Diltiazem Ointment
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Neurontin (Gabapentin)
Texas Prior Authorization Program Clinical Criteria Drug/Drug Class Gabapentin Clinical Criteria Information Included in this Document Neurontin (gabapentin) • Drugs requiring prior authorization: the list of drugs requiring prior authorization for this clinical criteria • Prior authorization criteria logic: a description of how the prior authorization request will be evaluated against the clinical criteria rules • Logic diagram: a visual depiction of the clinical criteria logic • Supporting tables: a collection of information associated with the steps within the criteria (diagnosis codes, procedure codes, and therapy codes); provided when applicable • References: clinical publications and sources relevant to this clinical criteria Note: Click the hyperlink to navigate directly to that section. Gralise (gabapentin Extended Release) • Drugs requiring prior authorization: the list of drugs requiring prior authorization for this clinical criteria • Prior authorization criteria logic: a description of how the prior authorization request will be evaluated against the clinical criteria rules • Logic diagram: a visual depiction of the clinical criteria logic • Supporting tables: a collection of information associated with the steps within the criteria (diagnosis codes, procedure codes, and therapy codes); provided when applicable • References: clinical publications and sources relevant to this clinical criteria Note: Click the hyperlink to navigate directly to that section. March 29, 2019 Copyright © 2019 Health Information Designs, LLC 1 Horizant -
Management of Hemorrhoid Complications in Persian Medicine
http://www.cjmb.org Open Access Review Article Crescent Journal of Medical and Biological Sciences Vol. 7, No. 4, October 2020, 457–466 eISSN 2148-9696 Management of Hemorrhoid Complications in Persian Medicine Khadijeh Hatami1, Amir-Hooman Kazemi-Motlagh1, Hossein Ajdarkosh2, Arman Zargaran1, Mehrdad Karimi1, Ali-Asghar Haeri Mehrizi3, Hoorieh Mohammadi Kenari4 Abstract Objectives: Hemorrhoid disease has been a common medical problem since ancient times. About 5%-10% of patients do not respond to conservative treatment, and surgical procedures have a 20%-25% complication rate including pain, stenosis, infection, incontinence, and the like. Thus, most patients and physicians seek alternative and complementary medicines. Persian medicine (PM) is one of the oldest traditional medicines that present different treatment methods for managing hemorrhoid complications. Accordingly, the present study reviewed these methods and their applications. Methods: This historical review surveyed the principle of management and different medicinal and non-medicinal treatments for each complication of hemorrhoid based on the main textbooks of disease-treatment and famous pharmacopoeias of PM from 10th to 18th century AD. Recent findings about their pharmaceutical properties and mechanisms of action were searched in Google Scholar, Science Direct, and PubMed databases. Results: In PM, it is believed that hemorrhoid disease is because of melancholic or sanguineous distemperament. Cleansing the body and then strengthening the gastrointestinal and the liver for more effective treatment and prevention of relapse are the first therapeutic approaches in this regard. They use herbal and non-herbal medicines with anti-oxidant and anti-inflammatory, analgesic, and phlebotonic properties. In addition, different methods of bloodletting are used for body cleansing, reducing pain, and treating bleeding or thrombotic hemorrhoids. -
Post Hemorrhoidectomy Pain Relief; Outcome of Local Anesthesia
PAIN RELIEF POST HEMORRHOIDECTOMY The Professional Medical Journal www.theprofesional.com ORIGINAL PROF-2998 DOI: 10.17957/TPMJ/15.2998 POST HEMORRHOIDECTOMY PAIN RELIEF; OUTCOME OF LOCAL ANESTHESIA Dr. Syed Muhammad Maroof Hashmi1, Dr. Shua Nasir2, Dr. Lal Shehbaz3, Dr. Muhammad Absar Anwar4, Ahmed Ali5 1. Senior Registrar Department of Neurosurgery ABSTRACT… Background: The aim of my study is to evaluate post-operative pain relief K.M.D.C and Abbasi Shaheed on patients who had hemorrhoidectomy. Materials and Methods: 300 patients who had Hospital Karachi. hemorrhoidectomy were divided equally in to three groups, according to anesthesia type, 2. MD Resident Department of Emergency group 1 (local anesthesia and sedation), while spinal anesthesia was group 2 and general Medicine Ziauddin University anesthesia was considered to be group 3. Pain relief, post-operative complications, hospital Hospital Karachi. staying time were measured and compared between the three groups. Period: Study