Showing posts with label benzodiazepines. Show all posts
Showing posts with label benzodiazepines. Show all posts

Tuesday, March 29, 2016

Using Client's Routine Urinalysis Records From Multiple Treatment Systems to Model Five-Year Opioid Substitution Treatment Outcomes

BACKGROUND:
At global, national, and local level, the need for ongoing, timely and cost efficient, comprehensive drug treatment monitoring, and evaluation systems have clearly been well recognized.

OBJECTIVES:
To test the feasibility of linking laboratory data and client intake data and its usefulness for modeling retrospectively, for the first time, 5-year longitudinal drug treatment outcomes in an Irish opiate treatment setting.

METHODS:
A multisite, retrospective, longitudinal cohort study was implemented to evaluate outcomes for opiate users based on 1.7 million routine urinalysis results collected from 4,518 individuals presenting for opioid substitution treatment in Ireland from January 2006 to December 2010.

RESULTS:
Analysis of opiates, cocaine, benzodiazepine, and cannabis use at treatment intake, 6 months and at 1-5 year follow-ups revealed differences in urinalysis protocols; significant differences in age of first drug use between those using and not using opiates at 5 years; significant decreases in opiate use; increases in benzodiazepine use and significant increasing effects of concurrent cocaine and benzodiazepine use on the odds of using opiates. Time series analysis of weekly proportions opiate positive predicted 16% (95% confidence interval: 7%-25%) of clients would be opiate positive 5 years postinitial intake. 

CONCLUSIONS: 
Underutilized urinalysis data can be used to address the need for cost effective, efficient evidence of drug-treatment outcomes across time, place, and systems. Linking and matching the cross-sectional data across sites and times also revealed where improvements in electronic records could be made.

Purchase full article at:   http://goo.gl/CH6vaI

By:  Comiskey CM1Snel A1.
  • 1 School of Nursing and Midwifery, Trinity College, University of Dublin , Dublin , Ireland.
  •  2016 Mar 20;51(4):498-507. doi: 10.3109/10826084.2015.1126738. Epub 2016 Mar 4. 



Friday, January 29, 2016

Management of Benzodiazepine Misuse and Dependence

There are well-recognised harms from long-term use of benzodiazepines. These include dependency, cognitive decline and falls. It is important to prevent and recognise benzodiazepine dependence. A thorough risk assessment guides optimal management and the necessity for referral. 

The management of dependence involves either gradual benzodiazepine withdrawal or maintenance treatment. Prescribing interventions, substitution, psychotherapies and pharmacotherapies can all contribute. Unless the patient is elderly, it is helpful to switch to a long-acting benzodiazepine in both withdrawal and maintenance therapy. 

The dose should be gradually reduced over weeks to lower the risk of seizures. Harms from drugs such as zopiclone and zolpidem are less well characterised. Dependence is managed in the same manner as benzodiazepine dependence.

Benzodiazepine and z-drugs half-life and conversion table
DrugApproximate half-life (hours)Dose of oral benzodiazepine approximately equivalent to diazepam 5 mg
Short- to intermediate-acting benzodiazepines
Triazolam1–30.25 mg
Oxazepam4–1515 mg
Temazepam5–1510 mg
Lorazepam12–161 mg
Bromazepam203 mg
Alprazolam6–250.5 mg
Flunitrazepam20–300.5 mg
Nitrazepam16–485 mg
Clobazam17–4910 mg
Long-acting benzodiazepines (includes effects of active metabolites)
Clonazepam22–540.5 mg
Diazepam20–805 mg
Z-drugs
Zolpidem2.410 mg
Zopiclone5.27.5 mg

Benzodiazepine withdrawal syndrome – clinical features

General

Headache
Palpitations
Sweating

Musculoskeletal

Tremor, fasciculations
Muscle pain, stiffness and aches (limbs, back, neck, jaw)

