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煙草制品管制科學(xué)基礎(chǔ)報(bào)告:WHO研究組第八份報(bào)告 讀者對象:吸煙與健康、煙草化學(xué)和公共衛(wèi)生學(xué)諸多應(yīng)用領(lǐng)域科學(xué)家
本報(bào)告介紹了WHO煙草制品管制研究小組第十次會議的結(jié)論和建議。該次會議討論了新型煙草制品,如電子煙堿傳輸系統(tǒng)(ENDS)、電子非煙堿傳輸系統(tǒng)(ENNDS)和加熱型煙草制品(HTP)管制科學(xué)基礎(chǔ)方面的優(yōu)先事項(xiàng)。研究小組審查了專門為會議編寫的九份背景文件和兩份補(bǔ)充文件,涉及以下專題:①HTP中的有害物質(zhì)及其暴露、健康影響和風(fēng)險(xiǎn)降低聲明;②HTP的吸引力和致癮性:對認(rèn)知和使用的影響及關(guān)聯(lián)效應(yīng);③HTP之間的差異:考慮因素和影響;④HTP的使用:產(chǎn)品轉(zhuǎn)換以及雙重或多重使用;⑤HTP、ENDS和ENNDS相關(guān)法規(guī)以及國家措施和監(jiān)管障礙;⑥電子煙堿傳輸系統(tǒng)和傳統(tǒng)卷煙的煙堿暴露評估;⑦ENDS、ENNDS和HTP相關(guān)個(gè)體風(fēng)險(xiǎn)的量化方法探索:對人體健康和監(jiān)管的影響;⑧新型煙草制品的風(fēng)味;⑨新型煙草制品的全球營銷和推廣及其影響;⑩煙草中的煙堿形態(tài)、化學(xué)修飾及其對電子煙堿傳輸系統(tǒng)的影響;電子煙堿傳輸系統(tǒng)或霧化產(chǎn)品使用相關(guān)肺損傷。研究組關(guān)于每個(gè)主題的建議在相關(guān)章節(jié)末尾列出,最后一章為總體建議。
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1986年畢業(yè)于南京化工學(xué)院(現(xiàn)南京工業(yè)大學(xué))獲學(xué)士學(xué)位,1991年獲碩士學(xué)位,2006年畢業(yè)于中國科學(xué)院合肥物質(zhì)科學(xué)研究院,獲博士學(xué)位。1995年—2001年,中國煙草標(biāo)準(zhǔn)化研究中心副主任。
2001年—2011年,國家煙草質(zhì)量監(jiān)督檢驗(yàn)中心常務(wù)副主任。
2011年至今,鄭州煙草研究院黨組成員、質(zhì)檢中心主任。國家煙草質(zhì)量監(jiān)督檢驗(yàn)中心主任、世界衛(wèi)生組織(煙草控制框架公約)第 9、10條工作組中國政府代表。兼任國家實(shí)驗(yàn)室認(rèn)可委員會主任評審員,全國煙草標(biāo)準(zhǔn)化技術(shù)委員會委員,全國煙草標(biāo)準(zhǔn)化卷煙分技委委員,國家認(rèn)可委食品技術(shù)委員會副主任等職。
目錄
譯者序 i WHO煙草制品管制研究小組第十次會議 iii 致謝 xi 縮略語 xv 1.引言 1 參考文獻(xiàn) 3 2.加熱型煙草制品中的有害物質(zhì)及其暴露、健康影響和風(fēng)險(xiǎn)降低聲明 5 摘要 5 2.1 背景 5 2.2 加熱型煙草制品釋放物中的有害物質(zhì) 7 2.2.1 測量有害物質(zhì)的實(shí)驗(yàn)室方法 7 2.2.2 煙堿 8 2.2.3 其他有害物質(zhì) 9 2.3 加熱型煙草制品的體外暴露和實(shí)驗(yàn)動(dòng)物暴露及影響 15 2.3.1 體外研究 15 2.3.2 實(shí)驗(yàn)動(dòng)物研究 17 2.4 加熱型煙草制品中有害物質(zhì)的人體暴露及健康影響 18 2.4.1 產(chǎn)品用途和使用模式 18 2.4.2 暴露和效應(yīng)生物標(biāo)志物 19 2.4.3 被動(dòng)暴露 22 2.4.4 健康影響 23 2.5 加熱型煙草制品風(fēng)險(xiǎn)或危害降低的證據(jù)審查 25 2.5.1 煙草制品危害降低 25 2.5.2 風(fēng)險(xiǎn)降低聲明 25 2.6 小結(jié)和公共衛(wèi)生影響 28 2.6.1 數(shù)據(jù)摘要 28 2.6.2 公共衛(wèi)生影響 29 2.7 研究差距和優(yōu)先事項(xiàng) 30 2.8 政策建議 31 2.9 參考文獻(xiàn) 31 3.加熱型煙草制品的吸引力和致癮性:對認(rèn)知和使用的影響及關(guān)聯(lián)效應(yīng) 40 摘要 40 3.1 背景 41 3.2 HTP的吸引力 42 3.2.1 WHO FCTC第9條和第10條中吸引力的定義 42 3.2.2 HTP的吸引力特性 42 3.2.3 了解ENDS和ENNDS并應(yīng)用到HTP 45 3.3 HTP的致癮性 46 3.3.1 致癮性 46 3.3.2 了解ENDS和ENNDS并應(yīng)用到HTP 49 3.3.3 HTP的總體濫用傾向 49 3.4 ENDS、ENNDS和HTP的吸引力和致癮性對風(fēng)險(xiǎn)、危害和使用認(rèn)知的影響 50 3.4.1 吸引力和致癮性對開始、轉(zhuǎn)換、補(bǔ)償和戒除傳統(tǒng)卷煙的貢獻(xiàn) 50 3.4.2 了解ENDS和ENNDS并應(yīng)用到HTP 51 3.5 討論 52 3.5.1 不同群體不同使用方式的行為影響 52 3.5.2 公共衛(wèi)生影響 53 3.5.3 研究差距、優(yōu)先事項(xiàng)和問題 53 3.5.4 政策建議 54 3.6 結(jié)論 54 3.7 參考文獻(xiàn) 55 附錄 IQOS、卷煙和JUUL產(chǎn)品中的薄荷醇濃度 62 4.