Professional Documents
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The acute care pediatric nurse practitioner (ACPNP) is a professional, who provides cost-effective, evidence-based
quality care for acutely, critically, and chronically ill infants, children, adolescents, and young adults in a variety of
settings. For many decades pediatric nurse practitioners (PNPs) in acute and critical care settings have been
responsible for the management of patients with illnesses characterized by impending or existing organ system
instability and failure. More recently the recognition of the unique competencies and the important contributions of
the ACPNP to continuity of care have contributed to the role's expansion (Kline, Reider, Rodriguez, & Van Roeyen,
2007; Jackson et al., 2001; Clinton & Sperhac, 2005).
The ACPNP meets the specialized physiologic and psychological needs of infants, children, adolescents, and young
adults with complex acute, critical, and chronic health conditions. The focus of care includes complex monitoring
and ongoing management of intensive therapies in a variety of settings, including but not limited to inpatient and
outpatient hospital settings, emergency departments, and home care settings. Specialty areas of practice are varied
and continue to emerge. Collaboration with an interdisciplinary team is essential for optimal patient care.
The ACPNP is an experienced nurse, masters or doctorally prepared, with education in acute care that includes
didactic and mentored clinical experiences in pediatric acute, critical, and chronic care settings. The ACPNP may
possess additional educational preparation to perform standardized procedures. Acute care PNP programs adhere to
curricular standards set by the Commission on Collegiate Nursing Education (CCNE) and the National Organization
of Nurse Practitioner Faculties (NONPF).
In 2004, the National Association of Pediatric Nurse Practitioners (NAPNAP) expanded its PNP Scope of Practice to
reflect the role of the PNP in providing care to infants, children, adolescents, and young adults who are acutely,
critically, and chronically ill. Specific components of the ACPNP role vary depending on the practice setting, the
patient population, and the type of employment arrangement (Percy & Sperhac, 2007). The scope of practice of an
ACPNP includes providing direct patient care management in a variety of settings. ACPNP practice includes
independent and interdependent decision-making and direct accountability for clinical judgment. Components of
management include, but are not limited to, performance of in-depth histories, physical examinations, interpretation
of diagnostic studies, prescribing/ordering medications and therapies, and developing and evaluating therapeutic
management plans (NAPNAP, 2008).
The ACPNP also performs a full complement of functions integral to the role including research activities,
interdisciplinary education, consultation, advocacy, and support of systems within the work environment (Kline et
al., 2007; Verger, Marcoux, Madden, Bojko, & Barnsteiner, 2005). Gaining practice privileges is a requirement for
an ACPNP as set forth by The Joint Commission. The process for becoming credentialed and obtaining practice
privileges is based on institutional policy and the state nurse practice act (NAPNAP, 2010).
NAPNAP advocates for:
1. ACPNP scope of practice that includes direct patient care responsibilities, education, leadership, and research.
2. Continued development of educational standards to prepare the ACPNP for practice.
3. Comprehensive ACPNP programs that focus on the management of complex health issues in acutely, critically,
and chronically ill infants, children, adolescents, and young adults and incorporates well-child growth and
development as well as basic health promotion and disease prevention.
4. Certification of the ACPNP in keeping with national accreditation standards for nurse practitioners (PNCB, 2010).
5. Ongoing evaluation of the impact and value of the ACPNP role for quality improvement using outcome measures.
In addition to providing direct evidence-based patient care to infants/children/adolescents/young adults with life-
threatening illnesses and organ dysfunction or failure, the ACPNP negotiates healthcare delivery systems, monitors
and ensures the quality of health care practice, provides family-centered care, and demonstrates cultural competency.
NAPNAP is an organization whose mission is promoting optimal health for children through leadership, practice,
advocacy, education, and research.
PURPOSE: Visualization of the vocal cords, end-tidal capnography, auscultation of bilateral chest and
epigastrium are the standard methods to confirm proper ETT placement, immediately post-intubation, in our
medical intensive care unit (MICU). A chest radiograph is also done to confirm ETT position. The goal of this
study was to determine the accuracy of US to confirm proper ETT placement, defined as, in the trachea with
bilateral lung ventilation, indicating an ETT position above the carina.
