INVESTIGATING the TRANSITION from CHRONIC LOW BACK OR NECK PAIN to WIDESPREAD PAIN and FIBROMYLGIA by Lindsay Lancaster Kindler

Total Page:16

File Type:pdf, Size:1020Kb

INVESTIGATING the TRANSITION from CHRONIC LOW BACK OR NECK PAIN to WIDESPREAD PAIN and FIBROMYLGIA by Lindsay Lancaster Kindler INVESTIGATING THE TRANSITION FROM CHRONIC LOW BACK OR NECK PAIN TO WIDESPREAD PAIN AND FIBROMYLGIA By Lindsay Lancaster Kindler, MSN, RN, CNS A Dissertation Presented to Oregon Health & Science University School of Nursing In partial fulfillment of the requirements for the degree of Doctor of Philosophy April 14, 2009 ii ACKNOWLEDGEMENTS This dissertation research was supported by a National Institute of Nursing Research Institutional National Service Research Award (5 T32 NR007061-15), a National Institute of Nursing Research Individual National Service Research Award (1 F31 NR010301-01), the Oregon Health & Sciences University Dean’s Award for Doctoral Dissertation, the Sigma Theta Tau Beta Psi Research Award, and a University Club Foundation Fellowship Award. The generous funding provided by these institutions enabled the participants of this study to be compensated for their time and energy and allowed me to express my appreciation to several individuals who assisted with testing a subset of these participants for fibromyalgia. This funding also allowed me to present my research twelve times at various regional, national, and international conferences. Equally as important, this financial support paid for necessary research materials and services such as printing and mailing study surveys and invitation letters. Without the support provided to me by these considerate institutions, this research would not have been possible. Lastly, the generous award from the University Club Foundation will help me move into the next phase of my research career; a post-doctoral fellowship at the University of Florida. Although I alone will be receiving this doctoral degree, it should really include the names of the many individuals who made this journey possible. Throughout this program I have come to appreciate how fortunate I have been to have a committee whose primary interest is helping me succeed. Dr. Kim Dupree Jones has consistently been an incredible cheerleader whose faith in me has helped me believe in myself as well. Throughout my work with her, Kim has served as a role model to demonstrate that a woman can be a successful researcher while maintaining a family life and being a kind person to others. Dr. Robert Bennett’s expansive knowledge of the field has piqued my iii own interest in the biological mechanisms of chronic pain and fibromyalgia, pushing me to further my research in this area through a post-doctoral fellowship. Finally, I am grateful to Dr. Nancy Perrin for patiently sharing her statistical expertise, all the while never making me feel inept. Although Nancy’s skills are requested on much higher level projects, she treated me as if my study were just as critical to the advancement of the University. I am grateful to my committee for providing me with the support, expertise, and encouragement necessary to successfully complete this study. Throughout my time in the program I was fortunate enough to work clinically with an incredibly supportive and flexible team of coworkers at the Kaiser Permanente Pain Clinic. Their flexibility allowed me to continue the work that has been the impetus for my research interests and stay connected with the patients whose courage in the face of continuous pain moves us to find better treatments. The Pain Clinic has truly been a second family whose love and support kept me motivated to continue this journey. When I felt unsure of myself as a researcher, my coworkers reminded me that I was a valued clinician and had the ability to develop myself as a researcher as I had done with my clinical work. Their confidence in me has maintained my motivation throughout this journey. Finally, words cannot express the gratitude I feel towards the people who truly deserve this degree, my parents and husband. The support given to me by my parents astonishes me every day. Their unconditional belief in my abilities has allowed me to accomplish things I never thought possible. When I have doubted myself (as can occur regularly in a doctoral program), a simple phone call to them renewed my self confidence as I gain a glimpse of myself through their eyes. They are my biggest, most loyal fans, which has been invaluable throughout my journey. Finally, my husband, iv Travis, has met my seemingly unending journey in school with patience and understanding. He has endured the emotional ups and downs that come with waiting for grant approval, working with the IRB, patient recruitment, months of data entry, and preparation for conferences. He has kindly modified his expectations of a “normal” relationship as he has allowed me to focus on my own career development. And when I informed him of this thing called a post-doc, he put his own vision of our future on hold to support me in this endeavor. He has