加熱型煙草制品之間的差異:考慮因素及影響 63 摘要 63 4.1 背景 63 4.1.1 概述 63 4.1.2 締約方大會FCTC/COP8(22)號決議 64 4.1.3 范圍與目標(biāo) 64 4.2 市場上產(chǎn)品的差異 64 4.2.1 產(chǎn)品類別和類型的概述 64 4.2.2 加熱型煙草制品之間的差異 66 4.2.3 產(chǎn)品類型和類別的市場分布 66 4.3 產(chǎn)品特征和設(shè)計(jì)特點(diǎn) 67 4.3.1 產(chǎn)品的溫度分布情況和操作性能 67 4.3.2 電池性能 68 4.3.3 煙草插片、煙棒和膠囊的特性 68 4.4 產(chǎn)品的成分、釋放物及總體設(shè)計(jì) 69 4.4.1 成分和釋放物 69 4.4.2 煙堿遞送 70 4.4.3 風(fēng)險(xiǎn)概況 71 4.4.4 加熱型煙草制品成分的監(jiān)管意義 72 4.4.5 釋放物的監(jiān)管意義 73 4.5 產(chǎn)品、制造商和銷售點(diǎn)的差異 73 4.5.1 制造商和銷售點(diǎn) 73 4.5.2 對客戶吸引力的影響 74 4.6 討論 75 4.7 結(jié)論 75 4.8 研究差距、優(yōu)先事項(xiàng)和問題 76 4.9 政策建議 77 4.10 參考文獻(xiàn) 77 5.加熱型煙草制品的使用:產(chǎn)品轉(zhuǎn)換以及雙重或多重使用 82 摘要 82 5.1 概述 82 5.2 關(guān)于HTP在人群層面使用的信息 83 5.3 從傳統(tǒng)卷煙轉(zhuǎn)向HTP的動(dòng)態(tài)情況:雙重或多重產(chǎn)品聯(lián)用是過渡態(tài)還是永久態(tài)? 85 5.4 HTP作為傳統(tǒng)卷煙替代品的潛在作用 87 5.5 雙重/多重使用者的煙堿暴露及潛在健康風(fēng)險(xiǎn) 88 5.6 動(dòng)物藥代動(dòng)力學(xué) 91 5.7 人體藥代動(dòng)力學(xué) 91 5.8 使用HTP和傳統(tǒng)卷煙的主觀效應(yīng) 95 5.9 討論和影響 96 5.10 研究差距 97 5.11 政策建議 97 5.11.1 戒煙政策 97 5.11.2 監(jiān)督政策 97 5.11.3 研究政策 97 5.11.4 合作政策 98 5.12 參考文獻(xiàn) 98 6.加熱型煙草制品和電子煙堿/非煙堿傳輸系統(tǒng)相關(guān)法規(guī)以及國家措施和監(jiān)管障礙 106 摘要 106 6.1 背景 106 6.1.1 締約方大會的介紹和要求(FCTC/COP8(22)) 106 6.1.2 范圍和目標(biāo) 108 6.1.3 來源 108 6.2 新型煙草制品的監(jiān)管情況 108 6.2.1 HTP的可用性 108 6.2.2 產(chǎn)品分類 109 6.2.3 減少煙草需求的監(jiān)管框架和措施 113 6.3 監(jiān)管、實(shí)施和執(zhí)行政策的考慮事項(xiàng)和障礙 118 6.3.1 實(shí)施政策時(shí)的監(jiān)管考慮 118 6.3.2 實(shí)施和執(zhí)行政策的障礙 119 6.3.3 其他考慮和意外后果 119 6.4 討論 120 6.5 結(jié)論 121 6.6 研究差距 121 6.7 政策建議 121 6.8 參考文獻(xiàn) 122 7.電子煙堿傳輸系統(tǒng)和傳統(tǒng)卷煙的煙堿暴露評估 127 摘要 127 7.1 背景 128 7.2 電子煙堿傳輸系統(tǒng)的煙堿暴露 129 7.2.1 電子煙堿傳輸系統(tǒng)的煙堿釋放 129 7.2.2 電子煙堿傳輸系統(tǒng)電功率對煙堿釋放的影響 129 7.2.3 電子煙堿傳輸系統(tǒng)煙油中煙堿和其他化合物濃度對煙堿釋放的貢獻(xiàn) 130 7.3 伴生物質(zhì)的暴露概述 131 7.4 電子煙堿傳輸系統(tǒng)的煙堿遞送 131 7.5 與使用有關(guān)的暴露行為模式 132 7.5.1 使用者群體和使用者模式的定義 132 7.5.2 影響行為模式的因素 133 7.6 被動(dòng)暴露于煙堿和其他有害成分 135 7.7 煙堿通量 135 7.8 討論 137 7.9 結(jié)論 138 7.10 研究差距、優(yōu)先事項(xiàng)和問題 138 7.11 政策建議 139 7.12 參考文獻(xiàn) 139 8.電子煙堿/非煙堿傳輸系統(tǒng)和加熱型煙草制品相關(guān)個(gè)體風(fēng)險(xiǎn)的量化方法探索:對人體健康和監(jiān)管的影響 148 摘要 148 8.1 背景 148 8.1.1 量化風(fēng)險(xiǎn)的挑戰(zhàn) 150 8.2 使用ENDS和ENNDS相關(guān)的風(fēng)險(xiǎn)評估與量化 151 8.2.1 與特定成分或無意添加的物質(zhì)相關(guān)的健康風(fēng)險(xiǎn) 152 8.2.2 ENDS和ENNDS的潛在健康影響 154 8.2.3 非使用者的風(fēng)險(xiǎn) 156 8.3 量化風(fēng)險(xiǎn)的方法 156 8.3.1 毒理學(xué)關(guān)注的閾值 158 8.3.2 基于單個(gè)化合物的風(fēng)險(xiǎn)評估 158 8.3.3 相對風(fēng)險(xiǎn)方法 159 8.3.4 暴露邊界值法 159 8.3.5 非致癌作用 159 8.3.6 評估框架 160 8.4 加熱型煙草制品 162 8.5 對監(jiān)管的影響 162 8.6 討論 164 8.7 建議 165 8.8 結(jié)論 166 8.9 參考文獻(xiàn) 166 9.