11.16 Other Gastrointestinal Disorders
Open Resources for Nursing (Open RN)
Overviews of other common gastrointestinal disorders are discussed in this section.
Liver Cirrhosis
Liver cirrhosis occurs due to chronic liver damage and is characterized by the development of liver nodules and liver fibrosis (stiffening/scarring of the liver). This chronic liver damage can be related to viruses like hepatitis C, toxic substances like drugs or alcohol, or autoimmune conditions. There is also a hereditary link.[1],[2]
When exposed to injurious substances, cells in the liver react by depositing excess collagen, which leads to fibrosis. Initially, this fibrosis does not result in loss of liver function. However, as the exposure is repeated over time, the majority of the liver will become fibrosed, and loss of function results. Ultimately, this leads to portal hypertension or elevated pressures in the blood vessels of the liver. Due to the elevated pressure, the body compensates by diverting blood to other veins. This increase in blood flow weakens these vessels and makes them prone to injury and bleeding.[3],[4]
Clients with liver cirrhosis may be asymptomatic, and the disorder may only be discovered incidentally. Clinical manifestations of cirrhosis may include nonspecific symptoms such as anorexia, weight loss, weakness, fatigue, or signs and symptoms of hepatic decompensation (jaundice, pruritus, signs of upper gastrointestinal bleeding, abdominal distension from ascites, and confusion due to hepatic encephalopathy). Physical examination findings may include jaundice, spider angiomas, gynecomastia, ascites, splenomegaly, palmar erythema, digital clubbing, and asterixis.[5] Clients with cirrhosis may experience bleeding from enlarged veins in the esophagus caused by portal hypertension called varices. As cirrhosis and portal hypertension continue to progress, the effects are widespread and affect multiple organs of the body. Clients with cirrhosis are also at an increased risk for liver cancer.[6],[7]
Lab results typically indicate elevated liver enzymes and prothrombin time. Albumin levels are typically decreased because this protein is produced in the liver. Decreased red blood cells, white blood cells, and platelets may also occur. Diagnostic tests include an ultrasound, CT scan, or MRI, but the best diagnostic tool is a liver biopsy. Additional tests may be performed to evaluate for the specific cause of liver cirrhosis.[8],[9]
Cirrhosis can not be reversed, so treatment is focused on preventing further injury to the liver. Liver transplantation may be an option for some clients.[10],[11]
Pancreatitis
Pancreatitis is inflammation of the pancreas, and it can be an acute or chronic condition. Although there are a variety of causes of acute pancreatitis, the most common causes are the presence of gallstones and excess alcohol use. Chronic pancreatitis is most commonly caused by alcohol abuse.[12]
In acute pancreatitis caused by gallstones, the pancreatic duct is obstructed and cannot release digestive enzymes. This leads to autodigestion, a process in which the enzymes of the pancreas digest pancreatic tissue, as well as inflammation. Alcohol use can lead to acute pancreatitis due to the toxic effect of alcohol on pancreatic tissues. Chronic pancreatitis occurs when the pancreas is repeatedly attacked, leading to scarring and pancreatic hypofunctioning.[13]
Common signs of acute pancreatitis are epigastric abdominal pain that spreads to the back, nausea, and vomiting. Jaundice may be present if the pancreatitis is caused by gallstones, and severe pancreatitis may lead to changes in mental status. Those with chronic pancreatitis may have nausea, vomiting, abdominal pain, weight loss, and steatorrhea. There is also the potential for the development of diabetes due to pancreatic damage.[14]
Acute pancreatitis can be diagnosed by the presence of elevated serum amylase and lipase levels. These levels may be increased or normal in those with chronic pancreatitis. Imaging, such as a CT scan, MRI or MRCP, may also be done.[15]
Treatment of acute pancreatitis consists of IV fluids, analgesics, and diet modification. The client typically has an NPO diet order because this stops the activity of the pancreas, but their diet is progressed and they can take food by mouth when their pain is well managed.[16] In severe cases, parenteral nutrition may be required. If acute pancreatitis is caused by the presence of gallstones, an ERCP and/or a cholecystectomy may be performed. Clients with chronic pancreatitis will require pain management, a low-fat diet, and education on alcohol abstinence and potentially exogenous pancreatic enzymes.[17]
View a supplementary YouTube video[18] on pancreatitis: Acute pancreatitis.