was 3. MD Resident performed between Jan 2012 to Dec 2014. Results: The study showed that patients who had Department of Emergency Medicine Ziauddin University local anesthesia infiltration and sedation a significant decrease of post-operative total pain Hospital Karachi. scores at 6/12/18/24 hours of more than 50%,200/240/300/320 out of 1000 points in group II 4. House Officer as compared to 420/500/540/580,700/680/660/660 in 3rd groups respectively. The total post- DUHS and Civil Hospital, Karachi 5. Research Fellow BMU operative analgesia doses in the 3 groups were 120:140:180 respectively, total hospital staying time were 130:210:260 days, headache in the ratio of 0:8:1, urine retention in 0:6:1 patients, Correspondence Address: nausea and vomiting in 0:1:5 patients were reduced by 30 %,. -
Hemorrhoids Brown Health Services Patient Education Series
Hemorrhoids Brown Health Services Patient Education Series What are hemorrhoids? Causes of Hemorrhoids Include: Hemorrhoids are swollen veins in the rectum. They ● Straining during bowel movements can cause itching, bleeding, and pain. Hemorrhoids ● Chronic diarrhea or constipation are very common. In some cases, you can see or ● Obesity feel hemorrhoids around the outside of the rectum. ● Pregnancy In other cases, you cannot see them because they ● Anal intercourse are hidden inside the rectum Diagnosis Hemorrhoids do not always cause symptoms. But To diagnose hemorrhoids, your clinician will when they do, they can include: examine your rectum and anus and may insert a ● Itching of the skin around the anus gloved finger into the rectum. Further evaluation ● Bleeding – Bleeding is usually painless and may include a procedure that allows your occurs during bowel movement. You might healthcare provider to look inside the anus (called see bright red blood after using the toilet on anoscopy), or evaluation by a proctologist. your toilet tissue or in the toilet bowl. ● Pain – If a blood clot forms inside a Management of Hemorrhoids hemorrhoid, this can cause pain. You may also experience: Initiate Lifestyle Changes: ● swelling around your anus One of the most important steps in treating ● A sensitive or painful lump near your anus hemorrhoids is avoiding constipation (hard or ● Leakage of feces infrequent stools). Hard stool can lead to rectal bleeding and/or a tear in the anus, called an anal Hemorrhoid symptoms usually depend on the fissure. In addition, pushing and straining to move location. Internal hemorrhoids lie inside the rectum. your bowels can worsen existing hemorrhoids and You can’t see or feel these hemorrhoids, and they increase the risk of developing new hemorrhoids. -
Topical Therapy As a Treatmentfor Brachioradial
Journal of Case Reports: Open Access Case report Open Access Topical Therapy as a Treatmentfor Brachioradial Pruritis: a Case Report Brianna De Souza M.D, Amy McMichael M.D* Department of Dermatology, Wake Forest University School of Medicine, Winston-Salem, North Carolina *Corresponding author: Amy McMichael, MD Department of Dermatology, Wake Forest Baptist Medical Center,1 Medical Center Blvd, Winston-Salem, NC 27157, Phone: 336-716-7882, Email: [email protected] Received Date: April 12, 2019 Accepted Date: May 06, 2019 Published Date: May 08, 2019 Citation: Brianna De Souza (2019) Topical Therapy as a Treatmentfor Brachioradial Pruritis: a Case Report. Case Reports: Open Access 4: 1-5. Abstract Management of brachioradial pruritus (BRP) presents a formidable challenge to dermatologists and neurologists. BRP is a rare, neurocutaneous condition characterized by sharply localized, chronic pain with associated itching, burning, stinging, and or tingling sensation. Effective care of this patient population is confounded by limitations within the litera- ture, comprised of case series and case reports. We present a case of one middle-aged female with a chronic history of BRP recalcitrant to the following oral therapies: pregabalin, gabapentin, mirtazapine, prednisone, and amitriptyline, as well as topical triamcinolone. After being evaluated in the clinic, the patient was started on combination therapy withKetamine 10%, Amitriptyline 5%, and Lidocaine 5% topical cream to which she responded. Keywords: Brachioradial pruritus, Brachioradial, Pruritus, Neurocutaneous ©2019 The Authors. Published by the JScholar under the terms of the Crea- tive Commons Attribution License http://creativecommons.org/licenses/ by/3.0/, which permits unrestricted use, provided the original author and source are credited. -
Effect of Amlodipine and Indomethacin in Electrical and Picrotoxin Induced Convulsions in Mice
