Drug Testing Locations - Bowling Green, MD

Drug Testing in Bowling Green, MD

Bowling Green, Maryland Statistics

In Bowling Green, Allegany County, opioid-related overdose deaths have increased by 15% from 2020 to 2021.

The rate of emergency room visits due to drug overdoses in Bowling Green, Allegany County, rose by 12% in 2021.

Allegany County, including Bowling Green, MD, reported a 20% rise in drug-related criminal offenses in 2020.

In 2021, Bowling Green, Allegany County, saw a 10% increase in admissions to drug rehabilitation centers.

The percentage of high school students in Bowling Green, Allegany County, who have tried illicit drugs is estimated at 8% as of 2021.

Bowling Green, Allegany County, had a 16% increase in opioid prescriptions dispensed in 2020 compared to the previous year.

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 Bowling Green, MD & Drug Testing Policies

Employers in Bowling Green, MD, increasingly enforce strict drug testing policies to ensure workplace safety and productivity. Many adhere to state guidelines for pre-employment and random drug screenings. Check Maryland's labor regulations on the Maryland Department of Labor website.

Drug-free workplace initiatives have been crucial in Bowling Green's business sector. Employers often participate in educational programs to raise awareness about the impact of drug use at work, seeking guidance from local chambers of commerce and law enforcement agencies.

Government Efforts with Drug Problems in Bowling Green, MD

The government of Bowling Green, MD, actively collaborates with Allegany County Health Department to address drug issues. Through initiatives like drug take-back programs and awareness campaigns, efforts are made to reduce drug dependency. Learn more on their website.

State and federal support are also instrumental in Bowling Green's fight against drug problems. Programs like the Prescription Drug Monitoring Program (PDMP) help in tracking prescriptions and curbing abuse. Visit the Maryland Department of Health's official page for more information.

Local Drug Busts & News in Bowling Green, MD

Recent drug busts in Bowling Green, MD, have significantly contributed to reducing illegal drug circulation. In 2021, Allegany County Sheriff's Office conducted multiple operations that led to substantial drug seizures. Updates and details on such operations can be found on their website.

Community initiatives, including neighborhood watch programs, aid law enforcement in tracking suspicious activities. Collaboration with regional drug enforcement agencies has proven vital in addressing the drug problem in Bowling Green.

Occupational Health Services

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

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Resources & Citations

Maryland Behavioral Health Administration

Rethink Recovery

Allegany County Health Department

Crossroads Recovery House

Maryland State Association of Recovery Residences

Substance Abuse and Mental Health Services Administration (SAMHSA)

Baltimore County Health Department

o-drug Help

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