METHODS: This was a prospective study. Eligible patients were 18 years or older, admitted to the MICU, that
required endotracheal intubation due to their underlying clinical condition. Endotracheal intubation was
performed by an anesthesiologist, intensivist or a critical care fellow under supervision. An immediate pre and
post intubation US examination was performed by an intensivist who was blinded to the result of the standard
confirmatory methods of ETT placement. A post-intubation chest radiograph was done in all the patients.
RESULTS: As per the standard methods of confirmation of ETT placement, 19/20 patients had a properly
placed ETT. US examination was able to confirm correct placement in all 19 cases. 1 patient, confirmed to have
a properly placed ETT by standard methods had a right main stem intubation, as seen on a post-intubation chest
radiograph. US examination was able to detect a right main stem intubation in this patient. The sensitivity of US
in identifying correct ETT placement was 100%, specificity 100%, diagnostic accuracy 100%, false positive rate
0% and a false negative rate of 0%.
CONCLUSION: This study demonstrates that US imaging is an accurate method to confirm proper ETT
placement in an acute care setting.
CLINICAL IMPLICATIONS: US is a rapid, readily available, and a noninvasive technique that can be used
as an additional tool to immediately confirm proper ETT placement in an acute care setting.
In a CNA job, a certified nursing assistant will start an eight hour shift at 7 am, 3 pm, or 11 pm. The twelve
hour assistant usually starts at 6am or 7am for day shirts, and 6pm or 7pm for the night shift. The
responsibilities for each shift may differ, but most tasks are the same regardless of the shift you work.
CNA Jobs
Nursing Schools
Nursing Jobs
The day shift assistants start by receiving an assignment and report on the patients in their care. In some
institutions, the report is CNA to CNA, but in other facilities, the CNAs may sit in on the overall nursing report.
When reporting is completed, the first responsibility usually involves taking the vital signs on the assigned
patients and assisting clients with breakfast. Both of these responsibilities involve direct patient contact and
documentation. The vital signs need to be recorded, regardless of the practice of your institution. Some facilities
allow the CNA to document directly in the chart or in the computer chart, and some just want it written on a
flow sheet for the nurse to transcribe. The intake and output sheet for a patient can be taped to the bathroom
door, the patient room, or in the chart. This is where the assistant will record what the patient drank for
breakfast and how much the patient ate.
In the acute care setting, linens are changed every day. The CNA is responsible for assisting the patient with a
bath, shaving, oral care, and changing the bed. Any assistance needed to use the bathroom or bedpan,
ambulating, or being taken in a wheelchair for x-rays during the course of the shift falls to the CNA.
Nurses give the medications, treatments, and conduct full assessments. Nurses may also assist the CNA with
turning and positioning patients or transferring the patient to a chair.
The shift for a certified nursing assistant goes quickly, and the activities are centered on patient care and
assisting the nurses during the shift. CNAs do not answer the phone, take physician orders, or do patient
treatments or dressing changes. Their role is non-technical, yet hands on. It is one of the most important parts of
direct patient care in the overall hospital stay. Most CNAs find providing direct patient care can also be the
most satisfying part of the job.
Tags: acute care cna course in so ca, Certified Nursing Assistant, Cna, cna acute, cna certificate, CNA Jobs,
Cna Nurses, duties of acute certified nursing assistant, duties of an acute care cna, nurse assisting patient to
bathroom, nursing assistant charts, Nursing Jobs, Nursing School Directory, oral care cna, what is a acute cna
Ans: bed baths, changing bed, transfers, transport, walking people, bed pans Very similar to SNF
Full Article Title: Skin failure in the acute care setting.(Preparing for Certification)(Report)
Article Excerpt
Skin is the largest organ of the human body and, like other organs, it can fail, especially in the geriatric
population. The aging process results in a loss of fatty tissue, collagen, and skin elasticity, as well as a decrease
in vascularity and sweat gland function (Langemo & Brown, 2006).
The acutely ill older adult is at even greater risk of skin failure as the body fights to provide more circulation to
the diseased system. The elder with multiple co-morbid conditions is at increased risk for skin breakdown.
Decreased mobility and malnutrition can lead to loss of fat and muscle mass. Nutrition and hydration are
essential in the plan of care for older adult patients, as well as good hygiene and frequent turning and
positioning to alleviate and redistribute the areas of pressure (Langemo & Brown, 2006).
A patient's skin integrity must be assessed and documented accurately on admission. Beginning in 2008, the
Centers for Medicare & Medicaid Services (CMS), no longer reimburses hospitals for "never events or serious
and costly errors in the provision of health care services that should never happen" (CMS, 2006).
Nutrition is a key consideration when treating the patient with pressure ulcers because of its direct correlation
with healing. A sound nutritional assessment on admission is vital, with a focus on adequate protein intake and
overall optimal nutrition for each patient. Other helpful interventions might include provision of small frequent
meals and/or use of nutritional supplements (Baranoski & Ayello, 2004).
Clear, concise documentation of skin integrity is a must. Documentation of any existing skin condition should
include size, location, and description of the wound or ulcer, stage of the ulcer, and a description of any
drainage or odor that may be exiting the wound. For additional information on staging, see the Academy of
Medical-Surgical Nursing's Core Curriculum for Medical-Surgical Nursing (Brozenec & Russell, 2004).
1. Jeannine Cooper, age 92, is admitted with altered mental status and to rule out sepsis. While performing the
initial admission assessment, the nurse notices that Ms. Cooper has an area of breakdown in her sacral area as
well as a round purple area on the left heel. It is most important that the nurse initially:
a. Calls Adult Protective Services to report suspicion of neglect in the patient's home setting.
b. Calls the doctor to report the findings and ask for an order to consult the wound care nurse for staging.
c. Ensures the nursing assistant turns and repositions the patient every 1-2 hours and applies barrier cream to the
patient's sacral area.
d. Documents clearly on the admission assessment the alterations in skin integrity noting size, location, and
stage of any injured area as well as performs a sound nutritional assessment.
2. Glenda Jones, age 65, is admitted for exacerbation of chronic bronchitis. While performing the shift
assessment, the nurse notices patches of erythema on the right side of the patient's.
Background
Palliative care has been defined by the World Health Organization (WHO) as "the active total care of patients whose
disease is not responsive to curative treatment. Control of pain, of other symptoms, and of psychological, social and
spiritual problems, is paramount. The goal of palliative care is achievement of the best quality of life for patients and their
families."
Another way to look at palliative care is the concept of a "good death," free of avoidable pain and suffering for the patient
and the patient's family. At first glance, this definition would seem to have little to do with acute care delivered in a setting
such as the emergency department. In fact, while up to 60% of patients die at home in the United States, reportedly as
few as 35% of patients want to die at home. Consequently, many patients who are terminally ill present to emergency
departments. They may do so when death is imminent, for treatment of an acute illness superimposed on their existing
disease, or for symptom control, especially of pain. This article focuses on symptom control.
Pain is the single most prevalent symptom for patients receiving palliative care. The pathophysiology varies with the
anatomic location of pain and the underlying disease process. In a large study of patients with cancer who were in
palliative care, approximately 55% of pain was somatic in origin, with the remainder nearly equally divided between
visceral and neuropathic causes.1
For example, patients with advanced cancer may have headache due to increased intracranial pressure from tumor
masses or from inflammation. Bone pain is the most common source of cancer pain and may occur with either
osteoblastic or osteolytic activity. Bone pain can originate directly from bone (direct invasion with microfracture, distortion
of the periosteum) or from nerve root compression or muscle spasm in the lesion area. Major pathologic fractures may
occur at the site of primary or metastatic tumor. Abdominal pain in patients with cancer may be due to solid organ masses
causing capsular distension. Ascites or tumor mass may lead to uncomfortable abdominal distention and constipation is
common. Chest pain is most often due to tumor invasion of bone or other pain sensitive structures. The pathophysiology
of pain in patients who do not have cancer and are in palliative care is a function of the specific nature and anatomic
location of the underlying disease process.
Shortness of breath in patients in palliative care is especially common with lung cancer or advanced congestive heart
failure. Sixty-five percent of patients with lung cancer and nearly all patients with heart failure experience dyspnea.
In patients with lung cancer, underlying chronic obstructive pulmonary disease (COPD), which may cause dyspnea, is
often present. More specific causes include pleural effusion, pericardial effusion or tamponade,superior vena cava
syndrome, pulmonary embolism, and pneumonia. Besides disease progression, patients with heart failure may also have
pleural effusion and pericardial effusion or tamponade. Each of these may cause increased dyspnea. Severe anemia is
another etiology of dyspnea, but chronic anemia may be very well tolerated in this population.