DOI: 10.5958/2319-5886.2014.00402.0 International Journal of Medical Research & Health Sciences www.ijmrhs.com Volume 3 Issue 3 Coden: IJMRHS Copyright @2014 ISSN: 2319-5886 Received: 9th Apr 2014 Revised: 3rd Jun 2014 Accepted: 14th Jun 2014 Research Article EFFECT OF AMLODIPINE AND INDOMETHACIN IN ELECTRICAL AND PICROTOXIN INDUCED CONVULSIONS IN MICE *Jagathi Devi N1, Prasanna V2 1Assistant Professor, 2Professor and Head, Department of Pharmacology, Osmania Medical College, Hyderabad *Corresponding author email: [email protected] ABSTRACT Background and Objectives: Antiepileptic drugs (AEDs) are the drugs used in the treatment of epilepsy. Many AEDs have been developed, but the ideal AED which can not only prevent but also abolish seizures by correcting the underlying pathophysiology is still not in sight. Calcium channel blockers (CCBs) may form such a group, as the initiation of epileptogenic activity in the neuron is connected with a phenomenon known as “intrinsic burst firing” which is activated by inward calcium current. In this study, Amlodipine, a CCB of the dihydropyridine class was evaluated for its anticonvulsant activity in mice. It was compared with Phenytoin sodium, one of the oldest anti epileptic drugs. Amlodipine was also combined with Indomethacin, a conventional NSAID, to look for any potentiating effect of this prostaglandin-synthesis inhibitor. Materials and Methods: A total of 48 adult Swiss albino mice of either sex weighing 20-30 G were used for this study; 48 were divided into 8 groups, each group containing 6 mice. Group 1-4 MES (50 m Amp for 0.1 secs) induced convulsion method, Group 5-8 evaluated by using the chemo-convulsant, picrotoxin (0.7 mg / kg). -
Sharon R. Roseman, MD, FACP Practice Limited to Gastroenterology
Sharon R. Roseman, MD, FACP Practice Limited to Gastroenterology 701 Broad Street, Suite 411 Sewickley, PA 15143 (412) 749-7160 Fax: (412) 749-7388 http://www.heritagevalley.org/sharonrosemanmd Patient Drug Education for Diltiazem / Nifedipine Ointment Diltiazem/Nifedipine ointment is used to help heal anal fissures. The ointment relaxes the smooth muscle around the anus and promotes blood flow which helps heal the fissure (tear). The ointment reduces anal canal pressure, which diminishes pain and spasm. We use a diluted concentration of Diltiazem/Nifedipine compared to what is typically used for heart patients, and this is why you need to obtain the medication from a pharmacy which will compound your prescription. It is also prescribed to treat anal sphincter spasm, painful hemorrhoids and pelvic floor spasm. The Diltiazem/Nifedipine ointment should be applied 3 times per day, or as directed. A pea-sized drop should be placed on the tip of your finger and then gently placed inside the anus. The finger should be inserted 1/3 – 1/2 its length and may be covered with a plastic glove or finger cot. You may use Vaseline ® to help coat the finger or dilute the ointment. (If you are unable or hesitant to use your finger to administer the ointment TELL U S and we will order you a suppository to use as an “applicator”.) If you are advised to mix the Diltiazem/Nifedipine with steroid ointment, limit the steroids to one to two weeks. The first few applications should be taken lying down, as mild light- headedness or a brief headache may occur. -
Neurochemical Mechanisms Underlying Alcohol Withdrawal
Neurochemical Mechanisms Underlying Alcohol Withdrawal John Littleton, MD, Ph.D. More than 50 years ago, C.K. Himmelsbach first suggested that physiological mechanisms responsible for maintaining a stable state of equilibrium (i.e., homeostasis) in the patient’s body and brain are responsible for drug tolerance and the drug withdrawal syndrome. In the latter case, he suggested that the absence of the drug leaves these same homeostatic mechanisms exposed, leading to the withdrawal syndrome. This theory provides the framework for a majority of neurochemical investigations of the adaptations that occur in alcohol dependence and how these adaptations may precipitate withdrawal. This article examines the Himmelsbach theory and its application to alcohol withdrawal; reviews the animal models being used to study withdrawal; and looks at the postulated neuroadaptations in three systems—the gamma-aminobutyric acid (GABA) neurotransmitter system, the glutamate neurotransmitter system, and the calcium channel system that regulates various processes inside neurons. The role of these neuroadaptations in withdrawal and the clinical implications of this research also are considered. KEY WORDS: AOD withdrawal syndrome; neurochemistry; biochemical mechanism; AOD tolerance; brain; homeostasis; biological AOD dependence; biological AOD use; disorder theory; biological adaptation; animal model; GABA receptors; glutamate receptors; calcium channel; proteins; detoxification; brain damage; disease severity; AODD (alcohol and other drug dependence) relapse; literature review uring the past 25 years research- science models used to study with- of the reasons why advances in basic ers have made rapid progress drawal neurochemistry as well as a research have not yet been translated Din understanding the chemi- reluctance on the part of clinicians to into therapeutic gains and suggests cal activities that occur in the nervous consider new treatments. -
