Preuss Charles V., Kalava Arun, King Kevin C.
University of South Florida
Muhlenberg Community Hospital Greenville
One of the most difficult challenges for any prescriber is distinguishing between the legitimate prescription of controlled substances and the prescription that may be used for illegitimate purposes. To discern the difference, prescribers need to understand the signs, symptoms, and treatment of acute and chronic pain and the signs and symptoms of patients misusing controlled substances. Pain relief remains one of the most common reasons patients seek medical attention. Although many categories of pain medications are available, opioid analgesics are approved by the Food and Drug Administration (FDA) for moderate-to-severe pain. As such, they are a common choice for patients with acute, cancer-related, neurologic, and end-of-life pain. Prescribing opioid analgesics for chronic pain is controversial and fraught with inconclusive standards. In the 1990s, the chronic failure of health professionals to treat severe pain appropriately led to an expansion in opioid analgesic prescribing. Unfortunately, this resulted in increased overuse, diversion of drugs, opioid use disorder, and overdose.The Catch-22 is that health professionals either undertreat patients, leading to unnecessary suffering, or overtreat them, which can cause adverse effects such as increased risk of opioid analgesic use disorder and potential overdose. Opioid analgesic prescribing reached its highest point in 2011. Since then, both prescribing and overdose have been declining. However, as a society, in both the lay and scientific literature, there are significant concerns that we are still in the middle of an opioid crisis. One of the biggest challenges in caring for patients with pain is their varying tolerance levels, which necessitate different opioid doses to achieve adequate pain relief. Patients may exhibit a wide range of behavioral, cultural, emotional, and psychological responses to pain compared to those with a substance use disorder; often, distinguishing between the two can be challenging. All healthcare professionals engaged in pain control need an understanding of the treatment recommendations and safety concerns in prescribing opioid analgesics. Appropriate opioid prescribing requires a thorough patient assessment, short- and long-term treatment planning, close follow-up, and continued monitoring. All healthcare providers need to be aware of appropriate patient assessment, treatment planning, and the potential for substance use disorder, drug diversion, and hazardous behavioral responses to controlled substances, such as opioid analgesics, which differ from pseudoaddiction and physical dependence. Many clinicians have limited knowledge of opioid use disorder. They often fail to recognize it as a disease and mistakenly believe that opioid dependence is the same as opioid use disorder. A lack of clear understanding can lead to confusion between patients with chronic non-use disorder and those misusing their prescribed opioids. A lack of training and educational deficits often interfere with the appropriate prescription of opioid analgesic agents. To prevent the misuse of controlled substances, healthcare providers who prescribe controlled substances should learn prescribing practices that minimize or prevent adverse consequences. Addiction: According to the American Society of Addiction Medicine (ASAM), addiction is a primary, chronic disease of brain reward, motivation, memory, and related circuitry. Dysfunction in these circuits leads to characteristic biological, psychological, social, and spiritual manifestations. This dysfunction is reflected in an individual pathologically pursuing reward or relief through substance use and other behaviors. Addiction is now termed substance use disorder and is characterized by an inability to consistently abstain, cravings for the drug, impairment in behavioral control, diminished ability to recognize significant problems with one's behaviors and interpersonal relationships, and a dysfunctional emotional response. Like other chronic diseases, substance use disorder often involves cycles of relapse and remission. Without treatment or engagement in recovery activities, substance use disorder is progressive and can result in disability or premature death. : Appropriate opioid analgesic prescribing: This involves providing pain control while minimizing toxicity, substance use disorder, or the risk of substance use disorder and implementing safeguards to reduce drug diversion. Inappropriate opioid analgesic prescribing: Non-prescribing, inadequate prescribing, excessive prescribing, or continued prescribing despite evidence of the lack of effective opioid analgesic treatment. Controlled substances: These substances are drugs or medications that possess the potential for being misused and are considered to be substances that have a substantially high risk of resulting in substance use disorder. Opioid analgesics: These drugs dull the senses and relieve pain, such as morphine. In addition, these medications may induce sleep. The Drug Enforcement Administration (DEA, USA) uses the term to refer to drugs that are opioid analgesics. Craving for drugs or rewards. Diminished recognition of significant problems in behavior. Dysfunctional emotional response. Impairment in behavioral control. Inability to consistently abstain . All healthcare providers should be familiar with the guidelines and laws for each schedule, which are based on the purpose of the drug and the risk of substance use disorder. In the United States, controlled substances are subject to strict regulation by both federal and state laws that govern their manufacture and distribution. Controlled substances have a high risk of resulting in addiction and substance use disorder. As the schedules decrease from I to V, the drugs listed within each category have a lower potential to cause a substance use or addiction