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Textbook Pain Medicine Board Review Anna Woodbury Et Al Ebook All Chapter PDF
Textbook Pain Medicine Board Review Anna Woodbury Et Al Ebook All Chapter PDF
Woodbury Et Al.
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Anna Woodbury, MD
Department ofAnesthesiology
Emory University School ofMedicine
Veterans Afiairs Medical Center
Atlanta, Georgia
Boris Spektor, MD
Department ofAnesthesiology
Emory University School ofMedicine
Atlanta, Georgia
Vinita Singh, MD
Department ofAnesthesiology
Emory University School ofMedicine
Atlanta, Georgia
Brian Bobzien, MD
Department ofAnesthesiology
Emory University School ofMedicine
Grady Memorial Hospital
Atlanta, Georgia
Trusharth Patel, MD
Department ofAnesthesiology
Emory University School ofMedicine
Atlanta, Georgia
Jerry Kalangara, MD
Department ofAnesthesiology
Emory University School ofMedicine
Veterans Aflairs Medical Center
Atlanta, Georgia
ELSEVIER
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Notices
Knowledge and best practice in this field are constantly changing. As new research and experience
broaden our understanding, changes in research methods, professional practices, or medical treat—
ment may become necessary.
Practitioners and researchers must always rely on their own experience and knowledge in evalu—
ating and using any information, methods, compounds, or experiments described herein. In using
such information or methods they should be mindful of their own safety and the safety of others,
including parties for whom they have a professional responsibility.
With respect to any drug or pharmaceutical products identified, readers are advised to check the
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of administration, and contraindications. It is the responsibility of practitioners, relying on their own
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To the fullest extent of the law, neither the Publisher nor the authors, contributors, or editors,
assume any liability for any injury and/ or damage to persons or property as a matter of products li-
ability, negligence or otherwise, or from any use or operation of any methods, products, instructions,
or ideas contained in the material herein.
The field of pain medicine is an ever-developing and expand- This question book is not intended as a stand-alone re-
ing field with an inherently multidisciplinary nature. The source, but as an aid to guide studying and highlight key
field continues to advance with research into newer, safer, points in pain management. It is a companion book to Prac—
and more comprehensive techniques for the management of tical Management of Pain, edited by Honorio Benzon et al.
pain. In the face of a widespread opioid epidemic, physicians Practical Management of Pain stands out as a comprehensive
from a variety of fields have become intensely interested in resource for those interested in the study of pain; it is ap—
nonnarcotic management of acute and chronic pain condi- propriate both for those seeking board certification as well
tions and learning how to appropriately assess opioid risk. As as for those who simply wish to gain a deeper understanding
those who study pain know, there are many varieties of pain of pain and its various treatments. Healthcare practitioners
and many ways to target these individual pain sources and from a variety of fields would benefit from information
interrupt their mechanisms of development. found in these books. In assessing currently available books
This question book highlights some key concepts in the regarding pain medicine for our fellows to use for self-study
pathophysiology and treatment of pain. It was compiled by and board review, we found that most books on the market
physicians from specialties and subspecialties including An— were inadequate and inherently flawed. We therefore en—
esthesiology, Emergency Medicine, Pain Medicine, Pallia- couraged them to read Practical Management of Pain and, as
tive Care, Physical Medicine and Rehabilitation, and Re- a group interested in furthering education and understand-
gional Anesthesia/Acute Pain, and it also includes editors ing regarding pain medicine, came together (fellows and
with expertise and special interests in Cancer Pain, Integra- faculty) to develop a question book based off of this com-
tive Medicine, and Pediatric Pain. Questions were written prehensive text. As such, this question book should be used
primarily by fellows during their subspecialty training at as an adjunct to specifically target areas in need of further
Emory University School of Medicine and reviewed/ edited study, whether for board preparation or simply as a “test
by their attendings. Editors represent four separate institu- your knowledge” guide to accompany Practical Management
tions associated with Emory University School of Medicine, ofPain.
bringing with them a wide range of backgrounds and exper-
tise with diverse patient populations.
vi
Acknowledgments
The editors would like to acknowledge helpful discussions (Emergency Medicine 8: Palliative Care), Lynn O’Neill
and input from their colleagues in multiple departments at (Geriatrics, Internal Medicine & Palliative Care), Michael
Emory University School of Medicine. The multidisciplinary Silver (Neurology), Taylor Harrison (Neurology 8c Electrodi—
pain fellowship at Emory and the development of this book agnostics), Natalie Strickland (Pediatric Pain), Jennifer
could not exist without the willingness and enthusiasm to Steiner (Pain Psychology), Nadine Kaslow (Pain Psychology),
teach that has come from the cohesive groups of individuals Howard Levy (Physical Medicine 8c Rehabilitation), William
within these departments. These departments include Anes- Beckworth (Physical Medicine & Rehabilitation),]ose Garcia
thesiology, Emergency Medicine, Hematology 8c Oncology, (Physical Medicine 8c Rehabilitation), Randy Katz (Occupa—
Interventional Radiology, Neurology, Palliative Care, Physical tional Medicine & Physical Medicine 8c Rehabilitation), Scott
Medicine and Rehabilitation, Primary Care, Psychiatry, Psy- Firestone (Psychiatry), Walter Carpenter (Radiology). And of
chology, Radiology, and many others. Specific individuals de— course, the field would not advance without the aid of those
serving of thanks for their support and their commitment to who have dedicated themselves to advancing research in
medical education include Laureen Hill (Chair, Department pain and neural networks, including Paul Garcia, Wei Huang,
of Anesthesiology), Anne Marie McKenzie—Brown (Director, Vitaly Napadow, Bruce Crosson, Ling Wei, and Shan Ping Yu.
Center for Pain), Colette Curtis (Acute Pain), Tammie Quest
(Emergency Medicine & Palliative Care), Paul Desandre Anna Woodbury, MD
vii
GENERAL CONSIDERATIONS
QUESTIONS
1. Which of the following anesthetics was administered for 3. Which of the following organizations is multidisci-
labor pain to Queen Victoria in 1874 and subsequently plinary, with members including but not limited to
cited as legitimizing analgesia during labor? physicians, dentists, psychologists, nurses, and physical
A. Chloroform therapists?
B. Nitrous oxide A. The American Academy of Pain Medicine (AAPM)
C. Cocaine B. The International Association for the Study of Pain
D. Morphine (IASP)
E. Procaine C. The International Spine Intervention Society
(SIS, formally ISIS)
2. Which of the following theories combines both physical D. The American Society of Interventional Pain
and psychological aspects of pain perception and is Physicians (ASIPP)
credited with revolutionizing pain research? E. The American Society of Regional Anesthesia
A. Pattern Theory (ASRA)
B. Sensory Interaction Theory
C. Gate Control Theory
D. The Fourth Theory of Pain
E. Specificity Theory
ANSWERS
I. A. Queen Victoria was given chloroform byjames Simp- techniques, are based on the Gate Control Theory.
son in 1847 for the delivery of her eighth child, at This theory is cited as ending the debate regarding
which point it became widely accepted that labor pain whether or not the cerebral cortex plays a role in pain.
should be medically managed. Prior to this, it was con— Development of imaging such as PET, fMRI, and
sidered against Christian beliefs to provide or accept SPECT later added credibility to this theory by demon—
analgesia during labor. strating the activation of the cerebral cortex in
response to pain.
