Anatomical Classification Guidelines V2020 EPHMRA ANATOMICAL
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
125559Orig1s000
CENTER FOR DRUG EVALUATION AND RESEARCH APPLICATION NUMBER: 125559Orig1s000 PHARMACOLOGY REVIEW(S) Tertiary Pharmacology/Toxicology Review Date: July 14, 2015 From: Timothy J. McGovern, Ph.D., ODE Associate Director for Pharmacology and Toxicology, OND IO BLA: 125559 Agency receipt date: November 24, 2014 Drug: PRALUENT (alirocumab) Sponsor: Sanofi-Aventis U.S. LLC Indication: Adult patients with primary hypercholesterolemia (non-familial and heterozygous familial) or mixed dyslipidemia Reviewing Division: Division of Metabolism and Endocrinology Products Introductory Comments: The pharmacology/toxicology reviewer and supervisor concluded that the nonclinical data support approval of PRALUENT (alirocumab) for the indication listed above. Alirocumab is a human IgG1 monoclonal antibody that binds to human PCSK9 (Proprotein Convertase Subtilisin Kexin Type 9). The recommended Established Pharmacologic Class for alirocumab is PCSK9 inhibitor antibody. There are no approved products in this class currently. An appropriate nonclinical program was conducted by the sponsor to support approval of alirocumab. Alirocumab elicited expected pharmacological responses in rats, hamsters, and monkeys; alirocumab lowered total cholesterol and LDL-cholesterol in the species tested and decreased HDL-cholesterol in rats and hamsters. The primary nonclinical toxicity studies of alirocumab were conducted in rats and monkeys for up to 6 months duration with weekly subcutaneous and intravenous dosing. No significant adverse findings were observed at the doses tested which achieved exposure multiples up to 11-fold in rats and 103-fold in monkeys compared to the maximum recommended human dose of 150 mg alirocumab administered subcutaneously once every two weeks. Findings in the liver and adrenal glands of rats were associated with exaggerated pharmacologic effects. -
Angiotensin-Converting Enzyme Inhibitors Or Angiotensin II Receptor Blockers and the Risk of Developing Rheumatoid Arthritis in Antihypertensive Drug Users
Jong, H.J.I. de, Vandebriel, R.J., Saldi, S.R.F., Dijk, L. van, Loveren, H. van, Cohen Tervaert, J.W., Klungel, O.H. Angiotensin-converting enzyme inhibitors or angiotensin II receptor blockers and the risk of developing rheumatoid arthritis in antihypertensive drug users. Pharmacoepidemiology and Drug Safety: 2012, 21(8), 835-843 Postprint Version 1.0 Journal website http://dx.doi.org/10.1002/pds.3291 Pubmed link http://www.ncbi.nlm.nih.gov/pubmed/22674737 DOI 10.1002/pds.3291 This is a NIVEL certified Post Print, more info at http://www.nivel.eu Angiotensin-converting enzyme inhibitors or angiotensin II receptor blockers and the risk of developing rheumatoid arthritis in antihypertensive drug users†‡ HILDA J. I. DE JONG1,2,3, ROB J. VANDEBRIEL1, SITI R. F. SALDI3, LISET VAN DIJK4, HENK VAN LOVEREN1,2, JAN WILLEM COHEN TERVAERT5, OLAF H. KLUNGEL3,* ABSTRACT Purpose: Angiotensin-converting enzyme (ACE) inhibitors and angiotensin II receptor blockers (ARBs) are effective in the