新型煙草制品的風(fēng)味 175 摘要 175 9.1 背景和引言 175 9.2 風(fēng)味電子煙的流行病學(xué)(使用頻率、模式和原因,按社會人口統(tǒng)計(jì)變量) 177 9.2.1 電子煙堿/非煙堿傳輸系統(tǒng) 178 9.2.2 傳統(tǒng)卷煙和無煙煙草制品 179 9.2.3 加熱型煙草制品 180 9.3 調(diào)味物質(zhì)對吸引力、嘗試使用、使用和持續(xù)使用的影響 180 9.3.1 青少年和年輕人 180 9.3.2 成年人 182 9.4 常見調(diào)味物質(zhì)特性、健康效應(yīng)及其對公眾健康的影響 183 9.4.1 電子煙和煙草制品中常見的調(diào)味物質(zhì) 183 9.4.2 風(fēng)味電子煙中常見調(diào)味物質(zhì)的化學(xué)和物理性質(zhì) 183 9.4.3 調(diào)味物質(zhì)的毒性 184 9.5 風(fēng)味產(chǎn)品的監(jiān)管 185 9.5.1 全球風(fēng)味電子煙監(jiān)管 185 9.5.2 全球風(fēng)味煙草制品監(jiān)管 186 9.5.3 常用方法的優(yōu)缺點(diǎn) 188 9.5.4 對煙堿產(chǎn)品特定風(fēng)味監(jiān)管產(chǎn)生的影響 188 9.5.5 調(diào)味物質(zhì)的未來監(jiān)管 189 9.6 討論 191 9.7 研究差距、優(yōu)先事項(xiàng)和問題 191 9.8 政策建議 192 9.9 參考文獻(xiàn) 192 10.新型煙草制品的全球營銷和推廣及其影響 206 摘要 206 10.1 背景 206 10.2 電子煙堿傳輸系統(tǒng)和電子非煙堿傳輸系統(tǒng) 208 10.2.1 引言 208 10.2.2 電子煙市場、產(chǎn)品和營銷策略 209 10.2.3 電子煙的全球使用情況和使用流行程度 212 10.2.4 電子煙的廣告、促銷和贊助趨勢 216 10.2.5 控制電子煙的廣告、促銷和贊助的措施 217 10.2.6 建議 218 10.2.7 電子煙的研究差距 220 10.3 加熱型煙草制品 221 10.3.1 引言 221 10.3.2 市場參與者、產(chǎn)品和策略 221 10.3.3 加熱型煙草制品的全球使用和流行情況 224 10.3.4 加熱型煙草制品的廣告、促銷和贊助趨勢 225 10.3.5 加熱型煙草制品廣告、促銷和贊助的控制措施 227 10.3.6 對監(jiān)測加熱型煙草制品的廣告、促銷和贊助趨勢的建議 227 10.3.7 對監(jiān)管機(jī)構(gòu)的建議 228 10.3.8 加熱型煙草制品研究的研究差距 229 10.4 總結(jié) 229 10.5 參考文獻(xiàn) 230 11.煙草中的煙堿形態(tài)、化學(xué)修飾及其對電子煙堿傳輸系統(tǒng)的影響 241 摘要 241 11.1 背景 241 11.2 煙堿的化學(xué)修飾及其對煙堿傳輸?shù)挠绊?243 11.2.1 烘烤對煙堿的影響 243 11.2.2 堿改性 244 11.2.3 酸改性 244 11.3 對電子煙堿傳輸系統(tǒng)產(chǎn)品和多樣性的影響 245 11.3.1 電子煙堿傳輸系統(tǒng)中游離態(tài)煙堿與煙堿鹽 245 11.3.2 有效濃度和濫用傾向 246 11.3.3 對產(chǎn)品刺激性可能的掩飾 247 11.3.4 健康影響和監(jiān)管考慮 247 11.4 討論 248 11.5 研究差距、優(yōu)先事項(xiàng)和問題 248 11.6 建議 249 11.7 考慮因素 249 11.8 參考文獻(xiàn) 249 12.電子煙堿傳輸系統(tǒng)或霧化產(chǎn)品使用相關(guān)肺損傷 258 摘要 258 12.1 背景 258 12.1.1 與電子煙和霧化產(chǎn)品相關(guān)的呼吸影響 258 12.1.2 電子煙堿傳輸系統(tǒng)或霧化產(chǎn)品使用相關(guān)肺損傷(EVALI) 259 12.1.3 與EVALI有關(guān)的產(chǎn)品和化學(xué)制品 259 12.2 EVALI 260 12.2.1 詳細(xì)說明和歷史記錄 260 12.2.2 癥狀 260 12.2.3 臨床表現(xiàn) 261 12.2.4 報(bào)告病例 261 12.3 EVALI的識別 261 12.4 對EVALI的監(jiān)測 262 12.4.1 國家監(jiān)測機(jī)制 262 12.4.2 地區(qū)監(jiān)測機(jī)制 262 12.4.3 國際監(jiān)測機(jī)制和驗(yàn)證 262 12.5 討論 262 12.6 考慮事項(xiàng) 263 12.7 建議 263 12.7.1 主要建議 263 12.7.2 其他建議 264 12.8 參考文獻(xiàn) 264 13.總體建議 266 13.1 主要建議 267 13.2 對公共衛(wèi)生政策的意義 268 13.3 對WHO規(guī)劃的影響 269 13.4 參考文獻(xiàn) 269 Contents Participants in the 10th meeting of the WHO study group on tobacco product regulation vii Acknowledgements xiii Abbreviations and acronyms xvii 1.Introduction 273 References 277 2.Toxicants in heated tobacco products, exposure, health effects and claims of reduced risk 278 Abstract 278 2.1 Background 279 2.2 Toxicants in heated tobacco product emissions 281 2.2.1 Laboratory methods for measuring toxicants 281 2.2.2 Nicotine 282 2.2.3 Other toxicants 284 2.3 Exposure and effects of HTPs in vitro and in laboratory animals 291 2.3.1 In-vitro studies 291 2.3.2 Studies in laboratory animals 293 2.4 Exposure of humans to toxicants in HTPs and implications for health 295 2.4.1 Product use and topography 295 2.4.2 