2. C. The Gate Control Theory, developed by Melzack
and Wall in 1965, states that nonnociceptive signals 3. B. The International Association for the Study of Pain
can override nociceptive signals, and, as a result, the (IASP) is the largest multidisciplinary international as-
perception of pain is reduced or eliminated. Interven- sociation, with a goal of furthering pain research by in-
tions such as peripheral nerve stimulators, TENS units, tegrating professionals with different backgrounds and
and spinal cord stimulators, as well as biofeedback disciplines.
2 Taxonomy and Classification
of Chronic Pain Syndromes
QUESTIONS
1. The International Association for the Study of Pain D. Serves to exclude new syndromes such as those
(LASP) classification focuses on chronic pain; however, involving painful legs and moving toes
it includes syndromes that are not acute in nature, E. Is entirely psychogenic in nature
including which of the following?
A. Acute herpes zoster . Migraines fall under which of the following diagnostic
B. Burns with spasm categories?
C. Pancreatitis Pain Disorder, Somatoform Persistent
£115.09”?
D. Prolapsed intervertebral disk Pain Disorder, Psychological Origin
E. All of the above Pain Disorder, Malingering
Pain Disorder, Neuropathic
. The classification of chronic pain specifies five axes for Psychological or Behavioral Factor Associated with
describing pain. The second axis is the system most re- Disorders or Disease Classified Elsewhere
lated to the cause of the pain. Which of the following
are systems identified? 7. While defining pain, it is important to recognize that
A. The central, peripheral, and autonomic nervous pain is always a subjective state related to which of the
systems and special senses following?
B. Psychological and social function of the nervous Emotional state
PLUGS”?
3. Which of the following is NOT part of the diagnosis of 8. According to the IASP Taxonomy Committee, chronic
complex somatic symptom disorder? pain is defined as pain that has been present for what
A. Emotional disturbances length of time?
B. Health anxiety 3 months
HUGE”?
ANSWERS
l. E. The LASP (International Association for the Study of based on a theoretical relationship to the sympathetic
Pain) focuses on the classification of chronic pain syn- nervous system.
drome, but includes some acute syndromes for compar-
ison (and because these acute conditions can often be- E. Pain that is due to known or inferred psychophysio-
come chronic). Acute herpes zoster, burns with spasm, logic mechanisms, such as muscle tension pain or mi—
pancreatitis, and prolapsed intervertebral disk are all graines, but is believed to have a psychogenic cause
examples of acute pain syndromes that are included. falls under the ICD-lO classification of Psychological or
Behavioral Factor Associated with Disorders or Disease
. E. The classifications are divided into five axes: (l) ana- Classified Elsewhere.
tomic, (2) system, (3) temporal characteristics and pat-
tern, (4) intensity, (5) etiology. The second axis systems D. The definition of pain by the IASP is “an unpleasant
include (a) central, peripheral, and autonomic nervous sensory and emotional experience associated with ac-
and special senses; (b) psychological and social function; tual or potential tissue damage or described in terms of
(c) respiratory and vascular; (d) musculoskeletal and such damage.” This addresses the situation of patients
connective tissue; (e) cutaneous and subcutaneous tissue who appear to have pain but do not have obvious tissue
and glands, gastrointestinal, genitourinary, and other damage and acknowledges that pain is always subjective
organs/viscera; and (g) unknown systems. and psychological, regardless of tissue damage.
. D. To be diagnosed with complex somatic symptom . C. Chronic pain is pain that persists beyond the normal
disorder by DSM-IV criteria, patients must report at healing process. Although the timeframe for this may
least one distressing somatic symptom as well as at least differ in practice and many types of pain become
one of “emotional/ cognitive/behavioral disturbances: chronic or persistent at 3 months, the 6—month division
high levels of health anxiety, disproportionate and was chosen for scientific purposes by the IASP as a
persistent concerns about the medical seriousness of good entry to the patient population treated by pain
the ‘symptoms’ and an excessive amount of time and physicians.
energy devoted to the symptoms and health concerns,”
for at least 6 months’ duration. . D. The words “disorder,” “syndrome,” and “disease”
are all in dispute regarding whether they reflect the
4. A. Persistent Somatoform Pain Disorder is persistent, true phenomena that physicians treat. However, the
severe, distressing pain that cannot be explained fully word “symptom” is not in dispute.
by physiologic mechanisms. Pain during schizophrenia
or depression is not included. 10. E. Relatively generalized syndromes include diffuse or
widespread pain that is poorly localized, such as rheu-
. B. The name of CRPS was changed from RSD based on matoid arthritis, fibromyalgia, polymyalgia rheumatica,
the advice of a special subcommittee. Steps taken have pain of psychological origin, syringomyelia, central
(1) defined CRPS type 1 by its clinical phenomena and pain, CRPS, phantom pain, stump pain, and periph-
(2) developed identifying diagnostic criteria for clinical eral neuropathy. Localized syndromes are divided by
agreement as well as for more stringent research pur- the area affected (head, neck, limbs, thorax, abdomen,
poses. The classification has also helped in understand- spinal/ radicular) .
ing relatively new syndromes. The old name, RSD, was
Organizing an Inpatient Acute
Pain Service
QUESTIONS
1. Which of the following factors is likely to influence C. 50%—60%
postoperative opioid requirements? D. 60%—70%
A. Preoperative pain sensitivity E. 80%—90%
B. Presurgical opioid tolerance or a history of drug
abuse . All of the following are examples of multimodal
C. Psychological factors, including catastrophizing and analgesia EXCEPT:
anxiety A. Neuraxial block and music therapy
D. Age B. IV morphine and fentanyl patch
E. All of the above C. PCA morphine and thoracic epidural
D. Acupuncture and TENS
2. Which is the best intervention for inhibition of surgical E. Femoral nerve block and stress reduction
stress responses?
A. Neuraxial steroids . Which is an important first step in organizing an inpa-
B. Neuraxial local anesthetics tient acute pain service?
C. Perineural local anesthetics A. Enlisting the support of hospital administration and
D. Systemic steroids defining resources
E. None of the above B. Assessment of need
C. Definition of service
. Postoperative pain is identified as one of the major D. Financing and business plan
fears of patients undergoing surgery. What percentage E. Nursing education
of patients consider it to be their primary fear?
