Webb Therapy Uncategorized Treatment-resistant Substance Use Disorder

Treatment-resistant Substance Use Disorder

There continues to be an ongoing gap between how addiction gets treated and how it actually works.

Knowledge and behaviour are handled by different systems. Insight lives largely in the prefrontal cortex — the part of the brain that plans, weighs consequences, and holds “I know this is bad for me.” But addiction increasingly reshapes subcortical circuits involved in craving, habit, and stress reactivity. Under cue exposure or stress, those older circuits can override the newer, knowledge-holding ones. This is why someone can recite their relapse triggers perfectly in a therapist’s office or recount pages of 12-step literature from memory and still act against that knowledge the moment they’re actually standing in the triggering situation.

Wiers and colleagues’ work on “dual process” models of addiction — explicit cognition versus automatic, implicit approach biases — captures this well. Cognitive bias modification research grew directly out of the finding that explicit knowledge doesn’t touch these automatic processes.

The transition from goal-directed use to habit. Everitt and Robbins’ work describes how repeated substance use shifts control from goal-directed brain circuits (which respond to consequences and knowledge) to habitual, and eventually compulsive, circuits centred in the dorsal striatum. Compulsive behaviour is, by definition, less responsive to knowing better. Decades of use can entrench this shift very deeply.

For example:

Early: goal-directed. Bad day → “I want to relax” → decide to drink. The action is chosen and tied to an expected outcome. If consequences got bad enough, the person could still stop — this runs through prefrontal cortex and ventral striatum.

Middle: habit. After years of stress → drink → relief, the sequence no longer needs a decision. Walking in the door at 6pm triggers pouring a drink before any conscious “do I want this?” moment happens. The cue now drives the action directly. Control has shifted to dorsolateral striatum — same circuitry as driving a familiar route on autopilot.

Late: Compulsive. In Everitt and Robbins’ animal studies, drug-seeking gets paired with a mild shock. Most animals stop once punished. But a subset — roughly a third, matching the rate of severe addiction in humans — keeps seeking the drug even though it now reliably delivers a shock. That’s the model for compulsion: behaviour persisting despite known, immediate harm.

The human version: Someone with DUI’s, lost relationships, health scares — every piece of proof the behaviour is destructive — still relapses. Not from lack of knowledge; they’ve lived the consequences repeatedly. The circuitry driving the behaviour at this stage doesn’t consult the consequence-tracking system the way it did early on.

This is also why pure education or insight-oriented therapy often under-performs at this stage — it’s arguing with a system that isn’t listening. Interventions that interrupt the cue-response link itself (contingency management, environmental restructuring, craving-blunting medication, removing triggers) tend to have more traction, because they target the habit/compulsion circuit rather than trying to out-inform it.

Koob and Volkow’s allostasis model. Their research reframes chronic addiction as a shift from positive reinforcement (seeking a high) to negative reinforcement (avoiding a increasingly severe dysphoric, anxious, irritable state without the substance). Long-term users aren’t chasing a reward anymore — they’re fleeing a state. That flight response is fast, automatic, and largely indifferent to intellectual understanding.

Unresolved comorbidity. A large fraction of people with treatment-resistant, decades-long relapse patterns have under-treated trauma, complex PTSD, personality disorders, or conditions like ADHD sitting underneath the substance use. If the underlying driver isn’t directly addressed, coping skills training treats the symptom while the engine keeps running. This is a common finding in dual-diagnosis literature — outcomes are much worse when co-occurring conditions go unaddressed even amid extensive substance-focused treatment.

Recovery capital, not just recovery knowledge. William White’s work on recovery capital argues sustained recovery depends on social, financial, physical, and community resources — stable housing, relationships, purpose, employment — not just internal coping skills. Someone can have excellent DBT (Dialectical Behaviour Therapy) skills and still relapse repeatedly if their environment, relationships, or life structure haven’t meaningfully changed.

Relapse as expected, not exceptional. Prochaska and DiClemente’s stages-of-change model treats relapse as a normal part of the cycle, not a failure of knowledge. But when relapse repeats over decades despite intensive treatment, researchers increasingly look at severity markers — poly-substance use, genetic loading, age of onset, impulsivity and risk-taking — that predict a harder course regardless of how much psychoeducation someone has absorbed.