Neurological

Dizziness, light-headedness
Paraesthesia, shooting pains in neck and spine
Visual disturbances (blurred vision, diplopia, photophobia, vision lags behind eye movements)
Tinnitus
Faintness and dizziness, sense of unsteadiness
Confusion, disorientation (may be intermittent) – a common cause of confusion in older patients
Delirium (in the absence of autonomic hyperactivity) – particularly in older patients
Delusions, paranoia
Hallucinations (visual, auditory)
Grand mal seizures 1–12 days after discontinuing benzodiazepines

Gastrointestinal

Nausea
Anorexia
Diarrhoea (may resemble irritable bowel syndrome)

Psychological

Rebound insomnia, nightmares
Anxiety, panic attacks
Irritability, restlessness, agitation
Poor memory and concentration
Perceptual distortions – sensory hypersensitivity (light, sound, touch, taste), abnormal sensations (e.g. ‘cotton wool’ sensations)
Metallic taste
Distortions of body image
Feelings of unreality, depersonalisation, derealisation
Depression, dysphoria

Full article at:   http://goo.gl/radrfW

By:  Brett J1Murnion B2.
  • 1Clinical Pharmacology and Addiction Medicine, Drug Health Services, Royal Prince Alfred Hospital.
  • 2Clinical Pharmacology and Addiction Medicine, Drug Health Services, Royal Prince Alfred Hospital ; Concord Repatriation General Hospital, Sydney. 
  •  2015 Oct;38(5):152-5. Epub 2015 Oct 1.




Attitudes Towards a Maintenance (-agonist) Treatment Approach in High-Dose Benzodiazepine-Dependent Patients

BACKGROUND:
High-dose benzodiazepine dependence constitutes a major clinical concern. Although withdrawal treatment is recommended, it is unsuccessful for a significant proportion of affected patients. More recently, a benzodiazepine maintenance approach has been suggested as an alternative for patients' failing discontinuation treatment. While there is some data supporting its effectiveness, patients' perceptions of such an intervention have not been investigated.

METHODS:
An exploratory qualitative study was conducted among a sample of 41 high-dose benzodiazepine (BZD)-dependent patients, with long-term use defined as doses equivalent to more than 40 mg diazepam per day and/or otherwise problematic use, such as mixing substances, dose escalation, recreational use, or obtainment by illegal means. A qualitative content analysis approach was used to evaluate findings.

RESULTS:
Participants generally favored a treatment discontinuation approach with abstinence from BZD as its ultimate aim, despite repeated failed attempts at withdrawal. A maintenance treatment approach with continued prescription of a slow-onset, long-acting agonist was viewed ambivalently, with responses ranging from positive and welcoming to rejection. Three overlapping themes of maintenance treatment were identified: "Only if I can try to discontinue…and please don't call it that," "More stability and less criminal activity…and that is why I would try it," and "No cure, no brain and no flash…and thus, just for everybody else!"

CONCLUSIONS:
Some patients experienced slow-onset, long-acting BZDs as having stabilized their symptoms and viewed these BZDs as having helped avoid uncontrolled withdrawal and abstain from criminal activity. We therefore encourage clinicians to consider treatment alternatives if discontinuation strategies fail.

...In this explorative study, participants often used the term “substitution” in their initial narrative, primarily while referring to the substitution of benzodiazepines for other psychotropic substances like alcohol or heroin. The statement of VP22 exemplifies this perception:

“…Initially I took mostly heroin and when I wanted to sleep I just waited until the flash wore off. But when I could not fall asleep this way, then I thought, instead of taking more Heroin, I take a benzodiazepine, then I did not just save money, but it also helped better to fall asleep. O.k. with heroin you can also fall asleep, but actually out of cost considerations I switched over to benzodiazepines...”
VP 22, male, 46 years

Furthermore, participants associated “substitution” with the replacement of BZDs with a non-BZD class of agents such as antipsychotics or antidepressants, which was something they had often experienced during treatment. In addition, some participants described a long-term BZD maintenance approach with a slow-onset, long-acting BZD, when referring to previous experiences and preferences for different kinds of BZDs. Only few participants had heard of a “maintenance” approach by their treating physicians, reflecting the heterogeneity of this sample in regard to treatment duration (weeks to years) and form of intervention, ranging from abstinence-oriented benzodiazepine discontinuation approach to the more permanent prescription of slow-onset, long-acting BZDs.

