Home Blog Page 354

New treatment is now available for patients with Non-Hodgkins Lymphoma and Multiple Myeloma

0

MozobilTM (plerixafor), a new treatment for the mobilization of stem cells in patients with non-Hodgkin’s Lymphoma (NHL) and multiple myeloma (MM), is now available in Canada. MozobilTM is designed to mobilize hematopoietic stem cells from the bone marrow into the bloodstream where they can be collected, making it more likely for patients with certain types of cancer to proceed to transplant. Currently, before a transplant takes place, patients receive growth factors and possibly chemotherapy to mobilize hematopoietic stem cells into the bloodstream, allowing them to be collected. A minimum number of 2 million stem cells per kilogram of body weight must be collected; for many patients this process can take three of four hours over multiple days to complete and ~15 to 20% of patients fail to mobilize enough cells. This new treatment option enhances the probability of a successful stem cell collection and subsequent transplant provides hope for those patients who otherwise would not have had this option.

Researchers develop rapid test strips for bacterial contamination in swimming water

0

Researchers at McMaster University have developed a rapid testing method using a simple paper strip that can detect E. coli in recreational water within minutes with much greater accuracy than existing portable technology. This new tool can contribute to improved global public safety. The work is described in a paper published in the journal Analytical and Bioanalytical Chemistry. “Coliforms are always a big problem,” says the paper’s lead author John Brennan, a McMaster chemistry professor who holds the Canada Research Chair in Bioanalytical Chemistry. “The methods used to detect outbreaks are slow, and tend not to be portable, as they often need a lab-based amplification step prior to testing, causing a time lag between an outbreak and a beach closure.” These new strips are coated with chemicals that react to the bacteria, and are printed using inkjet technology. Within 30 minutes of sampling, the paper changes colour to indicate the presence of E. coli, with colours coded to represent different forms and concentrations of the bacteria. Commercialization of a final product could take as little as two to three years.

Canadian cancer death rate is decreasing

0

Canadian Cancer Statistics 2012 released by the Canadian Cancer Society in collaboration with the Public Health Agency of Canada and Statistics Canada has revealed that the cancer death rate in Canada is decreasing. Between 1988 and 2007, overall death rates dropped by 21% in men and 9% in women, resulting in nearly 100,000 lives saved over the last 20 years. Declines in death rates were seen in all four major cancers: lung, colorectal, breast, and prostate. Although the death rate is dropping, cancer is still the leading cause of death in Canada. “A large body of evidence has accumulated over the last 30 years showing that about half of cancers can be prevented,” says Gillian Bromfield, Director, Cancer Control Policy, Canadian Cancer Society. “Even greater gains can be made in reducing cancer rates if more is done to help Canadians embrace healthy lifestyles and if governments do more to create policies that encourage people to make these changes.” For more information about Canadian Cancer Statistics 2012, visit the Society’s website at cancer.ca/ statistics

Researchers discover the gene for a rare disorder

0

Using next-generation sequencing technology, researchers at Alberta Children’s Hospital Research Institute (ACHRI) have identified the gene that causes Nager Syndrome, a condition that causes deformation in a child’s face and limbs, as well as deafness. This gene has eluded scientists for more than 60 years. “Genetic disorders of children are individually rare but collectively common, affecting the lives of hundreds of thousands of children in Canada. And most of the genes that cause these conditions have yet to be found,” says Dr. Francois Bernier. “While Nager Syndrome may be rare, it doesn’t feel like it when it’s your child whose future health is unknown.” This discovery was the result of an international collaboration between FORGE Canada and the University of Washington.

Home-based dialysis is more popular in developing versus developed countries

0

Researchers at Lawson Health Research Institute at London Health Sciences Centre have discovered that developing countries have faster growing rates of home-based peritoneal dialysis for kidney failure than the developed world. This is noteworthy since peritoneal dialysis is more cost effective than hospital-based hemodialysis. Records from 1997 to 2008 in 130 countries were analyzed and results revealed that 59% of peritoneal patients were treated in developing countries as opposed to 41% in developed countries. Throughout the 12 years of the study, peritoneal dialysis patients in developing countries increased by 24.9 patients per million populations versus 21.8 per million populations in developed countries. Despite this increase, the overall proportion of all dialysis patients treated with peritoneal dialysis in developed countries has actually declined by 5.3%, while developing countries have seen no change. The researchers believe that these findings may impact future business and research innovations.