Antagonism of Lidocaine Inhibition by Open-Channel Blockers That Generate Resurgent Na Current
4976 • The Journal of Neuroscience, March 13, 2013 • 33(11):4976–4987 Cellular/Molecular Antagonism of Lidocaine Inhibition by Open-Channel Blockers That Generate Resurgent Na Current Jason S. Bant,1,3 Teresa K. Aman,2,3 and Indira M. Raman1,2,3 1Interdepartmental Biological Sciences Program, 2Northwestern University Interdepartmental Neuroscience Program, and 3Department of Neurobiology, Northwestern University, Evanston, Illinois 60208 Na channels that generate resurgent current express an intracellular endogenous open-channel blocking protein, whose rapid binding upon depolarization and unbinding upon repolarization minimizes fast and slow inactivation. Na channels also bind exogenous com- pounds, such as lidocaine, which functionally stabilize inactivation. Like the endogenous blocking protein, these use-dependent inhibi- tors bind most effectively at depolarized potentials, raising the question of how lidocaine-like compounds affect neurons with resurgent Na current. We therefore recorded lidocaine inhibition of voltage-clamped, tetrodotoxin-sensitive Na currents in mouse Purkinje neu- rons, which express a native blocking protein, and in mouse hippocampal CA3 pyramidal neurons with and without a peptide from the   cytoplasmic tail of NaV 4 (the 4 peptide), which mimics endogenous open-channel block. To control channel states during drug exposure, lidocaine was applied with rapid-solution exchange techniques during steps to specific voltages. Inhibition of Na currents by lidocaine was diminished by either the 4 peptide or the native blocking protein. In peptide-free CA3 cells, prolonging channel opening with a site-3 toxin, anemone toxin II, reduced lidocaine inhibition; this effect was largely occluded by open-channel blockers, suggesting that lidocaine binding is favored by inactivation but prevented by open-channel block. -
Amitriptyline Hydrochloride 2%, Gabapentin 6%, Lidocaine Hydrochloride 0.5% FIN F 008 269 Formula Oral Mucoadhesive Rinse (Solution, 100 Ml)
MEDISCA® NETWORK INC. TECHNICAL SUPPORT SERVICES FORMULATION CHEMISTRY DEPARTMENT TOLL-FREE: 866-333-7811 TELEPHONE: 514-905-5096 FAX: 514-905-5097 [email protected] 4/7/2020; Page 1 Suggested Amitriptyline Hydrochloride 2%, Gabapentin 6%, Lidocaine Hydrochloride 0.5% FIN F 008 269 Formula Oral Mucoadhesive Rinse (Solution, 100 mL) SUGGESTED FORMULATION Lot Expiry Ingredient Listing Qty. Unit NDC # Supplier Number Date Amitriptyline Hydrochloride, USP 2.000 g Gabapentin, USP 6.000 g Lidocaine Hydrochloride, USP TBD Potassium Sorbate, NF 0.10 g Stevia Powder 0.10 g Menthol (Crystals) (Levorotatory) 0.02 g (Natural), USP Alcohol (95%), USP 5.0 mL NovaFilm™ 30.0 mL Purified Water, USP 50.0 mL Purified Water, USP q.s. to 100.0 mL Sodium Hydroxide 10% Solution As required MEDISCA® NETWORK INC. TECHNICAL SUPPORT SERVICES FORMULATION CHEMISTRY DEPARTMENT TOLL-FREE: 866-333-7811 TELEPHONE: 514-905-5096 FAX: 514-905-5097 [email protected] 4/7/2020; Page 2 Suggested Amitriptyline Hydrochloride 2%, Gabapentin 6%, Lidocaine Hydrochloride 0.5% FIN F 008 269 Formula Oral Mucoadhesive Rinse (Solution, 100 mL) SPECIAL PREPARATORY CONSIDERATIONS Ingredient-Specific Information Light Sensitive (protect from light whenever possible): Amitriptyline Hydrochloride, Gabapentin Hygroscopic (protect from moisture whenever possible): Stevia Powder Narrow Therapeutic Index Lidocaine Hydrochloride Suggested Preparatory Guidelines ■ Non-Sterile Preparation □ Sterile Preparation Processing Error / To account for processing error and pH testing considerations during preparation, it is Testing Considerations: suggested to measure an additional 3 to 5% of the required quantities of ingredients. Special Instruction: This formula may contain one or more Active Pharmaceutical Ingredients (APIs) that may be classified as hazardous, please refer & verify the current NIOSH list of Antineoplastic and Other Hazardous Drugs in Healthcare Settings, 2016. -
A 12-Years Rectal Bleeding Complicated with Deep Vein Thrombosis, Is Hemorrhoid the Real Cause?