Perceptions and beliefs about an agonist treatment (or “maintenance”) approach had to be elucidated using non-judgmental questions: “How would you feel about a substitution for benzodiazepines? Like, for example, heroin, that gets substituted with methadone?” Furthermore and in cases of highly knowledgeable participants, we gave more specific examples for slow-onset, long-acting benzodiazepines usually by mentioning specific brand names.

However, participants’ statements in regard to such a treatment strategy sometimes appeared to contradict their previous statements or explanations. Although we tried to clarify apparent inconsistencies using additional probes, they persisted in four instances:

“…For me, personally, that is nothing…I think that is a stupid question, but with heroin you have, but I never tried heroin, as far as I know you have a “high.” And that is something you don’t have with methadone. The “high” feeling is removed with methadone—it just eases withdrawal effects…And benzodiazepines do not make a “high,” so there is no “high” feeling, at least not with me…so I would not take (substituting drugs) since I don’t have side effects from benzodiazepines…if someone just overcomes feelings of anxiety and then does not need benzos anymore, then I think it is good, if there is such a development…but I am very happy that they are around...”
VP6, male, 30 years... 

Full article at:   http://goo.gl/NhY0yN

  • 1Department of Forensic Psychiatry, Institute of Legal Medicine, University of Bern, Bern, Switzerland. Michael.Liebrenz@fpd.unibe.ch.
  • 2Department of Psychiatry, Psychotherapy and Psychosomatics, Psychiatric Hospital, University of Zurich, Zurich, Switzerland. Michael.Liebrenz@fpd.unibe.ch.
  • 3Department of Surgery, Division of Visceral and Transplantation Surgery, University Hospital Zurich, Zurich, Switzerland. marcelandre.schneider@gmail.com.
  • 4Department of Psychiatry, Psychotherapy and Psychosomatics, Psychiatric Hospital, University of Zurich, Zurich, Switzerland. Anna.Buadze@puk.zh.ch.
  • 5Ulmenhof, Sozialtherapie, Ottenbach, Switzerland. marie-therese.gehring@diealternative.ch.
  • 6University of Pennsylvania Health System, Philadelphia, USA. Anish.Dube@gmail.com.
  • 7Department of Psychiatry, Psychotherapy and Psychosomatics, Psychiatric Hospital, University of Zurich, Zurich, Switzerland. Carlo.Caflisch@puk.zh.ch. 
  •  2016 Jan 8;13(1):1. doi: 10.1186/s12954-015-0090-x.




Wednesday, January 20, 2016

Essential Psychiatric Medicines: Wrong Selection, High Consumption & Social Problems

Background
The World Health Organization Essential Medicines List (WHO-LIST) and national essential medicines lists differ because many countries face significant challenges, such as product availability, cost, product quality and epidemiological disease profiles. In Brazil, governments pay for drugs that are included on the federal, state and municipal government (REMUME) lists. The extent to which municipal lists differ from state and national lists and from the WHO-LIST is unclear. We investigate the use of the WHO-LISTas a tool with which to evaluate the selection process for the essential psychiatric medicines in the public system coverage list of Brazilian communities (cities) and the use of the target drugs.

Methods
Municipal health secretaries were interviewed regarding the selection process for REMUMEs and the antidepressants and benzodiazepines included in REMUMEs and reference lists. We calculated the use of REMUME drugs that appeared or did not appear on reference lists according to the defined daily dose (DDD) per 10,000 inhabitants.