Canadian College of Naturopathic Medicine opens first integrative cancer centre in Eastern Canada

0

The Ottawa Integrative Cancer Centre (OICC), which is both a treatment clinic and an integrative oncology research centre, has opened its doors to provide multi- disciplinary complementary medicine and whole-person care for people with cancer. It is the first integrative oncology and research centre in Eastern Canada to provide whole-person cancer care that includes complementary medicine. The Centre’s clinical practice and visionary research agenda is led by Dugald Seely, ND, MSc, FABNO, the executive director and founder of the OICC who also serves as the Director of Research and Clinical Epidemiology at the Canadian College of Naturopathic Medicine (CCNM).“Providing complementary therapies in an evidence-based manner, supporting conventional medicine, is both desired by patientsandismuchneededinthecancer community,” says Seely. “Well over half of all cancer patients embrace complementary therapies alongside conventional treatments during their cancer journey and this proportion is growing. Often patients do not communicate their complementary care choices with conventional oncologists. A common concern among oncologists is the potential for complementary medicine to interfere with conventional therapies such as chemotherapy and radiation therapy. The OICC is committed to working with patients, their families and their health-care providers to develop a complementary, non-interfering therapeutic program to optimize overall wellness,” adds Seely.

Japanese bluefin tuna is carrying radioactive contamination

0

Massive bluefin tuna have carried radioactive contamination across 6,000 miles of the Pacific Ocean to the California shores. The Pacific bluefin tuna that can grow to 10 feet and weigh more than 1,000 pounds, spawn off the Japan coast and swim east at breakneck speed to school in waters off California and the tip of Baja California, Mexico. This is the first time a large migrating fish has been shown to carry radioactivity such a long distance. The levels of radioactive cesium were 10 times higher than the amount measured in tuna off the California coast in previous years. It is important to note that these levels are still far below safe-to-eat limits set by the U.S. and Japanese governments. Previously, smaller fish and plankton were found with elevated levels of radiation in Japanese waters after the March 2011 magnitude-9 earthquake that triggered a tsunami that damaged the Fukushima Dai-ichi reactors. Scientists report that bluefin tuna absorbed radioactive cesium from swimming in contaminated waters and feeding on contaminated prey such as krill and squid.

Gaia Integrative Clinic

0

Gaia Integrative Clinic 

Rural Canada welcomes naturopathic medicine

IHP is excited to introduce the Gaia Integrative Clinic, a multi-disciplinary wellness center located in downtown Yellowknife, Northwest Territories (NWT). Serving a relatively small ethnically diverse population of ~19 000 people, Gaia opened its doors in February 2012 and is already welcoming 150 to 175 patients through its doors each week. This is an excellent success story showcasing how a range of healthcare providers has come together within a circle of care to improve the health and wellbeing of a remote and under-serviced region of Canada

Despite a strong Aboriginal presence in Yellowknife, traditional healing methods are not commonly practiced and have been largely replaced by conventional healthcare treatment options. This motivated Naturopathic Doctor, Nicole Redvers, who was born and raised in the NWT, to bring her family back to the North after graduating from the Canadian College of Naturopathic Medicine. With a strong passion to offer Northerners different healthcare options, Nicole felt that Naturopathic Medicine’s holistic and respectful approach to healthcare could serve to bridge the gap between modern advances in medical science and more traditional forms of healing.