Colon Cancer
Colon cancer is cancer of the colon or rectum and is one of the top causes of death in the United States. Risk factors for colon cancer are a family history, the presence of colon polyps, a history of inflammatory bowel disease, prior radiation to the abdomen, obesity, tobacco or alcohol use, and the intake of red or processed meat.[19],[20]
Colon cancer forms after a number of genetic mutations result in cellular changes in the colon. Once colon cancer develops, it can be staged using the TNM system.[21],[22] For more information on this system of staging, please visit the “Malignancy and Autoimmune Alterations” chapter of this textbook.
Sometimes colon cancer is found incidentally during a colonoscopy or at-home colon cancer screening. A popular at-home screening is Cologuard, which looks for abnormal DNA and blood in a stool sample. Others may have symptoms such as blood in the stool, abdominal pain, anemia, and changes in bowel movements that prompt them to seek medical care. Colon cancer commonly spreads to the liver, lungs, and/or lymph nodes. Clients with metastasis may have additional signs and symptoms.[23],[24]
A definitive diagnosis of colon cancer requires a colonoscopy with a biopsy, but it could also be detected with a barium enema, CT scan, or MRI. A CEA test, a tumor marker blood test, may also be elevated with colon cancer. However, this test is used to monitor treatment response, not to diagnose.[25],[26]
Colon cancer can be treated with surgical removal of the cancerous area and affected lymph nodes, chemotherapy, immunotherapy, or other biologic agents. If the entire colon must be removed, the client will end up with a colostomy.[27],[28] For more information on nursing care of clients with cancer, please visit the “Malignancy and Autoimmune Alterations” chapter.
View a supplementary YouTube video[29] on Cologuard testing: Cologuard video: Colon Cancer Screening with Cologuard – Easy At-Home Kit Explained.
- Cleveland Clinic. (n.d.). Portal hypertension. https://my.clevelandclinic.org/health/diseases/4912-portal-hypertension ↵
- Hepatic Cirrhosis by Sharma & John is licensed under CC BY-NC-ND 4.0 ↵
- Cleveland Clinic. (n.d.). Portal hypertension. https://my.clevelandclinic.org/health/diseases/4912-portal-hypertension ↵
- Hepatic Cirrhosis by Sharma & John is licensed under CC BY-NC-ND 4.0 ↵
- Goldberg, E. & Chopra, S. (2023). Cirrhosis in Adults: Etiologies, Clinical Manifestations, and Diagnosis. https://www.uptodate.com/contents/cirrhosis-in-adults-etiologies-clinical-manifestations-and-diagnosis ↵
- Cleveland Clinic. (n.d.). Portal hypertension. https://my.clevelandclinic.org/health/diseases/4912-portal-hypertension ↵
- Hepatic Cirrhosis by Sharma & John is licensed under CC BY-NC-ND 4.0 ↵
- Cleveland Clinic. (n.d.). Portal hypertension. https://my.clevelandclinic.org/health/diseases/4912-portal-hypertension ↵
- Hepatic Cirrhosis by Sharma & John is licensed under CC BY-NC-ND 4.0 ↵
- Cleveland Clinic. (n.d.). Portal hypertension. https://my.clevelandclinic.org/health/diseases/4912-portal-hypertension ↵
- Hepatic Cirrhosis by Sharma & John is licensed under CC BY-NC-ND 4.0 ↵
- Pancreatitis by Mohy-ud-din & Morrissey is licensed under CC BY-NC-ND 4.0 ↵
- Pancreatitis by Mohy-ud-din & Morrissey is licensed under CC BY-NC-ND 4.0 ↵
- Pancreatitis by Mohy-ud-din & Morrissey is licensed under CC BY-NC-ND 4.0 ↵
- Pancreatitis by Mohy-ud-din & Morrissey is licensed under CC BY-NC-ND 4.0 ↵
- Medline Plus. (2023). Acute Pancreatitis. https://medlineplus.gov/ency/article/000287.htm ↵
- Pancreatitis by Mohy-ud-din & Morrissey is licensed under CC BY-NC-ND 4.0 ↵
- Animated Pancreas Patient. (2013, September 6). Acute pancreatitis [Video]. YouTube. All rights reserved. https://www.youtube.com/watch?v=inRSjh3bHPg ↵
- Cleveland Clinic. (n.d.). CEA test (carcinoembryonic antigen). https://my.clevelandclinic.org/health/diagnostics/22744-cea-test-carcinoembryonic-antigen ↵
- Colon Cancer by Lotfollahzadeh, Recio-Boiles, & Cagir is licensed under CC BY-NC-ND 4.0 ↵