Results
Local physicians and pharmacists without specific training or explicit criteria developed the REMUMEs. Of the 13 drugs and 24 products (i.e., the different dosages of these 13 drugs) in the REMUMEs, 8 drugs and 10 products were included in at least one reference list and in one municipal list; 4 drugs and 6 products were included in at least one reference list but in none of the municipal lists; and 7 drugs and 8 products were included in at least one municipal list but in none of the reference lists. The antidepressants that appeared in at least one municipal list but in none of the reference lists represented 25.1 % (mean 60.9 DDD/10,000 inhabitants-day) of the usage. The benzodiazepines that appeared in at least one of the municipal lists but in none of the reference lists represented 14.7 % mean 18.5 DDD/10,000 inhabitants-day) of the usage.

Conclusions
Brazilian cities have no rigorous processes for selecting the drugs that appear on their lists, and drugs that do not appear on the reference lists represent a significant proportion of antidepressant and benzodiazepine use, resulting in public health and social problems.

Full article at:   http://goo.gl/3NDXI0

By:  Izabela Fulone, Silvio Barberato-Filho, Michele Félix dos Santos, Carolina de Lima Rossi, Gordon Guyatt and  Luciane Cruz Lopes
Pharmaceutical Sciences Master’s Course, University of Sorocaba, UNISO






Monday, January 4, 2016

Risk Factors of Prescription Opioid Overdose among Colorado Medicaid Beneficiaries

Highlights
  • This article presents the risk factors of opioid overdose among the Colorado Medicaid population.
  • Six factors were associated with opioid overdose including mean morphine dose equivalent (>50 mg/day), methadone use, drug/alcohol abuse, psychiatric illness, benzodiazepine use, and the number of different pharmacies used by the beneficiary.
  • States and communities should ensure the availability of at-home intra-nasal naloxone for overdose rescue based on the presence of risk factors.
This study aims to determine risk factors of opioid overdose among the Colorado Medicaid population. A retrospective nested case-control study was undertaken. Medicaid beneficiaries who had a medical claim(s) for an emergency department visit or a hospitalization associated with an opioid overdose from July 2009 to June 2014 were defined as cases. Controls were selected using a nearest neighbor matching without replacement. The matched controls were selected based on age, gender, and opioid prescription. One case was matched with three controls. Multivariate conditional logistic regression was used to compare risk factors. 

A total of 816 cases with 2,448 controls were included. Six factors were associated with opioid overdose: mean morphine dose equivalent (>50 mg/day), methadone use (switching opioid to methadone vs. no methadone use), drug/alcohol abuse, other psychiatric illness, benzodiazepine use, and the number of pharmacies utilized by the beneficiary (≥4 pharmacies vs. 1 pharmacy). 

In conclusion, several factors are associated with opioid overdose. States and communities should ensure the availability of at-home intra-nasal naloxone for overdose rescue based on the presence of risk factors.

PERSPECTIVES:
This article presents the risk factors of opioid overdose among Colorado Medicaid population. Based on study findings, Colorado Medicaid is currently working with physicians, hospitals, and other health-system stakeholders to continue develop policies to identify and assist this subset of our population. One such policy will be to provide intranasal naloxone for overdose rescue.

Purchase full article at:  http://goo.gl/Zt8BmW

  • 1Center for Pharmaceutical Outcomes Research, Skaggs School of Pharmacy and Pharmaceutical Sciences (http://www.ucdenver.edu/academics/colleges/pharmacy/Pages/SchoolofPharmacy.aspx), University of Colorado Anschutz Medical Campus, Aurora, CO, USA; Center of Pharmaceutical Outcomes Research, Department of Pharmacy Practice, Faculty of Pharmaceutical Sciences, Naresuan University, Phitsanulok, Thailand. Electronic address: piyamethd@gmail.com.
  • 2Center for Pharmaceutical Outcomes Research, Skaggs School of Pharmacy and Pharmaceutical Sciences, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
  • 3Department of Health Care Policy and Financing, State of Colorado.
  • 4Peak Statistical Services, Evergreen, CO, USA.
  •  2015 Dec 22. pii: S1526-5900(15)00985-2. doi: 10.1016/j.jpain.2015.12.006.