Gastrointestinal symptoms are also common in the palliative care population. Anorexia, nausea, and vomiting are
common symptoms at the end of life, occurring in 62% of terminally ill cancer patients. Nausea and vomiting also occur
frequently in other terminal illnesses such as congestive heart failure, end-stage renal disease, and AIDS.
The most frequently cited etiologies in patients with cancer are chemical abnormalities (eg, metabolic, drugs, infection) in
33%, impaired gastric emptying in 44%, and visceral causes (eg, bowel obstruction, GI bleed, enteritis, constipation) in
31%. A study of 40 patients on a palliative care unit identified 59 reversible etiologies for GI symptoms, with medications
(51%) and constipation (19%) presenting most commonly. 2 Hypercalcemia is a cause of constipation that is common in
patients with cancer. Dry mouth is a bothersome symptom that may often be medication related.
Anxiety and depression are the most common psychological symptoms in patients with terminal illnesses.
Frequency
Because of the fragmented nature of health care in the United States, measuring the number of patients in palliative care
is difficult. A current estimate of patients receiving the Medicare benefit for hospice and palliative care is more than
500,000. Another estimate is that, in 2000, approximately 20% of patients dying in the United States received hospice
care.
In the United Kingdom, in 2005-2006, approximately 65,000 new patients enrolled in palliative care programs. According
to one estimate, approximately 70% of deaths in the developed world are preceded by a condition for which death is
predictable in the foreseeable future.
Cancer is the most common diagnosis among patients in palliative care. The traditional eligibility criterion for hospice care
in the United States includes an estimated lifespan of 6 months or less; this reflects the predominance of patients with
cancer who are in palliative care. However, lifespan may be easier to determine for cancer than for certain other terminal
diseases such as COPD, congestive heart failure (CHF), severe dementia, and stroke. Many patients request only
palliative care early in the course of a fatal, incurable disease. These patients may survive for years rather than 6 months
or less.
A 2006 study of the California population found that views on a patient's right to die varied significantly by ethnicity, with
whites much more willing to allow a loved one to die than any other ethnic group including African Americans, Asians, and
Latinos.3 Once a patient or family requests palliation only, medical care does not differ by ethnicity. Differences may also
exist in the ways that cultural groups express pain, and clinicians should consider this.
An article by Smith et al provides a comprehensive discussion regarding cultural issues that clinicians should be aware of
while caring for terminally ill patients of Latino heritage. Included are various recommendations on how to effectively utilize
interpreters and universal strategies for patient health communication. 4
History
Patients in palliative care already carry a diagnosis of terminal illness. The focus of the encounter is therefore different
than for other patients in acute care settings. New symptoms that may indicate a new disease process should be sought
when appropriate. Often though, the focus of the visit is explicitly for relief of long-standing symptoms that are progressive
or poorly controlled. Consulting the patient's medical history and treating physicians, when available, is often valuable in
learning the details of prior symptoms, diagnostic tests, and treatments.
With the exception of pain, there is poor concordance between symptom questionnaires as completed by the patient and
the physician history as recorded in the medical record.5 It is therefore often appropriate to ask specifically about other
symptoms such as anorexia, incontinence, gastrointestinal symptoms, respiratory symptoms, or level of functioning, in
order to best identify the patient's needs.
Physical
Physical examination for patients in palliative care should be based on knowledge of preexisting diseases and presenting
symptoms. As with the history, the primary goal is to determine if a new, acute condition needing further evaluation and
management is present or to verify that a preexisting condition needing further symptomatic treatment is responsible for
the presenting complaints.
Causes
The most common reason to enter palliative care is advanced cancer. According to the Centers for Disease Control and
Prevention, in the United States, the most common primary sites as causes of cancer death are (in order) lung, colon-
rectal, breast, and pancreas.6 Other diseases commonly leading to palliative care are HIV/AIDS, congestive heart failure,
chronic obstructive pulmonary disease, renal failure, liver failure, dementia, and stroke.
Laboratory Studies
Laboratory studies are dictated by the suspicion of a specific acute disease that would require treatment if discovered.
