquat from blood, prevent cellular damage by oxygen radicals and in some cases to suppress the immune system. The study then elaborated on the specific agents used to achieve these aims. ‘Fuller’s earth, bentonite and activated charcoal are usually administered to prevent gastrointestinal absorption. Haemodialysis and haemoperfusion are conducted in order to remove paraquat from blood. Antioxidants such as vitamin C & E, salicylic acid and N-acetylcysteine are used to prevent further cellular damage. In addition to this glucocorticoids (cyclophosphamide, methylprednisolone, dexamethasone) are used to suppress the immune system and prevent the acute inflammatory response from occurring.’ In some studies, patients are given a cocktail of treatments covering all the bases, that is to prevent GI absorption, prevent generation of oxygen radicals, immunosuppression, and removal of paraquat from blood while some studies investigate the superiority of certain methods of treatment over others. In a study conducted by Sandhu(18), 17 patients were studied over a 5 year period. All these patients received the same standard treatment: gastric lavage using tap water (5mL/kg body weight), activated charcoal (1g/kg dissolved in 250-400mL of water), hydrocortisone injection 100mg IV 6 hourly for 3-5 days, Vitamin C 500mg twice daily and Vitamin E 400mg twice 14 | P a g e daily. The study recorded a 35% mortality rate using this regimen. The causes of mortality in these patients were attributed to respiratory failure, multi-organ failure and shock. In a study done by Li et al (19) a review was done to assess the effects of glucocorticoid with cyclophosphamide on mortality in patients with paraquat induced lung fibrosis. Only RCTs were included in this review. All patients were to receive standard care, plus the intervention or control. The intervention was glucocorticoid with cyclophosphamide in combination versus a control of a placebo, standard care alone or any other therapy in addition to standard care. They reviewed 3 randomised controlled trials with a combined total of 164 patients who had moderate to severe paraquat poisoning. They calculated the relative risk (0.72) and found that the group receiving cyclophosphamide and steroids with standard care had a reduced risk of death of about 28% compared with patients given standard care alone. However, the RCT conducted were small and one of them was of low methodological quality so the conclusions drawn from the results have some degree of uncertainty. Gawarammama(16) suggests that management of paraquat poisoning is determined by two philosophies. Firstly, when there is no hope of recovery palliative care is provided using lowrisk intervention such as charcoal, IV fluids and maybe an antioxidant. Secondly, when it is recognised that the outcome is dire and that no treatment is likely to be worse than the disease, then treatment includes haemoperfusion or haemodialysis, immunosuppresion and a mixture of treatments. However, a report by the World Health Organisation(10) regarding clinical management of acute pesticide intoxication states that the treatment should suit the patient needs. Studies(10,16,22) suggest that more research is needed to determine effective treatment guidelines and appropriate therapeutic doses. ‘We would encourage anyone seeing a substantial number of paraquat poisonings to adopt a consistent strategy for a number of patients, measure the 15 | P a g e paraquat concentration and report their outcomes’(10). ‘There is a great need of additional and better quality information related both to the extent and nature of pesticide poisoning and its clinical and public health management’(16). ‘If the occurrence and lethality of pesticide ingestions cannot be prevented then improved medical management is crucial(22).’ The prognosis of a patient who has ingested paraquat depends on the amount that is ingested. Winchester(2) classified paraquat ingestion as moderate and severe poisoning. In his study moderate poisoning was defined as ingesting small quantities (4-30mL of the liquid concentrate) whereas severe poisoning was defined as ingesting massive amounts (more than 30mL of the concentrate). According to Winchester(2), death in patients who ingest moderate amounts occurs within one to two weeks whereas death in patients who ingest massive amounts occurs within several hours to a few days. The classification and prognosis outlined in Martindale(3) differs slightly from that of Winchester(2). Martindale(3) suggests that most patients who ingest 7.5 to 15mL of the concentrate die within 2 or 3 weeks after ingestion. Patients who ingest more than 15mL of the concentrate die 1-7 days