Drug Testing Locations - Vandiver, AL

Drug Testing in Vandiver, AL

Vandiver, Alabama Statistics

Vandiver, AL, in Shelby County, reports a 4% increase in drug-related arrests over the past two years.

Shelby County's opioid prescription rate remains 10% above the national average.

In Vandiver, AL, 15% of youth have reported illicit drug use in surveys.

Drug overdose deaths in Shelby County have doubled in the last decade.

Vandiver, AL, has seen a 25% rise in drug treatment admissions over the past year.

Prescription drug misuse was reported by 8% of adults in Vandiver, AL, in 2022.

How does the body eliminate Drugs

Drug elimination is the sum of the processes of removing an administered drug from the body. In the pharmacokinetic ADME scheme (absorption, distribution, metabolism, and excretion), it is frequently considered to encompass both metabolism and excretion. Hydrophobic drugs, to be excreted, must undergo metabolic modification making them more polar. Hydrophilic drugs, on the other hand, can undergo excretion directly, without the need for metabolic changes to their molecular structures.

Although many sites of metabolism and excretion exist, the chief organ of metabolism is the liver, while the organ primarily tasked with excretion is the kidney. Any significant dysfunction in either organ can result in the accumulation of the drug or its metabolites in toxic concentrations.

A variety of other factors impact elimination — intrinsic drug properties, such as polarity, size, or pKa. Also other factors include genetic variation among individuals, disease states affecting other organs, and pathways involved in the way the drug distributes through the body, such as first-pass metabolism.

Issues of Concern

Drug elimination is the removal of an administered drug from the body. It is accomplished in two ways, either by excretion of an unmetabolized drug in its intact form or by metabolic biotransformation followed by excretion. While excretion is primarily carried out by the kidneys, other organ systems are involved as well. Similarly, the liver is the primary site of biotransformation, yet extrahepatic metabolism takes place in a variety of organ systems affecting multiple drugs.

Given the multiple organ systems and the variety of metabolic transformations present, drug elimination can entail a significant degree of complexity. Hydrophilic drugs are typically directly excreted by the kidneys, while hydrophobic drugs undergo biotransformation before excretion. The purpose here is twofold – biotransformation serves both detoxify the exogenous substances as well as to increase their hydrophilicity, ensuring their elimination via the kidneys.

Two broad metabolic pathways of hepatic drug transformation exist. Phase I is the direct modification of the target molecule, whereas phase II entails conjugation of the target to a polar molecule of low molecular weight. Phase I prepare the drug to enter phase II, but single-phase metabolism also exists.

Phase I involves oxidation, reduction, and hydrolysis of the exogenous molecule. These reactions are accomplished by hepatic microsomal enzymes, which reside in the smooth endoplasmic reticulum of the hepatocytes. Best known among them is the cytochrome P450 system, whose enzymes are predominantly involved in oxidative metabolism. Within the cytochrome P450 family (CYP), the enzyme responsible for the metabolism of more than 50% of existing drugs is the CYP3A4. Its activity encompasses various classes of medications, including opioids, immunosuppressants, antihistamines, and benzodiazepines. The enzymes can also be induced or inhibited by a variety of substances they interact with, including pharmaceuticals. The increase in metabolic activity with CYP induction results in a diminished activity of drugs targeted by that particular isoform. Conversely, CYP inhibition will result in increased drug plasma concentration, potentially leading toxicity. The CYP3A4 is induced by phenytoin, phenobarbital, and St. John's wort, while diltiazem, erythromycin, and grapefruit inhibit it. Caution is, therefore, necessary when administering CYP3A4-metabolized drugs in the presence of any of the inhibitors or inducers.