  • More at:  https://twitter.com/hiv insight
  • And: http://twitter.com/Prison Health



Illustration via:  http://goo.gl/k5I5L2

Focused Use of Drug Screening in Overdose Patients Increases Impact on Management

Abstract
Drug poisoning is a common cause for attendance in the emergency department. Several toxicology centres suggest performing urinary drug screens, even though they rarely influence patient management.

STUDY OBJECTIVES:
Measuring the impact on patient management, in a University Emergency Department with approximately 40,000 admissions annually, of a rapid urinary drug screening test using specifically focused indications. Drug screening was restricted to patients having a first psychotic episode or cases demonstrating respiratory failure, coma, seizures, a sympathomimetic toxidrome, severe opiate overdose necessitating naloxone, hypotension, ventricular arrhythmia, acquired long QT or QRS >100 ms, and high-degree heart block.

METHODS:
Retrospective analysis of Triage® TOX drug screen tests performed between September 2009 and November 2011, and between January 2013 and March 2014.

RESULTS:
A total of 262 patients were included, mean age 35 ± 14.6 (standard deviation) years, 63% men; 29% poisoning with alcohol, and 2.3% deaths. Indications for testing were as follows: 34% were first psychotic episodes; 20% had acute respiratory failure; 16% coma; 8% seizures; 8% sympathomimetic toxidromes; 7% severe opioid toxidromes; 4% hypotension; 3% ventricular arrhythmias or acquired long QT intervals on electrocardiogram. A total of 78% of the tests were positive (median two substances, maximum five). The test resulted in drug-specific therapy in 6.1%, drug specific diagnostic tests in 13.3 %, prolonged monitoring in 10.7% of methadone-positive tests, and psychiatric admission in 4.2%. Overall, 34.3% tests influenced patient management.

CONCLUSIONS:
In contrast to previous studies showing modest effects of toxicological testing, restricted use of rapid urinary drug testing increases the impact on management of suspected overdose patients in the ED.

Below:  Indications for urinary drug screening (n = 369) in 262 patients.
Arrhythmia or long QT = QT prolongation >480 ms, or ventricular tachycardia or flutter, or torsade de pointes tachycardia; Hypotension = systolic hypotension (<80 mm Hg); Opiate toxidrome = if requiring antagonist administration; Psychosis = first psychotic episode; Resp failure = acute respiratory failure (pCO2 45‑80 mm Hg or emergency intubation); Sympathomimetic = clinical signs of sympathomimetic toxicity



Below:  Spectrum of substances detected with the Triage® TOX screen (204 positive urine samples with 348 substances detected). AMP = amphetamines; BAR = barbiturates; BZO = benzodiazepines; COC = cocaine; MAMP = metamphetamines; MTD = methadone; OPI = opiates; PAR = paracetamol; TCA = tricyclic antidepressants; THC = tetrahydrocannabinoids



Below:  Impact of test results on clinical decisions (in %, n = 90) consecutive to the detection of substances with the Triage®TOX drug screen (n = 262 tests). Toxin-specific administration of naloxone, flumazenil or N-acetycysteine or other drug-specific treatments after test results.
Diagnostic tests = drug-related diagnostic tests ordered after test result; disposition = psychiatry transfer influenced by negative screening / somatic transfer if positive; prolonged monitoring = longer monitoring when methadone positive



Full article at:   http://goo.gl/MGRtlR

By:   Erdmann A1Werner D2Hugli O3Yersin B3.
  • 1Emergency Department, University Hospital (CHUV), Lausanne, Switzerland; Angiology Department, University Hospital (CHUV), Lausanne, Switzerland.
  • 2Laboratory of clinical chemistry, University Hospital (CHUV), Lausanne, Switzerland.
  • 3Emergency Department, University Hospital (CHUV), Lausanne, Switzerland.
  •  2015 Dec 28;145:w14242. doi: 10.4414/smw.2015.14242. eCollection 2015.