after ingestion. The study done by Gawarrammana(16) goes on to explain the relationship between the amount ingested and the prognosis of the patient. Gawarammana(16) explains that ingestion of small quantities initially affects the kidney and lungs and toxicity of other organs occur gradually, thus these patients live for a few weeks. Ingestion of large amounts simultaneously affects the lungs, heart, kidneys, liver and the brain leading to multi-organ failure, thus these patients only live a few hours or days. Another study(18) conducted by Sandhu et.al reviewed the outcome of paraquat poisoning patients admitted in Dayanand Medical College and Hospital in Ludhiana over a 5 year period (1998-2002). In this study, the degree of poisoning was assessed by number of mouthful of 16 | P a g e paraquat concentrate ingested i.e. <1 mouthful as mild, 1 mouthful as moderate and 2 or more as severe. In this study, 1 mouthful was equated to approximately 20mL of paraquat. The different classification methods are creating confusion and differences in classifying patients among different researchers. The study outlined below is an example reflecting this confusion. A study (17) conducted in China reporting the successful treatment of patients with paraquat intoxication, used a different classification to compare its results with. This study utilised a method that compared the milligrams of paraquat ion ingested per kg of body weight. They classified mild poisoning as ingesting < 20mg of paraquat ion/kg body weight, moderate to severe poisoning as ingesting 20-40mg of ions/kg and acute fulminant poisoning as >40mg of ion/kg body weight. The study then went on to say that since its patients had ingested >20mL of concentrate, according to the classification above, they categorised it as acute fulminant poisoning. Their classification was based on mg of ions /kg of body weight, and equating >20mL of concentrate as fulminant poisoning is contradictory as the measures are totally different. Two studies (21,22) (one being a large prospective cohort study consisting of 451 patients and the other that did a systematic review of 17 studies) highlight the fact that a validated method of predicting outcome of patients is needed so that appropriate treatment may be selected based on likelihood of survival. Furthermore, once methods of predicting outcomes are validated, it may be used to assess the effectiveness of new treatments in improving prognosis. 17 | P a g e CHAPTER 3: RESEARCH METHODOLOGY 3.1. STUDY TYPE AND VARIABLES A non-experimental descriptive cross-sectional study design was used. 3.2. SAMPLING Convenient sampling was done of doctors, nurses and pharmacists who were then given questionnaires. Personnel Inclusion Criteria Wards/ Departments where selection was made. Doctors and nurses working All other hospital staff working in the wards in Accidents and apart from those stated in the inclusion criteria were Emergency Ward, Stress not given the questionnaire. Management Ward, Intensive Care Unit were included. Pharmacists working in inpatients and outpatients department. Exclusion Criteria 18 | P a g e 3.3. DATA COLLECTION TECHNIQUES Data collection commenced after written approval was obtained from the Department Research Committee (DRC), College Research and Ethics Committee (CREC) and the Ministry of Health: National Health Research Committee (NHRC). Approval was also obtained from the Medical Superintendent of Colonial War Memorial Hospital before conducting the research. Data collection commenced on 11th August 2014. Twenty (20) self-administered questionnaires were distributed to doctors (7), nurses (7) and pharmacists (6) to obtain data regarding treatment. The questionnaire contained seven questions and has been enclosed in Annex 4. De-identified data (regarding gender, ethnicity and age groups) of patients diagnosed with paraquat poisoning (including data from Labasa, Lautoka and Colonial War Memorial hospital) was sourced from Health Information Unit of Ministry of Health upon approval. The data was used for demographic mapping of paraquat poisoning cases in Fiji. Additional data regarding demographics was sourced from Mental Health Alliance of Fiji. 3.4. DATA PROCESSING AND ANALYSIS EpiInfo software was used to analyse the data collected from the questionnaires. The central tendencies of this data was also calculated. Microsoft Excel software was used to present the analysis in the form of graphs and pie-charts. 