The consistent variable across all of this: Insight is necessary but nowhere near sufficient. Addiction at that level of chronicity behaves more like a deeply conditioned neurobiological and habitual process than an information deficit. That’s also part of why chronic relapse is increasingly framed like a chronic illness — closer to diabetes or hypertension in its relapsing-remitting course — rather than something insight alone should be expected to resolve.

Here’s what the literature and clinical guidelines point to for people who’ve cycled through standard treatment repeatedly without sustained success. I’ll organise by approach type.

Pharmacological — often underused

  • For opioid use disorder, methadone and buprenorphine substantially outperform abstinence-only approaches in treatment-resistant populations — this is some of the strongest evidence in the entire addiction field, yet many long-term relapsers have never actually been offered maintenance medication, often due to program philosophy (abstinence-only 12-step programs) rather than clinical reasoning.
  • For alcohol, naltrexone (blocks the reward), acamprosate (reduces post-acute withdrawal dysregulation), and disulfiram (aversive) are under-prescribed. Naltrexone specifically blunts the reward signal that drives compulsive use — targeting the biology rather than relying on willpower.
  • Emerging: psychedelic-assisted therapy (psilocybin, ketamine) is showing promise in trials for alcohol and other use disorders, though this is newer evidence and not yet standard of care everywhere.

Interrupting the cue-response cycle directly

  • Contingency management — tangible rewards for verified abstinence — has some of the best effect sizes in the literature, particularly for stimulant use disorders where no strong pharmacological option exists. It works by directly competing with the habit circuit rather than arguing with it.
  • Environmental restructuring — changing routes, routines, social circles, physically removing cues — matters more than intellectual insight at this stage, because the behaviour has become cue-triggered rather than decision-driven.

Treating what’s underneath

  • Systematic assessment for under-treated trauma, complex PTSD, ADHD, and personality disorders. Trauma-focused therapies (EMDR, prolonged exposure, Seeking Safety) address the driver rather than just the symptom, and are often skipped in standard programs focused on the substance alone.
  • Integrated dual-diagnosis treatment (treating psychiatric conditions and addiction concurrently, by the same team) outperforms sequential or parallel treatment where the person bounces between separate providers.

Building recovery capital, not just coping skills

  • Housing First and supported employment models — stabilising the environment before or alongside treatment — show better outcomes than clinical treatment alone in chronic, treatment-resistant cases. William White’s recovery capital framework: outcomes track with social support, stable housing, purpose, and community as much as with therapy itself.
  • Recovery community centres and mutual-aid alternatives beyond 12-step (SMART Recovery, Refuge Recovery) matter for people whose repeated 12-step involvement hasn’t translated to sustained sobriety — fit between the person and the model isn’t universal.

Reframing the model of care itself

  • Treating addiction like a chronic relapsing-remitting illness (the diabetes/hypertension model) rather than an acute, curable event changes what “treatment resistant” even means. Long-term, low-intensity, indefinite maintenance care (medication, periodic check-ins, ongoing peer support) shows better outcomes than repeated cycles of intensive short-term treatment followed by discharge.
  • Harm reduction as a bridge or destination — not necessarily full abstinence — for people who haven’t achieved abstinence-based sobriety after years of trying. This reduces mortality and morbidity even when abstinence isn’t currently achievable, and can sometimes become a pathway toward it later.
  • Multidimensional Family Therapy / systemic approaches — treating the family/relational system rather than the individual alone — show better outcomes for people whose relapse is tangled up in unchanged relational dynamics.

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Why We Choose Now Over Later: Instant vs Delayed Gratification and CostWhy We Choose Now Over Later: Instant vs Delayed Gratification and Cost

We all know the feeling of eating the last Tim Tam even though we said we’d stop, or putting off the gym even though we know we’ll feel better after. There’s a simple psychological framework behind this tug-of-war, and it’s more nuanced than “willpower” or “laziness.”