Biomarkers of exposure and effect 296 2.4.3 Passive exposure 300 2.4.4 Impact on health outcomes 302 2.5 Review of the evidence for reduced risk or harm with use of HTPs 304 2.5.1 Harm reduction in the context of tobacco products 304 2.5.2 Claims of reduced risk 304 2.6 Summary and implications for public health 308 2.6.1 Summary of data 308 2.6.2 Implications for public health 310 2.7 Research gaps and priorities 311 2.8 Policy recommendations 312 2.9 References 312 3.The attractiveness and addictive potential of heated tobacco products: effects on perception and use and associated effects 320 Abstract 320 3.1 Background 321 3.2 Attractiveness of HTPs 323 3.2.1 Definition of attractiveness in the context of Articles 9 and 10 of the WHO FCTC 323 3.2.2 Attractive features of HTPs 323 3.2.3 What we can learn from studies on ENDS and ENNDS and relevance to HTPs 327 3.3 Addictiveness of HTPs 328 3.3.1 Addictiveness 328 3.3.2 What we can learn from ENDS and ENNDS and relevance to HTPs 332 3.3.3 Overall abuse liability of HTPs 332 3.4 Effects of the attractiveness and addictiveness of ENDS, ENNDS and HTPs on perceptions of risk and harm and use 333 3.4.1 Contributions of attractiveness and addictiveness to initiation, switching, complementing and quitting conventional tobacco products 333 3.4.2 Learning from ENDS and ENNDS and application to HTPs 334 3.5 Discussion 335 3.5.1 Behavioural implications of different patterns of use in different groups 335 3.5.2 Implications for public health 336 3.5.3 Research gaps, priorities and questions 337 3.5.4 Policy recommendations 338 3.6 Conclusions 339 3.7 References 339 Annex 3.1.Menthol concentrations in IQOS, cigarettes and JUUL products 345 4.Variations among heated tobacco products: considerations and implications 346 Abstract 346 4.1 Background 347 4.1.1 Overview 347 4.1.2 Decision FCTC/COP8(22) of the Conference of the Parties 347 4.1.3 Scope and objectives 347 4.2 Variations among products on the market 348 4.2.1 Overview of product categories and types 348 4.2.2 Variations among heated tobacco products 350 4.2.3 Market distribution of product types and categories 350 4.3 Characteristics and design features of products 352 4.3.1 Temperature profiles of products and operational capabilities 352 4.3.2 Battery characteristics 352 4.3.3 Properties of tobacco inserts, sticks and capsules 352 4.4 Content, emissions and general design of products 353 4.4.1 Content and emissions 353 4.4.2 Nicotine delivery 356 4.4.3 Risk profiles 356 4.4.4 Regulatory implications of the contents of heated tobacco products 357 4.4.5 Regulatory implications of emissions 358 4.5 Variations among products, manufacturers and selling points 359 4.5.1 Manufacturers and