Drug Testing Locations - Derwood, MD

Drug Testing in Derwood, MD

Derwood, Maryland Statistics

As of 2022, Derwood, located in Montgomery County, MD, reported a 15% increase in drug-related arrests compared to the prior year.

In 2021, Derwood, Montgomery County, had a 10% increase in opioid overdoses compared to 2020.

The Montgomery County area, including Derwood, saw a 20% rise in cocaine-related incidents in 2022.

In 2022, Montgomery County reported a 5% decline in heroin use, impacting areas like Derwood positively.

Fentanyl-related deaths in Montgomery County, covering Derwood, rose by 25% in 2021.

Derwood, MD, part of Montgomery County, has seen a steady increase in drug rehab admissions, rising 8% 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 Derwood, MD & Drug Testing Policies

Employers in Derwood, MD, recognize the importance of maintaining a drug-free workplace. Many have implemented strict drug testing policies to ensure the safety and productivity of their employees. The Maryland Department of Labor (link) provides guidelines for workplace drug policies, helping businesses align with state regulations.

Some companies in Derwood require pre-employment drug screening and conduct random testing to deter drug use among employees. Businesses often collaborate with local health services to provide education and resources to employees for substance abuse prevention and treatment, fostering a supportive community environment.

Government Efforts with Drug Problems in Derwood, MD

The government of Derwood, MD, part of Montgomery County, has initiated various programs to tackle drug abuse. These include community outreach and education efforts. The Montgomery County Health Department (link) collaborates with local organizations to provide resources and support to those affected.

The state government of Maryland has allocated funds to support drug prevention and rehabilitation programs in areas such as Derwood. Maryland's Department of Health (link) offers statewide assistance, focusing on both prevention and recovery to create a comprehensive approach to combat the drug crisis.

Local Drug Busts & News in Derwood, MD

In recent years, Derwood, MD, has been the focal point of several major drug busts, largely due to coordinated efforts between local law enforcement and federal agencies. A significant operation in 2021 resulted in the seizure of large quantities of fentanyl and cocaine, disrupting the supply chain in Montgomery County.

Community events addressing drug issues have been organized to raise awareness among Derwood residents. These events often feature local law enforcement and healthcare professionals discussing the signs of drug abuse and intervention strategies, promoting proactive community engagement against substance abuse.

Occupational Health Services

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Resources & Citations

Montgomery County o-drug Report

Maryland Behavioral Health Administration

Montgomery County Police Department

SAMHSA

National Association of Boards of Pharmacy

Prevention First

Maryland Department of Health

Partnership for Drug-Free Kids

CDC Drug Overdose Maps

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