A. 30%—40%
B. 40%—50%
ANSWERS
l. E. Achieving satisfactory acute pain management can be 4. B. A time-, energy—, and cost-effective acute pain pro-
challenging. It is often difficult to estimate a patient’s gram should optimally provide multimodal and multidis-
postoperative analgesic requirements. The following ciplinary interventions, including systemic and regional
factors may influence postoperative opioid require— pharmacologic treatments, stress reduction, transcuta—
ments: preoperative pain sensitivity, coexisting medical neous electrical nerve stimulation, music therapy, and
conditions and associated multiple drug administration, acupuncture. Extracting and integrating the relevant
presurgical opioid tolerance or a history of drug abuse, expertise from multiple health care disciplines often
psychological factors (including catastrophizing and allows individualized and optimized pain management.
anxiety), age, and type of surgery. Disciplines commonly involved include psychology,
pharmacy, physical therapy, and nutrition.
. B. Surgical stress responses are best inhibited by neur-
axial administration of local anesthetics; the adminis- 5. A. Enlisting the support of hospital administration and
tration of other agents—systemically, neuraxially, or defining resources are a Vital first step in organizing an
perineurally—appears to contribute little additional inpatient acute pain service. Once the challenge of or—
reduction of the endocrine (metabolic and catabolic) ganizing an acute pain service is accepted, assessment
stress response following operative procedures. of need is mandatory. Once the mission statement has
been formulated in response to the perceived institu-
. C. Inadequacy of pain relief has been highlighted as a tional and community needs, it is necessary to define
quality-of—care measure and a focus of patients’ con- the resources that will be required. The next step in the
cern. In a questionnaire survey, 57% of patients identi- process of organizing an inpatient acute pain service is
fied pain after surgery as their primary fear. to construct the business plan.
Measurement-Based
Stepped Care Approach to
Interdisciplinary Chronic
Pain Management
QUESTIONS
1. Which of the following is FALSE regarding the World 5. All of the following are aberrant drug behaviors
Health Organization cancer pain analgesic ladder? EXCEPT:
A. It is focused on the relief of intensity of cancer pain. A. Self-induced oversedation
B. It incorporates relief of suffering of the cancer pain B. Continuing medication despite report of feeling
patient. intoxicated
C. It emphasizes treating the intensity of pain even at C. Early refill requests
the expense of function. D. Calling the office to report worsening pain
D. It includes three steps in its analgesic strategy. E. Self-directed dose increase
E. The goal of the ladder is complete freedom from
pain. . The 2006 Trends and Risks of Opioid Use for Pain
(TROUP) study found opioid use to be higher in pa-
. Which the following pain treatment domains should tients with mental health disorders and what other
ideally be included in a measurements-based stepped health problem?
care pain treatment algorithm? A. Chronic pelvic pain
A. Physical and emotional function B. Substance use disorders
B. Quality of sleep C. Chronic back pain
C. Risk for chemical dependency D. Postsurgical patients
D. Self-reported quality of life E. Patients with whiplash history
E. All of the above
. All of the following are validated opioid risk scales
. The Patient Health Questionnaire 4 (PHQ—4) is a EXCEPT:
screening tool for depression and anxiety. Which of the A. ORT
following is NOT assessed on this questionnaire? B. COMM
A. Feeling nervous, anxious, or on edge C. SOAPP—R
B. Not being able to stop or control worrying D. DIRE
C. Feeling down, depressed, or hopeless E. DOLOPLUS
D. Having little interest or pleasure in doing things
E. Feeling better off dead 8. Which of the following is true about patient access to
pain specialists?
4. Which of the following is true about daily morphine A. There is an overabundance of pain care providers in
equivalent dose (MED) and relative risk of mortality in the United States today.
patients on chronic opioid therapy? B. There is currently a significant shortage in pain
A. As daily morphine equivalent dose increases, providers relative to the number of people with
mortality risk also increases in tandem. chronic pain.
B. As daily morphine equivalent dose increases, C. The number of patients with chronic pain is cur-
mortality risk tends to plateau. rently well matched to the number of board-certified
C. As daily morphine equivalent dose increases, providers in pain care.
mortality risk decreases. D. In the United States, fewer than 1000 physicians
D. The 50—100 mg morphine equivalent dose has the were board-certified in pain care between 2000 and
highest risk for mortality. 2009.
E. Using between 20 and 50 mg morphine equivalents E. The current shortage in pain care expertise leaves
per day does not increase mortality risk relative to more than 100,000 people with chronic pain for
less than 20 mg daily. every pain specialist in the United States.
6 PART 1 — GENERAL CONSIDERATIONS
ANSWERS
1. B. The WHO cancer pain analgesic ladder is focused 6. B. Presence of substance use disorder in addition to
strictly on alleviating the intensity of pain and does not mental health disorders predisposed patients to higher
incorporate suffering of the cancer pain patient in its opioid use in the TROUP study.
analgesic strategy. Other answer choices listed are true
statements regarding the ladder. 7. E. The first four options are validated opioid risk
screening tools: Opioid Risk Tool (ORT), the Screener
2. E. All of the listed pain treatment domains should and Opioid Assessment for Patients with Pain—Revised
ideally be included in a stepped care pain treatment (SOAPP—R) ; the Current Opioid Misuse Measure
algorithm. (COMM); and the Diagnosis, Intractability, Risk, and
Efficacy (DIRE). The DOLOPLUS scale, though vali-
3. E. The question regarding suicidality comes from the dated, is used for behavioral pain assessment in elderly
PHQ—Q screening tool rather than the simpler PHQ—4 with verbal communication problems, not for opioid
questionnaire. risk screening.
4. A. Relative risk of mortality with chronic opioid therapy . B. There is currently a significant shortage of
increases in parallel with escalating morphine equiva- board-certified pain physicians in the United States
lent dose. relative to the number of patients with chronic pain.
5. D. Contacting the office to report worsening pain is . D. Age greater than 50 is a risk factor for OSA per the
considered appropriate behavior meriting reevaluation. STOP-BANG criteria.
CHAPTER 4 — Measurement-Based Stepped Care Approach to Interdisciplinary Chronic Pain Management
10. E. While anxiety is often associated with chronic pain, 13. A. The patients at highest opioid risk are being
its presence alone is not considered sufficient for psy- prescribed the highest opioid doses.
chiatrist referral according to the stepped care model
unless deemed poorly controlled despite conservative 14. E. Greater than 120 mg MED.
measures.
15. E. All are true except obesity, which is one of the risk
11. D. This patient has an opioid risk tool score 28 and factors for sleep medicine referral.
thus merits referral to an addiction medicine specialist.