Many patients may have a high pretest probability of disease yet not require testing. For example, it would often be of little
benefit to confirm an elevated serum creatinine level in a patient in palliative care who has end-stage renal disease and
presents with an unrelated complaint such as a minor soft tissue infection.
Imaging Studies
As with laboratory studies, imaging studies should be reserved for the identification of conditions that will change
treatment when present. For example, merely documenting known findings such as a lung mass in a patient with lung
cancer who has symptoms unrelated to the chest is unnecessary. Conversely, a patient with a cough and a fever may
warrant a chest radiograph provided that he or she would wish antibiotic treatment for pneumonia, if discovered.
Procedures
Common procedures in patients in palliative care include intravenous or subcutaneous clysis fluids for
dehydration,thoracentesis for symptomatic pleural effusion, paracentesis for symptomatic ascites, and placement of a
urinary catheter for hygienic purposes or to ameliorate obstruction. One study reported on a collaboration of emergency
physicians and palliative care specialists in performing sonographically guided paracentesis at home. 7
Nasogastric (NG) tubes may be used temporarily to supplement oral intake. However, they are uncomfortable and
significantly increase the risk of aspiration. When patients desire artificial nutrition, arrangements for a semipermanent
type of feeding tube, such as a percutaneous endoscopic gastrotomy (PEG) tube, may be considered. An NG tube can be
an acceptable short-term bridge to a longer-term solution. A Foley catheter may be used as a short-term replacement for
an extruded or blocked gastrotomy tube needing replacement.
Care for patients in a palliative acute care setting is primarily concerned with symptom relief. At times, specific treatment
aimed at an acute condition is appropriate. For these situations, other sections of this text or other references should be
consulted. This section focuses on treatment strategies for pain, the most common symptom in patients receiving
palliative care. Pain is the most common symptom of patients with cancer who are in palliative care and seeking acute
care. Other patients in palliative care may also experience continuous or intermittent pain, and the principles of treatment
are the same. The WHO has disseminated a 3-step "stepladder" outlining an approach to treating pain in patients with
cancer. While not specifically formulated for other types of patients in palliative care, the scheme is clearly applicable.
According to the WHO8 :
If pain occurs, there should be prompt oral administration of drugs in the following order: nonopioids (aspirin and
acetaminophen); then, as necessary, mild opioids (codeine); then strong opioids (such as morphine), until the
patient is free of pain. To calm fears and anxiety, additional drugs – "adjuvants" – should be used. To maintain
freedom from pain, drugs should be given "by the clock", rather than "on demand." This three-step approach of
administering the right drug in the right dose at the right time is inexpensive and 80-90% effective. Surgical
intervention on appropriate nerves may provide further pain relief if drugs are not wholly effective.
The stepladder approach has been questioned but is generally considered to be a valuable tool in guiding treatment of
chronic cancer pain. The basic principle of reserving opioids for pain that cannot be successfully treated with nonopioids,
and continuing nonopioid treatments when possible, is important for both patients with cancer and patients without cancer
who are in palliative care settings. For a description of the ladder, see WHO's pain relief ladder.
The time course of pain may be continuous, intermittent, or breakthrough pain. In one study, 48% of patients with cancer
had continuous pain, with 75% experiencing breakthrough pain at some time. The other 52% experienced intermittent
pain.1 Inadequately treated continuous pain is also common with studies reporting frequent deviation from evidence-based
guidelines for treatment. A specific type of inadequately treated chronic pain is known as end-of-dose pain. Each type
requires a somewhat different therapeutic approach and, therefore, being able to differentiate them is important.
Patients in palliative care may present with chronic pain to an acute care setting early in the course of their disease. In
that situation, as suggested by the WHO ladder, nonopioids or mild opioids are the most appropriate symptomatic
pharmacological treatment. The initial treatment of pain that requires opioids should be with short-acting/rapid-onset
preparations. More commonly, patients present with inadequately controlled chronic pain and are already receiving
narcotic pain medication. In that circumstance, end-of-dose pain needs to be differentiated from breakthrough pain.
Breakthrough pain is described as an acute pain exacerbation in the setting of chronic pain. A specific precipitating event,
such as coughing in a patient with rib metastases, may occur, or it may occur with no identifiable precipitant.