Phase II consists of covalent bonding of polar groups to nonpolar molecules to render them water-soluble and allow renal or biliary excretion. Target molecules enter phase II directly or via initial processing through phase I. A variety of polar adjuncts is transferred, including amino acids, glucuronic acid, glutathione, acetate, and sulfate. Glucuronidation is one of the major pathways of phase II biotransformation. The UDP-glucuronosyltransferase (UGT) enzyme family performs this activity. Typically, glucuronide derivatives possess less or no activity of the original drug, but in some cases, pharmacologically active compounds result. Morphine-6-glucuronide is a phase II metabolite of morphine with significant analgesic activity. As with the CYP enzymes, inducers, and inhibitors of phase II, enzymes exist and may influence the efficacy of drugs that rely on conjugation before excretion.

The first-pass effect is a feature of hepatic metabolism that also plays a role in the elimination of multiple drugs. Here, the enteric consumed drugs are exposed directly to the liver via the portal vein, where they undergo biotransformation before entering the systemic circulation. This activity reduces the bioavailability and needs to be factored into the dose administered to the patient. Intravenously administered drugs are not subject to the first-pass effect.

Extrahepatic drug metabolism takes place in the GI tract, kidneys, lungs, plasma, and skin.

Renal excretion completes the process of elimination that begins in the liver. Polar drugs or their metabolites get filtered in the kidneys and typically do not undergo reabsorption. They subsequently get excreted in the urine. Urinary pH has a significant impact on excretion, as drug ionization changes depending on the alkaline or acidic environment. Increased excretion occurs with weakly acidic drugs in basic urine and weakly basic drugs in acidic urine.

Excretion in the bile is another significant form of drug elimination. The liver can actively secrete ionized drugs with a molecular weight greater than 300 g/mol into bile, from where they reach the digestive tract and are either eliminated in feces or reabsorbed as part of the enterohepatic cycle.

Other pathways of excretion include the lungs, breast milk, sweat, saliva, and tears

Employers in Vandiver, AL & Drug Testing Policies

Employers in Vandiver, AL, are adopting proactive measures to ensure a drug-free workplace. Many businesses are integrating regular drug testing policies to maintain safety standards. SHRM provides guidelines that help employers create policies within legal frameworks. Employers emphasize education and rehabilitation for employees who struggle with substance misuse.

While some companies in Vandiver prefer pre-employment testing, others have opted for periodic testing based on job functions. Random drug testing policies are also being instituted where safety is critical, such as in transportation and manufacturing sectors. Employers collaborate with local healthcare providers to offer support services for affected employees.

Government Efforts with Drug Problems in Vandiver, AL

The government of Vandiver, AL, along with Shelby County, has implemented several initiatives to combat drug abuse. Local authorities are working closely with community-based programs to provide education and rehabilitation services. Efforts are ongoing to increase the accessibility of treatment facilities and promote public awareness about the dangers of substance misuse.

Alabama Department of Mental Health has launched statewide campaigns to reduce drug misuse, emphasizing prevention and intervention. They provide funding for local programs to enhance the community’s capacity to deal with drug-related issues. Collaborative efforts are being made at local and state levels to create a supportive environment for individuals in recovery.

Local Drug Busts & News in Vandiver, AL

In recent months, Vandiver, AL, has witnessed several significant drug-related events. Local law enforcement, in collaboration with Shelby County Sheriff's Office, conducted a major drug bust leading to multiple arrests. The operation targeted a network suspected of distributing opioids and other illicit substances within the community.

Community awareness events, such as drug take-back days, are being organized to safely dispose of unused prescriptions. These efforts are part of broader initiatives aimed at curbing the availability of drugs and promoting safer neighborhoods. Public forums and informational sessions are regularly held to engage residents in open discussions on drug issues.

Occupational Health Services

Accredited Drug Testing offers fast, reliable employment screening services in Vandiver, AL. Trusted by employers nationwide for accurate results and exceptional service.

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Resources & Citations

National Institute on Drug Abuse

Substance Abuse and Mental Health Services Administration

Alabama Drug Information Network

Alabama Department of Public Health

Alabama Public Health Department

Crisis Center Birmingham

Alabama AIDS Task Force

Narcan Access and Information

Behavioral Health Care Services Alabama

Angelina House Substance Abuse Services

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