After receiving a federal grant and choosing a fantastic eclectic all-female team of healthcare providers, Nicole opened the Gaia Integrative Clinic and has been working to educate the public that complimentary methods of healthcare are acceptable and effective. Since it can take Northerners upwards of six to seven weeks to see their medical doctors, Gaia wanted to offer an extensive array of services to meet a variety of needs. Nicole, who is licensed as a Naturopathic Doctor in British Columbia (the NWT lacks naturopathic regulation), has advanced training in intravenous therapies and cosmetic acupuncture. She is also trained as a labor doula and is beginning her post-graduate training to become a naturopathic midwife. Dr. Carrie Lehman is a chiropractor whose additional training includes inspiral paediatrics, kinesiotaping, rock-taping, Active Release Technique, Graston Technique, clinical acupuncture, and custom orthotics. Corina Pletscher is a Registered Massage Therapist with additional training in Thai massage, myofascial release, craniosacral work, muscle energy, manual lymph drainage, trigger point therapy, deep tissue massage, and gentle relaxation. Simone Goudreau is a Life Coach, Weight Coach, and Visual Coach with additional Intuitive Eating PRO Skills training. Krystal Thompson practices Yoga therapy to help individuals achieve health and wellness through the application of yoga techniques and practices. Rhonda Miller is an Art Therapist who believes that the creative process involved in artistic self-expression helps people resolve conflicts and problems, develop interpersonal skills, reduce stress, and increase self-esteem and self-awareness. Olga Kovalenko, a certified massagist who focuses on deep tissue massage and aromatherapy, completes the team.

Screen Shot 2014-06-30 at 12.40.23 PM

Nicole is currently in discussions with local Elders about adding a Dene Natural Healer to the team since attempts to incorporate a traditional natural healer into the hospital have thus far been unsuccessful. Gaia is hopeful and optimistic that the addition of this unique service will shed further light on traditional Aboriginal healing methods.

Gaia’s clinic occupies 1900 square feet in a renovated house in downtown Yellowknife that is conveniently located across the street from a large medical clinic. The building boasts six treatment rooms, an infrared sauna room, an intravenous therapy area, and a meeting room that can comfortably accommodate 12-16 people for a meeting or 6-8 people for a yoga class. The clinic also has a laboratory and dispensing room. Completing all on site blood draws for laboratory testing, Gaia utilizes Rocky Mountain Analytical, Metamatrix, and Doctor’s Data and most commonly requisitions IgE and IgG food analyses and comprehensive stool analyses. The dispensary consists of a wide variety of high quality nutraceuticals, botanicals, topical creams, meal shakes, food bars, and homeopathics from such companies as AOR, NFH, Seroyal, Metagenics, Thorne, Biotics, Heel, Boiron, Pascoe, Ferlow Botanicals, St. Frances Herb Farm, Signature Supplements, Nordic Naturals, Elevate Me, The Simply Bar, and Purity Professionals. Individualized formulations (i.e., demulcents) can also be compounded as per patient requirement.

Supplying the dispensary and offering lab testing to patients presents unique challenges given Gaia’s remote geographical location. For example, instead of the typical one to two day delivery time most practitioners can expect upon placing a supplement order, shipments take ten to 14 days to arrive in Yellowknife and require extra ice packs for quality preservation. Ice road closures that may occur for up to four weeks provide additional complications as they prevent road access to Yellowknife and require that supplies must be flown in. Further, biological samples must be shipped to Edmonton at a cost of $60 per sample, thereby increasing test prices significantly while laboratory testing requiring time-sensitive samples must be avoided altogether. These restrictions mean that Gaia must generally rely on the cooperation of medical physicians to requisition standard blood work. Luckily, Gaia is already developing a trusted reputation within the medical community; a number of general practitioners have been quite supportive of the new clinic and are hoping to learn more about Gaia’s services from an upcoming grand rounds presentation by Nicole at the local hospital.

Gaia offers a variety of programs to the public, including: “Body Love Yoga Therapy” and “Make Peace Mondays”. Additional naturopathic-focused programs (i.e., detoxification, weight management, and smoking cessation) are available and will eventually be expanded to include other practitioners’ expertise.

Gaia has employed minimal formal advertising. Word of mouth, advertisements on Yellowknife’s popular YKTrader.com website, and posters placed in local grocery stores have proven successful. Gaia’s practitioners have attended health and wellness fairs held by the diamond mines, which has led to the development of a positive relationship and hopes for the future of one day having on site treatments as mine employees have excellent third party health insurance. The clinic’s massage therapists have also developed relationships with local hotels to offer treatments to weekend travelers. IHP would like to thank Gaia for allowing us to highlight this highly successful clinic in a remote area of our beautiful country. We hope that this clinic profile will serve as motivation for practitioners who are anxious about opening a clinic in a small community!

Screen Shot 2014-06-30 at 12.40.31 PM

Liver Cirrhosis

0

Liver Cirrhosis Naturopathic strategies

Abstract

Liver injury exists on a continuum from transiently elevated liver enzymes, to fatty deposits for example in non-alcoholic steatohepatitis (NASH), to liver fibrosis, which is the beginning of liver cirrhosis. Once the process has begun, liver cirrhosis can progress asymptomatically for years until the point where a critical threshold is reached, and remaining hepatocytes can no longer compensate for lost function – decompensated liver disease. This article reviews staging of liver cirrhosis, and focuses on naturopathic treatment strategies than can maximize liver function in cases of moderate to advanced cirrhosis as well as hepatic encephalopathy (HE). These strategies include adequate dietary intake of calories and protein, and restriction of sodium. Nutritional supplementation strategies include branched chain amino acids, probiotics, acetyl-L-carnitine, zinc, silymarin, LOLA (L-ornithine, L-aspartate), and phosphatidylcholine. This paper reviews the evidence supporting these interventions as well as dosing recommendations based on the literature.

Introduction

Cirrhosis is the 12th leading cause of death in the United States, accounting for almost 30 thousand deaths per year (Starr 2011). The leading causes of cirrhosis include chronic alcohol abuse and viral hepatitis; however cirrhosis is the common end pathway of several types of liver injury, including non-alcoholic fatty liver disease (NAFLD), autoimmune hepatic or biliary disease, and obstructive tumors of the liver or biliary ducts (Starr 2011). Liver cirrhosis or “scarring” leads to gradual loss of liver function and the eventual emergence of decompensated liver disease, including hepatic encephalopathy and ascites. This paper will discuss naturopathic strategies that can assist in the management of cirrhosis, particularly decompensated cirrhosis. Intervention with a selection of natural agents offers the potential for delaying and/ or alleviating some of the symptoms associated with this condition, for which conventional treatments remain limited.

Pathophysiology

Cirrhosis is “a late stage of hepatic fibrosis that has resulted in widespread distortion of normal hepatic architecture… characterized by regenerative nodules surrounded by dense fibrotic tissue” (Merck 2011). The replacement of functional hepatocytes with non-functioning fibrous tissue results in progressive loss of liver function. Table 1 describes the sequelae of advanced cirrhosis. According to Wolf, these arise from three common underlying malfunctions: “decreased hepatic synthetic function (eg, coagulopathy), decreased detoxification capabilities of the liver (eg, hepatic encephalopathy), [and] portal hypertension (eg, variceal bleeding)” (2011).

Conventional treatment

Cirrhosis is non-reversible, and current treatments are supportive in nature (Merck 2011). These include lactulose to promote bowel elimination of ammonia; neomycin or rifaximin, antibiotics that decreased ammonia producing bacteria in the gut; and salt restrction, diuretics, and paracentesis (peritoneal “tap” procedure with fluid removal) if necessary for ascites (Foster 2010, Starr 2011). The last resort for liver failure is an organ transplant (Merck 2011).

Cirrhosis is staged using the Child-Turcotte-Pugh Scoring System (See Table 2). Severity is scored as (Merck 2011):

• Child Class A=5-6 points (1y survival 100%);

• Child Class B=7-9 points (1y survival 80%);

• Child Class C=10-15 points (1y survival 45%)

Hepatic encephalopathy (HE) ranges from minimal encephalopathy (grade 1-2) to coma (grade 4) in end stage liver disease (ESLD). Minimal encephalopathy is present in 30-84% of patients with cirrhosis (Chadalavada 2010); patients may have an apparently normal mental status, with abnormalities detected only with psychometric testing, but may have intermittent episodes of worsened encephalopathy that may be triggered by infection, diuretic therapy, hypovolemia, renal failure, GI bleeding, infection, and constipation (Chadalavada 2010, Wolf 2011). Certain pscyhoactive medications may also worsen HE (Wolf 2011). HE is graded symptomatically (Merck 2011):

• Grade 1) Sleep disturbance; impaired concentration; depression, anxiety, or irritability

• Grade 2) Drowsiness, disorientation, poor short-term memory; uninhibited behaviour

• Grade 3) Somnolence, confusion, amnesia, anger, paranoia, bizarre behaviour

• Grade 4) Coma

Table 1. Sequelae of Cirrhosis (Merck 2011, Wolf 2011)
Table 1. Sequelae of Cirrhosis (Merck 2011, Wolf 2011)
Table 2. Child-Turcotte-Pugh Scoring System for Cirrhosis (adapted from Wolf 2011).
Table 2. Child-Turcotte-Pugh Scoring System for Cirrhosis (adapted from Wolf 2011).

Dietary Guidelines

The goals of dietary treatment for cirrhosis are three-fold:

1) Maintain adequate caloric intake (30-35 kcal/kg dry weight = 1800 kcal/ 60kg person) (Bemeur 2010). Patients with cirrhosis are often undernourished due to anorexia and poor nutrient absorption. Recommendations for dietary composition are 50-60% of calories as carbohydrate; 20-30% as protein; and 10-20% as fat (Chadalavada 2010).

2) Adequate protein intake (1.2 – 1.5 g/kg protein daily) (Bemeur 2010). Traditionally, a low-protein diet (0-40g/d) has been advocated, since ammonia is derived from protein. Recently there is a growing consensus that this strategy is counterproductive. Inducing a state of protein and/ or calorie malnutrition results in catabolism of muscle protein, and has the double effect of increasing ammonia and causing malnutrition & loss of muscle mass; and patients with cirrhosis have increased protein requirements (Cabral 2011). Instead protein restriction should be limited to a small number of protein-intolerant patients in grade 3-4 HE, if there is a lack of response to other therapies, and only for short periods of time (Bemeur 2010). Wolf says, “the vast majority of patients can tolerate a protein-rich diet (>1.2 g/kg/d) including well-cooked chicken, fish, vegetable protein, and, if needed, protein supplements” (2011).

Recent studies have shown that protein intake is safe and has little impact on HE (Cordoba 2004), and a trial by Gheorghe found that a casein-vegetable-based, high-protein high-calorie (HPHC) diet decreased serum ammonia levels and resulted in improved mental status in patients with overt HE (2005).

3) Salt restriction. To minimize sodium/ water retention and ascites, an initial limit of <2000mg sodium/d is utilized; if this is ineffective, a limit of <500mg/d is used.

Dietary changes (eg. fibre intake) to ensure regular elimination through the gut should also be implemented.

Supplemental Interventions

Select nutritional supplements have been shown to improve liver function and decrease ammonia levels, resulting in clinical improvements in patients with HE.

Branched chain amino acids (leucine, isoleucine, valine) are probably the best- studied supplemental intervention for HE. Although their use has been debated, the discussion seems to have settled in favour of BCAAs (Cabral 2011). The European Society for Parenteral and Enteral Nutrition (ESPEN) has strengthened its recommendation for BCAAs in decompensated liver cirrhosis to grade B (Plauth 2006). BCAAs promote protein synthesis and decrease blood ammonia levels (Cabral 2011); compete with aromatic amino acids (phenylalanine, tyrosine, tryptophan) for uptake into the CNS, where these are thought to contribute to HE (Cabral 2011, Iwasa 2003); stimulate human growth factor (HGF), which promotes hepatic regeneration; and there is some indication that they might lower risk of hepatocellular carcinoma (Kobayashi 2008). Clinical trials have shown that BCAA administration improves neurophysiological function and psychometric testing in HE (Egberts 1986, Higuchi 1994, Plauth 1993). In a randomized double blind trial, Marchesini found that BCAA supplemented at 0.24 g/kg (approx. 14g for a 60kg person) for three months rapidly improved neuropsychologic function, and resulted in mild improvement in nutritional parameters and liver function tests (1990).

Kawamura found that in patients with early cirrhosis (Child class A), administration of 12.45g/d BCAAs for 3.2y resulted in significantly slower changes in markers of progression (2009). In addition, BCAAs lowered the incidence of overall major cirrhotic complications to 14.8% (4 of 27 patients) compared to 30.4% (7 of 23 patients) in the control group at 3 years (P = 0.043); potentially prolonging the waiting period until liver organ transplantation is necessary (Kawamura 2009). