Pain transcends borders. Latin America (LatAm), with a population of about 639 million, is a diverse geographical region facing public health challenges in helping patients who must deal with different forms of moderate to severe pain. Opioid consumption varies among the LatAm countries but ranges from low to moderate based on international standards [1–10 mg/morphine equivalents (ME) per capita annually]. Formularies in LatAm may offer opioid analgesics, and international guidelines discuss the appropriate use of opioids for various painful conditions, but in LatAm access can limit the use of opioids even when indicated. The appropriate role of opioid analgesics for treating cancer and noncancer pain has fallen under scrutiny as the United States and nations in Western Europe face the public health crisis of widespread opioid use disorder (OUD). At a time when key opinion leaders in North America may be advocating a much more limited role for opioid pain relievers, the nations of LatAm must evaluate and even consider expanding the role of opioids in the care of pain patients. Lessons learned from the United States may help guide their considerations. Of particular interest is the role of strong opioids in the management of pain of moderate to severe intensity.

A variety of analgesic products are available: paracetamol (acetaminophen), nonsteroidal anti-inflammatory drugs (NSAIDs), and a range of opioid analgesics such as codeine, morphine, oxycodone, and others. Buprenorphine is a strong opioid analgesic with a unique pharmacology that may offer certain advantages over other opioid analgesics in the treatment of certain pain syndromes. This article is based on previously conducted studies and does not contain any studies with human participants or animals performed by any of the authors.

Latin America

For the purposes of this article, Latin America (LatAm) is composed of the many nations in Central America, South America, much of the Caribbean, and Mexico. As such, LatAm is large, populous, and extremely diverse. While recent decades have seen an ongoing migration of the population to urban centers, LatAm retains a large rural population with more limited access to healthcare. There is great racial and ethnic diversity in LatAm. While most LatAm citizens have at least some European ancestry, intermarriage among Europeans, indigenous peoples, and others of African or Asian ancestry has produced a genetically mixed population. Historically, the Spanish who settled in LatAm encouraged conversion to Catholicism (today LatAm is 70% Roman Catholic) and cultural assimilation (nearly all of LatAm speaks Spanish or Portuguese), but discrimination was dissimilar to that which occurred in the U.S.. For example, racial slavery was not widespread in LatAm and miscegenation was legal, in that the Spanish seemed to expect mixed-race marriages. The so-called Columbian Exchange initiated when Christopher Columbus transferred a variety of life forms (including humans) to the New World from the Old World had a pronounced effect on LatAm [1], allowing for genomes in LatAm to be evolutionarily novel in that haplotypes have combined in unprecedented ways [2]. Early genetic research has determined that most LatAm individuals today have paternal connections to Europe and maternal connections to indigenous populations [3]. While much work remains to be done, genetics may explain, for example, why LatAm has a comparatively high prevalence of type II diabetes (risk associated with Native American ancestry) [4].

The healthcare system in LatAm is complex, imperfect, and still evolving. While some form of universal healthcare is available in at least eight LatAm countries [5], healthcare resources in many regions may generally be described as being out of alignment with healthcare demand [6]. Universal healthcare is available in Argentina, Brazil, Chile, Colombia, Costa Rica, Guatemala, Mexico, and Brazil [5], but each nation has its own unique system with peculiarities. Colombia made healthcare a constitutional right for its citizens in 1991 and runs a national insurance program with government subsidies. Mexico has two nationally supported systems: one for retired people and the other for the rest of the population, but private insurance is increasingly popular [7]. Brazil’s system likewise is a hybrid of a taxpayer-funded health system and private insurance products that are used by about 25% of the population to supplement care [7]. However, gaps in the system can be daunting. About 30% of LatAm citizens have no access to healthcare for any number of reasons, including financial restrictions, geographic impediments, and lack of available services [8]. Nevertheless, there appears to be an increased social and political drive to expand and improve health coverage. Some of the challenges facing LatAm healthcare are summarized in Table 1.

Table 1 Important healthcare challenges faced by LatAm nations moving forward

Epidemiological data show that LatAm has made and continues to make considerable progress in healthcare [9]. In the last three decades, life expectancy has increased by about 9 years, and is now approximately 65 years for men and 74 years for women [10]. The “graying” of LatAm is one aspect of these extended life expectancies and better healthcare, such as “managed” cancer patients. LatAm has a comparatively high rate of healthcare expenditure associated with injury, with about 20% of all potential years of life lost in LatAm caused by trauma [11]. About 50% of all potential years of life are lost to some form of noncommunicable disease (such as cardiovascular disease, stroke, or cancer) [11]. As is evident in much of the rest of the world, smoking rates in LatAm are declining overall [12]. In LatAm, an inverse relationship has been observed between income and prevalence of tobacco consumption [12]. Obesity remains a public health crisis in LatAm, where body mass indices (BMI) of 30 or more occur in 37.6% of citizens of Uruguay (highest) and 13.3% of Cubans (lowest) [13]. It has been estimated that every 5-point gain in BMI confers on the individual a 30% greater risk of mortality, typically due to vascular disease, diabetes, cancer, kidney dysfunction, liver disease, or respiratory disorders [14]. Thus, the increasing rates of obesity are a major public health concern.

Pain is prevalent in LatAm. This may be exacerbated by obesity, which is associated with pain, particularly joint-related pain [15]. Obesity-associated inflammation may also induce paroxysmal pain via neural damage [16]. In addition, chronic pain tends to increase with advancing age. As the population of LatAm ages, rates of cancer and obesity increase, and the area maintains its relatively high rate of injuries, treating pain safely and effectively will emerge as a growing (and possibly unmet) urgent medical need.

Opioid Analgesics in Latin America

Pain in LatAm is not always effectively treated because of limited access to opioid analgesics, widespread use of less-effective nonopioid pain relievers, regulatory and legal barriers, a lack of clinician training in opioid prescribing, and cultural reservations among patients about the use of such drugs [17]. Concern about the public health crisis in the United States involving opioids may make clinicians, regulators, politicians, and patients uneasy about the use of opioids as pain relievers when there are nonopioid products available.

Optimal pain control requires analgesic therapy to be individualized to meet each patient’s needs; for this, the prescriber must have access to the full armamentarium of pain relievers, including opioids. Medical key opinion leaders in LatAm have recently advocated changes to pain control guidelines that would allow the broader use of opioids in selected cases of chronic noncancer pain [18]. Opioids were advocated for the control of cancer pain by the World Health Organization over a quarter century ago with its now-famous “pain ladder” that called for increasingly strong pharmacological options to address increasingly severe cancer pain intensity levels [19]. About 20–50% of cancer patients experience pain, and 80% of patients with advanced-stage cancer have moderate to severe pain [20, 21]. This pain can occur at multiple sites [22]. Cancer patients experience pain related to the growth of tumors but also pain associated with treatments (chemotherapy-induced peripheral neuropathy [23] and postsurgical pain), and may have unrelated painful conditions as well. Obesity may compound these risks [24].

Large-scale broad epidemiologic studies have not been conducted in LatAm to provide more specific data on pain, its burden to the healthcare system, and opioid use patterns by country or population groups [25]. Opioid consumption is low to moderate in LatAm by international standards, which suggests that much pain is inadequately treated [26]. However, opioids may not be universally available to all indicated patients in LatAm [27]. Where pain is under-treated or ignored, there are usually multiple factors in play, including legal restrictions, regulatory issues, limited access to care, deficits in provider education and training, cultural attitudes, patient prejudices against opioids or pain relief in general, limited or no reimbursement, or other financial restrictions [28]. In some parts of LatAm, opioid analgesics may be considered too expensive for other than very short-term use [27]. It is not known how much the opioid crisis in the United States is shaping the decisions of international prescribers.

The Potential Role of Buprenorphine in Latin America

Buprenorphine is increasingly being explored by leading medical centers around the world as an important opioid analgesic option, in that it is associated with fewer and less intense psychoactive effects compared to other strong opioids, such as oxycodone [29]. Buprenorphine is not particularly sought by drug-seekers as it has been shown to have low “likeability” [30]. Its withdrawal symptoms are typically less severe than those of other strong opioids [31]. Anecdotally, it is known to the authors that in the U.S., where buprenorphine is a Schedule III controlled substance rather than a Schedule II controlled substance such as oxycodone or morphine, some prescribers prefer buprenorphine to other strong opioids such as oxycodone because it has a lower risk for misuse. In addition, the transdermal formulation of buprenorphine provides convenience and may improve patient adherence [32]. Transdermal buprenorphine may be helpful for patients who require strong analgesics but have difficulty swallowing, have a high pill burden, are involved in complicated treatment protocols that already require taking multiple oral drugs, tend toward noncompliance, or are cognitively impaired or extremely stressed with their treatment protocol.

Buprenorphine possesses a unique pharmacology in that it acts as a partial agonist at the µ-opioid receptors although it provides analgesia as a full agonist; it also acts on the κ-opioid receptors [30, 33]. It is more potent than morphine and has a “ceiling effect” for respiratory depression (meaning that beyond a certain dose, the risk of respiratory depression does not increase), but not for analgesia [34]. In humans, buprenorphine undergoes extensive metabolization, with only a small amount of the parent drug excreted by the kidneys [35, 36]. Most of this metabolism corresponds to N-dealkylation to norbuprenorphine via the cytochrome (CYP)450-3A4/5 enzymes [37, 38]. Buprenorphine and norbuprenorphine are subject to glucuronidation via the UDP-glucuronosyltransferase (UGT) enzymes to buprenorphine-3-glucuronide (B3G) and norbuprenorphine-3-glucuronide (N3G) [39]. Peak plasma concentrations of norbuprenorphine exceed those of buprenorphine [40]. Originally, the metabolism of buprenorphine to norbuprenorphine was considered an inactivation pathway [41], but subsequent research indicated that it may actually be a pathway to bioactivation instead [39]. Glucuronidination is generally considered a form of detoxification and an inactivation pathway. To date, the pharmacological effects of norbuprenorphine glucuronides remain to be elucidated [39]. Norbuprenorphine is a powerful opioid agonist that appears to be more potent than buprenorphine [42]. Norbuprenorphine has affinities for the µ-, δ-, and κ-opioid receptors [43].

The transdermal delivery system for buprenorphine relies on a matrix (patch) to deliver buprenorphine through the skin, avoiding first-pass hepatic metabolism. In many LatAm countries, transdermal buprenorphine is available in low doses (5, 10, and 20 µg/h) that are designed to be applied once every 7 days for prolonged release. The transdermal patch eliminates the issue of patient adherence in that the patient need not remember to take oral medications on a by-the-clock schedule. It is eliminated hepatically (2/3 as norbuprenorphine) and renally (1/3) [33]. Buprenorphine is a potent opioid, but when delivered at low doses it can provide adequate analgesia with adverse effects similar to those of other opioids [44].

Clinical Results

The authors were unable to find randomized clinical study data from trials conducted in LatAm, although there are numerous clinical studies on the role of buprenorphine in a variety of painful conditions. The paucity of clinical trials in LatAMm extends beyond buprenorphine and pain management and may reflect an overall low scientific productivity in the region, financial constraints, lack of a clinical infrastructure suitable for running large randomized trials (such as limited numbers of institutional positions), and an expectation that studies be conducted in developed nations [45]. Thus, we present clinical trials from other parts of the world with the expectation that these are relevant to pain patients in LatAm. A review of low-dose transdermal buprenorphine in the treatment of chronic noncancer pain found that the patch (5, 10, or 20 µg/h) was better tolerated than sublingual buprenorphine and provided effective analgesia for patients with osteoarthritis (OA), low back pain, and other forms of chronic nonmalignant pain [46]. Specific study results for transdermal buprenorphine follow.

Long-Range Studies

In a study of 321 pain patients (mean age 72.4 ± 13.8 years, 85.4% with musculoskeletal pain, mean pain intensity 6.1 ± 1.2), buprenorphine transdermal patches (5 and 10 µg/h) were initiated (89.7% of patients started at the lower dose), and patients were followed over 6 months during which non-interventional observational data were collected. Doses stabilized to 5, 10, or 20 µg/h over the course of the study and the average pain intensity decreased at 6 months from 5.1 ± 1 (absolute) to 1.0 ± 1.0, while pain-related quality of life improved by 97.3%. The low-dose, seven-day transdermal buprenorphine system with stable dose management was reported to be associated with a remarkable improvement in the quality of life and pain relief in this elderly population [47].

A randomized double-blind parallel-group multicenter study in Europe evaluated 199 (OA) patients with a 7-day buprenorphine patch or sham patch. The initial active patch was a 5 µg/h patch which could be titrated up to 10 or 20 µg/h, as needed over the course of the 6-month study. Rescue medication was available in the form of 0.5–4 g of paracetamol (acetaminophen) per day. Twelve placebo and seven active-group patients withdrew from the study for lack of effective pain control. Buprenorphine patients had significantly less pain with movement (p = 0.029) and significantly improved Patient Global Impression of Change scores (p = 0.017). The primary and secondary endpoints of the Western Ontario and McMaster Universities (WOMAC) OA Index for Pain and the WOMAC OA [48] functional scores were statistically similar. Sleep quality improved in both groups.

Transdermal buprenorphine (initiated at 11.7 µg/h and then titrated, as needed, to a maximum of 35 µg/h) provided effective pain control in 146 real-world patients with moderate to severe chronic noncancer pain over 6 months. Patients experienced significant pain relief over baseline in terms of pain at rest and pain in movement, and had improved quality of life versus baseline [49].

Comparative Studies

A clinical study of 134 patients with moderate to severe chronic pain associated with OA compared pain control over 12 weeks using low-dose transdermal buprenorphine patches (n = 69) to oral prolonged-release tramadol (n = 65). Buprenorphine patches were available at 5, 10, and 20 µg/h and tramadol was administered twice daily at doses of 75, 100, 150, and 200 mg; maximum doses were 20 µg/h of buprenorphine or 400 mg/day of tramadol. Both groups achieved clinically relevant pain relief over baseline pain scores, and low-dose buprenorphine patches were deemed non-inferior to prolonged-release tramadol tablets. Adverse events were similar between groups and occurred in 88.4% of buprenorphine and 78.5% of tramadol patients. More tramadol than buprenorphine patients discontinued treatment (32% vs. 20%, respectively). It was reported that 70% of patients in both groups would prefer the 7-day low-dose transdermal buprenorphine patch to continue their future analgesic therapy. This study also concludes that the effect of 7-day low-dose transdermal buprenorphine was not inferior to that of oral tramadol tablets [50].

Low-dose transdermal buprenorphine was tested in 1160 opioid-experienced patients with chronic moderate-to-severe low back pain using patches of 5, 10, and 20 µg/h buprenorphine compared to an active control group (immediate-release oxycodone 40 mg/day) over 84 days in a double-blind study. The primary study endpoint was the average pain in the last 24 h at weeks 4, 8, and 12. This score was significantly lower in patients in the buprenorphine 20 µg/h group compared to patients in the 5 µg/h group; oxycodone was significantly more effective than buprenorphine 5 µg/h (p < 0.001). Buprenorphine 20 µg/h was found to be safe and efficacious in controlling chronic low back pain. Adverse events occurred in 77% of the buprenorphine 20 µg/h group and 73% of the oral oxycodone 40 mg group. In this study, 1 patient in the buprenorphine group died of causes deemed unrelated to the study drug, and < 1% of patients experienced a treatment-emergent serious adverse event [51].

In a similar study, the seven-day buprenorphine transdermal system was evaluated in opioid-naïve patients with moderate-to-severe chronic low back pain in an enriched, open-label, randomized, placebo-controlled study. Patients were provided with a buprenorphine 10 or 20 µg/h patch (n = 257) or placebo (n = 284) and were evaluated for pain control over 12 weeks. At week 12, the buprenorphine group had significantly lower pain scores (least squares mean treatment difference − 0.58, p = 0.010). Adverse events were similar between groups (55% vs. 52% for buprenorphine and placebo, respectively). In this study, the 7-day-buprenorphine transdermal system showed efficacy and safety in opioid-naïve patients with chronic low back pain [52].

A comparative non-inferiority study of transdermal buprenorphine in the treatment of moderate-to-severe musculoskeletal pain (n = 280) randomized patients to receive low-dose 7-day buprenorphine patches (5, 10, or 20 µg/h) or sustained-release oral tramadol (100–400 mg/day) over 8 weeks. Both groups experienced significant pain relief over baseline, and buprenorphine was not inferior to sustained-release tramadol [53].

In an eight-week, double-blind, placebo-controlled trial, transdermal buprenorphine (10–40 µg/h) was more effective than placebo at reducing pain in 78 opioid-experienced pain patients suffering moderate-to-severe low back pain, and these benefits were sustained over a six-month open-label study extension [54].

In a study of 220 patients ≥ 60 years old with hip and/or knee OA, patients were randomized to be treated with the 7-day transdermal buprenorphine patch plus oral paracetamol (5–25 µg/h of buprenorphine plus 1000 mg of paracetamol four times a day, n = 110) or co-codamol (two 8/500, two 30/500 mg tablets twice a day, n = 110). Medication was titrated over 10 weeks and then patients were evaluated over 12 weeks. Buprenorphine patches plus oral paracetamol was deemed to be not inferior to co-codamol tablets for pain relief [55].

Other Studies

In an open-label observational study of 114 patients with severe chronic musculoskeletal pain, low-dose transdermal buprenorphine patches provided effective pain control over 11 weeks with acceptable tolerability [56]. Yarlas and colleagues published results from two randomized controlled trials that found transdermal buprenorphine improved the quality of sleep in both opioid-naïve and opioid-experienced patients suffering from moderate-to-severe chronic low back pain; benefits emerged at about 4 weeks and were maintained over the 12-week course of the study [57].

Buprenorphine for Cancer Pain

In a phase IV real-world clinical study of 520 patients suffering chronic cancer pain, the four opioids tested (oral morphine, oral oxycodone, transdermal fentanyl, and transdermal buprenorphine) were similarly effective at 28 days in terms of pain control. About 14.4% of patients were nonresponders to buprenorphine (highest rate), compared to 11.5% of morphine patients being nonresponders (lowest rate), which was not statistically significant [58]. A study of 62 patients with severe cancer pain were evaluated over 28 days and grouped into those treated with oral morphine, oral oxycodone, transdermal fentanyl, and transdermal morphine. All of the opioids in this study were found to be effective and well tolerated [59]. A Cochrane review and meta-analysis indicated that transdermal buprenorphine might be effective in treating cancer pain patients but that its use would be limited to a subset of patients (responders) [60].

Safety and Adverse Events

In an Asian open-label observational study of transdermal buprenorphine (n = 114), 78% of patients reported at least one treatment-emergent adverse event (TEAE), and 22.8% of patients discontinued treatment because of side effects [56]. In a comparative study of low-dose transdermal buprenorphine (5, 10, and 20 µg/h) and oral sustained-release tramadol, the incidence of adverse events over the 12-week study was similar for the two groups [53]. In a six-month study of transdermal buprenorphine (n = 146, patches from 11.7 to 35 µg/h), 23 patients (15.75%) discontinued the patch because of adverse events, most of which were related to either the central nervous system or the gastrointestinal system [49].

A post-marketing surveillance study (n = 13,179) of patients with a mean treatment duration of 2 months and transdermal buprenorphine doses ranging from 35 to 70 µg/h found that the most commonly reported adverse events were nausea (3.95%), cutaneous reactions (2.3%), confusion (1.91%), vomiting (1.59%), and constipation (0.97%) [61].

Application site reactions have been reported with the use of buprenorphine transdermal systems. Using integrated data from 16 controlled and uncontrolled phase 3 studies involving chronic pain patients (n = 6566), the overall incidence of application site reactions was 23.4%, most of which (98.3%) could be considered mild to moderate in intensity; 4.4% led to discontinuation of buprenorphine patch therapy [62]. From a subset of integrated data on double-blind phases of five enriched, placebo-controlled studies (n = 1806), the rate of application site reactions was higher in buprenorphine patch patients (16.6%) than in patients with a sham patch (12.7%) [62]. The most commonly reported application site reactions (in both datasets and in data from an international postmarketing safety database) were pruritus, erythema, and rash. Relevant results of this study were that buprenorphine relieved pain in both groups of patients (cancer pain and non-cancer pain) regardless of age, and that the development of tolerance was not relevant throughout this study [62].

Special Populations

A Cochrane review examined the literature regarding the role of opioid therapy in the treatment of chronic noncancer pain in pediatric patients (children/adolescents), but found no studies that met its rigorous inclusion criteria [63]. A study of 16 pediatric oncology patients treated with transdermal buprenorphine for moderate-to-severe pain on a 72-h schedule with rescue oral tramadol found that 68.75% of patients responded to transdermal buprenorphine at 2 weeks with a significant decrease in pain over baseline (p < 0.001) along with a significant improvement in quality of life [64]. There is anecdotal evidence that transdermal buprenorphine could be of use in children with cancer pain [65], but clinicians must be aware that data on the pediatric use of transdermal buprenorphine are very limited.

Geriatric patients appear to be particularly good candidates for buprenorphine therapy in that buprenorphine dosing need not be adjusted for older versus younger patients. In fact, buprenorphine may be administered to patients with renal dysfunction [30, 66]. Its efficacy and safety for chronic OA pain has been evaluated specifically in older subjects by Uberall et al., who found that in more than 800 subjects 65 years old or older, transdermal buprenorphine was safe and effective [67]. Its pharmacokinetics in older subjects have also been shown to be similar to those of younger subjects [68]. Low-dose transdermal buprenorphine was efficacious in reducing persistent noncancer pain in geriatric patients (n = 891, mean age 72.8 years) over 12 weeks, with most patients reporting improvements in quality of life and function (activities of daily living) [67].

Elderly patients in cognitive decline may be undertreated for pain because their ability to articulate their concerns diminishes and they may be unable to adequately describe pain intensity using conventional metrics such as visual analog or numeric scales. (Some special scales for cognitively impaired patients have been created.) Clinicians may have to assess pain by understanding the patient’s potential pain etiologies (e.g., osteoarthritis) and observing the patient’s behaviors (e.g., facial expressions, vocalizations, changes in interpersonal interactions, and so on). When available, caregivers or family members may be able to offer insight to the clinical team about possible painful conditions. In some cases, an analgesic regimen may be trialed in a patient with cognitive dysfunction suspected of suffering pain to determine if the patient’s behaviors reflect pain relief [69].

The pharmacokinetics of buprenorphine in geriatric patients were evaluated in a multiple-dose open-label parallel-group study of healthy volunteers [68]. The volunteers were grouped by age into a younger group (age 50–60 years) and an older group (≥ 75 years). Two consecutive 7-day buprenorphine 5 µg/h patches were applied to the subjects, and blood samples were taken during the second patch (days 7, 8, 9, 10, 12, and 14, where day 7 corresponded to a pre-dose). The area under the plasma concentration–time curve at steady state (AUCtau) was similar for both age groups (the mean for older patients was 9940 pg/h/ml and the mean for younger patients was 11,309 pg/h/ml). Adverse events were reported more frequently among the younger than the older patients (216 vs. 164 events, respectively). This suggests that the dosing of transdermal buprenorphine 7-day patches does not need to be adjusted for older patients [68].


LatAm is the large, growing, vibrant, diverse home to over 8% of the world’s population. It is likely to emerge in the coming decades as an economic powerhouse. Its tremendous cultural, genetic, and political diversity makes it difficult to discuss as a single geographic region, but there are some important considerations for LatAm as a whole with respect to pain. Pain is a universal condition and pain control has been put forth by respected international bodies as a fundamental human right [70, 71]. Pain should not be ignored, particularly since modern medicine has made available to clinicians a myriad of pain-control products. The current public health crisis of opioid abuse in the United States should not fuel opiophobia in LatAm, but rather help guide LatAm prescribers in how to optimize the role of opioids rather than just avoid them. In fact, LatAm may be in a unique and important position to craft opioid policy and practices that support pain control and minimize risk of OUD by considering lessons learned in the United States in the past decades (see Table 2).

Table 2 Experiences in the U.S. with opioids and potential lessons to be derived from these experiences

Physicians in LatAm have a unique advantage in that they can help to shape their nations’ pain control policies in ways that confer analgesic benefits to pain patients without undue public health risk. OUD is a serious concern and must not be taken lightly, but pain is also an important consideration. Unrelenting moderate-to-severe pain can destroy lives, tear apart families, derail careers, contribute to disability, and cause financial devastation. Patients facing untreated pain have a decreased quality of life; suicide rates are higher among those with unrelenting pain [72]. The appropriate pain control regimen can improve patient function and boost quality of life.

The role of strong opioids in pain control is important. This article focused on transdermal buprenorphine, as it appears to be an excellent all-round choice of opioid analgesic for both cancer and noncancer pain. It is a strong, effective drug; it can be safely used in those with impaired renal function and geriatric patients (without dose adjustment); it has a ceiling for respiratory depression; it is not a drug that drug-seekers tend to “like” and abuse; and it is available in a transdermal patch system that may confer its own advantages over oral opioids. This is not to say that transdermal buprenorphine should be the only consideration. Pain control regimens should be the result of shared decision-making between prescribers and patients and, in some cases, their families. There are numerous nonpharmacological and pharmacological methods for pain control, and combination therapy is often helpful. Opioid therapy may not be the first-line approach. Opioids may be combined with nonopioids such as NSAIDs for effective pain relief with a net opioid-sparing effect. When it is determined that a patient is indicated for opioids and deemed to be a suitable candidate, opioids should be trialed with a specific “exit plan” in mind, as many patients find opioids ineffective or cannot tolerate opioid-associated side effects. The lowest possible effective dose should be used. For other than short-term use, titration is often required over several days or weeks. Patients may find certain opioids less effective or less tolerable than others; opioid rotation (to another opioid agent) may be helpful in some cases [73]. Opioids may be combined with nonopioid agents for a net opioid-sparing effect.

There is no “one size fits all” solution to pain. Each patient must be reviewed and considered individually and holistically. A very old terminal cancer patient in severe pain at the end of their life is a different case than a younger active patient with moderate occasional knee pain from OA. A patient with a lifelong history of substance abuse and vague pain complaints is a different case than a patient with no such history trying to cope with a few days of postsurgical pain in the hospital setting. Physicians must be advised that, just as each case is unique, each case changes over time. Risk factors for opioid use disorder may be described as dynamic [74]. Physicians and other clinicians should develop relationships of trust with their pain patients, utilize strategies of shared decision-making to find the most appropriate solutions for the pain of each individual, and monitor patients closely to be sure that pain control is effective and its side effects are tolerable. As such, patient education as well as provider training are crucial.


Pain in LatAm may be undertreated, but learning from the U.S. experience with opioids may help guide the diverse nations of LatAm toward a better opioid policy that treats pain effectively without encouraging opioid abuse. There are many reasons that opioids are underutilized in LatAm compared to other parts of the world, including regulations, culture, and accessability. Buprenorphine may be a particularly useful opioid for LatAm patients in that it has a unique pharmacology (ceiling effect for respiratory depression), is appropriate for geriatric as well as younger patients without dosing adjustments, is less well “liked” by drug seekers than other strong opioids, and is available in a transdermal system that may provide enhanced patient convenience and possibly drive better compliance. Pain should not be ignored, and finding better pain control solutions is a global concern.