Breakthrough pain is best treated with a short-acting narcotic as a "rescue" medication. End-of-dose pain is diagnosed by
the characteristic time course. It occurs fairly predictably prior to the next scheduled dose of analgesic. End-of-dose pain
is treated by increasing the dosing frequency or switching to a longer-acting narcotic.
When pain relief from a long-acting opioid is inadequate, the primary approach is to increase the dose. Opioids have no
ceiling effect and, therefore, no specific maximum dose, whatever amount the patient is receiving. The correct dose is the
dose needed to relieve pain. Fear of addiction or respiratory depression is not appropriate in this setting. At times, rather
than simply increasing the dose, switching from one opioid preparation to another is reasonable. Side effects may differ
with different preparations, and cross-tolerance is incomplete. When switching, begin the new drug at 50% (or more) of
the published equianalgesic dose. Less than this dose will almost certainly be inadequate.
Opioid side effects can be anticipated and treated prophylactically. Nausea and vomiting are common in the first few days
after initiating treatment. An antiemetic such as metoclopramide or a serotonin antagonist is often effective and should be
prescribed for the first week or so of narcotic treatment.
In certain circumstances, specific types of pain may be targeted with relatively specific therapies. The mechanism of
specific pain relief varies and, in some cases, is not well understood. Some pharmacological examples of specific pain
treatments are listed below.
In addition to pharmacologic treatment of pain, nonpharmacologic treatments are available. Radiation, radiofrequency
ablation, or surgery may be used to treat a tumor in a specific area causing pain. Physical modalities such as splinting or
the application of heat or cold may be used. Cold application with ice packs, gel packs, and coolant sprays reduces nerve
conduction, muscle spasm, inflammation, and edema. Ice massage, in which skin overlying tender tissue is rubbed with a
block of ice, produces analgesia after several minutes. No controlled studies of cold-induced analgesia for treatment of
cancer pain have been completed. Cold should be avoided in ischemic and irradiated tissues.
Heating has long been used to relieve muscle, bone, and joint pain. The analgesic effect of heat is due in part to
increased blood flow and also decreasing joint stiffness. Heat also induces mental relaxation and relieves stress. Hot
packs, heating pads, or hot baths improve cutaneous blood flow and relax muscles and ligaments.
Psychological treatment may play a long-term role. In the ED, recognition of the role of anxiety and depression may lead
to referral to a mental health provider or to pharmacologic treatment with anxiolytics or antidepressants. Both anxiety and
depression can decrease pain thresholds and increase opioid requirements. Anxiolytics can be an extremely important
adjunct in achieving pain control acutely, and anxiolytics or antidepressants may play a bigger role in the management of
chronic pain.
There are also interventional techniques that are effective for relief of pain. Neurolytic blocks of the sympathetic axis may
be used to relieve visceral pain in the abdominal or thoracic cavity. Implantable devices, such as epidural or intrathecal
catheters, are beneficial for patients on high-dose opioids when side effects are debilitating. These devices provide
analgesia that targets the selected regions, dependent on the catheter tip location. These devices allow significant
reduction in the amount of opioids required. Some authors consider interventional techniques as a "fourth step" on the
WHO ladder.9
Patients with end-stage lung disease or congestive heart failure are invariably dyspneic, and 75% of all dying patients
experience dyspnea. This may represent a progression of their disease or a complicating illness. In cases of disease
progression, when the patient desires no further treatments for the primary condition, palliation is
appropriate. Patients may already be using supplemental oxygen, and the oxygen concentration may be increased or
oxygen therapy begun.
Increased dyspnea is often associated with anxiety, and a positive feedback loop may exist in which difficulty breathing
leads to anxiety that causes an increased respiratory rate and oxygen demand leading to even more severe dyspnea. In
this situation, medications are appropriate. Concerns about respiratory depressant effects are not well founded and
should not be a concern.
Benzodiazepines are often effective. For patients not already taking opioids, low-dose opioids may relieve dyspnea. For
example, codeine, 30 mg orally every 4 hours may provide relief of mild dyspnea. For those already using opioids, the
dose may be increased.
When the evaluation reveals a potentially treatable cause of dyspnea, such as pneumonia, pneumothorax, pleural
effusion, or superior vena cava syndrome, the ratio of the risk and discomfort of diagnostic and therapeutic interventions
needs to be considered in light of the patients projected lifespan and probability of the therapy being successful.