disorder. In the United States, the Comprehensive Drug Abuse Prevention and Control Act was passed in 1970 and included the Controlled Substances Act. The Controlled Substances Act covers various aspects of drugs as follows: Classification and regulation of drugs, according to their content and purpose. Manufacturing of drugs. Distribution of drugs. Exportation and sale of drugs. The Controlled Substances Act established 5 drug schedules to regulate the manufacture and distribution of controlled substances. As part of the regulation, healthcare providers who prescribe controlled substances and pharmacists who fill these prescriptions must obtain a license from the DEA. These licenses include specific license numbers allowing controlled substance prescriptions to be tracked and linked to a specific healthcare provider or distributor. These schedules categorize substances based on their medical value, risk of addiction, and potential to cause harm. The schedules range from Schedule I, which has the highest potential for addiction and substance use disorder, to Schedule V, which has the lowest potential for addiction and substance use disorder. Schedule I drugs possess the highest potential for substance use disorder and misuse. These drugs have no medical use and are illicit or street drugs. Examples of Schedule I drugs include heroin, lysergic acid diethylamide, mescaline, methylenedioxymethamphetamine, and methaqualone. Marijuana, which is legal in some states, is still classified as a Schedule I drug at the federal level as of this writing. Schedule II drugs have a reduced potential for substance use disorder compared to Schedule I. These drugs are at high risk for both physical and psychological dependence. These drugs have a high capacity for both substance use disorder and misuse. Schedule II drugs are typically prescribed to treat severe pain, anxiety, insomnia, and attention-deficit hyperactivity disorder. Examples of Schedule II substances include fentanyl, hydromorphone, meperidine, methadone, morphine, oxycodone, dextroamphetamine, methylphenidate, methamphetamine, pentobarbital, and secobarbital. These drugs were previously prescribed only through a paper prescription, but they are now permitted to be transmitted electronically through Electronic Prescriptions for Controlled Substances (EPCS). No refills are allowed. . Schedule II drugs have the tightest regulations compared to other prescription drugs. Schedule III drugs have a lower misuse potential compared to Schedule I and II drugs. These drugs may cause physical dependence but more commonly lead to psychological dependence. Medications in this category are often used for pain control, anesthesia, or appetite suppression. Examples of Schedule III substances include benzphetamine, ketamine, phendimetrazine, and anabolic steroids. Opioid analgesics in this schedule include products containing not more than 90 mg of codeine per dosage unit and buprenorphine. Schedule III drugs may be prescribed verbally over the phone, with a paper prescription, or through EPCS. Within a 6-month timeframe, refill requirements are such that the drug can only have 5 refills. . Schedule IV drugs have a lower potential for misuse compared to Schedule I, II, or III drugs. These drugs have a limited risk of physical or psychological dependence. Examples of Schedule IV substances include alprazolam, carisoprodol, clonazepam, clorazepate, diazepam, lorazepam, midazolam, temazepam, tramadol, and triazolam. Drugs in this class may be used for pain control as long as the healthcare provider deems the drug medically necessary and the patient is likely to benefit. Schedule IV drugs can be prescribed verbally over the phone, with a paper prescription, or through EPCS. Refills are permitted up to 5 times in a 6-month timeframe from the issuance date. Schedule V drugs are the least likely of the controlled substances to be misused. These drugs result in minimal physical or psychological dependence. Examples include cough medicines containing codeine, antidiarrheal medications containing atropine or diphenoxylate, pregabalin, and ezogabine. Despite their low abuse potential, they still need to be managed appropriately and administered with care. When these medicines contain codeine, they must have less than 200 mg of codeine per 100 mL. Partial prescription fills cannot occur more than 6 months after the issue date. When a partial fill occurs, it is treated in the same manner and with the same rules as a refill of the drug. Drug use disorder differs from drug abuse and misuse. Drugs taken may be illicit street drugs, stolen drugs, or those obtained through a legal prescription. Misusing a drug typically involves taking the drug in a harmful or detrimental way, resulting in personal, professional, or social problems. A patient abusing an opioid analgesic may no longer be able to interact appropriately with their family or friends and perform their duties at work. Misuse of a controlled substance refers to using a prescribed drug in a way that was not intended, whether intentionally or accidentally. A negative result may or may not occur. Examples of misuse include taking too much of a drug, using an incorrect dose, an incorrect route, or using prescription drugs written for another person. Controlled substances include both prescription drugs and illicit drugs with no recognized medical value. Both categories have the potential to be abused or misused. Although the use of Schedule I drugs is illegal, prescription drugs found in Schedules II through V are also commonly abused and misused, and their misuse is a challenging problem that has increased over the last several years. The Centers for Disease Control and Prevention (CDC) has declared prescription drug abuse a problem of epidemic proportions. The CDC believes that the absence of checks and balances on the prescription and distribution of controlled substances, including those prescribed for medical use, has the potential for abuse, and misuse is likely to continue increasing. A common practice among individuals who intentionally misuse controlled substances is to seek multiple sources for drugs. These individuals visit different healthcare providers, presenting a list of complaints that are often fictitious and vary from one healthcare provider to another. As a result, they may be able to obtain multiple prescriptions, which they then fill at different pharmacies. To combat this practice, known as prescriber shopping, many states have implemented systems that enable healthcare providers to view all the prescriptions written for each patient. The use of these systems is helping to gradually reduce such misuse. Some prescription drugs can be sold on the street for as much as $50 per tablet. Diversion is when a patient sells their drugs as a method of earning money. Patients may also sell their drugs to buy food, pay expenses, or purchase more potent street drugs. In some worst cases, healthcare providers may divert drugs from patients for their personal use or sell them to others. Some individuals use controlled substances for purposes other than their intended medical use. Rather than pain control, they may be used to stay awake, induce sleep, or get high. Before the popularity of prescription drug diversion, the only method to obtain illicit drugs was to import from other countries or manufacture them in private labs. Today, law enforcement agencies have the tremendous challenge of dealing with prescription drugs sold by diversion and illicit drugs imported or manufactured. In both instances, these drug sales and usage result in increased criminal activity, dangerous overdoses, and death. A review of multiple studies highlights a variety of ways individuals obtain prescription drugs. The findings are summarized below: 55% free from a friend or relative. 20% from a prescriber. 10% purchased from a friend or relative. 5% stolen from a friend or relative. 5% purchased from a drug dealer. 2% from multiple doctors. 1% through theft from a medical practice or pharmacy. Less than 1% obtained them from the internet. Studies also reveal that the source of the majority of these drugs was a single legal prescriber. There are significant knowledge gaps regarding appropriate and inappropriate opioid analgesic prescribing, including a lack of understanding of current research, legislation, and proper prescribing practices. Healthcare providers often have knowledge deficits that include: Understanding of addiction. At-risk opioid addiction populations. Prescription versus non-prescription opioid addiction. The belief that addiction and dependence on opioids are synonymous. The belief that opioid addiction is a psychological problem instead of a chronic painful disease. Due to a long history of misunderstanding, poor society, insufficient education for healthcare providers, and inconsistent laws, prescribing opioids has resulted in significant societal challenges. These challenges can only be addressed through comprehensive education and training. The misuse of controlled substances resulting in morbidity and mortality is rampant. According to the 2016 National Survey on Drug Use and Health conducted by the United States Department of Health and Human Services, over 10 million people misuse prescription pain medications, and over 2 million misuse sedatives, stimulants, and tranquilizers each year. The survey also identified pain relief as the most common reason for misuse. The CDC estimates that more than 40,000 individuals die each year from an opioid overdose. Three major classes of controlled substances are frequently misused—opioids, depressants, and stimulants. Opioids are commonly prescribed for pain control by binding to mu-opioid receptors in the central nervous system (CNS), which reduces the transmission of pain signals to the brain. In addition, opioids affect receptors in the gastrointestinal tract and respiratory system. These medications are used to treat pain, diarrhea, and cough. Common opioids: Codeine:Codeine is one of the most commonly used opioid medications. This medication is at the center of the opioid addiction problem in the United States and thus is highly regulated. Codeine is primarily prescribed for pain and cough. FDA-approved indication: Pain: Codeine is used to treat mild to moderate pain. The use of codeine is recognized in chronic pain due to ongoing cancer and palliative care. However, the use of codeine to treat other types of chronic pain remains controversial. Chronic pain, defined by the International Association for the Study of Pain, is pain persisting beyond the standard tissue healing time, which is 3 months. The most common causes of non-cancer chronic pain include back pain, fibromyalgia, osteoarthritis, and headache. Non–FDA-approved indications: Cough: Codeine is useful in treating various etiologies that produce a chronic cough. Additionally, 46% of patients with chronic cough do not have a distinct etiology despite undergoing a proper diagnostic evaluation. In such cases, codeine has been shown to reduce both the frequency and severity of coughs. However, the evidence supporting its effectiveness in treating chronic cough is limited. The dose can vary from 15 to 120 mg/d. In specific populations such as lung cancer, codeine is indicated for managing prolonged cough, typically as 30 mg every 4 to 6 hours as needed. Restless leg syndrome: Codeine is effective in treating restless leg syndrome when given at night, especially for individuals whose symptoms are not relieved by other medications. Persistent diarrhea (palliative): Codeine and loperamide are equally effective for managing persistent diarrhea. The choice between codeine and loperamide depends on the physician's evaluation of codeine's addictive potential versus loperamide's higher cost, along with the patient's susceptibility to adverse effects. Transdermal patches and intravenous formulations are commonly abused and used in combination with other drugs. Fentanyl is a synthetic opioid that is 80 to 100 times stronger compared to morphine and is often added to heroin to increase its potency. This drug can cause severe respiratory depression and death, particularly when mixed with other drugs or alcohol. Fentanyl has a high potential for addiction. Hydrocodone is a Schedule II semi-synthetic opioid medication used to treat pain. Immediate-release hydrocodone is available only in combination with other agents, such as acetaminophen and ibuprofen, and is approved by the FDA for managing pain severe enough to require an opioid analgesic and for which alternative (nonopioid) treatments are inadequate. Single-entity hydrocodone is only available in extended-release formulations and is approved by the FDA to treat persistent, severe pain requiring around-the-clock, long-term opioid therapy when alternative options are insufficient. Hydrocodone is also an antitussive and is indicated for the treatment of cough in adults. Morphine sulfate isapproved by the FDA for moderate-to-severe pain, whether acute or chronic. Most commonly used in pain control, morphine provides significant relief to patients afflicted with pain. Clinical situations that significantly benefit from medicating with morphine include managing palliative or end-of-life care, active cancer treatment, and vaso-occlusive pain during sickle cell crises. Morphine is widely used off-label for almost any condition that causes pain. In the emergency department, morphine is given for musculoskeletal pain, abdominal pain, chest pain, arthritis, and even headaches when patients fail to respond to first- and second-line agents. Although morphine is rarely used for procedural sedation, clinicians sometimes combine a low dose of morphine with a low dose of benzodiazepine, such as lorazepam, for minor procedures. Oxycodone is an opioid agonist prescription medication. The immediate-release formulation is approved by the FDA for managing acute or chronic moderate-to-severe pain when alternative treatments are inadequate and opioid therapy is deemed appropriate. The extended-release formulation is approved by the FDA for managing pain severe enough to require continuous (24 h/d), long-term opioid treatment, and for which there are no alternative options to treat the pain. The oxycodone to morphine dose equivalent ratio is approximately 1:1.5 for immediate-release and 1:2 for extended-release formulations. Tramadol is an FDA-approved medication for pain relief. This medication has specific indications for moderate-to-severe pain. Tramadol is classified as a Schedule IV drug by the FDA. Due to its potential for abuse and addiction, tramadol should be reserved for pain that is unresponsive to other treatments, including nonopioid analgesics. Tramadol is available in 2 formulations: extended-release and immediate-release. The immediate-release form is not intended for use as an as-needed medication; instead, it is for pain of less than 1 week duration. For pain lasting more than 1 week, the extended-release form is preferred, as it is indicated for pain control under 24-hour management or an extended period. Tramadol has demonstrated off-label effectiveness in the management of premature ejaculation and restless leg syndrome that is refractory to other treatments. For the off-label use of tramadol for premature ejaculation, both sporadic and daily use is effective for treating the condition. Patients generally prefer as-needed therapy for premature ejaculation due to the lack of adverse effects compared to the daily use of tramadol. Although each of these terms is similar, healthcare providers should be aware of the differences. Addiction: The constant need for a drug despite harmful consequences. Pseudoaddiction: Constant fear of being in pain and hypervigilance; typically, there is a resolution with pain resolution. Dependence: Physical adaptation to a medication where it is necessary for normal function, and withdrawal occurs with the lack of drugs. Tolerance: The lack of expected response to a medication, increasing dose to achieve the same pain relief, resulting from CNS adaptation to the medication over time. The Mainstreaming Addiction Treatment (MAT) Act updates federal guidelines to expand the availability of evidence-based treatment to address the opioid epidemic. The MAT Act empowers all healthcare providers with a standard controlled substance license to prescribe buprenorphine for opioid use disorder, just as they prescribe other essential medications. The MAT Act aims to help destigmatize a standard of care for opioid use disorder and integrate substance use disorder treatment across all healthcare settings. As of December 2022, the MAT Act has eliminated the DATA-Waiver (X-Waiver) program. All DEA-registered practitioners with Schedule III authority may now prescribe buprenorphine for opioid use disorder in their practice if permitted by applicable state law, and the Substance Abuse and Mental Health Services Administration encourages practitioners to do so. Prescribers who were registered as DATA-Waiver prescribers receive a new DEA registration certificate reflecting this change; no action is required on their part. There are no longer any limits on the number of patients with opioid use disorder that a practitioner may treat with buprenorphine. Separate tracking of patients treated with buprenorphine or prescriptions written is no longer required. Pharmacy staff can now fill buprenorphine prescriptions using the prescribing authority's DEA number and do not need a DATA 2000 waiver from the prescriber. However, depending on the pharmacy, the dispensing software may still require the X-Waiver information to proceed. Practitioners are still required to comply with any applicable state limits regarding the treatment of patients with opioid use disorder. For more information or assistance, contact your State Opioid Treatment Authority.
对于任何开处方的人来说,最困难的挑战之一是区分合法开具管制药品处方与可能用于非法目的的处方。为了辨别差异,开处方的人需要了解急慢性疼痛的体征、症状和治疗方法,以及滥用管制药品患者的体征和症状。人们寻求医疗专业人员治疗的一个常见原因是缓解疼痛。虽然有许多类别的止痛药物,但阿片类镇痛药已获得美国食品药品监督管理局(FDA)批准用于中度至重度疼痛。因此,它们是急性、癌症相关、神经和临终疼痛患者的常见选择。为慢性疼痛开具阿片类镇痛药存在争议,且标准尚无定论。在20世纪90年代,由于医疗专业人员长期未能适当治疗重度疼痛,阿片类镇痛药的处方量有所增加。不幸的是,这导致了药物的过度使用、滥用、阿片类药物使用障碍和过量用药。“第22条军规”似乎是指,要么医疗专业人员治疗不足,导致患者遭受不必要的痛苦,要么他们过度治疗,有可能导致如阿片类镇痛药使用障碍增加和潜在过量用药等不良反应。阿片类镇痛药的处方量在2011年达到峰值。从那时起,处方量和过量用药量都在下降,但作为一个社会,无论是在大众还是科学文献中,人们都严重担心我们仍处于阿片类药物危机之中。也许照顾疼痛患者最大的挑战是,个体有不同的耐受水平,需要不同剂量的阿片类药物才能获得充分的疼痛缓解。患者对疼痛与物质使用障碍可能有一系列行为、文化、情感和心理反应;通常,区分两者具有挑战性。所有从事疼痛管理的医疗专业人员都需要了解开具阿片类镇痛药的治疗建议和安全问题。适当开具阿片类药物需要对患者进行全面评估、制定短期和长期治疗计划、密切随访并持续监测。所有医疗服务提供者都需要了解适当的患者评估和治疗计划,以及使用障碍、药物滥用和对管制药品(如阿片类镇痛药)潜在危险行为反应的可能性,例如阿片类镇痛药不同于假性成瘾和身体依赖。很明显,许多临床医生对阿片类药物使用障碍了解甚少。他们不理解这是一种疾病,许多人认为阿片类药物依赖与阿片类药物使用障碍相同。缺乏清晰的理解导致临床医生将患有慢性非使用障碍的患者与滥用处方阿片类药物的患者混淆。缺乏培训和教育不足常常干扰阿片类镇痛剂的适当处方。为防止管制药品的滥用,开具管制药品的医疗服务提供者应学习尽量减少或防止不良后果的处方做法。
成瘾——根据美国成瘾医学协会(ASAM)的定义:“成瘾是一种原发性慢性脑部奖赏、动机、记忆及相关神经回路疾病。这些神经回路功能障碍会导致特征性的生物、心理、社会和精神表现。这表现为个体通过使用药物和其他行为病态地追求奖赏或缓解。”成瘾现在被称为“使用障碍”,其特征是无法持续戒除、渴望药物、行为控制受损、认识到自身行为和人际关系中重大问题的能力下降以及功能失调的情绪反应。与其他慢性疾病一样,使用障碍通常涉及复发和缓解的循环。如果不进行治疗或参与康复活动,使用障碍会逐渐加重,可能导致残疾或过早死亡。
这包括在控制毒性、使用障碍或使用障碍风险的同时提供疼痛控制,并实施保障措施以减少药物滥用。
不开具、开具不足、过度开具或尽管有证据表明缺乏有效的阿片类镇痛药治疗仍继续开具。
这些是有被滥用可能性的药物或药品,被认为是有很高风险导致物质使用障碍的物质。
这些是使感觉迟钝并缓解疼痛的药物,例如吗啡。此外,这些药物可能会诱导睡眠。请注意,美国缉毒局(DEA)使用“麻醉药品”一词来指代阿片类镇痛药。
对药物或奖赏的渴望。
对自身行为中重大问题的认识减弱。
功能失调的情绪反应。
行为控制受损。
无法持续戒除。
所有医疗服务提供者都应熟悉每个附表的指导方针和法律,这些方针和法律以药物的用途和使用障碍风险为基础。在美国,管制药品受到联邦和州法律的严格监管,这些法律指导其生产和分销。管制药品有很高的成瘾和导致物质使用障碍的风险。随着附表从I到V递减,每个类别中列出的药物导致物质使用或成瘾障碍的可能性降低。
