Drug Testing Locations - West Hattiesburg, MS

Drug Testing in West Hattiesburg, MS

West Hattiesburg, Mississippi Statistics

West Hattiesburg, located in Lamar County, has experienced a 25% increase in opioid-related hospitalizations over the past decade.

Law enforcement in Lamar County reports that methamphetamine is the most commonly seized illegal drug in West Hattiesburg.

West Hattiesburg ranks third in the state for highest number of drug overdose deaths per capita according to the recent health department report.

The youth in West Hattiesburg show a 15% higher rate of recreational drug use compared to the national average, as per the latest survey.

Emergency services in Lamar County recorded a 30% increase in drug-related calls in West Hattiesburg from the previous year.

A local study reveals that 40% of West Hattiesburg's homeless population report active substance abuse issues.

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 West Hattiesburg, MS & Drug Testing Policies

Employers in West Hattiesburg, working within Lamar County guidelines, are vigilant about maintaining drug-free workplaces. Many implement routine drug testing for employees to ensure a safe working environment, following protocols set by the U.S. Department of Labor.

Adherence to these strict policies not only deters drug use among employees but also aligns with state safety regulations. Such measures are pivotal in industries like transportation and manufacturing, where safety is paramount, increasing productivity and reducing workplace incidents.

Government Efforts with Drug Problems in West Hattiesburg, MS

The state government, alongside local authorities in West Hattiesburg and Lamar County, have rolled out comprehensive measures to combat drug issues. They focus on prevention, treatment, and law enforcement to curtail drug misuse in the area, collaborating with entities like the Mississippi State Department of Health.

Enhanced efforts by the DEA include targeting drug trafficking in Lamar County. Community programs also aim to educate residents on the dangers of drug use, providing alternatives and support through rehabilitation services to foster a healthier community.

Local Drug Busts & News in West Hattiesburg, MS

In recent months, West Hattiesburg has experienced several significant drug busts orchestrated by local law enforcement in cooperation with federal agencies. These operations, crucial to dismantling local drug networks, have resulted in numerous arrests, particularly targeting methamphetamine distribution.

The community has also witnessed an uptick in drug awareness events aimed at educating residents and curbing youth drug experimentations. These events highlight the city's commitment to addressing and reducing drug use, signaling a community-driven response to a pervasive problem.

Occupational Health Services

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

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