consistently demonstrated his love by allowing me to partake in the opportunities that advance my career, while placing his needs on the back burner. I am forever indebted to the people who made this journey not only possible, but enjoyable. You have given me an invaluable gift that I will never forget. v ABSTRACT Objectives: Emerging evidence suggests that chronic low back pain, chronic neck pain, widespread pain (WSP), and fibromyalgia (FM) share a common underlying mechanism, namely central sensitization. Research demonstrates that a majority of individuals with WSP and FM and some people with chronic low back or neck pain (termed chronic regional spinal pain, CRSP) exhibit altered pain processing which is characteristic of the neuroplastic changes of central sensitization. Perhaps due to this shared pathophysiology, recent studies have demonstrated that a subset of individuals with chronic low back or neck pain develop WSP and/or FM over time. Less clear are the specific risk factors that predispose a person with chronic low back or neck pain to the development of these widespread pain disorders. The purpose of this study was to determine the frequency with which patients with chronic low back or neck pain develop WSP or FM and to determine the risk factors which place a person at risk for this transition. Knowing the predictive factors for the development of WSP and FM in patients with CRSP is critical in that numerous studies have demonstrated that WSP and FM are associated with more severe clinical outcomes as compared to CRSP. Identifying a group of patients with CRSP who are at a higher risk of developing WSP or FM would provide an opportunity for the nursing and medical community to intervene in this downward trajectory. Methods: 2,256 patients previously seen by a multidisciplinary pain clinic in 2001 or 2002 for evaluation and treatment of a chronic low back or neck pain disorder were invited to participate in this study in 2007. The researchers used data collected on two questionnaires, one completed by the patients in 2001 or 2002 and one sent to them by the study team in 2007. Predictive factors investigated in this study fell broadly into three categories; features thought to influence the development of central sensitization, risk vi factors known to precede WSP and FM, and clinical features that frequently co-occur with WSP and FM. Both questionnaires included a body drawing, allowing the study team to determine which participants, who had CRSP in 2001 or 2002, had developed WSP by 2007. Those participants who had developed WSP by 2007 were invited to undergo an examination to evaluate the presence of a FM diagnosis. The 2001/2002 questionnaire was used to determine participant status on proposed risk factors prior to their development of WSP or FM. Results: Out of the 512 participants who had presented with CRSP in 2001/2002, 114 (22.3%) had developed WSP by 2007. Risk factors present in 2001/2002 that were associated with the development of WSP included moderate or severe pain intensity, female gender, history of abuse, family history of WSP, severe interference with general activity, morbid obesity, having one or more central sensitivity syndromes, and using more pain management strategies. Out of the 23.6% of subjects with WSP who were willing to report to the study site for an examination, 22 (75.9%) were diagnosed with FM. These 22 participants were added to the 18 participants who had been diagnosed with FM by their health plan provider between 2003 and 2007 for a total of 40 study participants who had presented with chronic low back or neck pain in 2001/2002 and developed FM by 2007. Risk factors present in 2001/2002 that were associated with a transition to FM included moderate or severe pain intensity, female gender, history of abuse, having a sibling with WSP, having one or more central sensitivity syndromes, and using more pain management strategies. Risk factors from 2001/2002 that did not significantly predict the development of WSP or FM in these participants with CRSP included depression, age, pain duration, number of back or neck surgeries, number of medication classes used to treat pain, tobacco pack year history, or receipt of disability benefits. vii Conclusions: This study demonstrated that nearly a quarter of patients with CRSP developed WSP over a six-year period. Interestingly, 75.9% if those participants who were willing to be examined also had FM. Several risk factors were shown to be predictive of the development of WSP and FM which allows practitioners to identify a group of patients with CRSP who are at increased risk for progression to a worsening clinical condition. Information gained from this study can guide the management of this group of high risk patients in an attempt to mitigate this progression. The identification of clinical features that are characteristic of this high risk group could also inform future studies that investigate individual differences in pain processing and prospective investigations into the development of other central sensitivity syndromes.