19 | P a g e 3.5. ETHICAL CONSIDERATION Prior to administering questionnaires, participants were provided with a participant information sheet (Annex 2) and were required to fill the consent form (Annex 3). All data obtained during the course of the research was kept confidential. Participant names were not recorded or revealed. The data collection tools were kept in a file. The file was stored in a locked drawer. Furthermore, the analysis of results was kept in a password protected computer in order to restrict access. Questionnaire answers were coded using the EpiInfo software. The analysis of the results were presented in the form of graphs and pie charts, therefore no one was able to connect specific answers to any one individual. 20 | P a g e CHAPTER 4: RESULTS 4.1. RESULTS Figure 1: Trends of paraquat poisoning cases in past 6 years. Paraquat Poisoning trends (past 6 years) 60 50 51 49 51 40 39 30 21 20 17 10 0 2008 2009 2010 2011 2012 2013 Explanation: Paraquat poisoning cases in the past 6 years have been increasing except in the year 2011 when a decrease in cases was reported. Figure 2: A comparison of Paraquat Poisoning cases between genders. Paraquat poisoning cases by Gender 35 30 33 32 29 25 23 20 15 10 17 18 16 15 13 5 22 6 4 0 2008 2009 2010 Male 2011 2012 2013 Female Explanation: In all 6 years, male patients were greater in number than female patients. In the past 6 years 145 cases (64%) reported were Male whereas 83 cases (36%) reported were female. 21 | P a g e Figure 3: A comparison between ethnicity of Paraquat Poisoning cases. Paraquat Poisoning Cases by Ethnicity 100% 0 1 1 0 1 90% 80% 70% 60% 50% 14 40 44 14 43 36 40% 30% 20% 10% 0% 6 9 2 2008 6 2009 2010 I-taukei 8 3 2011 Fijian [Indo] 2012 2013 Others Explanation: Indo Fijians make up majority of the paraquat poisoning cases. In the past 6 years, cases revealed that 34 (15%) were I-taukei , 191 (84%) were Indo-fijians and 3 (1%) were Others. Figure 4: Comparison of paraquat poisoning cases by age group Distribution of paraquat poisoing cases by age group 35 30 25 20 15 10 5 0 0-16 16-25 2008 2009 2010 2011 26+ 2012 2013 Explanation: The highest number of cases reported was in the year 2013 and occurred in patients 26 years and over. However, reported cases of patients in the 16-25 age group increased in the year 2009 and 2010. Overall in the past 6 years, 21 cases (9%) were reported in 0-16 age group, 82 cases (36%) reported for 17-25 year age group, and 125 (55%) cases were reported for 26 years and over age group. 22 | P a g e Figure 5: A comparison between attempted and completed paraquat poisoning cases. A comparison b/w attempted and completed paraquat poisoning cases 60 50 40 50 45 30 30 20 18 10 7 10 4 17 1 22 21 3 0 2008 2009 2010 2011 Attempted 2012 2013 Completed Explanation: The attempted cases of paraquat poisoning has been increasing for the past 3 years. In the past 2 years, a greater number of completed paraquat poisoning cases was recorded. In total, in the past 6 years 61cases (27%) were reported as attempted suicide, and 167 cases (73%) were reported as completed suicide cases due to paraquat poisoning. The percentage of completed suicide cases, reflects the lethal nature of paraquat. Figure 6: Cases Reported in Divisional Hospitals Cases Reported in Divisional Hospitals 25 20 15 10 5 0 2009 2010 2011 CWMH Lautoka 2012 2013 Labasa Explanation: In the past 5 years Colonial War Memorial Hospital has seen the highest number-79 (55%) of reported cases of poisoning due to herbicides/fungicides. Lautoka Hospital reported 20 cases (14%) whereas in Labasa Hospital 44 cases (31%) of poisoning due to herbicides/fungicides was recorded. Thus poisoning by herbicides/fungicides is not only confined to the western and northern areas of Fiji, where most of the farming communities reside. It is also happening in urban areas such as Suva. 23 | P a g e Figure 7. Number of cases observed in a year. Coded: 2= one-ten cases 3= eleven-twenty cases 7= greater than 50 cases. Explanation: 85.7% of participants have observed about 1-10 cases in a year. 7.1% of participants have observed between 11-20 cases in a year whereas 7.1% of the participants have observed greater than 50 cases. Figure 8. Diagnosis of Paraquat Poisoning Patients Explanation: 9 participants said that diagnosis was made according to clinical symptoms. 1 participant said that other biochemical tests were done. Majority (11) participants said that diagnosis was done according to information provided by relatives. 24 | P a g e Figure 9: Treatment Options Utilised by Colonial War Memorial Hospital (CWMH) Explanation: The most commonly used treatment option is Fullers Earth (all 14 participants chose this option), followed by activated charcoal (10 participants) and mannitol (8 participants). 