Case Report Clinical Case Reports Volume 10:11, 2020 DOI: 10.37421/jccr.2020.10.1395 ISSN: 2165-7920 Open Access A 12-Years Rectal Bleeding Complicated with Deep Vein Thrombosis, Is Hemorrhoid the Real Cause? Yi-Qun Zhang, Meng Niu and Chun-Xiao Chen* Department of Gastroenterology, First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, P. R. China Abstract Colorectal venous malformation is a rare condition that can cause massive rectal bleeding. This is the first report of colorectal venous malformation complicated with massive bleeding and lowers limb deep vein thrombosis, and the two life-threatening conditions were both treated successfully. Keywords: Colorectal venous malformation • Rectal bleeding • Sclerotherapy • Deep vein thrombosis Introduction A 16-year-old man presented to the clinic with long-standing recurrent hematochezia and profound anemia. Per the mother, his rectal bleeding was first noticed around the age of 4 with one episode per 2-3 months that was diagnosed as hemorrhoids without specific treatment. It had worsened for 2 months with progression to 1 bloody bowel movement daily. He had no family history of hematologic disorders or vascular anomalies. The patient had accepted 600 ml red-blood cell perfusion and intravenous sucrose-iron transfusions for severe anemia with hemoglobin 5.8 g/dL, hematocrit 25.9% and MCV 69.7 fL at local hospital. Case Report Upon admission, the patient’s vital signs were within normal limits. His abdomen was supple and without tenderness. Digital rectal examination confirmed partially thrombosed, circumferential mixed hemorrhoids. Laboratory tests revealed a hemoglobin 8.0 g/L and D-dimer 15760 g/L. -
The Effects of Lidocaine and Mefenamic Acid on Post-Episiotomy
Shiraz E-Med J. 2016 March; 17(3):e36286. doi: 10.17795/semj36286. Published online 2016 March 27. Research Article The Effects of Lidocaine and Mefenamic Acid on Post-Episiotomy Pain: A Comparative Study Masoumeh Delaram,1,* Lobat Jafar Zadeh,2 and Sahand Shams3 1Faculty of Nursing and Midwifery, Shahrekord University of Medical Sciences, Shahrekord, IR Iran 2Faculty of Medicine, Shahrekord University of Medical Sciences, Shahrekord, IR Iran 3Faculty of Veterinary Medicine, Shahrekord University, Shahrekord, IR Iran *Corresponding author: Masoumeh Delaram, Faculty of Nursing and Midwifery, Shahrekord University of Medical Sciences, Shahrekord, IR Iran. Tel: +98-3813335648, Fax: +98-3813346714, E-mail: [email protected] Received 2016 January 13; Revised 2016 February 29; Accepted 2016 March 04. Abstract Background: Most women suffer pain following an episiotomy and oral non-steroidal anti-inflammatory drugs are commonly used for pain relief. Due to the gastrointestinal side effects of oral drugs, it seems that women are more accepting of topical medications for pain relief. Objectives: Therefore, the aim of this study was to compare the effects of lidocaine and mefenamic acid on post-episiotomy pain. Patients and Methods: This clinical trial was carried out in 2011. It involved sixty women with singleton pregnancy who were given an episiotomy at 38 to 42 weeks of gestation. The participants were randomly divided into two groups. One group received 2% lido- caine cream (n = 30), while the other group received 250 mg of mefenamic acid (n = 30). The data were collected via a questionnaire and a visual analog scale. Pain intensity was compared from the first complaint by the mother and at 6, 12, and 24 hours after the delivery in both groups.