Recommended publications
  • The Relation Between Tender Points and Fibromyalgia Symptom Variables
    268 Annals of the Rheumatic Diseases 1997;56:268–271 CONCISE REPORTS Ann Rheum Dis: first published as 10.1136/ard.56.4.268 on 1 April 1997. Downloaded from The relation between tender points and fibromyalgia symptom variables: evidence that fibromyalgia is not a discrete disorder in the clinic Frederick Wolfe Abstract Fibromyalgia represents the intersection of a Objective—To investigate the relation considerably abnormal and reduced pain between measures of pain threshold and threshold with a series of clinical distress vari- symptoms of distress to determine if ables, including pain, fatigue, sleep distur- fibromyalgia is a discrete construct/ bance, anxiety, and depression, among others. disorder in the clinic. In the clinic, it is best diagnosed by counting Methods—627 patients seen at an the number of tender points a patient has. In outpatient rheumatology centre from 1993 the presence of 11 or more tender points and to 1996 underwent tender point and dolor- widespread pain, fibromyalgia is diagnosed (classified) according to American College of imetry examinations. All completed the Rheumatology (ACR) Criteria.1 assessment scales for fatigue, sleep The ability to diagnose fibromyalgia with disturbance, anxiety, depression, global commonly agreed upon criteria has stimulated severity, pain, functional disability, and a research into basic and clinic aspects of the composite measure of distress con- syndrome. In general, research has used structed from scores of sleep disturbance, ‘normals’ or patients with other rheumatic dis- fatigue, anxiety, depression, and global eases as control subjects. This comparison, of severity—the rheumatology distress index fibromyalgia with such control subjects, (RDI). implies that fibromyalgia is a discrete entity.
    [Show full text]
  • Pain” in the Modern Neurosciences: a Historical Account of the Visualization Technologies Used in the Development of an “Algesiogenic Pathology”, 1850 to 2000
    Brain Sci. 2015, 5, 521-545; doi:10.3390/brainsci5040521 OPEN ACCESS brain sciences ISSN 2076-3425 www.mdpi.com/journal/brainsci/ Review Objectifying “Pain” in the Modern Neurosciences: A Historical Account of the Visualization Technologies Used in the Development of an “Algesiogenic Pathology”, 1850 to 2000 Frank W. Stahnisch Department of Community Health Sciences & Department of History, The University of Calgary, 3280 Hospital Drive NW, Calgary T2N 4Z6, AB, Canada; E-Mail: [email protected]; Tel.: +1-403-210-6290. Academic Editor: Patrick W. Stroman Received: 31 August 2015 / Accepted: 9 November 2015 / Published: 17 November 2015 Abstract: Particularly with the fundamental works of the Leipzig school of experimental psychophysiology (between the 1850s and 1880s), the modern neurosciences witnessed an increasing interest in attempts to objectify “pain” as a bodily signal and physiological value. This development has led to refined psychological test repertoires and new clinical measurement techniques, which became progressively paired with imaging approaches and sophisticated theories about neuropathological pain etiology. With the advent of electroencephalography since the middle of the 20th century, and through the use of brain stimulation technologies and modern neuroimaging, the chosen scientific route towards an ever more refined “objectification” of pain phenomena took firm root in Western medicine. This article provides a broad overview of landmark events and key imaging technologies, which represent the long developmental path of a field that could be called “algesiogenic pathology.” Keywords: pain; history of medicine; Leipzig; Montreal; New York; nineteenth century; precursors to functional neuroimaging of pain; twentieth century “The past of a present-day science is not the same thing as that science in the past.” (Georges Canguilhem) [1] 1.