QUESTIONS
1. Which of these statements is part of the International basic safety profile and pharmacokinetics of the drug
Association for the Study of Pain (IASP) Declaration of in human subjects?
Montreal? A. Preclinical Investigational New Drug (IND) application
A. Only pain that has been objectively verified must be B. Phase I
treated. C. Phase II
B. Pain must be treated by a medical doctor specialty- D. Phase III
trained in pain management. E. Phase IV
C. Patients should receive analgesia based on their
ability to pay. 3. Which of the following is NOT identified as a barrier to
D. Access to effective pain management is a basic access to pain treatment around the world?
human right. A. Education of patient population
E. Patients must have a history negative for substance B. High cost of treatment
abuse to qualify for opioids. C. Lack of government policy on pain treatment and
drug supply
2. Which of the following phases of the Food and Drug D. Poor training of health care workers
Administration Center for Drug Evaluation and Re— E. Fear among health care workers of legal action
search (FDA CDER) approval process focuses on the
ANSWERS
I. D. The Declaration of Montreal, published in 2010, states 0 Phase III: Confirmation of the safety and effective-
that effective pain management is a basic human right. ness of the drug, its dosages, and drug interactions
It underscores the importance of government to enact in 1000—4000 human subjects.
legislature that promotes access to pain management 0 Phase IV: New or expanded use for patient population
for all. It consists of three articles, including: and long—term risks vs. benefits.
0 Article I: The right of all people to have access to
pain management without discrimination. . A. Access to appropriate pain management worldwide
0 Article 2: The right of people in pain to have their remains largely inadequate. Seventy-eight percent of
pain acknowledged and to be informed about how morphine consumed in 2010 went to only six countries.
it can be assessed and managed. Inexpensive oral medications are unobtainable in many
0 Article 3: The right of all people with pain to have countries. Reasons cited include:
access to appropriate assessment and treatment 0 Failure of governments to put functioning drug supply
of the pain by adequately trained health care systems in place.
professionals. 0 Failure to enact policies on pain treatment and
palliative care.
2. B. The phases of the FDA CDER approval process are 0 Poor training of health care workers.
tiered as follows: 0 Existence of unnecessarily restrictive drug control
0 Preclinical IND application: Animal data used to regulations and practices.
justify testing of the drug in humans. 0 Fear among health care workers of legal sanctions
0 Phase I: Basic safety profile and pharmacokinetics of for legitimate medical practice.
the drug in 50—100 human subjects. 0 Unnecessarily high cost of pain treatment.
0 Phase II: Drug dosage, efficacy, and safety in 100—500
human subjects.
Quality Assessment and 6
Improvement and Patient
Safety in the Pain Clinic
QUESTIONS
1. The majority of errors that take place in health care are C. Lack of evidence-based benchmarks or national “best
due to which of the following? practices”
A. Patient factors D. Lack of cooperation from patients
B. System defects E. Lack of government regulation to support such
C. Provider carelessness programs
D. Equipment malfunction
E. Resource misallocation 3. Which of the following tools has been shown to signifi-
cantly lower the death rate, reduce patient complica-
2. Which of the following is identified as the biggest hurdle tions, and is especially helpful in emergencies?
to establishing Continuous Quality Improvement (CQI) A. E-conferencing/ telecommuting
in pain medicine? B. Speech recognition software
A. Lack of additional reimbursement to justify higher C. Electronic prescriptions
quality care D. Safety checklist
B. Lack of support from hospital administration E. Patient portals
ANSWERS
1. B. According to the Institute of Medicine (IOM), a ma- 3. D. Using a checklist has been shown to reduce patient
jority of errors in health care are more likely attributable complications, which is thought to be due to decreases
to system defects (as opposed to individual errors). in human error. Data shows that simply implementing a
safety checklist can substantially reduce patient mortality
2. C. Because evidence available in peer-reviewed litera- rates. Checklists are critical in emergency situations,
ture is insufficient for chronic pain interventions, estab- such as local anesthetic toxicity, where a checklist/
lishing a CQI in the field of pain medicine largely relies protocol should be readily available.
on consensus expert opinion instead.
Education, Training, and
Certification in Pain Medicine
QUESTIONS
1. Which of the following describes the design of current D. Introduction of devices to the market often outpaces
pain medicine training programs? practitioner familiarity.
Comprehensive and multidisciplinary E. Creation of new devices becomes cost prohibitive for
cow?
ANSWERS
1. A. The original fellowship training programs in pain market if the FDA deems the risks and benefits are
medicine were extensions of the department of anesthe- comparable to a device that has been previously ap-
siology. Since that time, there has been a broadening proved. The FDA’s 510(k) “substantially similar device”
of specialties seeking training in pain medicine. In an process can require little additional efficacy data. In
effort to standardize and ensure quality of pain medi- some cases, practitioners are overwhelmed with new
cine training programs, four specialties have agreed to technology available and are not able to keep pace with
ACGME requirements for fellowship programs, includ- the skills and knowledge required to use the device.
ing anesthesiology, neurology, physical medicine and
rehabilitation, and psychiatry, since 2007. This collabo- 3. B. The trend in medicine favoring evidence—based therapy
ration between specialties echoes the views of the has highlighted a relative lack of randomized controlled
American Academy of Pain Medicine and the American trials in the pain medicine subspecialty to validate treat-
Board of Pain Medicine, emphasizing a multidisciplinary ments. At the same time, patients with chronic pain re-
and multimodal approach to pain medicine. quire treatment and are often willing to try novel proce—
dures. Practitioners must monitor their own outcomes to
. D. In order to expedite innovation and the introduc- aid in making decisions in patient care as well as use best
tion of new technology, devices can be cleared for judgment of risk vs. benefit for each individual patient.
10
BASIC CONSIDERATIONS
QUESTIONS
1. What is the primary termination site for sensory integra- 5. Prolonged membrane hyperpolarization has what effect
tion in the pain pathway? on the role of GABA—B receptors?
A. Thalamus A. Change from inhibition to more inhibition
B. Medulla B. Change from inhibition to excitation
C. Basal ganglia C. Change from excitation to inhibition
D. Dorsal columns D. Increased threshold for depolarization
E. Frontal cortex E. No effect
. What are the small unmyelinated axonal fibers with slow 6. Which of the following is the primary afferent excitatory
conduction velocities that relay noxious input from the neurotransmitter?
skin and other tissues to the central nervous system? A. Substance P
A. A-delta fibers B. CGRP
B. A—beta fibers C. IL—I
C. C fibers D. Glutamate
D. Free nerve endings E. Norepinephrine
E. Dorsal root ganglia
. Noxious cutaneous input is relayed by which of the
The dorsal horn is anatomically organized in laminae. following lamina projection neurons as the crossed
Small unmyelinated fibers terminate in laminae , spinothalamic tract pathway traveling in the lateral
while large myelinated fibers terminate in laminae and ventrolateral white matter en route to the VPL?
A. II—III, IV—V
B. I—II, III—V
C. III—V, I—II
D. II—IV, I—III
E. V, I—II
. The substantia gelatinosa is associated with which of the . The gray matter of the dorsal horn includes the following
following lamina? Rexed laminae:
A. Lamina I A. I—IV
B. Lamina II B. I—VI
C. Lamina III C. II—IV
D. Lamina IV D. II—VI
E. Lamina V E. I—X
ll
12 PART 2 — BASIC CONSIDERATIONS
9. All of the following are considered ascending medial 10. Which of the following structures most likely contrib-
pain pathways EXCEPT: ute to memory and learning related to painful stimuli
A. Spinoamygdalar as indicated by fMRI imaging studies?
B. Spinohypothalamic A. The VPL thalamus, SI, and S11 cortices
C. Spinoreticular B. The ACC, cerebellum, and lentiform nucleus
D. Spinothalamic C. The insula, cerebellum, and frontal cortex
E. Medial spinothalamic D. The ACC, PCC, SI, and S11 cortices
E. The insula, lentiform nucleus, and periaqueductal
gray
ANSWERS
I. A. The primary termination site for sensory integration D. Glutamate is an excitatory amino acid and plays
is the thalamus. Peripheral nociceptors transmit nox— key roles in neural activation throughout the nervous
ious information to second-order neurons at the spinal system. It is the primary neurotransmitter in afferent
cord and brainstem levels, which are then sent by pro- nociception.
jection neurons of the pain system to integration sites
in the brainstem. Though the primary site for integrat- C. Noxious cutaneous input from lamina I, IV, and V
ing sensory information is the thalamus, many other is relayed by projection neurons along the crossed STT
brain structures are also involved. (spinothalamic tract) in the lateral and ventrolateral
white matter to the VPL (ventral posterolateral) and
. C. C fibers (group IV) are small unmyelinated nocicep- posterior thalamus.
tors with conduction velocities less than 2.5 m/ sec.
A—delta fibers (group III) are small fibers with a conduc- . B. Laminae I—X are all considered gray matter, but the
tion velocity of 4—30 m/ sec and conduct faster because dorsal horn includes only laminae I—VI. Some deeper
of a thin myelin sheath produced by Schwann cells. laminae are also involved in nociceptive processing.
Both of these axonal fibers carry noxious input from
tissue to the CNS. . D. The spinoamygdalar, spinohypothalamic, medial spi-
nothalamic and spinoreticular pathways, and connec-
. B. Small unmyelinated C—fiber nociceptor endings for tions to the anterior cingulate and prefrontal and insu-
somatic sensation are distributed mainly in focused lar limbic cortices are all medial pain pathways. The
areas of laminae I and II, though visceral afferents can spinothalamic tract is a nonoverlapping but parallel
extend multiple segments and are widely dispersed in lateral pathway.
ipsilateral laminae I, II, V, and X, or contralateral V and
X. Large myelinated A—beta fibers carrying nonnocicep- 10. C. Centers for higher processing can modulate aware—
tive input terminate in laminae III—V. ness of and responses to pain as well as regulate emo-
tional, autonomic, and motor responses. The insula,
B. Interneurons of lamina II (substantia gelatinosa) syn- cerebellum, and frontal cortex contribute to avoidance
thesize inhibitory (GABA) and excitatory (glutamate) behaviors and other types of memory and learning re-
neurotransmitters. Opioid receptors are also found on lated to the painful stimulus. The VPL thalamus and
these nerve cells. SI and 811 cortices are somatosensory—proeessing regions.
The ACC (anterior cingulate cortex) may be involved
. B. GABA (y-aminobutyric acid) primarily reduces neu- in interpreting emotional significance of pain via the
ronal excitability and provides presynaptic inhibition, limbic system.
though with prolonged hyperpolarization/nociceptive
input, GABA—B receptors can change their role from
inhibition to excitation, leading to a positive feedback
loop that can establish chronic pain.
A Review of Pain-Processing
Pharmacology
QUESTIONS
1. What are the two key inhibitory neurotransmitters? Which of the following receptors are activated by cold
A. NMDA, glycine or menthol?
B. Somatostatin, substance P A. TRPM8
C. AMPA, glutamate B. TRPVl
D. GABA, glycine C. ASIC
E. Somatostatin, NMDA D. TRPV2
E. TRPVS
. Following a peripheral nerve injury, ongoing pain from
ectopic activity is due to the up—regulation of what type . Which of the following protein kinases phosphory—
of channels? lates the NMDA receptor to lower its threshold for
A. Calcium activation?
B. Sodium A. PKA
C. Potassium B. PKC
D. Chloride C. MAPK
E. Fluoride D. AMPA
E. All of the above
. All of the following are effects of substance P binding
EXCEPT: . Blockage of the facilitated state called “wind-up” has
A. Mast cell degranulation been reported with the use of:
B. Swelling of skin A. Opioids
C. Local erythema B. Prostaglandins
D. Vomiting C. Nitric oxide
E. Vasoconstriction D. NMDA antagonists
E. 5-HT3 inhibitors
. After nerve injury there is an increase in axonal excit—
ability that is associated with which of the following? . Chemical injury to a nerve is MOST LIKELY to be
A. Up—regulation of potassium channels and down- characterized by:
regulation of sodium channels A. Reddening at the site of the stimulus
B. Up—regulation of sodium channels and down-regulation B. An initial burst of afferent firing
of potassium channels C. Increased capillary permeability
C. Down-regulation of sodium and potassium channels D. Local arterial dilation
D. Up—regulation of sodium and potassium channels E. Regional hyperalgesia
E. Up—regulation of calcium channels and down-
regulation of sodium channels 10. Which of the following occurs after nerve injury?
A. Increased local catecholamine release
. All of the following mediators are released with tissue B. Alpha-adrenergic antagonists increase excitation of
injury and depolarize and sensitize primary afferent the injured axon
terminals EXCEPT: C. Down-regulation of alpha-l-adrenergic receptor
A. TNF—alpha expression
B. Substance P D. Decreased local catecholamine release
C. Bradykinin E. Decreased activity at the DRG or injured neuroma
D. Histamine
E. Glycine
l3
IA PART 2 — BASIC CONSIDERATIONS
ANSWERS
1. D. GABA and glycine act on GABA—A/GABA—B and gly— 5. E. Following tissue injury, a variety of cytokines and
cine receptors, reducing excitation. Glycine is an inhibi- inflammatory neurotransmitters are released, leading
tory amino acid. Somatostatin is classified as an inhibi- to sensitization. Glycine, however, is an inhibitory neu-
tory hormone with a range of functions throughout the rotransmitter and has not been shown to result in
body including modulating peripheral inflammation, increased afferent sensitization.
the gastrointestinal tract, and the brain. The NMDA
(N—methyl—D—aspartate) receptor requires glutamate or 6. A. Transducer channels on afferent terminals have dif—
aspartate binding for activation. Substance P contributes ferent sensitivities to specific stimuli. Some channels
to enhanced nociception. AMPA (d-amino-S-hydroxy- transducing a physical sensation are also activated by
5-methyl—4—isoxazolepropionate) receptors, like NMDA chemicals and can reproduce the physical sensation
receptors, are activated by glutamate. Glutamate is a main when exposed to the chemical. For example, the
excitatory neurotransmitter. GABA (”y-aminobutyric acid) TRPVl (>43OC) vanilloid receptor is activated by
primarily reduces neuronal excitability and provides presyn— capsaicin (heat sensation), while the TRPM8 (QB—28°C)
aptic inhibition, though with prolonged hyperpolarization/ receptor is activated by menthol (cold sensation), and
nociceptive input, GABA—B receptors can change their the TRPA (<17 oC) receptor is activated by mustard oil.
role from inhibition to excitation, leading to a positive
feedback loop that can establish chronic pain. B. It has been shown that PKG (protein kinase C)
phosphorylates sites on NMDA and AMPA receptors,
B. Sodium channel expression is increased in neuromas which can lower threshold for activation and increase
and dorsal root ganglia following nerve injury. Lidocaine membrane permeability.
can block ectopic activity and attenuate hyperpathic
states after nerve injury. There are a variety of sodium E. Through the bulbospinal pathway, C fibers make
channels in primary afferent neurons (Navl.6—Navl.9). contact with neurons that project into the brainstem
Navl.8 and Navl.9 are resistant to a sodium channel contacting serotonergic neurons, which then project
blocker (TTX) and found primarily in G fibers. Variants to the spinal dorsal horn contacting lamina V neurons.
such as Navl.8 are important because, for example, Cells of lamina V in the deep dorsal horn are noted
Navl.8 reverses nerve-injury—evoked pain states in animal for their ability to display a state known as “wind-up.”
models. Mutations in Navl.7 in humans can cause Blockage of this pathway using 5-HT?) inhibitors has
extremely painful conditions, while loss-of—function been reported to reduce “wind-up” facilitation.
mutations can lead to prominent insensitivity. Gain of
function mutations (i.e., to the sodium ion channel B. Following nerve injury, afferent axons display an
alpha subunit gene SCN9A) can result in syndromes initial burst of afferent firing followed by electrical
like erythromelalgia, characterized by severe periodic silence for hours—days and finally the appearance of
pain from blocked blood vessels. spontaneous bursting activity for hours-days. This is
correlated to an initial degeneration of the injured
. E. Substance P acts on the neurokinin—l (NK—l) recep- nerve followed by new sprouting. Answer choices A, C,
tor and is involved in inflammation, pain perception D, and E are associated with tissue injury.
(along with glutamate), and the vomiting centers.
Substance P is also a potent vasodilator in conjunction 10. A. Stimulation of these postganglionic axons and
with nitric oxide. increased catecholamine release can excite the injured
axon and DRG, but this activation can be blocked by
B. Following nerve injury, sodium channel expression alpha—adrenergic antagonism.
has been found to be significantly increased, while po-
tassium (K+) currents have been shown to be reduced,
suggesting down-regulation of K+ channels.
Pain and Brain Changes
QUESTIONS
15
16 PART 2 — BASIC CONSIDERATIONS
10. The dimension of pain thought to include interaction 13. You are performing a neurologic sensory exam. The
with previous experience and involve the prefrontal patient shows normal sensation to light touch in the
cortex is termed: distributions of the radial and median nerves and in-
A. Sensory-discriminative creased sensitivity to pinprick. What most accurately
B. Cognitive-evaluative describes this phenomenon?
C. Affective-motivational A. Allodynia
D. Behavioral-cortical B. Hypesthesia
E. Emotional—receptive C. Paresthesia
D. Hyperalgesia
11. Which of the following is true of placebo analgesia? E. Secondary sensitization
A. It cannot be blocked by naloxone.
B. The endogenous opioid system is involved. 14. Chronic pain conditions are consistently associated
C. The somatosensory cortex is involved. with decreased activity in which brain structure(s)?
D. There is no correspondence between placebo A. Prefrontal cortex
analgesia and reward. B. Thalamus
E. All of the above C. Reticular activating system
D. Pons
12. Which of the following is TRUE regarding bone E. All of the above
cancer pain?
A. Substance P and other neuropeptides, such as 15. Based on brain-imaging studies, which of the following
CGRP, are unregulated. is implicated as a cause for the autonomic symptoms
B. Up—regulation of galanin and neuropeptide Y experienced in cluster headaches?
occurs. A. Activation of the first (ophthalmic) division of the
C. Neuropathic pain and bone cancer pain have trigeminal nerve
similar changes with substance P and CGRP. B. Activation of cranial parasympathetic outflow from
D. The greatest change observed in the spinal cord in the seventh cranial nerve
response to metastatic bone cancer pain is activa— C. Cortical spreading depression
tion of astrocytes. D. Activation of the trigeminovascular system
E. All of the above E. Hyperemia in the occipital cortex
ANSWERS
l. D. The TRPVl receptor responds to stimuli including 7. B. While the pain may be described as inflammatory
heat, acidity, and hot pepper capsaicin. These stimuli and/ or neuropathic as well, the patient is clearly expe—
can enhance each other. riencing an abnormal response to mechanical light
touch. This would be described as tactile allodynia, an
2. D. Glutamate is the dominant excitatory nociceptor experience where a typically innocuous sensation such
neurotransmitter. as light touch becomes painful.
3. B. Intracranial recordings show that the earliest pain— 8. E. Neuromas are sensitive to multiple sensations and
induced signals originate near the SH cortex, implicat— generate spontaneous ectopic activity from both A and
ing SH and adjacent insula regions as the primary brain C fibers. Noradrenergic sensitization can result in cou-
areas for receiving nociceptive input. pling of sympathetic and sensory inputs.
4. C. Secondary sensitization leads to enhanced neural 9. B. In sensitization, opioid receptors are down—regulated
transmission distant from the site of injury, thought to with neuropathic pain, though C) up—regulated with
result from reorganized spinal cord nociceptive circuitry. inflammatory pain; A) there is an increased release of
Primary sensitization, in contrast, leads to increased excitatory neurotransmitters; D) KCl receptor down-
transmission near the site of injury. regulation decreases the effects of GABA release; E)
these peptides open the NMDA channel, leading to
5. B. A—delta and C fibers are the primary nociceptors in increased sensitization.
healthy organisms. A—beta afferents are large nonnoci—
ceptive, heavily myelinated touch receptors. However, 10. B. Traditionally, pain perception consists of the following
following central sensitization, input from these touch dimensions: sensory-discriminative, cognitive-evaluative,
receptors can result in the sensation of pain. and affective-motivational. The cognitive-evaluative di—
mension includes previous experiences and cognitive
6. E. Currently, there is no objective measure of brain activ— influences on perception of pain intensity and, tradi-
ity that can conclusively determine whether an individual tionally, the prefrontal cortex is thought to be involved
is in pain. However, fMRI and PET are able to provide in this dimension. Note: Neuroimaging studies have
valuable information regarding the pathologic process— assessed paradigms that do not easily fit into these
ing of nociception and pain perception. three traditional dimensions and tend to discuss
CHAPTER 10 — Pain and Brain Changes 17
cortical areas and brain regions involved in specific sensation. E) Secondary sensitization is enhanced sensa-
functions instead. tion at sites distant from the site of injury.
ll. B. The placebo response involves the endogenous opi- 14. B. Clinical brain imaging studies show reduced activ-
oid system and can be blocked by naloxone. Studies ity in and transmission through the thalamus for
have shown a correspondence between placebo anal- chronic clinical pain (as opposed to experimentally
gesia and reward pathways. The PAG and amygdala are induced acute pain). There is, however, increased ac-
involved, as well as the prefrontal/rostral ACC. tivity in the prefrontal cortex in chronic pain. These
changes support the idea that chronic pain condi—
12. D. A unique set of neurochemical changes occur at the tions are associated with increased involvement of
level of the spinal cord and dorsal root ganglion for brain regions for cognition and emotion. Meanwhile,
each type of pain: inflammatory, neuropathic, or cancer the sensory and nociceptive regions of the brain (thala-
pain. The greatest change in metastatic bone cancer mus) show decreased activity. There is also a reduc-
pain is activation of astrocytes at the spinal cord. tion in neocortical gray matter.
13. D. Hyperalgesia describes the abnormally increased 15. B. Activation of cranial parasympathetic outflow from
response to pain for a stimulus that would typically cause cranial nerve VII is thought to result in the autonomic
pain, but not to the extent observed. A) Allodynia de- symptoms in cluster headaches. A) Activation of V1 is
scribes a painful response to a normally nonnoxious thought to mediate the excruciating unilateral pain
stimulus such as light touch. B) Hypesthesia describes in cluster headaches. Answer choices C—E apply to
diminished sensation. C) Paresthesia describes abnormal migraine headaches.
An Introduction to
Pharmacogenetics In Pain
Management: Knowledge of
How Pharmacogenomics May
Affect Clinical Care
QUESTIONS
1. Polymorphism of an enzyme involved in tetrahydrobiop- C. Codeine
terin (BH4) synthesis in primary sensory neurons of the D. Oxycodone
dorsal root ganglion following nerve injury results in E. Hydrocodone
which of the following?
A. Increased sensitivity to painful stimuli . Analgesics that require breakdown in the liver through
B. Reduced sensitivity to painful stimuli CYP45O to achieve analgesic effects are metabolized by
C. Increased sensitivity to analgesic medications which of the following?
D. Reduced sensitivity to analgesic medications A. CYP1A2
E. Reduced ability to heal following injury B. CYP2D6
C. CYP2C9
2. Which of the following phenotypes is consistent with D. CYP2C19
either multiple copies of a functional allele or an allele E. CYP3A4
with increased gene transcription?
A. Nonmetabolizer . Which of the following is the name for a field of medi-
B. Poor metabolizer cine that includes a patient’s genetic background and
C. Intermediate metabolizer uses the information to predict how a patient will
D. Extensive metabolizer respond in terms of efficacy and side effects when
E. Ultra-rapid metabolizer given a medication?
A. Pharmacognosy
3. A patient with known mutation in the CYP450 enzyme B. Pharmacokinetics
requires analgesic medication. Which of the following C. Pharmacogenomics
are NOT metabolized through this system at standard D. Genesiology
prescribed doses? E. Pharmacodynamics
A. Hydromorphone
B. Tramadol
ANSWERS
1. B. Patients with increased pain tolerance are thought 2. E. Classification of phenotypes for enzymes includes the
to have a polymorphism (a genetic variant) in GTP cy- following:
clohydrolase, which is the rate-limiting enzyme involved 0 Poor metabolizers: Two nonfunctional enzyme alleles.
in tetrahydrobiopterin (BH4) synthesis. BH4 has been 0 Intermediate metabolizers: At least one reduced
shown to be involved in regulation of inflammatory and functional allele.
neuropathic pain. It is estimated that this polymor- 0 Extensive metabolizers: At least one functional allele.
phism is associated with increased pain tolerance and is 0 Ultra-rapid metabolizers: Multiple copies of a func-
present in 15% of the population. Similarly, reduced tional allele or an allele with a promoter mutation
pain tolerance has been linked to polymorphisms in that confers increased transcription of that gene.
other genes. Different responses to analgesics among Phenotype variations can be responsible for the vast
patients can be attributed to genetic variance as well. difference in clinical effect as well as side effects
18
CHAPTER 1 l — An Introduction to Pharmacogenetics in Pain Management: Knowledge of How Pharmacogenomics May AtfectCIinical Care 19
between two patients taking the same weight-based form, for example conversion of codeine to the active
dosage of medication. metabolite morphine.
3. A. Although 40%—50% of medications are metabolized . C. By preemptively identifying patients at risk for ad-
in the liver through the CYP450 family of enzymes, verse side effects or poor efficacy from medication, the
three opioids are not, including hydromorphone, field of pharmacogenomics may improve health care
morphine, and oxymorphone. outcomes and efficiency, including higher success rate
after medication administration, lower incidence of side
. B. Analgesics that are metabolized by CYP450 include effects, and reduction of cost. As a relatively new field, it
codeine, dextromethorphan, oxycodone, and tramadol. shows promise in terms of tailoring medication regi-
Prodrugs require CYP2D6 for conversion to the active mens to each patient.
2 Psychosocial Aspects
of Chronic Pain
QUESTIONS
1. Chronic pain is best understood using which of the C. Positive reinforcement
following models? D. Both A and B
A. Biomedical E. All of the above
B. Biopsychosocial
C. Psychogenic . What is an exaggerated negative orientation toward
D. Secondary-gain actual or anticipated pain experiences?
E. Both A and C A. Self-efficacy
B. Fear avoidance
. In regards to psychological factors that play an important C. Pain catastrophizing
role in the experience of pain, which of the following is D. Anxiety
an affective factor rather than a cognitive factor? E. Negative reinforcement
A. Anger
B. Catastrophic thinking 6. Your patient had significant pain following his physical
C. Beliefs about pain therapy sessions, and now every time he drives by the
D. Self-efficacy facility he becomes tense and his back pain increases in
E. Coping severity. This is considered:
A. Classical conditioning
3. All of the following are examples of passive coping strat- B. Operant conditioning
egies EXCEPT: C. Negative reinforcement
A. Inactivity D. Punishment
B. Distraction E. Fear avoidance
C. Medications
D. Alcohol . According to one study, the target of a patient’s anger
E. Avoidance was most commonly acknowledged to be the:
A. Health care worker
4. According to the operant conditioning principles of re- B. Attorney
inforcement, the following response to a specific behav- C. Insurance company
ior will likely decrease the probability of the behavior D. Patient themselves
recurring: E. Significant other
A. Neglect
B. Negative reinforcement
A NSWE RS
1. B. In chronic pain, there may or may not be an identifi— the response to the illness and treatments, can be
able pathologic process or organic cause. Pain can also understood more completely by using this model.
take a significant emotional toll on the patient leading
to feelings of demoralization, helplessness, hopeless- 2. A. Affective factors are emotions, and in chronic pain,
ness, depression, and anxiety, to name a few. Since peo- they are mainly negative emotions such as depression,
ple rarely live in complete isolation, there is a larger anxiety, and even anger. The other factors listed are
social context that impacts and influences a person’s cognitive factors, which are involved in how someone
chronic pain. Given the multidimensional nature of thinks, perceives, and reasons. Catastrophic thinking is
chronic pain, a biopsychosocial approach is best used defined as an exaggerated negative orientation toward
to understand this condition. This model focuses on the actual or anticipated pain experiences. It can also be
illness as a whole, which is the result of a complex inter- described as a set of maladaptive beliefs. Beliefs about
action of biologic, psychological, and social variables. the meaning of pain influence a person’s expectations
Both the patient’s perception of his/her pain, as well as about pain and can be either positive or negative.
2O
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Worora, known vernacularly as “wirrauwa,” is beyond doubt an
indigenous evolution. It is much like a bushman’s billycan in shape—
a cylindrical vessel closed at one end and with a handle at the other,
measuring from four to twelve inches in height, and from six to nine
inches in width. A circular piece of woolly-butt bark is cut for the
base, and this is surrounded by another sheet which forms the
cylinder. The joints are carefully stitched together with threads of split
cane, using a bone-awl to prick the holes; then melted resin from the
eucalyptus tree is applied over the seam to render it water-tight. The
edge of the open mouth may be strengthened by cross-stitching and
applying resin. The handle is made of human hair-string, several
pieces of which are threaded diametrically across the open end of
the bucket, through holes previously made with a bone-awl, and tied.
The outer surfaces of the vessel are often painted. The usual device
consists of alternate bars of red and white or red and black, joined at
the top and bottom by horizontal lines of red; occasionally the whole
surface may be splashed or daubed with white, or the above designs
may be embellished with regularly spaced dots and “emu tracks.”
Lastly we shall briefly refer to the skin water-bag which is used (or
has been used) by the desert tribes of central Australia, from central
Western Australia to Western Queensland. A kangaroo, wallaby,
euro, or dingo is killed and the animal’s skin removed almost in toto
by making a circular cut around its neck, and, whilst one or two men
hold on to the head, others detach the skin from the carcase and pull
it off inside-out. The neck-hole forms the mouth of the bag, but all the
other openings are tied, stitched, or pinned together. The limbs are
cut off near the paws, the tail near its root, and the resulting holes
securely tied with string. The limb-pieces are tied together and act as
straps to assist the native carrying the bag when filled with water.
To fill these vessels with water, bailers are available either in the
form of specially constructed or of naturally occurring objects; no
matter which they are, they usually also answer the purpose of
drinking cups. Along the north coast of Australia the large melon
shell is perhaps the handiest; it is either used as it is found or its
inner whorls and columella are broken away, leaving just the
spacious outer shell to hold the water like a bowl. The same remarks
apply to the large Fusus pricei, and other molluscs.
The Narrinyerri and other tribes south of Adelaide used human
calvaria as drinking vessels. The facial skeleton of a complete skull
was broken away so as only to leave the brain-box; and this held the
water.
The broken shells of the large boabab nuts are similarly used in
the Northern Kimberleys of Western Australia, and now and then the
broken shell of the emu egg also makes a very serviceable cup.
A miniature bark-cooleman is constructed by the Wongapitcha,
Aluridja, and Arunndta tribes, like that described on page 92, about
eight inches long and half as wide, which serves the purpose of a
bailer, drinking-vessel, fire-shovel, and special food-carrier. It is
strongly convex lengthwise, and therefore comparatively deep.
The Bathurst Islanders tear or cut a piece of bark from a tree,
usually the ti-tree or “paper-bark,” out of which they fashion a cup.
The piece of bark measures about twelve inches in length, and eight
in width. It is first folded longitudinally at about its middle, and then
both ends of the doubled piece are folded transversely at about one-
quarter the whole length. The overturned parts of the inner sheet of
the first fold are clasped between the fingers on the inside and the
thumb on the outside, when the cup is ready for use.
The natural water supplies available over so vast an expanse of
territory as is embraced by the continent of Australia and its
subjacent islands, occur, as one might have expected, in great
variety. There is no need for us to consider such familiar supplies as
rivers, creeks, lakes, billabongs, waterholes, and springs; we shall
just briefly consider a few of the more uncommon cases, which are
of special interest. The native has a wonderful instinct for locating
hidden supplies of water; and many a European wanderer has
perished in the Australian bush, within a stone’s throw of the life-
saving fluid, all for the want of that gift, which to the primitive
inhabitant of the desert central regions means his very existence.
Along the superficially dry, sandy beds of “rivers” in arid Australia,
he is able to pick sites, at which, by shallow digging with his hands
and yam-stick, he can in quick time produce a “native well,” sufficient
to supply the needs of all the camp. The water is often exposed
within a foot or two of the surface, but at times he has to dig to a
depth of from five to six feet, which so far as my experience goes
seems to be the limit. When not in use, or when the camp moves on,
the natives always take care to cover the mouth of the well in order
that wild animals cannot reach the water and pollute it. When the
well is deep, its sides are made secure with pieces of timber and
brushwood, and cross-pieces are left to serve as a ladder whereby
the native can attain the water. Similar wells are constructed in the
catchment basins adjacent to the hills.
PLATE XII
Juvenile Types.
PLATE XIV