treatment of cardiovascular disease. Next to effects on hypertension and cardiac function, these drugs have anti-inflammatory and immunomodulating properties which may either facilitate or protect against the development of autoimmunity, potentially resulting in autoimmune diseases. Therefore, we determined in the current study the association between ACE inhibitor and ARB use and incident rheumatoid arthritis (RA). Methods: A matched case–control study was conducted among patients treated with antihypertensive drugs using the Netherlands Information Network of General Practice (LINH) database in 2001–2006. Cases were patients with a first-time diagnosis of RA. Each case was matched to five controls for age, sex, and index date, which was selected 1 year before the first diagnosis of RA. -
Abstracts from the 5Th World Psoriasis & Psoriatic Arthritis Conference 2018
ISSN 0001-5555 ActaDV Volume 98 2018 Supplement No. 219 ADVANCES IN DERMATOLOGY AND VENEREOLOGY A Non-profit International Journal for Interdisciplinary Skin Research, Clinical and Experimental Dermatology and Sexually Transmitted Diseases Abstracts from the 5th World Psoriasis & Psoriatic Arthritis Conference 2018 Official Journal of June 27–30, 2018 - European Society for Dermatology and Psychiatry Affiliated with Stockholm, Sweden - The International Forum for the Study of Itch Immediate Open Access Acta Dermato-Venereologica www.medicaljournals.se/adv DV cta A enereologica V ermato- D cta A DV cta A dvances in dermatology and venereology A Abstracts from the 5th World Psoriasis & Psoriatic Arthritis Conference 2018 www.medicaljournals.se/acta doi: 10.2340/00015555-2978 Journal Compilation © 2018 Acta Dermato-Venereologica. Acta Derm Venereol 2018; Suppl 219 2 5th World Psoriasis & Psoriatic Arthritis Conference 2018 Ref.no Title Biomarkers and Imaging 001 A metagenomics study of the elbow of psoriasis subjects and their healthy relatives Clinical phenotypes 002 Nail disorders in patients with Psoriasis vulgaris 003 Psoriasis hidden in Gottron’s papules Comorbidities 004 Characteristics of psoriasis in obese patients versus non-obese patients; a multicenter study 005 Psoriasis and comorbidity 006 Risk of periodontal disease in patients with chronic plaque psoriasis 007 Splenomegaly and Psoriasis - A case report 008 Psoriasis as predictor for cardiovascular and metabolic comorbidity in middle-aged women 009 A Case of Concurrent Psoriasis and Vitiligo 010 Successful long-term double disease control by adalimumab in a patient with psoriasis vulgaris and hidradenitis suppurativa 011 Clinical and epidemiological caracterization of psoriasis and psoriatic arthritis on a multidisciplinary assesment model. -
No Name of Drug Branded/Generic Drug Class 1 Acipimox Capsule 250Mg Olbetam Nicotinic Acid 1.50 2.14 2 Atorvastatin Calcium 10Mg