- Cleveland Clinic. (n.d.). CEA test (carcinoembryonic antigen). https://my.clevelandclinic.org/health/diagnostics/22744-cea-test-carcinoembryonic-antigen ↵
- Colon Cancer by Lotfollahzadeh, Recio-Boiles, & Cagir is licensed under CC BY-NC-ND 4.0 ↵
- Cleveland Clinic. (n.d.). CEA test (carcinoembryonic antigen). https://my.clevelandclinic.org/health/diagnostics/22744-cea-test-carcinoembryonic-antigen ↵
- Colon Cancer by Lotfollahzadeh, Recio-Boiles, & Cagir is licensed under CC BY-NC-ND 4.0 ↵
- Cleveland Clinic. (n.d.). CEA test (carcinoembryonic antigen). https://my.clevelandclinic.org/health/diagnostics/22744-cea-test-carcinoembryonic-antigen ↵
- Colon Cancer by Lotfollahzadeh, Recio-Boiles, & Cagir is licensed under CC BY-NC-ND 4.0 ↵
- Cleveland Clinic. (n.d.). CEA test (carcinoembryonic antigen). https://my.clevelandclinic.org/health/diagnostics/22744-cea-test-carcinoembryonic-antigen ↵
- Colon Cancer by Lotfollahzadeh, Recio-Boiles, & Cagir is licensed under CC BY-NC-ND 4.0 ↵
- UC Davis Health. (2023, October 16). Colon cancer screening with Cologuard - Easy at-home kit explained [Video]. YouTube. All rights reserved. https://www.youtube.com/watch?v=ZcFGgFFY3Eo ↵
ABCDE: A mnemonic for assessing for melanoma developing in moles: Asymmetrical, Borders are irregular in shape, Color is various shades of brown or black, Diameter is larger than 6 mm., and the shape of the mole is Evolving.
Acne: A skin disturbance that typically occurs on areas of the skin that are rich in sebaceous glands, such as the face and back.
Apocrine sweat gland: Sweat glands associated with hair follicles in densely hairy areas that release organic compounds subject to bacterial decomposition causing odor.
Blanching: To make white or pale by applying pressure.
Cyanosis: A bluish discoloration caused by lack of oxygenation of the tissue.
Dermis: The inner layer of skin with connective tissue, blood vessels, sweat glands, nerves, hair follicles, and other structures.
Diaphoretic: Excessive, abnormal sweating.
Ecchymosis: Bruising.
Eccrine sweat gland: Sweat gland that produces hypotonic sweat for thermoregulation.
Epidermis: The thin, uppermost layer of skin.
Erythema: A red color of the skin.
First-degree burn: A superficial burn that affects only the epidermis.
Fourth-degree burn: Severe burn damaging the dermis and the underlying muscle and bone.
Hypodermis: The layer of skin beneath the dermis composed of connective tissue and used for fat storage.
Jaundice: A yellowing of the skin or sclera caused by underlying medical conditions.
Keloid: A raised scar caused by overproduction of scar tissue.
Lesion: An area of abnormal tissue.
Lymphedema: A type of swelling that occurs when lymph fluid builds up in the body's soft tissues due to damage to the lymph system.
Melanin: Skin pigment produced by melanocytes scattered throughout the epidermis.
Melanoma: Skin cancer characterized by the uncontrolled growth of melanocytes that commonly develops from a mole. Melanoma is the most fatal of all skin cancers because it is highly metastatic. Melanomas usually appear as asymmetrical brown and black patches with uneven borders and a raised surface.
Pallor: A reduced amount of oxyhemoglobin the skin or mucous membranes. Skin and mucous membranes present with a pale skin color.
Petechiae: Tiny red dots caused by bleeding under the skin.
Pressure injury: Skin breakdown caused when a patient’s skin and soft tissue press against a hard surface for a prolonged period of time, causing reduced blood supply and resulting in damaged tissue.
Rule of Nines: A tool used in the emergency department to assess the total body surface area burned to quickly estimate intravenous fluid requirements.
Second-degree burn: Burn affecting both the epidermis and a portion of the dermis, resulting in swelling and a painful blistering of the skin.
Skin turgor: The skin's elasticity and its ability to change shape and return to normal when gently grasped between two fingers.
Third-degree burn: Severe burn that fully extends into the epidermis and dermis, destroying the tissue and affecting the nerve endings and sensory function.
ABCDE: A mnemonic for assessing for melanoma developing in moles: Asymmetrical, Borders are irregular in shape, Color is various shades of brown or black, Diameter is larger than 6 mm., and the shape of the mole is Evolving.
Acne: A skin disturbance that typically occurs on areas of the skin that are rich in sebaceous glands, such as the face and back.
Apocrine sweat gland: Sweat glands associated with hair follicles in densely hairy areas that release organic compounds subject to bacterial decomposition causing odor.
Blanching: To make white or pale by applying pressure.
Cyanosis: A bluish discoloration caused by lack of oxygenation of the tissue.
Dermis: The inner layer of skin with connective tissue, blood vessels, sweat glands, nerves, hair follicles, and other structures.
Diaphoretic: Excessive, abnormal sweating.
Ecchymosis: Bruising.
Eccrine sweat gland: Sweat gland that produces hypotonic sweat for thermoregulation.
Epidermis: The thin, uppermost layer of skin.
Erythema: A red color of the skin.
First-degree burn: A superficial burn that affects only the epidermis.
Fourth-degree burn: Severe burn damaging the dermis and the underlying muscle and bone.
Hypodermis: The layer of skin beneath the dermis composed of connective tissue and used for fat storage.
Jaundice: A yellowing of the skin or sclera caused by underlying medical conditions.
Keloid: A raised scar caused by overproduction of scar tissue.
Lesion: An area of abnormal tissue.
Lymphedema: A type of swelling that occurs when lymph fluid builds up in the body's soft tissues due to damage to the lymph system.
Melanin: Skin pigment produced by melanocytes scattered throughout the epidermis.
Melanoma: Skin cancer characterized by the uncontrolled growth of melanocytes that commonly develops from a mole. Melanoma is the most fatal of all skin cancers because it is highly metastatic. Melanomas usually appear as asymmetrical brown and black patches with uneven borders and a raised surface.
Pallor: A reduced amount of oxyhemoglobin the skin or mucous membranes. Skin and mucous membranes present with a pale skin color.
Petechiae: Tiny red dots caused by bleeding under the skin.
Pressure injury: Skin breakdown caused when a patient’s skin and soft tissue press against a hard surface for a prolonged period of time, causing reduced blood supply and resulting in damaged tissue.
Rule of Nines: A tool used in the emergency department to assess the total body surface area burned to quickly estimate intravenous fluid requirements.
Second-degree burn: Burn affecting both the epidermis and a portion of the dermis, resulting in swelling and a painful blistering of the skin.
Skin turgor: The skin's elasticity and its ability to change shape and return to normal when gently grasped between two fingers.
Third-degree burn: Severe burn that fully extends into the epidermis and dermis, destroying the tissue and affecting the nerve endings and sensory function.
Learning Objectives
- Safely administer medication orally, rectally, and via enteral tubes
- Accurately check medication administration rights three times
- Calculate correct amount of medication to administer
- Explain medication information to patient
- Collect appropriate assessment data prior to and after medication administration
- Modify procedure to reflect variations across the life span
- Document actions and observations
“Enteral” means related to the intestines. The term enteral medication describes medications that are administered into the gastrointestinal tract, including orally (PO), rectally (PR), or through a tube such as a nasogastric (NG) tube, nasointestinal (NI) tube, or percutaneous endoscopic gastrostomy (PEG) tube.
This chapter will review overall concepts related to safe medication administration, as well as specific information regarding the administration of oral medication, rectal medication, and medication via a gastric tube. Information regarding administering injections and intravenous medications can be found in "Administration of Parenteral Medications" and additional information about administering medications via other routes can be found in "Administration of Medications via Other Routes."
Learning Objectives
- Safely administer medication orally, rectally, and via enteral tubes
- Accurately check medication administration rights three times
- Calculate correct amount of medication to administer
- Explain medication information to patient
- Collect appropriate assessment data prior to and after medication administration
- Modify procedure to reflect variations across the life span
- Document actions and observations
“Enteral” means related to the intestines. The term enteral medication describes medications that are administered into the gastrointestinal tract, including orally (PO), rectally (PR), or through a tube such as a nasogastric (NG) tube, nasointestinal (NI) tube, or percutaneous endoscopic gastrostomy (PEG) tube.
This chapter will review overall concepts related to safe medication administration, as well as specific information regarding the administration of oral medication, rectal medication, and medication via a gastric tube. Information regarding administering injections and intravenous medications can be found in "Administration of Parenteral Medications" and additional information about administering medications via other routes can be found in "Administration of Medications via Other Routes."