Four combinations, not two

Most people think of this as one axis — instant vs delayed — but really there are two separate questions: when something happens, and whether it’s a reward or a cost. That gives four combinations:

  • Instant gratification: reward now (a cigarette, a scroll through social media, a splurge on payday)
  • Delayed cost: the price paid later (lung damage, lost hours, an empty bank account)
  • Instant cost: effort or discomfort now (a hard training session, saying no to dessert)
  • Delayed gratification: the pay-off later (fitness, health, savings)

These naturally pair up in everyday life — instant gratification tends to travel with a delayed cost (gluttony, addiction, procrastination), and instant cost tends to travel with delayed gratification (discipline, exercise, saving). But they’re not the same thing by definition; they’re just common bundles. Sometimes you get gratification with barely any real cost (an afternoon nap), or cost with barely any real reward (over-saving to the point of never enjoying your money).

Why the future feels so much less real

The underlying mechanism is called temporal discounting — our tendency to value a reward less the further away it sits. Offer someone $50 today or $100 in a year, and plenty will take the $50. The future reward gets “discounted” in the mind, even though it’s objectively worth more. This isn’t a flaw exclusive to people struggling with addiction or avoidance — everyone discounts the future to some degree. What differs from person to person is how steeply.

A more specific quirk sitting inside this is present bias — an extra, disproportionate pull toward anything happening right now, over and above normal discounting. The classic sign of it is a preference reversal: someone might happily choose $100 in 31 days over $50 in 30 days when both options are off in the future. But offer them $50 today versus $100 tomorrow, and many flip to taking the smaller amount immediately. Nothing about the maths changed — only whether “now” was on the table. This is the same mechanism behind grand plans made the night before that evaporate the next morning: the plan looked easy when “now” was still hypothetical.

Why does this happen? Economists originally assumed we discount the future smoothly and consistently — a steady, predictable decline in value the further out a reward sits. Real behaviour doesn’t work that way. Instead, people follow what’s called a hyperbolic discounting curve — value declines really fast for anything in the near future (i.e., pushing a reward from today to next week costs it a lot of its appeal) then flattens out for anything further away. But pushing a reward from five years away to six years away barely changes how appealing it feels at all. The decline is steep early and flat later. That steep early drop is what makes “right now” so magnetic, and the flat tail is why consequences six months away can feel almost as unreal as consequences five years away, even though they’re nothing alike in real terms.

Where this shows up in society

This isn’t just an economics quirk — it explains a lot of everyday human struggle:

  • Addiction runs almost entirely on this pattern: an intensely immediate reward (a drink, a hit, a bet) paired with a cost that’s not just delayed but sitting on that flat, barely-felt part of the curve.
  • Avoidance behaviours (procrastination, dodging a hard conversation, skipping medical checkups) work in reverse — the relief of avoiding discomfort is instant, while the cost of avoidance quietly compounds somewhere out on the flat tail.
  • Overeating or “gluttony” fits the same shape — the pleasure of eating is immediate and vivid; weight gain or health decline is real but distant and abstract, so it barely registers in the moment of choosing.
  • Under-saving and impulse spending are the financial version — a purchase feels good today; retirement or a rainy-day fund is decades away and easy to discount to near zero.

Why this matters practically

The useful reframe here is that struggling with this isn’t a personal failing or a lack of insight — it’s the human valuation system doing exactly what it evolved to do, just more steeply in some people than others. That points toward practical fixes that work with the curve rather than fighting it: shrinking the delay before a good choice pays off (visible progress, milestone rewards), making the cost of a bad choice show up sooner rather than later (a streak, a check-in, immediate feedback), or removing the in-the-moment choice altogether through precommitment (automatic savings transfers, not keeping temptation in the house). Trying to simply convince someone to “care more” about the distant future tends not to work, because the problem was never a lack of caring — it’s that the future is quietly, structurally, worth less to the mind than the present.

What Alcohol does to the Human BodyWhat Alcohol does to the Human Body

1. Alcohol (ethanol) enters the body through the oral cavity (i.e., the mouth). The inner surface of the oral cavity is mucosal tissue to keep the cavity lubricated and it is capable of absorbing alcohol into the bloodstream. This absorption is considered “insignificant”.