MEDICATIONS FOR TREATMENT OF HIGH BLOOD LIPIDS (HYPERLIPIDEMIA) PRICE RANGE (S$) PER NO NAME OF DRUG BRANDED/GENERIC DRUG CLASS TABLET/ CAPSULE/ SACHET 1 ACIPIMOX CAPSULE 250MG OLBETAM NICOTINIC ACID 1.50 - 2.14 STATIN & CALCIUM 4.40 - 4.90 2 ATORVASTATIN CALCIUM 10MG AMLODIPINE BESYLATE 10MG TABLET CADUET CHANNEL BLOCKERS STATIN & CALCIUM 3.88 - 4.00 3 ATORVASTATIN CALCIUM 10MG AMLODIPINE BESYLATE 5MG TABLET CADUET CHANNEL BLOCKERS STATIN & CALCIUM 4.33 - 4.90 4 ATORVASTATIN CALCIUM 20MG AMLODIPINE BESYLATE 10MG TABLET CADUET CHANNEL BLOCKERS STATIN & CALCIUM 4.05 - 4.80 5 ATORVASTATIN CALCIUM 20MG AMLODIPINE BESYLATE 5MG TABLET CADUET CHANNEL BLOCKERS 6 ATORVASTATIN CALCIUM 10MG LIPITOR STATIN 2.60 - 2.60 7 ATORVASTATIN CALCIUM 20MG LIPITOR STATIN 2.99 - 3.00 8 ATORVASTATIN CALCIUM 40MG LIPITOR STATIN 4.10 - 8.20 9 ATORVASTATIN CALCIUM 80MG LIPITOR STATIN 8.45 - 8.95 10 BEZAFIBRATE SR TABLET 400MG BEZALIP FIBRATES 0.00 - 0.00 11 CHOLESTYRAMINE 4G/SACHET GENERIC FIBRATES 1.35 - 2.25 12 CIPROFIBRATE TABLET 100MG MODALIM FIBRATES 1.60 - 1.75 13 FENOFIBRATE CAPSULE 200MG APO-FENO-MICRO FIBRATES 0.71 - 1.07 14 FENOFIBRATE CAPSULE 200MG LIPANTHYL FIBRATES 1.45 - 1.45 15 FENOFIBRATE CAPSULE 145MG LIPANTHYL PENTA 145 FIBRATES 1.75 - 2.05 16 FENOFIBRATE TABLET 160MG LIPANTHYL SUPRA 160 FIBRATES 1.45 - 1.45 17 FLUVASTATIN SODIUM CAPSULE 20MG LESCOL STATIN 1.85 - 1.86 18 FLUVASTATIN SODIUM CAPSULE 40MG LESCOL STATIN 3.29 - 3.39 19 FLUVASTATIN SODIUM CAPSULE 80MG LESCOL XL STATIN 3.60 - 3.93 20 GEMFIBROZIL CAPSULES 300MG GENERIC-IPOLIPID FIBRATES -
(12) United States Patent (10) Patent No.: US 9,498,481 B2 Rao Et Al
USOO9498481 B2 (12) United States Patent (10) Patent No.: US 9,498,481 B2 Rao et al. (45) Date of Patent: *Nov. 22, 2016 (54) CYCLOPROPYL MODULATORS OF P2Y12 WO WO95/26325 10, 1995 RECEPTOR WO WO99/O5142 2, 1999 WO WOOO/34283 6, 2000 WO WO O1/92262 12/2001 (71) Applicant: Apharaceuticals. Inc., La WO WO O1/922.63 12/2001 olla, CA (US) WO WO 2011/O17108 2, 2011 (72) Inventors: Tadimeti Rao, San Diego, CA (US); Chengzhi Zhang, San Diego, CA (US) OTHER PUBLICATIONS Drugs of the Future 32(10), 845-853 (2007).* (73) Assignee: Auspex Pharmaceuticals, Inc., LaJolla, Tantry et al. in Expert Opin. Invest. Drugs (2007) 16(2):225-229.* CA (US) Wallentin et al. in the New England Journal of Medicine, 361 (11), 1045-1057 (2009).* (*) Notice: Subject to any disclaimer, the term of this Husted et al. in The European Heart Journal 27, 1038-1047 (2006).* patent is extended or adjusted under 35 Auspex in www.businesswire.com/news/home/20081023005201/ U.S.C. 154(b) by Od en/Auspex-Pharmaceuticals-Announces-Positive-Results-Clinical M YW- (b) by ayS. Study (published: Oct. 23, 2008).* This patent is Subject to a terminal dis- Concert In www.concertpharma. com/news/ claimer ConcertPresentsPreclinicalResultsNAMS.htm (published: Sep. 25. 2008).* Concert2 in Expert Rev. Anti Infect. Ther. 6(6), 782 (2008).* (21) Appl. No.: 14/977,056 Springthorpe et al. in Bioorganic & Medicinal Chemistry Letters 17. 6013-6018 (2007).* (22) Filed: Dec. 21, 2015 Leis et al. in Current Organic Chemistry 2, 131-144 (1998).* Angiolillo et al., Pharmacology of emerging novel platelet inhibi (65) Prior Publication Data tors, American Heart Journal, 2008, 156(2) Supp. -
Ontario Drug Benefit Formulary Edition 43
Ministry of Health and Long-Term Care Ontario Drug Benefit Formulary/Comparative Drug Index Edition 43 Drug Programs Policy and Strategy Branch Ontario Public Drug Programs Ministry of Health and Long-Term Care Effective February 28, 2018 Visit Formulary Downloads: Edition 43 Table of Contents Part I Introduction ....................................................................................................... I.1 Part II Preamble .......................................................................................................... II.1 Part III-A Benefits List ........................................................................................... III-A.1 Part III-B Off-Formulary Interchangeable Drugs (OFI) ........................................ III-B.1 Part IV Section Currently Not In Use ......................................................................... IV Part V Index of Pharmacologic-Therapeutic Classification .................................... V.1 Part VI-A Facilitated Access - HIV/AIDS .............................................................. VI-A.1 Part VI-B Facilitated Access - Palliative Care ..................................................... VI-B.1 Part VI-C Temporary Facilitated Access - Rheumatology ................................. VI-C.1 Part VII Trillium Drug Program ................................................................................ VII.1 Part VIII Exceptional Access Program (EAP) ........................................................ VIII.1 Part IX-A Nutrition Products ................................................................................ -
Lipid-Lowering Therapy and Low-Density Lipoprotein Cholesterol
Kristensen et al. BMC Cardiovascular Disorders (2020) 20:336 https://doi.org/10.1186/s12872-020-01616-9 RESEARCH ARTICLE Open Access Lipid-lowering therapy and low-density lipoprotein cholesterol goal attainment after acute coronary syndrome: a Danish population-based cohort study Marie Skov Kristensen1, Anders Green2,3, Mads Nybo4, Simone Møller Hede2, Kristian Handberg Mikkelsen5, Gunnar Gislason1,6,7,8, Mogens Lytken Larsen9 and Annette Kjær Ersbøll1* Abstract Background: Patients with acute coronary syndrome (ACS) are at high risk of recurrent cardiovascular (CV) event. The European guidelines recommend low-density lipoprotein cholesterol (LDL-C) levels < 1.8 mmol/L and early initiation of intensive lipid-lowering therapy (LLT) to reduce CV risk. In order to reduce the risk of further cardiac events, the study aimed to evaluate LDL-C goal attainment and LLT intensity in an incident ACS population. Methods: A cohort study of patients with residency at Funen in Denmark at a first-ever ACS event registered within the period 2010–2015. Information on LLT use and LDL-C levels was extracted from national population registers and a Laboratory database at Odense University Hospital. Treatments and lipid patterns were evaluated during index hospitalization, at 6-month and 12-month follow-up. Results: Among 3040 patients with an LDL-C measurement during index hospitalization, 40.7 and 39.0% attained the recommended LDL-C target value (< 1.8 mmol/L) within 6- and 12-month follow-up, respectively. During 6- and 12-month follow-up, a total of 89.2% (20.2%) and 88.4% (29.7%) used LLT (intensive LLT). -