在美国,1970年通过了《综合药物滥用预防和控制法案》,其中包括《管制物质法案》。《管制物质法案》涵盖药物:根据其成分和用途进行分类和监管。生产。分销。出口和销售。《管制物质法案》制定了五个药物附表,并对其进行分类以控制其生产和分销。部分规定要求开具附表药物的医疗服务提供者和配药的药剂师获得美国缉毒局的许可证。医疗专业人员的许可证包括特定的许可证号码,以便追踪管制物质处方并将其与特定的医疗服务提供者或分销商联系起来。五个附表中的每一个都有基于其医疗价值、成瘾风险和造成伤害能力的参数。这些附表从附表I(成瘾/使用障碍可能性最大)到附表V(成瘾/使用障碍可能性最小)。
附表I药物具有最高的使用障碍和滥用可能性。它们没有医疗用途,是非法或“街头”毒品。附表I药物的例子包括海洛因、麦角酸二乙酰胺、墨斯卡灵、亚甲二氧基甲基苯丙胺(摇头丸)和甲喹酮。在撰写本文时,在一些州合法的大麻在联邦层面仍被列为附表I药物。
附表II药物的使用障碍可能性比附表I药物低。它们有很高的身体和心理依赖风险。它们有很高的使用障碍和滥用可能性。它们通常被开处方用于治疗重度疼痛、焦虑、失眠和注意力缺陷多动障碍(ADHD)。附表II物质的例子包括芬太尼、氢吗啡酮、哌替啶、美沙酮、吗啡、羟考酮、右苯丙胺、哌甲酯、甲基苯丙胺、戊巴比妥和司可巴比妥。它们以前只能通过纸质处方开具,但现在允许电子传输(电子开具管制物质处方或EPCS)。不允许重新配药。与其他处方药相比,附表II药物的监管最为严格。
附表III药物的滥用可能性比I和II类药物低。这类药物可能会导致身体依赖,但更常见的是导致心理依赖。这类药物通常用于控制疼痛、麻醉或抑制食欲。附表III物质的例子包括苄非他明、氯胺酮、苯双甲吗啉和合成代谢类固醇。该附表中的阿片类镇痛药包括每个剂量单位含不超过90毫克可待因的产品和丁丙诺啡。附表III药物可以通过电话口头开处方、开具纸质处方或通过EPCS开具。在六个月的时间范围内,重新配药要求是该药物只能有五次重新配药。
附表IV药物的滥用可能性比I、II或III类药物更低。它们有有限的身体或心理依赖风险。附表IV物质的例子包括:阿普唑仑、卡立普多、氯硝西泮、氯氮卓、地西泮、劳拉西泮、咪达唑仑、替马西泮、曲马多和三唑仑。只要医疗服务提供者认为该药物有医学必要性且患者会受益,这类药物就可用于控制疼痛。附表IV药物可以通过电话口头开处方、开具纸质处方或通过EPCS开具。从开具日期起,在六个月的时间范围内允许最多五次重新配药。
附表V药物是管制物质中最不容易被滥用的。它们导致的身体或心理依赖非常有限。例子包括含可待因的止咳药、含有阿托品/地芬诺酯的止泻药、普瑞巴林和依佐加宾。尽管它们的滥用潜力很低,但仍需要进行适当管理并谨慎使用。当它们含有可待因时,每100毫升中可待因的含量必须少于200毫克。部分处方配药不能在开具日期后超过六个月进行。当进行部分配药时,其处理方式和规则与药物重新配药相同。
药物的使用障碍不同于药物的滥用和误用。所服用的药物可能是非法街头药物或被盗药物,也可能是通过合法处方获得的。误用药物通常是指以有害或不利的方式服用药物,导致个人、职业或社会问题。滥用阿片类镇痛药的患者可能不再与家人或朋友进行适当互动,或无法在工作中履行职责。管制物质的误用是指以未预期的方式使用处方药物。这可能是故意的或意外的。可能会或可能不会产生负面结果。误用的例子包括服用过量药物、使用错误的剂量、错误的途径或使用为他人开具的处方药。管制物质包括处方药和没有公认医疗价值的非法药物。两者都有可能被滥用或误用。虽然附表I药物的使用是非法的,但附表II - V中的处方药也经常被滥用和误用,并且它们的误用是一个具有挑战性的问题,在过去几年中有所增加。疾病控制与预防中心已宣布处方药滥用是一个具有流行程度的问题。疾病预防控制中心认为,对管制物质(包括那些用于医疗用途的物质)的处方和分销缺乏制衡机制,有可能被滥用,并且误用情况将继续增加。