selling points 359 4.5.2 Implications for customer pulling power 360 4.6 Discussion 361 4.7 Conclusions 362 4.8 Research gaps, priorities and questions 363 4.9 Policy recommendations 363 4.10 References 365 5.Use of heated tobacco products: product switching and dual or poly product use 369 Abstract 369 5.1 Introduction 370 5.2 Information on HTP use at population level 370 5.3 Dynamics of switching from conventional cigarettes to HTPs: Is dual or poly use a transitional or permanent state? 373 5.4 Potential role of HTPs as a substitute for conventional cigarettes 376 5.5 Exposure to nicotine and potential health risks among poly users 377 5.6 Pharmacokinetics in animals 380 5.7 Pharmacokinetics in people 380 5.8 Subjective effects of use of HTPs and conventional cigarettes 385 5.9 Discussion and implications 386 5.10 Research gaps 387 5.11 Policy recommendations 387 5.11.1 Cessation policy 387 5.11.2 Surveillance policy 387 5.11.3 Research policy 388 5.11.4 Cooperation and partnership policy 388 5.12 References 388 6.Regulations on heated tobacco products, electronic nicotine delivery systems and electronic non-nicotine delivery systems, with country approaches, barriers to regulation and regulatory considerations 395 Abstract 395 6.1 Background 396 6.1.1 Introduction and the request of the Conference of the Parties (FCTC/COP8(22)) 396 6.1.2 Scope and objectives 397 6.1.3 Sources 398 6.2 Regulatory mapping of novel and emerging nicotine and tobacco products 398 6.2.1 Availability of HTPs 398 6.2.2 Product classification 399 6.2.3 Regulatory frameworks and measures to reduce tobacco demand 404 6.3 Considerations and barriers to regulation, implementation and enforcement of policies 411 6.3.1 Regulatory considerations in implementing policies 411 6.3.2 Barriers to implementing and enforcing policies 413 6.3.3 Other considerations and unintended consequences 413 6.4 Discussion 414 6.5 Conclusions 415 6.6 Research gaps 416 6.7 Policy recommendations 416 6.8 References 417 7.Estimation of exposure to nicotine from use of electronic nicotine delivery systems and from conventional cigarettes 421 Abstract 421 7.1 Background 422 7.2 Exposure to nicotine from ENDS 424 7.2.1 ENDS nicotine emission 424 7.2.2 Influence of ENDS electrical power on nicotine emission 424 7.2.3 Contribution of the concentrations of nicotine and other compounds in ENDS liquids to nicotine emissions 425 7.3 Overview of exposure to accompanying substances 426 7.4 Nicotine delivery from ENDS 427 7.5 Behavioural patterns of exposure according to use 428 7.5.1 Definition of user groups and user patterns 428 7.5.2 Factors that influence behavioural patterns 428 7.6 Passive exposure to nicotine and other toxicants 430 7.7 