The In¯Uence of Medication on Erectile Function
International Journal of Impotence Research (1997) 9, 17±26 ß 1997 Stockton Press All rights reserved 0955-9930/97 $12.00 The in¯uence of medication on erectile function W Meinhardt1, RF Kropman2, P Vermeij3, AAB Lycklama aÁ Nijeholt4 and J Zwartendijk4 1Department of Urology, Netherlands Cancer Institute/Antoni van Leeuwenhoek Hospital, Plesmanlaan 121, 1066 CX Amsterdam, The Netherlands; 2Department of Urology, Leyenburg Hospital, Leyweg 275, 2545 CH The Hague, The Netherlands; 3Pharmacy; and 4Department of Urology, Leiden University Hospital, P.O. Box 9600, 2300 RC Leiden, The Netherlands Keywords: impotence; side-effect; antipsychotic; antihypertensive; physiology; erectile function Introduction stopped their antihypertensive treatment over a ®ve year period, because of side-effects on sexual function.5 In the drug registration procedures sexual Several physiological mechanisms are involved in function is not a major issue. This means that erectile function. A negative in¯uence of prescrip- knowledge of the problem is mainly dependent on tion-drugs on these mechanisms will not always case reports and the lists from side effect registries.6±8 come to the attention of the clinician, whereas a Another way of looking at the problem is drug causing priapism will rarely escape the atten- combining available data on mechanisms of action tion. of drugs with the knowledge of the physiological When erectile function is in¯uenced in a negative mechanisms involved in erectile function. The way compensation may occur. For example, age- advantage of this approach is that remedies may related penile sensory disorders may be compen- evolve from it. sated for by extra stimulation.1 Diminished in¯ux of In this paper we will discuss the subject in the blood will lead to a slower onset of the erection, but following order: may be accepted. -
Statins and Lipid Lowering Agents
CARDIOVASCULAR Z/Ks^h>ZZh'^͗ ^dd/E^E>/W/>KtZ/E''Ed^ /E^d/Ɛ EEZd/Ɛ W/Ɛ x/d'Zs/Z ;ŝŬƚĂƌǀLJͿ x>s/d'Zs/Zͬ x KZs/Z/E ;WŝĨĞůƚƌŽ͕ x &s/ZE ;^ƵƐƚŝǀĂ͕ ŽŽƐƚĞĚǁŝƚŚƌŝƚŽŶĂǀŝƌ xK>hd'Zs/Z ;dŝǀŝĐĂLJ͕ K//^dd ;^ƚƌŝďŝůĚ͕ ĞůƐƚƌŝŐŽͿ ƚƌŝƉůĂͿ ;EŽƌǀŝƌͿŽƌĐŽďŝĐŝƐƚĂƚ dƌŝƵŵĞƋ͕:ƵůƵĐĂ͕ŽǀĂƚŽͿ 'ĞŶǀŽLJĂͿ x Z/>W/s/Z/E ;ĚƵƌĂŶƚ͕ x dZs/Z/E ;/ŶƚĞůĞŶĐĞͿ xdEs/Z ;ZĞLJĂƚĂnj͕ xZ>d'Zs/Z ŽŵƉůĞƌĂ͕KĚĞĨƐĞLJ͕ x Es/ZW/E ǀŽƚĂnjͿ ;/ƐĞŶƚƌĞƐƐͿ :ƵůƵĐĂͿ ;sŝƌĂŵƵŶĞͿ xZhEs/Z ;WƌĞnjŝƐƚĂ͕ WƌĞnjĐŽďŝdž͕^LJŵƚƵnjĂͿ x>KW/Es/Z ;<ĂůĞƚƌĂͿ ^dd/E^ xƚŽƌǀĂƐƚĂƚŝŶ WŽƚĞŶƚŝĂůĨŽƌ nƐƚĂƚŝŶ WŽƚĞŶƚŝĂůĨŽƌ pƐƚĂƚŝŶ WŽƚĞŶƚŝĂůĨŽƌ nƐƚĂƚŝŶ͘hƐĞ ;>ŝƉŝƚŽƌͿ ůŽǁĞƐƚƐƚĂƚŝŶĚŽƐĞƉŽƐƐŝďůĞ ;ŵĂdžŝŵƵŵϮϬŵŐ ĂƚŽƌǀĂƐƚĂƚŝŶĚĂŝůLJͿ͘ xZŽƐƵǀĂƐƚĂƚŝŶ WŽƚĞŶƚŝĂůĨŽƌ nƐƚĂƚŝŶ WŽƚĞŶƚŝĂůĨŽƌ nƐƚĂƚŝŶ͘hƐĞ ;ƌĞƐƚŽƌͿ ůŽǁĞƐƚƐƚĂƚŝŶĚŽƐĞƉŽƐƐŝďůĞ ;ŵĂdžŝŵƵŵϭϬŵŐ ƌŽƐƵǀĂƐƚĂƚŝŶĚĂŝůLJͿ͘ xWŝƚĂǀĂƐƚĂƚŝŶ ;>ŝǀĂůŽͿ xWƌĂǀĂƐƚĂƚŝŶ WŽƚĞŶƚŝĂůĨŽƌ nƐƚĂƚŝŶ WŽƚĞŶƚŝĂůĨŽƌ nƐƚĂƚŝŶ ;WƌĂǀĂĐŚŽůͿ x>ŽǀĂƐƚĂƚŝŶ WŽƚĞŶƚŝĂůĨŽƌ nƐƚĂƚŝŶĂŶĚ WŽƚĞŶƚŝĂůĨŽƌ pƐƚĂƚŝŶ WŽƚĞŶƚŝĂůĨŽƌ nƐƚĂƚŝŶĂŶĚ ;DĞǀĂĐŽƌͿ͕ ƚŽdžŝĐŝƚLJ ƚŽdžŝĐŝƚLJ ƐŝŵǀĂƐƚĂƚŝŶ ;ŽĐŽƌͿ CARDIOVASCULAR INSTIs NNRTIs PIs xBICTEGRAVIR (Biktarvy) xELVITEGRAVIR/ x DORAVIRINE (Pifeltro, x EFAVIRENZ (Sustiva, Boosted with ritonavir xDOLUTEGRAVIR (Tivicay, COBICISTAT (Stribild, Delstrigo) Atripla) (Norvir) or cobicistat Triumeq, Juluca) Genvoya) x RILPIVIRINE (Edurant, x ETRAVIRINE (Intelence) xATAZANAVIR (Reyataz, xRALTEGRAVIR Complera, Odefsey, x NEVIRAPINE Evotaz) (Isentress) Juluca) (Viramune) xDARUNAVIR (Prezista, Prezcobix, Symtuza) xLOPINAVIR (Kaletra) FIBRATES xFenofibrate, bezafibrate, gemfibrozil CHOLESTEROL ABSORPTION INHIBITOR xEzetimibe -