    [Show full text]
  • Download Article (PDF)
    ORIGINAL CONTRIBUTION Osteopathic manipulative treatment in conjunction with medication relieves pain associated with fibromyalgia syndrome: Results of a randomized clinical pilot project RUSSELL G. GAMBER, DO; JAY H. SHORES, PHD; DAVID P. RUSSO, BA; CYNTHIA JIMENEZ, RN; BENARD R. RUBIN, DO Osteopathic physicians caring for patients with fibro- treatments for FM incorporate nonpharmacologic ap- myalgia syndrome (FM) often use osteopathic manipu- proaches such as OMT. lative treatment (OMT) in conjunction with other forms of (Key words: osteopathic manipulative treatment, standard medical care. Despite a growing body of evi- orthopedic manipulation, fibromyalgia, clinical trials) dence on the efficacy of manual therapy for the treatment of selected acute musculoskeletal conditions, the role of ibromyalgia (FM) syndrome is a common nonarticular, OMT in treating patients with chronic conditions such Frheumatic musculoskeletal pain disorder for which a as FM remains largely unknown. definite cause has yet to be identified.1 Diffuse muscu- Twenty-four female patients meeting American Col- loskeletal pain and aching, the presence of multiple tender lege of Rheumatology criteria for FM were randomly points (TP), disturbed sleep, fatigue, and morning stiffness assigned to one of four treatment groups: (1) manipulation characterize the syndrome. Central to the American College group, (2) manipulation and teaching group, (3) moist of Rheumatology’s FM diagnostic criteria are the presence of heat group, and (4) control group, which received no addi-
    [Show full text]
  • Psychological Interventions for Needle-Related Procedural Pain and Distress in Children and Adolescents (Review)
    Psychological interventions for needle-related procedural pain and distress in children and adolescents (Review) Uman LS, Birnie KA, Noel M, Parker JA, Chambers CT, McGrath PJ, Kisely SR This is a reprint of a Cochrane review, prepared and maintained by The Cochrane Collaboration and published in The Cochrane Library 2013, Issue 10 http://www.thecochranelibrary.com Psychological interventions for needle-related procedural pain and distress in children and adolescents (Review) Copyright © 2013 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd. TABLE OF CONTENTS HEADER....................................... 1 ABSTRACT ...................................... 1 PLAINLANGUAGESUMMARY . 2 BACKGROUND .................................... 2 OBJECTIVES ..................................... 4 METHODS ...................................... 4 RESULTS....................................... 10 Figure1. ..................................... 13 Figure2. ..................................... 14 DISCUSSION ..................................... 17 AUTHORS’CONCLUSIONS . 20 ACKNOWLEDGEMENTS . 21 REFERENCES ..................................... 22 CHARACTERISTICSOFSTUDIES . 33 DATAANDANALYSES. 103 Analysis 1.1. Comparison 1 Distraction, Outcome 1 Self-reportedpain.. 105 Analysis 1.2. Comparison 1 Distraction, Outcome 2 Observer-reported pain. 106 Analysis 1.3. Comparison 1 Distraction, Outcome 3 Self-reported distress. 107 Analysis 1.4. Comparison 1 Distraction, Outcome 4 Observer-reported distress. 107 Analysis 1.5. Comparison 1 Distraction, Outcome
    [Show full text]
  • Advances in Spinal Cord Stimulation
    From DEPT OF CLINICAL NEUROSCIENCE Karolinska Institutet, Stockholm, Sweden ADVANCES IN SPINAL CORD STIMULATION ENHANCEMENT OF EFFICACY, IMPROVED SURGICAL TECHNIQUE AND A NEW INDICATION Göran Lind Stockholm 2012 All previously published papers were reproduced with permission from the publisher. Published by Karolinska Institutet. Printed by Larserics Digital Print AB, Bromma © Göran Lind, 2012 ISBN 978-91-7457-938-3 ABSTRACT Introduction and aim: Spinal cord stimulation (SCS) has been used for treatment of otherwise therapy-resistant chronic neuropathic pain for about four decades. However, 30-40 % of the patients do not benefit from SCS, despite careful case selection and technical advances. In search of ways to improve the outcome mechanisms underlying the pain relieving effect of SCS have been extensively explored. Experimental findings suggest a possibility to enhance the effect of SCS by concomitant intrathecal (i.t.) administration of pharmaceuticals, such as baclofen, clonidine and adenosine. Animal research has indicated that hypersensitivity to colonic dilatation can be attenuated by SCS. This finding, as well as related clinical observations, forms a basis for the possibility of treating irritable bowel syndrome (IBS) with SCS. Implantation of an SCS system with a plate electrode requires extensive surgery. This can be painful and cumbersome for the patient, since finding an optimal electrode position demands patient cooperation with reporting of stimulation evoked sensations. Aims of the thesis were to study: 1) if co-administration of baclofen (Study I and III), clonidine (Study III) or adenosine (Study I) can enhance the effect of SCS, 2) if long-term i.t. administration of a drug will continue to support the effect of SCS over time (Study II), 3) if implantation of plate electrodes can be performed in spinal anesthesia, retaining the possibility for the patient to feel and report stimulation evoked paresthesias and 4) if SCS can be used as a treatment option for IBS, otherwise resistant to therapy.