Up to 50% of patients who receive morphine and derivatives develop significant constipation. This is due to narcotic-
induced suppression of intestinal motility. A rectal examination should be performed to determine if fecal disimpaction is
needed. Enemas and stimulant cathartics that promote intestinal motility are a logical treatment.
A comparative study of the efficacy of lactulose and senna was conducted in patients with terminal cancer. Both laxatives
were found to be equally effective in treating narcotic-induced constipation, but senna was recommended because of its
lower cost.10 Stool softening agents may also help prevent narcotic-induced constipation. Bulk-forming laxatives are not
appropriate in opioid-induced constipation. They allow the colon to stretch but do not stimulate peristalsis. The use of
these agents may result in bowel "pseudo obstruction."
A relatively new agent, methylnaltrexone bromide (Relistor), is an opioid antagonist indicated for opioid-induced
constipation. Relistor is a peripherally acting agent and is able to reverse the undesired peripheral affects of opiates, like
constipation, without diminishing the analgesic nature of the drug class. In two clinical trials reported on the package
insert, Relistor was shown to reverse opioid-induced constipation in 48-62% of patients within 4 hours. 11 Relistor is
administered as a subcutaneous injection and is dosed in a weight-based fashion. It is typically used every other day if
needed.
Regardless of the etiology, up to 90% of patients with terminal illness report constipation. Treatment is similar to opioid-
induced constipation. Bowel obstruction may present as constipation but will have additional signs or symptoms such as
vomiting, abdominal pain or distension, or peritoneal signs that point toward the diagnosis. If there is doubt, plain
abdominal films usually help differentiate simple constipation from obstruction. More sophisticated imaging, such as CT
scanning, should be used rarely in this population.
Hypercalcemia occurs in 10-20% of patients with lung cancer and is also common in breast cancer and myeloma. The
most common symptom is constipation. Many patients may elect not to treat hypercalcemia in the setting of terminal
illness. In that case, symptomatic treatment with laxatives and enemas may be helpful.
Nausea and vomiting are common in patients with cancer, congestive heart failure, end-stage renal disease, and AIDS.
This may be a reflexive response to bowel distention from constipation, the most common reversible cause. The second
most commonly identified reversible cause of nausea and vomiting is medications. Narcotics often cause nausea and
vomiting when treatment is initiated. Tolerance usually develops during the first week of treatment. An antiemetic such as
metoclopramide or a serotonin antagonist may be effective. Another narcotic may be substituted. If another medication is
suspected, it should be discontinued with substitution as needed. When no specific etiology is identified, an antiemetic
should be used.
Depressive symptoms are common at the end of life. While many people believe that depression is "normal" among dying
patients, it is not a necessary element of terminal illness and may be treatable. Major depression needs to be
differentiated from the expected anger, sadness, and anxiety associated with a serious illness. The degree and
persistence of symptoms are a key to considering major depression, which is estimated to occur in fewer than 25% of
patients with terminal illness. An open-ended question such as "how much of the time do you feel depressed?" may be the
best screening tool. A previous history of depression or a family history increases the likelihood of developing depression
in response to a serious illness.
As with other cases of depression, selective serotonin reuptake inhibitors are the mainstay of treatment. Low doses may
be started in the acute care setting with upward titration as needed. Therapeutic effects may be delayed for weeks, so
these are appropriate when a patient has a prognosis of at least a few months. Some authors have advocated use of
stimulants for patients with a very short-term prognosis. 12,13 They may be effective within a day or two and may be
particularly helpful in patients who have severe fatigue as part of their symptom complex. Dextroamphetamine and
methylphenidate are amphetamine stimulants that have been used. Pemoline is a nonamphetamine stimulant that has
also been used in this context.
Anxiety is common in patients in palliative care. It is often a component of a depressive syndrome and, in that case,
treatment of depression usually results in improvement. Anxiety may also be a primary psychiatric disorder or represent
an exaggerated response to the stress and worry associated with a terminal illness. Anxiety disorders may increase the
requirements of opioids in acute and chronic pain management, and anxiolytics should be considered as an adjunct in
these patients. Benzodiazepines or neuroleptics are reasonable options for the pharmacologic treatment of anxiety.