1 participant said that Vitamins C and E may also be given. Analgesics and IV fluids were also given as answers although these options were not provided in the questionnaire. Figure 10: Guidelines used to treat paraquat poisoning patients Guidelines Utilised for management of paraquat poisoning patients SUICIDE PROTOCOL 1 ANTIDOTE HANDBOOK 1 INTERNAL MEDICINE GUIDELINE 1 TREATED ACCORDING TO CLINICAL PRESENTATION 3 CONSULTATION WITH OVERSEAS POISON CENTRES 1 MARTINDALE 1 EMERGENCY GUIDELINES 6 0 1 2 3 4 5 6 7 Explanation: The most commonly used guidelines utilised is emergency guidelines (6 participants mentioned it), followed by treatment according to clinical presentation (3 participants), other treatments that were mentioned by single (1) participants included using martindale, consultation with overseas poison centres, using the internal medicine guideline, using an antidote handbook and following the suicide protocol. 25 | P a g e Figure 11: Change in Treatment Explanation: Majority of participants (83.3%) said that amount of paraquat ingested did not change treatment options. The reason given was that there is a set protocol for management regardless of whether a sip or a gulp of paraquat is ingested. 16.7% said that treatment options changed according to amount ingested. These participants explained that significant paraquat poisoning carried poor prognosis and in these patients there are less treatment options available. Figure 12: Drug Shortage Explanation: Most participants (78.6%) felt that treatment was not hindered by drug shortages. 21.4% of participants said that there had been drug shortages and Fullers Earth was usually the treatment short in supply. However, at the time, other treatments such as activated charcoal were available, so treatment wasn’t necessarily hindered. 26 | P a g e Figure 13: Opinion on Banning Paraquat Explanation: Majority (57.1%) of participants felt that paraquat use should be banned. 42.9% of participants felt that paraquat should not be banned. Figure 14: Reasons given by participants saying yes: Ban paraquat use 33% 34% Fatal Commonly abused Safer alternatives available 33% Figure 15: Reasons given by participants saying no: Do not ban paraquat 25% 25% Others are just as lethal create awareness instead farming affected 50% Explanation: Some reasons provided for banning paraquat were: that it was fatal (34%), it is commonly abused (33%), alternatives and more environmentally friendly herbicides are available eg. Roundup-glyphosate (33%). 27 | P a g e Discussion: Some reasons for not banning paraquat include: other herbicides can also be lethal (banning one won’t solve the problem) [25%], stringent laws and awareness should be created instead of banning it [50%], farming will be adversely affected, observed that farmers utilising it don’t usually abuse it, the people that abuse it just buy it for the sake of suicide [25%]. Comparison between 2 data sets: Mental Health Alliance of Fiji (MHAF) & Health Information Unit (HIU) Table 1: Percentage Distribution of paraquat poisoning cases (MHAF) Variable Total Finding (past 6 years) Gender 145 (64%) Male, 83 (36%) Female Ethnicity I-taukei 34 (15%), Indo-fijians 191 (84%) Others 3 (1%) Age Group 21(9%) aged 0-16 years,82 (36%) aged 17-25 years, 125 (55%) aged 26 years and over Table 2: Percentage Distribution of Herbicide and Fungicide poisoning cases (HIU) Variable Total Finding (past 5 years) Gender 111 (59%) Male, 76 (41%) Female Ethnicity 27 (15%) Fijian, 156 (83%) Indo-Fijian, 4 (2%) Others, 0 Rotumans. Age Group 1 (0.5%) <1 year, 3 (2%) 1-4 years,0 in 5-9 years, 2 (1%) 10-14 years, 30 (16%) 15-19 years, 36(19%) 20-24 years, 37 (20%) 25-29 years, 27 (15%) 30-34 years, 14 (7%) 35-39 years, 8(4%) 40-44 years, 12(6%) 45-49 years, 5(3%) 50-54 years, 3(2%) 55-59 years, 4(2%) 60-64 years, 1 (0.5%)65-69 years, 4 (2%) in 70 years and over. Discussion: Data from both sources indicate that the gender, ethnicity and age groups most susceptible to poisoning (either from paraquat or other herbicides/fungicides) was found to be males, Indo-fijians and in age group of 26 years and over (for paraquat) and between 2529 years (for herbicides and fungicides) respectively. 