    [Show full text]
  • Psychological Interventions for Needle-Related Procedural Pain and Distress in Children and Adolescents (Review)
    Psychological interventions for needle-related procedural pain and distress in children and adolescents (Review) Uman LS, Chambers CT, McGrath PJ, Kisely S This is a reprint of a Cochrane review, prepared and maintained by The Cochrane Collaboration and published in The Cochrane Library 2007, Issue 3 http://www.thecochranelibrary.com Psychological interventions for needle-related procedural pain and distress in children and adolescents (Review) 1 Copyright © 2007 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd TABLE OF CONTENTS ABSTRACT ...................................... 1 PLAINLANGUAGESUMMARY . 2 BACKGROUND .................................... 2 OBJECTIVES ..................................... 3 CRITERIA FOR CONSIDERING STUDIES FOR THIS REVIEW . ......... 3 SEARCH METHODS FOR IDENTIFICATION OF STUDIES . ....... 5 METHODSOFTHEREVIEW . 6 DESCRIPTIONOFSTUDIES . 8 METHODOLOGICALQUALITY . 10 RESULTS....................................... 11 DISCUSSION ..................................... 14 AUTHORS’CONCLUSIONS . 16 POTENTIALCONFLICTOFINTEREST . 17 ACKNOWLEDGEMENTS . 17 SOURCESOFSUPPORT . 18 REFERENCES ..................................... 18 TABLES ....................................... 23 Characteristics of included studies . ....... 23 Characteristics of excluded studies . ....... 38 ADDITIONALTABLES. 40 Table 01. Definitions of Medical Procedures . ......... 40 Table02.Distraction . 41 Table 03. Information / Preparation . ........ 41 Table04.Hypnosis . 41 Table05.VirtualReality . 42 Table06.MemoryAlteration. .... 42
    [Show full text]
  • Evidence-Based Management of Acute Musculoskeletal Pain
    cute Neck Pain Acute Neck Pain Acute Neck Pain Acute Neck Pain Acute Neck Pain Acute Neck Pain Acute te Shoulder Pain Acute Shoulder Pain Acute Shoulder Pain Acute Shoulder Pain Acute Shoulder Pain Acute Acute Shoulder Pain Acute Shoulder Pain Acute Shoulder Pain Acute Shoulder Pain Acute Shoulder Pain Ac Acute Thoratic Spinal Pain Acute Thoratic Spinal Pain Acute Thoratic Spinal Pain Acute Thoratic Spinal Acute Thoratic Spinal Pain Acute Thoratic Spinal Pain Acute Thoratic Spinal Pain Acute Thoratic Spinal Pa Acute Thoratic Spinal Pain Acute Thoratic Spinal Pain Acute Thoratic Spinal Pain Acute Thoratic Spinal Acute Thoratic Spinal Pain Acute Thoratic Spinal Pain Acute Thoratic Spinal Pain Acute Thoratic Spinal Pa Acute Thoratic Spinal Pain Acute Thoratic Spinal Pain Acute Thoratic Spinal Pain Acute Thoratic Spinal Acute Thoratic Spinal Pain Acute Thoratic Spinal Pain Acute Thoratic Spinal Pain Acute Thoratic Spinal Pa Acute Thoratic Spinal Pain Acute Thoratic Spinal Pain Acute Thoratic Spinal Pain Acute Thoratic Spinal Acute Low Back Pain Acute Low Back Pain Acute Low Back Pain Acute Low Back Pain Acute Low Back Pain Acute Low Back Pain Acute Low Back Pain Acute Low Back Pain Acute Low Back Pain Acute Lo Back Pain Acute Low Back Pain Acute Low Back Pain Acute Low Back Pain Acute Low Back Pain Acute Anterior Knee Pain Anterior Knee Pain Anterior Knee Pain Anterior Knee Pain Anterior Knee Pain Anterior Anterior Knee Pain Anterior Knee Pain Anterior Knee Pain Anterior Knee Pain v Anterior Knee Pain Ant Anterior Knee Pain Anterior Knee Pain
    [Show full text]
  • Fibromyalgia and Diffuse Myalgia
    RHEUMATOLOGY 1522–5720/05 $15.00 + .00 FIBROMYALGIA AND DIFFUSE MYALGIA James M. Gill, MD, MPH, and Anna Quisel, MD PREVALENCE, PRESENTATION, AND PROGRESSION OF THE PATIENT WITH FIBROMYALGIA Chronic pain is one of the most common complaints encountered by primary care clinicians. Often, patients present not with well localized pain but with diffuse and nonspecific myalgias. Fibromyalgia is the most common etiology for this type of pain. In community-based studies, 2% [1] and 1.2% to 6.2% of school-age children screened positive for fibromyalgia [2–4]. Women and girls are at higher risk than males, and risk increases with age, peaking between 55 and 79 years [1,5]. Persons suffering from fibromyalgia most commonly complain of widespread pain. The pain is usually bilateral and is usually worse in the neck and trunk [6]. Additional symptoms include fatigue, waking unrefreshed, morning stiffness, paresthesias, and headaches [6–12]. Compared with patients with other rheumatologic conditions, persons with fibromyalgia more often suffer from comorbid conditions [13], including chronic fatigue syndrome, migraine headaches, irritable bowel syndrome, irritable bladder symptoms, temporomandibular joint syn- drome, myofascial pain syndrome, restless leg syndrome, and affective disorders [13–15]. Fibromyalgia can cause significant morbidity [1,16,17]. Patients with fibromyalgia require an average of 2.7 drugs at any time for fibromyalgia- related symptoms and have an average of 10 outpatient visits per year, with one hospitalization every 3 years [13]. Fibromyalgia
    [Show full text]
  • Challenges in Pain Assessment: Pain Intensity Scales
    [Downloaded free from http://www.indianjpain.org on Monday, August 18, 2014, IP: 218.241.189.21] || Click here to download free Android application for this journal Review Article Challenges in pain assessment: Pain intensity scales Praveen Kumar, Laxmi Tripathi1 Department of Pharmaceutical Chemistry, Moradabad Educational Trust, Group of Institutions, Moradabad, 1S. D. College of Pharmacy and Vocational Studies, Muzaffarnagar, Uttar Pradesh, India ABSTRACT Pain assessment remains a challenge to medical professionals and received much attention over the past decade. Effective management of pain remains an important indicator of the quality of care provided to patients. Pain scales are useful for clinically assessing how intensely patients are feeling pain and for monitoring the effectiveness of treatments at different points in time. A number of questionnaires have been developed to assess chronic pain. They are mainly used as research tools to assess the effect of a treatment in a clinical trial but may be used in specialist pain clinics. This review comprises the basic information of pain intensity scales and questionnaires. Various pain assessment tools are summarized. Pain assessment and management protocols are also highlighted. Key words: Pain assessment, pain intensity scales, pain assessment tools, pain assessment and management protocols, questionnaires Introduction observational (behavioral), or physiological data [Table 1]. Self-report is considered primary and should French philosopher Simone Weil noted that “Pain is the be obtained if possible. Pain scales are available root of knowledge.” In 1982, singer John Mellencamp for neonates, infants, children, adolescents, adults, proudly sang that it “Hurts so good.” Everywhere, seniors, and persons whose communication is impaired.
    [Show full text]
  • Evidence-Based Management of Acute Musculoskeletal Pain
    RESCINDED This publication was rescinded by National Health and Medical Research Council in 2013 and is available on the Internet ONLY for historical purposes. Important Notice This notice is not to be erased and must be included on any printed version of this publication. This publication was rescinded by the National Health and Medical Research Council in 2013. The National Health and Medical Research Council has made this publication available on its Internet Archives site as a service to the public for historical and research purposes ONLY. Rescinded publications are publications that no longer represent the Council’s position on the matters contained therein. This means that the Council no longer endorses, supports or approves these rescinded publications. The National Health and Medical Research Council gives no assurance as to the accuracy or relevance of any of the information contained in this rescinded publication. The National Health and Medical Research Council assumes no legal liability or responsibility for errors or omissions contained within this rescinded publication for any loss or damage incurred as a result of reliance on this publication. Every user of this rescinded publication acknowledges that the information contained in it may not be accurate, complete or of relevance to the user’s purposes. The user undertakes the responsibility for assessing the accuracy, completeness and relevance of the contents of this rescinded publication, including seeking independent verification of information sought to be relied upon for the user’s purposes. Every user of this rescinded publication is responsible for ensuring that each printed version contains this disclaimer notice, including the date of recision and the date of downloading the archived Internet version.
    [Show full text]
  • Proof and Evaluation of Pain and Suffering in Personal Injury Litigation Jack H
    PROOF AND EVALUATION OF PAIN AND SUFFERING IN PERSONAL INJURY LITIGATION JACK H. OLENDER* PAST, PRESENT AND FUTURE "pain and suffering" are well- recognized elements of damages in personal injury actions.' Medical science in its present state of development offers considerable aid in determining existence of pain resulting from personal injury and in predicting probabilities of future pain. Unfortunately, it is less helpful in establishing the severity of pain and suffering with much precision. Therefore, as would be expected, the problem of evaluating pain and suffering is a difficult one for juries. The current split of authority on the propriety of plaintiff's counsel utilizing mathematical formulae for evaluating pain and suffering in argument before the jury is a result of these inherent difficulties in evaluation of pain. In this article, first the legal theories for evaluating pain and suffer- ing are considered. Then, the nature of pain and methods for its measurement are discussed. Next, the methods of proving pain and suffering are examined, and last, pain and suffering as an element of damages is evaluated. I. WHAT IS PAIN AND SUFFRING "WORTH"? The fact-finder determines what pain and suffering is worth, or, * A.B. 1957, LL.B. 596o, University of Pittsburgh; LL.M. i96i, George Washing- ton University. Member of the District of Columbia Bar. This article is based on a thesis submitted in partial fulfillment of the LL.M. degree requirements at the George Washington University School of Law. The author gratefully acknowledges the helpful guidance of Professor J. Forrester Davison. ' Recovery for past pain and suffering is also allowed in survival actions.
    [Show full text]
  • Role of TRPV1 in Colonic Mucin Production and Gut Microbiota Profile
    bioRxiv preprint doi: https://doi.org/10.1101/2020.04.17.046011; this version posted April 18, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC 4.0 International license. 1 Role of TRPV1 in colonic mucin production and gut microbiota profile 2 Vijay Kumar1,2, Neha Mahajan1,3, Pragyanshu Khare1, Kanthi Kiran Kondepudi1, Mahendra 3 Bishnoi 1# 4 1National Agri-Food Biotechnology Institute (NABI), Knowledge City-Sector 81, SAS 5 Nagar, Punjab 140306, India. 6 2Department of Biotechnology, Panjab University, Sector-25, Chandigarh 160014, India. 7 3Regional Centre for Biotechnology, Faridabad-Gurgaon expressway, Faridabad, Haryana 8 121001, India. 9 Running title: TRPV1 and mucin production 10 #Corresponding author 11 Mahendra Bishnoi, PhD 12 Scientist and Group Leader, TR(I)P for Health Laboratory 13 Department of Food and Nutritional Biotechnology 14 National Agri-Food Biotechnology Institute (NABI), 15 Knowledge City-Sector 81, SAS Nagar, Punjab 140306, India. 16 Email: [email protected]; [email protected] 17 Phone no. +91-172-5220261; +91-9914469090 1 bioRxiv preprint doi: https://doi.org/10.1101/2020.04.17.046011; this version posted April 18, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC 4.0 International license. 18 ABSTRACT 19 PURPOSE: This study focuses on exploring the role of sensory cation channel Transient 20 Receptor Potential channel subfamily Vanilloid 1 (TRPV1) in gut health, specifically mucus 21 secretion and microflora profile in gut.
    [Show full text]