Zebrafish Behavioral Profiling Links Drugs to Biological Targets and Rest/Wake Regulation
www.sciencemag.org/cgi/content/full/327/5963/348/DC1 Supporting Online Material for Zebrafish Behavioral Profiling Links Drugs to Biological Targets and Rest/Wake Regulation Jason Rihel,* David A. Prober, Anthony Arvanites, Kelvin Lam, Steven Zimmerman, Sumin Jang, Stephen J. Haggarty, David Kokel, Lee L. Rubin, Randall T. Peterson, Alexander F. Schier* *To whom correspondence should be addressed. E-mail: [email protected] (A.F.S.); [email protected] (J.R.) Published 15 January 2010, Science 327, 348 (2010) DOI: 10.1126/science.1183090 This PDF file includes: Materials and Methods SOM Text Figs. S1 to S18 Table S1 References Supporting Online Material Table of Contents Materials and Methods, pages 2-4 Supplemental Text 1-7, pages 5-10 Text 1. Psychotropic Drug Discovery, page 5 Text 2. Dose, pages 5-6 Text 3. Therapeutic Classes of Drugs Induce Correlated Behaviors, page 6 Text 4. Polypharmacology, pages 6-7 Text 5. Pharmacological Conservation, pages 7-9 Text 6. Non-overlapping Regulation of Rest/Wake States, page 9 Text 7. High Throughput Behavioral Screening in Practice, page 10 Supplemental Figure Legends, pages 11-14 Figure S1. Expanded hierarchical clustering analysis, pages 15-18 Figure S2. Hierarchical and k-means clustering yield similar cluster architectures, page 19 Figure S3. Expanded k-means clustergram, pages 20-23 Figure S4. Behavioral fingerprints are stable across a range of doses, page 24 Figure S5. Compounds that share biological targets have highly correlated behavioral fingerprints, page 25 Figure S6. Examples of compounds that share biological targets and/or structural similarity that give similar behavioral profiles, page 26 Figure S7. -
Ace Inhibitors (Angiotensin-Converting Enzyme)
Medication Instructions Ace Inhibitors (Angiotensin-Converting Enzyme) Generic Brand Benazepril Lotensin Captopril Capoten Enalapril Vasotec Fosinopril Monopril Lisinopril Prinivil, Zestril Do not Moexipril Univasc Quinapril Accupril stop taking Ramipril Altace this medicine Trandolapril Mavik About this Medicine unless told ACE inhibitors are used to treat both high blood pressure (hypertension) and heart failure (HF). They block an enzyme that causes blood vessels to constrict. This to do so allows the blood vessels to relax and dilate. Untreated, high blood pressure can damage to your heart, kidneys and may lead to stroke or heart failure. In HF, using by your an ACE inhibitor can: • Protect your heart from further injury doctor. • Improve your health • Reduce your symptoms • Can prevent heart failure. Generic forms of ACE Inhibitors (benazepril, captopril, enalapril, fosinopril, and lisinopril) may be purchased at a lower price. There are no “generics” for Accupril, Altace Mavik, and of Univasc. Thus their prices are higher. Ask your doctor if one of the generic ACE Inhibitors would work for you. How to Take Use this drug as directed by your doctor. It is best to take these drugs, especially captopril, on an empty stomach one hour before or two hours after meals (unless otherwise instructed by your doctor). Side Effects Along with needed effects, a drug may cause some unwanted effects. Many people will not have any side effects. Most of these side effects are mild and short-lived. Check with your doctor if any of the following side effects occur: • Fever and chills • Hoarseness • Swelling of face, mouth, hands or feet or any trouble in swallowing or breathing • Dizziness or lightheadedness (often a problem with the first dose) Report these side effects if they persist: • Cough – dry or continuing • Loss of taste, diarrhea, nausea, headache or unusual fatigue • Fast or irregular heartbeat, dizziness, lightheadedness • Skin rash Special Guidelines • Sodium in the diet may cause you to retain fluid and increase your blood pressure. -
Apremilast and Systemic Retinoid Combination Treatment for Moderate to Severe Palmoplantar Psoriasis
CASE LETTER Apremilast and Systemic Retinoid Combination Treatment for Moderate to Severe Palmoplantar Psoriasis Tali Czarnowicki, MD, MSc; B. Peter Rosendorff, PhD; Mark G. Lebwohl, MD copy accumulating evidence suggests that it is accompanied PRACTICE POINTS by a multitude of systemic inflammatory comorbidities.5 • Palmoplantar psoriasis is challenging to treat and is This insight supports the concept of systemic treatment unresponsive to many modalities. for patients with moderate to severe psoriasis. As a • Combination, rotational, and sequential treatment chronic disease, psoriasis requires continuous therapy. approaches may minimize side effects and loss of The treatment approach should focus on achieving efficacy as well as enhance treatment responses. efficacynot and minimizing side effects. These goals can • Apremilast and acitretin combination therapy led to be achieved by combination, rotational, and sequential 90% skin improvement in a case of severe recalcitrant treatment approaches.6 Many therapeutic combinations palmoplantar psoriasis. have proven effective, using beneficially different mecha- nisms of action (MOAs) and toxicity profiles.7 We present a patient with moderate to severe recalcitrant palmo- Doplantar psoriasis who demonstrated improvement with To the Editor: combination therapy. Psoriasis is a chronic inflammatory papulosquamous skin A 50-year-old man presented with palmoplantar pso- disease affecting 2% to 3% of the population.1 Its patho- riasis of 7 years’ duration. His medical history included genesis is multifactorial, consisting of a disrupted skin mild hyperlipidemia treated with atorvastatin. Prior topi- barrier and dysregulated immune activation.2 cal treatments including calcipotriene, betamethasone A wide armamentarium of topical and systemic treat- dipropionate, and tacrolimus ointment did not result in ments targeting different aspects of the disease patho- improvement.