Drug Testing Locations - Old Fort, NC

Drug Testing in Old Fort, NC

Old Fort, North Carolina Statistics

In 2022, McDowell County reported a 15% increase in opioid-related overdoses compared to the previous year.

Old Fort, in McDowell County, saw a 25% rise in drug-related arrests during 2021.

According to McDowell County's health department, 45% of substance abuse cases in 2021 involved methamphetamines.

In 2021, 60% of rehabilitation admissions in McDowell County were from Old Fort residents.

Old Fort Police reported drug seizures totaling over $150,000 in street value in 2020.

McDowell County experienced a 30% increase in drug-related deaths in 2019, with a significant portion from Old Fort.

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 Old Fort, NC & Drug Testing Policies

Employers in Old Fort, NC, are increasingly adopting stringent drug testing policies to ensure a safe and productive work environment. Many local businesses require pre-employment drug screening as well as random tests during employment. These measures help in maintaining workplace safety and reducing the likelihood of accidents associated with substance abuse.

Companies in Old Fort often follow guidelines set out by the U.S. Department of Labor to implement comprehensive drug-free workplace programs. Employers are also encouraged to provide resources and support for employees struggling with substance abuse, promoting a culture of recovery and accountability.

Government Efforts with Drug Problems in Old Fort, NC

Government efforts to combat drug abuse in Old Fort, NC, have been ramped up in recent years. Initiatives include increased funding for local law enforcement to enhance drug patrol and surveillance activities. The McDowell County Health Department has been instrumental in organizing community outreach programs aimed at educating the public about the risks of drug use and addiction.

At the state level, the North Carolina Department of Health and Human Services partners with local authorities to implement prevention and recovery programs in McDowell County. Additionally, the National Institute on Drug Abuse supports research and intervention strategies tailored to the unique challenges faced in areas like Old Fort.

Local Drug Busts & News in Old Fort, NC

Old Fort, NC, has been the scene of several significant drug busts in recent years. In 2021, McDowell County Sheriff's Office led a major operation that resulted in the confiscation of methamphetamine and heroin valued at over $100,000. This operation led to the arrest of multiple suspects and was part of a broader effort to curb drug trafficking in the area.

Local authorities have also organized community events to raise awareness about the dangers of drug abuse. These events often feature guest speakers from law enforcement and rehabilitation centers, aiming to educate residents and provide them with resources for support. Such proactive measures are vital in fostering a drug-free environment.

Occupational Health Services

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

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Resources & Citations

CDC Drug Overdose

NC Department of Health and Human Services

National Institute on Drug Abuse

McDowell County Health Department

Men's Sana

CRC Health

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MAR

Wellness Recovery Information

Carolina Treatment Centers

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