2. Alcohol flows down the oesophagus to the stomach where 10-20% of ethanol will be absorbed into the bloodstream. Alcohol enters the bloodstream via the mucosal tissue of the stomach wall, and travels straight to the liver. Alcohol can take 5-10 minutes to reach the brain because of the ethanol absorbed via the stomach. If you drink alcohol on an empty stomach, the pyloric sphincter [gateway between the stomach and the small intestine] is going to be more open, and the alcohol is going to immediately enter the small intestine after reaching the stomach. If food is also present in the stomach, the sphincter will open and close at a rate that allows food to enter the small intestine gradually, therefore if alcohol is also in the stomach, it will gradually enter the small intestine.

3. Alcohol flows through the pyloric sphincter into the small intestines where most alcohol absorption occurs. Human intestines are attached the to the posterior abdominal wall by a fold of membrane called the mesentery. Alcohol is absorbed into the mesentery via veins and then travels to the liver.

4. One function of the liver is that it detoxifies toxic elements into non-toxic elements before passing it to the heart and then the rest of the body. The liver sustains considerable “abuse” from a variety of toxic elements and chemicals, and therefore it needs to be capable of full regeneration. NOTE: Many diseases and exposures can harm it beyond the point of repair. These include cancer, hepatitis, certain medication overdoses, and fatty liver disease.

In the liver, ethanol is met with an enzyme called alcohol dehydrogenase and converts ethanol into acetaldehyde [ass-eh-tal-de-hide]. This chemical is more toxic than ethanol, so the liver uses another enzyme to convert acetaldehyde into acetate, which is non-toxic to the human body. NOTE: the amount of alcohol consumed + the timeframe it is consumed [and a variety of other factors] will influence the ability of the liver to effectively convert acetaldehyde all the way into acetate. The liver can’t handle the entire workload effectively therefore ethanol (before being metabolised) will go straight from the liver to the bloodstream and make its way directly to the heart.

NOTE: Genetics will play a role! Certain people do not produce the liver enzymes in enough quantity to properly breakdown ethanol.

5. Blood leaves the liver through the hepatic veins. The hepatic veins carry blood to the inferior vena cava—the largest vein in the body—to the right side of the heart. The heart will beat and send the incoming blood to the lungs to oxygenate and expel carbon dioxide as we breath out. This is how ethanol can be on your breath. Inside the lungs, at the very end of the bronchioles, are hollow air sacs called alveoli where there is a gas exchange. Ethanol evaporates through capillaries into the air sacs and exhaled out of the body. Breathalysers can detect the quantity of ethanol in a person’s system based on the quantity of ethanol in our breath.

6. Not all the ethanol will expel from the body via the breath. The rest will flow back to the heart, with newly oxygenated blood, and then get pumped all the way up to the brain and around the body. NOTE: Ethanol is water soluble. It will be distributed to every cell in the body except bone and fatty tissue [some will enter fat cells but not easily]. Ethanol will interact with every other cell i.e., every organ, gland, nerve, muscle etc.

7. Ethanol will affect and compromise protein synthesis inside muscle tissue. Therefore, if you have been training at the gym, running, swimming etc., your muscles will not effectively be able to repair.

8. Once ethanol has reached the brain, it will cross the blood-brain barrier and begin to affect chemical messengers [neurotransmitters] in the grey matter of the brain. It affects serotonin, dopamine, gamma-amino-butyric-acid (aka GABA), glutamate, endorphins etc. The person will experience pleasure, euphoria, lowered inhibitions [related to dopamine], lowered cognitive ability (e.g., decision making/problem solving, emotion regulation) and lowered coordination and reflexes.