  • More at:  https://twitter.com/hiv insight
  • And: http://twitter.com/Prison Health


Thursday, December 31, 2015

Patterns of Abstinence or Continued Drug Use among Methadone Maintenance Patients & Their Relation to Treatment Retention

The efficacy and effectiveness of methadone maintenance treatment (MMT) in the medical management of opioid addiction has been well-established, but treatment outcomes are compromised by the continued use of licit and illicit drugs during MMT. 

The present study examined the relationship between in-treatment illicit drug use and retention and dropout of 604 MMT patients in Washington, D.C. Sixty-eight percent of patients did not test positive for an unprescribed drug during the study period. 

Of patients who tested positive for an illicit drug during the baseline period, 55% tested positive for cocaine, 44% for opiates, 23% for THC, 20% for benzodiazepines, 7% for PCP, and 4% for amphetamines. Those testing positive were three times more likely to leave treatment than those who did not test positive. Testing positive for one drug doubled the rate of attrition; testing positive for multiple drugs quadrupled the risk of attrition. Non-prescribed opioid or benzodiazepine use was a predictor of MMT dropout, but prescribed opioid or benzodiazepine use was not. 

Continued illicit drug use poses significant risk for subsequent premature termination of MMT. Assertive clinical management of continued illicit drug use could provide mechanisms to enhance MMT retention and long-term recovery outcomes.

Purchase full article at:   http://goo.gl/xG1nEe

  • 1a Emeritus Senior Research Consultant, Chestnut Health Systems , Punta Gorda , FL. 


Sunday, December 6, 2015

Patterns of Substance Use & Correlates of Lifetime & Active Injection Drug Use among Women in Malaysia

BACKGROUND:
While drug use is associated with HIV risk in Southeast Asia, little is known about substance use behaviors among women, including drug injection.

OBJECTIVES:
To describe patterns of substance use among women using alcohol and drugs in Malaysia and identify correlates of lifetime and active drug injection, a risk factor for HIV transmission.

METHODS:
A survey of 103 women who used drugs in the last 12 months assessed drug use history and frequency, including drug injection and drug use during pregnancy, self-reported HIV-status, childhood and adulthood physical and sexual abuse, and access to and utilization of harm reduction services, including needle-syringe exchange programs (NSEP) and opioid agonist maintenance therapy (OAT). Principal component analyses (PCA) were conducted to assess drug use grouping.

RESULTS:
Amphetamine-type substances (ATS; 82.5%), alcohol (75.7%) and heroin (71.8%) were the most commonly used drugs across the lifetime. Drug injection was reported by 32.0% (n = 33) of participants with 21.4% (n = 22) having injected in the last 30 days. PCA identified two groups of drug users: opioids/benzodiazepines and club drugs. Lifetime drug injection was significantly associated with lower education,homelessness, prior criminal justice involvement, opioid use, polysubstance use, childhood physical and sexual abuse, and being HIV-infected, but not with prior OAT.

CONCLUSION:
Women who use drugs in Malaysia report high levels of polysubstance use and injection-related risk behaviors, including sharing of injection equipment and being injected by others. Low OAT utilization suggests the need for improved access to OAT services and other harm reduction measures that prioritize women.

Purchase full article at:  http://goo.gl/OIVWNY

  • 1 Yale University School of Medicine , Department of Internal Medicine, Infectious Diseases Section, AIDS Program , New Haven , CT , USA.
  • 2 University of Malaya, Centre of Excellence for Research in AIDS , Kuala Lumpur , Malaysia.
  • 3 Yale University School of Public Health , Department of Epidemiology of Microbial Diseases , New Haven , CT , USA.