28 | P a g e 4.2. DISCUSSION The use of paraquat to inflict self-harm is a major concern as the number of paraquat poisoning cases reported are increasing (figure 1). The results (figure 2, 3 & 4) indicate that the gender, ethnicity and age groups most susceptible to paraquat poisoning was found to be males, Indo-fijians and in age group of 26 years and over respectively. These results were also reflected in cases of poisoning by herbicides and fungicides reported at Divisional Hospitals (Table 1 & 2). The results of this study are similar to another study that was conducted by Peiris-John(14), where the incidence and characteristics of poisoning fatalities and hospital admissions in Viti Levu among I-Taukei and the Indo-Fijians were compared. The study found that most intentional poisonings occurred among women (58.3%), over two thirds of poisonings occurred among people of Indian ethnicity and was most common within the 15-29 year age group. The number of completed suicide cases due to paraquat poisoning has been increasing (Figure 5) which gives an indication about the lethality of the herbicide. Contrary to popular belief, paraquat poisoning is not only prevalent predominantly in farming communities such as western or northern divisions, it also exists in urban areas such as Suva (Figure 6). Therapeutic management of paraquat poisoning patients at Colonial War Memorial Hospital is initiated in the Accidents and Emergency Department. About 1-10 cases are commonly observed in a year (figure 7). A diagnosis of paraquat poisoning is mostly made according to clinical symptoms of the patient and also on information provided by relatives (figure 8). 29 | P a g e These methods are not very reliable as illustrated by a case report in one study (17). ‘A 27 year old woman was sent to a local hospital after ingesting 30mL of herbicide. According to her relatives, she had ingested glyphosate, and she was therefore treated with gastric lavage, atropine and fluid administration. The patient was given oxygen before it was clear that the herbicide was paraquat.’ According to figure 9 the most commonly used treatment options utilised are Fullers Earth, activated charcoal and mannitol. Analgesics and IV fluids are also given for symptomatic relief. The treatment is given according to clinical presentation and according to protocol outlined in the Emergency Drug Guidelines (figure 10). Patients are treated in the Accidents and Emergency department until the patient is in a stable condition. Once the patient is stable, they are shifted to the stress management ward where the suicide protocol is followed. According to the suicide protocol the patient is classified as either Severe Suicidal Risk (SSR), Possible Suicidal Risk (PSR) or Watch Closely (W/C). The results regarding treatment options and guidelines in this study is consistent with other studies: “The search for an antidote for paraquat poisoning is still on-going. Since there is no antidote, standard treatments are often altered according to the patients’ needs in an effort to obtain a better prognosis. It is suggested that part of the lethality of paraquat is due to the lack of effective treatment” (10,20). The treatment options do not change according to the amount of paraquat ingested (figure 11). Furthermore, results reflect that drug shortages have not been implicated in causing hindrance to treatment of paraquat poisoning patients (figure 12). A solution to paraquat poisoning could be to ban the use of paraquat. Opinions vary in this regard (figure 13). Both participants who support the statement that paraquat use should be banned, and those that oppose the statement have provided valid reasons for their answers (figure 14 & 15). 30 | P a g e 4.3. CONCLUSION The vulnerable patient groups that are commonly involved in paraquat poisoning cases are males, Indo-fijians, and young people aged 26 years and over. Thus future campaigns regarding the dangers of paraquat use could be focused mainly on these groups. The fact that paraquat poisoning does not have an antidote, coupled with the toxicity of paraquat, pose a challenge in the therapeutic management of paraquat poisoning patients. This challenge is exacerbated by the rising number of paraquat poisoning cases observed in recent years. There is a need for more reliable diagnostic tests and further research is needed to determine the possibility of banning paraquat use. 31 | P a g e 4.4. LIMITATIONS • The data only reflects the number of cases that have been reported. The study does not reflect unreported suicide cases due to paraquat ingestion. • Doctors, nurses & pharmacists who were not working in the wards/departments specified, that may have encountered paraquat poisoning cases have not been included in this study. RECOMMENDATION • There is a need for more reliable diagnostic tests and further research is needed to determine the possibility of banning paraquat use. 32 | P a g e APPENDIX ANNEX 1- REFERENCES 1. Goundar, D.S et.al. Paraquat Toxicity In Man. Fiji Medical Journal, 1984: 74-75. 2. Winchester J. Paraquat Poisoning. UpToDate.Com.[cited 21st January 2013]; Available from: http://www.fsm.ac.fj/index.php?option=com_wrapper<emid=343 3. Sweetman SC,editor. Martindale. 37th ed. London: Pharmaceutical Press: 2011. 