The more ethanol ingested, the more dopamine is secreted and communicated between neurons (i.e., nerve cells). One of dopamine’s functions is to make you feel pleasure or ‘rewarded’ for doing things that are good for humans, hence, from an evolutionary perspective, we are likely to do them again to help us thrive in our environment and social world. Dopamine is secreted when we:

  • eat healthy foods (but also recently developed processed foods that are high in sugar and salt)
  • exercise
  • achieve goals
  • be productive (e.g., finish a task like cleaning, cooking, work-related tasks)
  • master new skills (e.g., learning an instrument or a new talent), and
  • have positive and stimulating social interactions

Ethanol influences so much dopamine secretion and communication that the brain becomes unable to make responsible decisions cognitively. The simultaneous experience of euphoria and lowered cognitive ability means we are more likely to be “happy” about making irresponsible decisions.

Increased dopamine is how drinking alcohol “blocks” unpleasant emotions like fear, stress, anxiety, and insecurity. When we don’t feel these unpleasant, yet necessary, emotions we will behave in ways that are dangerous, abnormal, potentially embarrassing, and generally problematic.

Another significant brain region affected by ethanol is the hypothalamus and the pituitary glad [together known as the hypothalamic-pituitary axis]. These structures control the entire hormonal system. The hypothalamus monitors the body, and it will send instructions to the pituitary gland based on information it receives from the hypothalamus. The hypothalamus is aware that ethanol is flooding the brain and it starts adjusting the secretion of hormones via the pituitary gland.

One of the instructions it gives the pituitary gland is to start modulating the adrenal glands to secrete cortisol (i.e., stress hormone) and epinephrine and norepinephrine (i.e., adrenaline).

Now, our cognitive capacity is diminished, inhibitions are lowered, and we will experience a rush of stress hormones and adrenaline coursing through the body. Cortisol and adrenaline will provide a boost of energy. It will increase the heart rate, blood pressure, body sweat, sugar levels in the bloodstream, and enhances the brain’s ability to use glucose. Glucose is a “fuel” source for brain functioning, including the generation of neurotransmitters. Behaviourally, we can see this in children when we say they are “hyperactive” because they’ve ingested too much sugar.

The pituitary gland will also slow the secretion of anti-diuretic hormone (aka. vasopressin). A diuretic is something that makes us urinate. If the anti-diuretic hormone (also called vasopressin) slows down, then we won’t be “holding on” to water as effectively, hence we begin to urinate more. People call this “breaking the seal”.

9. South of the body, blood is pumped into the kidneys via the renal artery which spreads through the renal cortex. The blood is then filtered into urine and expelled from the body. The lowered anti-diuretic hormone will dilate (become wider/bigger or more open) blood vessels in the kidneys which means more blood gets passed through and filtered, but it also means we lose a lot more body water which leads to dehydration. Vasopressin is essential in the control of osmotic balance, blood pressure regulations, and kidney function, therefore, when vasopressin is lowered, we are losing essential water and minerals/electrolytes. Electrolytes are involved in urination because the kidneys need them to make the process of filtering blood more efficient.

The loss of water and electrolytes will contribute to a hangover. Electrolytes play a role in cellular water absorption so if we are losing more water than we are bringing in, and we are losing the electrolytes that support the absorption of water, we become dehydrated very quickly.

10. The Hangover

Symptoms: nausea, fatigue, diarrhoea, vomiting, paranoia, anxiety, anorexia (i.e., loss of appetite), increased thirst, muscle weakness, irritability, sweating, increased blood pressure, and headache.

The exact cause of a “hangover” is not yet known however variables affecting the hangover are:

  • individual differences such as sex, size, body fat, genetics etc
  • lack of sleep
  • general health
  • drinking behaviour e.g., frequency, duration, quantity
  • food intake before and during
  • water intake before and after
  • your body’s ability to metabolise alcohol i.e., excessive amounts of acetaldehyde due to fewer enzymes to metabolise alcohol in the liver before entering the bloodstream
  • general behaviour while drinking e.g., poly-substance use, dancing, sexual activity, risk-taking behaviours etc.

Strategies for Controlled Drinking

  • Setting personal drinking limits and sticking to it
  • Alternating alcoholic drinks with soft drinks i.e., one alcoholic drink then a water, soft drink, or juice
  • Have a meal before drinking
  • Switching to low alcohol drinks
  • Having regular alcohol-free days/weeks/months
  • Identifying high risk situations for heavy drinking and creating a management plan

Engaging in alternative activities to drinking