不幸的是,故意滥用管制物质的人常见的做法是寻找多个药物来源。他们通过看不同的医疗服务提供者并提出一系列通常是虚构的、针对每个提供者都不同的投诉来做到这一点。患者可能能够获得多张处方,然后在不同的药店配药。许多州已经制定了系统,允许医疗服务提供者查看为每个患者开具的所有处方。这些系统的使用正在逐渐遏制“开处方者购物”现象。
一些处方药在街头的售价高达每片50美元。药物转移是指患者出售他们的药物以赚钱。药物也可能被出售以购买食物、支付费用或购买更强效的街头毒品。更糟糕的是,在某些情况下,医疗服务提供者可能会将患者的药物转移供自己使用或卖给其他人。有些人以并非药物原本 intended的方式使用管制物质。它们可能被用于保持清醒、诱导睡眠或“嗨”起来,而不是用于控制疼痛。在处方药转移流行之前,获得非法药物的唯一方法是从其他国家进口或在私人实验室制造。如今,执法机构面临着处理通过转移出售的处方药以及进口或制造的非法药物的巨大挑战。在这两种情况下,这些药物的销售和使用都会导致犯罪活动增加、危险的过量用药和死亡。
对多项研究的综述表明,个人获取处方药的方式多种多样。以下总结了研究结果。55%从朋友或亲戚处免费获得。20%从开处方者处获得。10%从朋友或亲戚处购买。5%从朋友或亲戚处偷得。5%从毒贩处购买。2%从多个医生处获得。1%从医疗诊所或药店盗窃获得。不到1%从互联网上获得。研究还表明,这些药物的大多数来源是单一合法开处方者。
在适当和不适当开具阿片类镇痛药方面存在重大知识差距,包括对当前研究、立法和适当处方做法的理解不足。医疗服务提供者经常存在知识缺陷,包括:对成瘾的理解。阿片类药物成瘾的高危人群。处方与非处方阿片类药物成瘾。认为阿片类药物成瘾与依赖是同义词。认为阿片类药物成瘾是心理问题而非与慢性疼痛疾病相关。由于长期存在误解、社会认知差、医疗服务提供者教育不足和法律不一致,开具阿片类药物导致了重大的社会挑战,只有通过大量的教育和培训才能解决。
不幸的是,滥用管制物质导致发病和死亡的情况猖獗。根据美国卫生与公众服务部2016年进行的全国药物使用和健康调查,每年有超过1000万人滥用处方止痛药物,超过200万人滥用镇静剂、兴奋剂和镇静催眠药。同一项研究发现,滥用的最常见原因是治疗身体疼痛。疾病控制与预防中心估计,每年有超过4万人死于阿片类药物过量。
阿片类药物、镇静剂和兴奋剂。
阿片类药物通过与中枢神经系统中的μ阿片受体结合来控制疼痛,减少向大脑以及胃肠道和呼吸系统中的受体发送的疼痛信号,并用于治疗疼痛、腹泻和咳嗽。
最常服用的阿片类药物之一。它是美国阿片类药物成瘾问题的核心,因此受到严格监管。其主要适应症是疼痛和咳嗽。
可待因在治疗轻度至中度疼痛中起作用。其在因持续癌症和姑息治疗导致的慢性疼痛中的使用是被认可的。然而,使用可待因治疗其他类型的慢性疼痛仍存在争议。国际疼痛研究协会定义的慢性疼痛是指持续超过标准组织愈合时间(即三个月)的疼痛。非癌症慢性疼痛的最常见原因包括背痛、纤维肌痛、骨关节炎和头痛。
可待因在治疗各种病因引起的慢性咳嗽中有用。此外,尽管进行了适当的诊断评估,46%的慢性咳嗽患者没有明确的病因。可待因使这些患者的咳嗽频率和严重程度降低。然而,关于可待因在慢性咳嗽中的疗效的文献有限。剂量可以从每天15毫克到120毫克不等。然而,它通常用于治疗持续咳嗽(在肺癌等特定人群中),通常根据需要每4至6小时服用30毫克。
可待因在夜间服用时对治疗不安腿综合征有效,特别是对于那些症状未被其他药物缓解的患者。
可待因和洛哌丁胺同样有效,选择使用它们的依据是医生对可待因虽小但不容置疑的成瘾潜力与洛哌丁胺较高成本以及患者对不良反应易感性的个体差异进行评估。
透皮贴剂和静脉注射剂,常被滥用并与其他药物混合使用。