4. Pesticide Action Network. Germany.2003. [cited 9th March 2013]; Available from: <http://www.pan-germany.org/download/fact_paraquat2.pdf> 5. Watts M .Pesticide Action Network Asia and the Pacific. Malaysia.2011 [cited 9th March 2013]; Available from: < http://wssroc.agron.ntu.edu.tw/note/Paraquat.pdf> 6. Paraquat in Fiji-What is to be Done. Fiji Medical Journal. 1984;12(5):72-3. 7. Watts M. Pesticide Action Network Asia and the Pacific, Malaysia.2012. [cited 9th March 2013]; Available from: <http://www.groundwork.org.za/Resources/FactSheets/PAN%20AP/ pesticidesfactsheet-hhpsparaquat.pdf> 8. Booth H. Gender, Power and Social Change: Youth Suicide Among Fiji Indians and Western Samoans. The Journal of the Polynesian Society. 1999;108(1):39-68. 9. WHO Suicide Prevention (SUPRE). World Health Organisation. [cited 8th April 2013]; Available from: http://www.who.int/mental_health/prevention/suicide/suicideprevent/en/ 10. Clinical Management of Acute Pesticide Intoxication: Prevention of Suicidal Behaviours. Geneva: World Health Organisation; 2008. 11. Smith, M. The Facts of Suicide.The Fiji Times. 1st October 2011. [cited 4th April 33 | P a g e 2013]; Available from: http://www.fijitimes.com/story.aspx?id=182096 12. Fiji Facts and Figures. Fiji Bureau of Statistics; 2010.[cited 8th April 2013]; Available from: http://www.statsfiji.gov.fj/releases/FFF2010.pdf 13. Henson C, Taylor A, Cohen J, Waqabaca A, Chand S. Attempted Suicide in Fiji. Suicidology Online. 2012;3:83-91. 14. Peiris-John R,Kafoa B, Wainiqolo I, Reddy RK, McCaig E, Ameratunga SN. Population-based characteristics of fatal and hospital admissions for poisoning in Fiji : TRIP Project-11. 2012 [cited 4th April 2013]; Available from: http://injuryprevention.bmj.com/content/early/2013/01/24/injuryprev-2012040651.full 15. Aghanwa HS. Attempted suicide by drug overdose and by poison-ingestion methods seen at the main general hospital in the Fiji Islands: a comparative study. General Hospital Psychiatry. 2001 ;23(5):266-71 16. Gawarammana IB, Buckley NA. Medical Management of Paraquat Ingestion. British Journal of Clinical Pharmacology. 2011;72: 745-757. 17. Zhang Q, Wu W, Lu Y, Wand J, Shang A, Yao F, Chen Y. Successful Treatment of patients with paraquat intoxication: three case reports and review of the literature. Journal of Zhejiang University. 2012;13(5):413-418. 18. Sandhu JS, Dhiman A, Mahajan R, Sandhu P. Outcome of Paraquat Poisoning-a five year study. Indian Journal of Nephrology. 2003;13:64-68. 19. Li LR, Sydenham E, Chaudhary B, You C. Glucocorticoid with cyclophosphamide for paraquat-induced lung fibrosis (Review). The Cochrane Library. 2012;(7) 34 | P a g e 20. Gunnel D, Eddleston M. Suicide by intentional ingestion of pesticides: a continuing tragedy in developing countries. International Journal of Epidemiology. 2003;32(6):902-909 21. Senarathna L, Eddleston M, Wilks MF, Woollen BH, Tomenson JA, Roberts DM, Buckley NA. Prediction of outcome after paraquat poisoning by measurement of the plasma paraquat concentration. British Medical Journal. 2009;102:251-259. 22. Eddleston M, Wilks M, Buckley N.Prospects for treatment of paraquat-induced lung fibrosis with immunosuppressive drugs and the need for better prediction of outcome: a systematic review. British Medical Journal. 2003 November; 96(11):809-824. 23. Santiago C.T. Paraquat. Toxipedia; 2010.[cited 12th June 2014]; Available from: http://www.toxipedia.org/display/toxipedia/Paraquat 35 | P a g e 2. ANNEX 2 – INFORMATION SHEET Research Topic: Therapeutic Management of Paraquat Poisoning at Colonial War Memorial Hospital Description of the research and your participation You are invited to participate in a research study conducted by Shayna Khan (Year 4 Pharmacy Student at the College of Medicine, Nursing and Health Sciences). The aim of this research is to determine the therapeutic management of paraquat poisoning patients at Colonial War Memorial Hospital. The objectives of this research are to determine how paraquat poisoning is diagnosed and to determine the treatment options available for paraquat poisoning patients at Colonial War Memorial Hospital. Your participation will involve answering a questionnaire which will contain 7 questions. These questions will explore the frequency of paraquat poisoning cases observed by you, the treatment options available and your personal opinions regarding issues such as ban of paraquat in Fiji. Risks There are no known risks associated with this research Potential Benefits There are no direct benefits associated with this research for the participant. However, through this research, you will be able to contribute your knowledge and expand the existing body of research conducted on paraquat poisoning. 36 | P a g e Protection of Confidentiality The participant details will be kept confidential. Your names will not be recorded and your responses will be coded and analysed. Thus the responses cannot be traced to any one individual. Your identity will not be revealed in any publication resulting from this study. Voluntary Participation Participation in this research is voluntary. If you wish to withdraw from participating in the research, you can do so freely at any point in time. You will not be penalized in any way should you decide not to participate or to withdraw from this study. Utilisation of Results The information obtained from these questionnaires will be analysed first and disseminated to the lecturers and students of the pharmacy department. It will also be available to the Ministry of Health. Contact Information If you have any questions or queries regarding any aspect of the research, please do not hesitate to contact me or my supervisor: Researcher: Shayna Khan Mobile: 9914580 Email: [email protected] Supervisor: Mr Arnold Ram Lecturer of Pharmacology Mobile: 9273029 Email: [email protected] 37 | P a g e 3. ANNEX 3 - CONSENT FORM Therapeutic Management of Paraquat Poisoning Patients Reporting to Colonial War Memorial Hospital This document is to certify that I _____________________(name of participant) have read the participant information and have been given the opportunity to ask questions. All of my questions have been answered to my satisfaction. I understand that all data will remain confidential with regard to my identity. I understand that my participation in this research project is voluntary and that I am free to withdraw my consent and discontinue participation at any time. I freely give my consent to participate in this study. _________________ Participant’s Signature _______________ Date I, the undersigned, have fully explained the research to the above subject. Researchers Name: Shayna Khan ________________ Signature ________________ Date 38 | P a g e 4. ANNEX 4 - DATA COLLECTION TOOLS Questionnaire Therapeutic Management of Paraquat Poisoning Patients at Colonial War Memorial Hospital Designation: Doctor Nurse Pharmacist Years of experience at the Colonial War Memorial Hospital _______________ 1. On average, in a year how many paraquat poisoning cases do you observe? None 1-10 11-20 21-30 31-40 41-50 >50 2. Based on your experience, how are paraquat poisoning patients diagnosed? Based on clinical symptoms Urine test Based on information provided by relatives plasma concentration test other biochemical tests 3. The following are some drug treatment options for paraquat poisoning. Please place a tick beside the options utilised at CWM Hospital for paraquat poisoning: Fullers Earth Activated Charcoal Mannitol Haemoperfusion/Haemodialysis N-acetyl cysteine Methyl-prednisolone Cyclophosphamide Vitamins C and E 4. What guidelines do you use to determine treatment options for paraquat poisoning patients? ___________________________________________________________________________ ___________________________________________________________________________ ___________________________________________________________________________ _______________________________________ 39 | P a g e 5. Do treatment options change according to the amount of paraquat ingested ? No Please Yes explain. __________________________________________________________________________________ __________________________________________________________________________________ __________________________________________________________________________________ __________________________________________ 6. In your experience, has treatment of paraquat poisoning ever been hindered due to drug shortages? Yes No If yes, then which drugs are commonly short of supply? ___________________________________________________________________________ ___________________________________________________________________________ ___________________________________________________________________________ _______________________________________ 7. “Paraquat use as an herbicide should be banned in Fiji”. Do you support this statement? Yes No Please state your reasons for agreeing or disagreeing with the statement. __________________________________________________________________________________ __________________________________________________________________________________ __________________________________________________________________________________ __________________________________________ Thank You for Your Participation 40 | P a g e 5. ANNEX 5 – APPROVAL LETTERS. 41 | P a g e 42 | P a g e Powered by TCPDF (www.tcpdf.org)