Nicotine flux 431 7.8 Discussion 433 7.9 Conclusions 434 7.10 Research gaps, priorities and questions 435 7.11 Policy recommendations 436 7.12 References 436 8.Exploration of methods for quantifying individual risks associated with electronic nicotine and non-nicotine delivery systems and heated tobacco products: impact on population health and implications for regulation 444 Abstract 444 8.1 Background 445 8.1.1 Challenges to quantifying risk 447 8.2 Risk assessment and quantification of risks associated with use of ENDS and ENNDS 449 8.2.1 Health risks associated with specific ingredients or unintentionally added substances 450 8.2.2 Potential health effects of ENDS and ENNDS 453 8.2.3 Risks for bystanders 455 8.3 Methods for quantifying risk 455 8.3.1 Threshold of toxicological concern 458 8.3.2 Risk assessment based on individual compounds 458 8.3.3 Relative risk approaches 459 8.3.4 Margin-of-exposure approach 459 8.3.5 Non-carcinogenic effects 460 8.3.6 Evaluation frameworks 460 8.4 Heated tobacco products 463 8.5 Implications for regulation 463 8.6 Discussion 466 8.7 Recommendations 467 8.8 Conclusions 468 8.9 References 469 9.Flavours in novel and emerging nicotine and tobacco products 476 Abstract 476 9.1 Background and introduction 477 9.2 Epidemiology of flavoured products (frequency, patterns and reasons for use by sociodemographic variables) 479 9.2.1 Electronic nicotine and non-nicotine delivery systems 480 9.2.2 Traditional smoked and smokeless tobacco products 481 9.2.3 Heated tobacco products 482 9.3 Effects of flavours on appeal, experimentation, uptake and sustained use 483 9.3.1 Adolescents and young adults 483 9.3.2 Adults 484 9.4 Common flavours, properties, health effects and implications for public health 486 9.4.1 Common flavours in electronic nicotine delivery systems and tobacco products 486 9.4.2 Chemical and physical properties of common flavours in flavoured products 486 9.4.3 Toxicity of flavours 487 9.5 Regulation of flavoured products 488 9.5.1 Global regulation of flavoured ENDS 488 9.5.2 Global regulation of flavoured tobacco products 490 9.5.3 Pros and cons of common approaches 492 9.5.4 Impact of regulation of specific flavoured nicotine products 492 9.5.5 Future regulation of flavours 493 9.6 Discussion 495 9.7 Research gaps, priorities and questions 496 9.8 Policy recommendations 497 9.9 References 497 10.Global marketing and promotion of novel and emerging nicotine and tobacco products and their impacts 509 Abstract 509 10.1 Background 510 10.2 Electronic nicotine delivery systems and electronic non-nicotine delivery systems 512 10.2.1 Introduction 512 10.2.2 Markets, products and strategies used in marketing ENDS and ENNDS 513 10.2.3 Global use of ENDS and prevalence of use 518 10.2.4 Trends in advertising, promotion and sponsorship of ENDS products 521 10.2.5 Measures to control advertising, promotion and sponsorship of ENDS products 523 10.2.6 Recommendations 524 10.2.7 Research gaps for ENDS and ENNDS 527 10.3 Heated tobacco products 528 10.3.1 Introduction 528 10.3.2 Market players, products and strategies 529 10.3.3 Global use and prevalence of use of HTPs 532 10.3.4 Trends in advertising, promotion and sponsorship of HTPs 533 10.3.5 Measures to control advertising, promotion and sponsorship of HTPs 535 10.3.6 Recommendations for monitoring trends in marketing, advertising, promoting and sponsorship of HTPs 536 10.3.7 Recommendations for regulators 536 10.3.8 Gaps in research on HTPs 538 10.4 Summary 538 10.5 References 539 Supplementary sections 548 11.Forms of nicotine in tobacco plants, chemical modifications and implications for electronic nicotine delivery systems products 549 Abstract 549 11.1 Background 550 11.2 Chemical modification of nicotine and influence on nicotine delivery 553 11.2.1 Brief summary of the effect of curing on nicotine 553 11.2.2 Modification with alkali 553 11.2.3 Modification with acid 554 11.3 Implications for ENDS products and diversity 554 11.3.1 Free-base nicotine vs nicotine salt in ENDS 554 11.3.2 Feasible concentrations and abuse liability 556 11.3.3 Potential masking of the harshness of products 557 11.3.4 Health implications and potential regulations 557 11.4 Discussion 558 11.5 Research gaps, priorities and questions to members regarding further work or a full paper 558 11.6 Recommendation 559 11.7 Considerations 559 11.8 References 560 12.EVALI: e-cigarette or vaping product use-associated lung injury 567 Abstract 567 12.1 Background 568 12.1.1 Respiratory effects associated with e-cigarettes and vaping 568 12.1.2 E-cigarette or vaping product use-associated lung injury (EVALI) 568 12.1.3 Products and chemicals implicated in EVALI 569 12.2 EVALI 569 12.2.1 Detailed description and history 569 12.2.2 Symptoms 570 12.2.3 Clinical presentation 570 12.2.4 Reported cases 571 12.3 Identification of EVALI 571 12.4 Surveillance for EVALI 571 12.4.1 National surveillance mechanisms 571 12.4.2 Regional surveillance mechanisms 572 12.4.3 International surveillance mechanisms and validation 572 12.5 Discussion 572 12.6 Considerations 573 12.7 Recommendations 574 12.7.1 Key recommendations 574 12.7.2 Other recommendations 574 12.8 References 574 13.Overall recommendations 576 13.1 Main recommendations 577 13.2 Significance for public health policies 579 13.3 Implications for the Organization’s programmes 580 13.4 References 581
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