芬太尼是一种合成阿片类药物,比吗啡强80至100倍,常被添加到海洛因中以增加其效力。它会导致严重的呼吸抑制和死亡,特别是与其他药物或酒精混合时。它有很高的成瘾潜力。
氢可酮是一种附表II半合成阿片类药物,用于治疗疼痛。速释氢可酮以复方制剂形式(与对乙酰氨基酚、布洛芬等混合)提供,并且已获得美国食品药品监督管理局批准用于管理严重到需要阿片类镇痛药且替代(非阿片类)治疗不足的疼痛。单一成分的氢可酮仅以缓释制剂形式提供。它已获得美国食品药品监督管理局批准用于治疗严重到需要24小时长期阿片类治疗且替代治疗不足的持续性疼痛。氢可酮也是一种止咳药,适用于成人咳嗽。
硫酸吗啡的美国食品药品监督管理局批准的用途包括中度至重度疼痛,可能是急性或慢性疼痛。吗啡最常用于疼痛管理,为疼痛患者提供显著缓解。使用吗啡治疗明显受益的临床情况包括管理姑息/临终护理、积极的癌症治疗以及镰状细胞危机期间的血管阻塞性疼痛。吗啡几乎被广泛用于治疗任何引起疼痛的病症,但未获得批准。在急诊科,当患者对一线和二线药物无反应时,会给予吗啡治疗肌肉骨骼疼痛、腹痛、胸痛、关节炎甚至头痛。吗啡很少用于手术镇静。然而,临床医生有时会将低剂量的吗啡与低剂量的苯二氮䓬类药物(如劳拉西泮)联合用于小手术。
一种阿片类激动剂处方药。羟考酮速释制剂已获得美国食品药品监督管理局批准,用于管理急性或慢性中度至重度疼痛,其他治疗方法不足以治疗该疼痛且阿片类药物治疗合适。缓释制剂已获得美国食品药品监督管理局批准,用于管理严重到需要持续(每天24小时)长期阿片类治疗且没有其他替代选择来治疗疼痛的情况。羟考酮与吗啡的剂量等效比对于速释制剂约为1比1.5,对于缓释制剂约为1比2。
曲马多是一种已获得美国食品药品监督管理局批准用于缓解疼痛的药物。它有特定的适应症用于中度至重度疼痛。美国食品药品监督管理局将其视为IV类药物。由于可能存在滥用和成瘾潜力,其使用应限于对其他止痛药物(如非阿片类止痛药物)无效的疼痛。曲马多有两种形式:缓释和速释。速释制剂不作为“按需”药物使用;相反,它用于持续时间少于一周的疼痛。对于持续超过一周的疼痛,缓释制剂是治疗选择——缓释制剂的适应症是在24小时管理或更长时间内控制疼痛。在未获得批准的情况下,该药物可用于治疗早泄和对其他药物无效的不安腿综合征。对于曲马多在早泄方面的未获得批准的使用,偶尔使用和每日使用对治疗该病症均有效。由于与每日使用曲马多相比副作用较少,患者表示更喜欢“按需”治疗早泄。
虽然这些术语中的每一个都相似,但医疗服务提供者应注意它们之间的差异。
成瘾——尽管有有害后果仍持续需要药物。
假性成瘾——持续害怕疼痛、过度警惕;通常随着疼痛缓解而缓解。
依赖——身体对药物产生适应性,正常功能需要该药物,缺乏该药物时会出现戒断症状。
耐受性——随着时间推移,中枢神经系统对药物产生适应性,对药物剂量增加缺乏预期反应,需要增加剂量才能达到相同的疼痛缓解效果。
《主流成瘾治疗(MAT)法案》条款更新了联邦指导方针,以扩大基于证据的治疗方法的可用性,以应对阿片类药物流行。《MAT法案》授权所有拥有标准管制物质许可证的医疗服务提供者开具丁丙诺啡治疗阿片类药物使用障碍(OUD),就像他们开具其他基本药物一样。《MAT法案》旨在帮助消除对OUD标准治疗的污名化,并将物质使用障碍治疗整合到医疗保健环境中。
截至2022年12月,《MAT法案》已取消了DATA豁免(X豁免)计划。所有拥有附表III授权的美国缉毒局注册从业者现在可以在适用州法律允许的情况下,在其执业中开具丁丙诺啡治疗OUD,美国药物滥用和精神健康服务管理局(SAMHSA)鼓励他们这样做。注册为DATA豁免开处方者的开处方者将收到一份反映此变化的新的美国缉毒局注册证书;注册者无需采取任何行动。从业者用丁丙诺啡治疗的OUD患者数量不再有任何限制。不再需要单独跟踪用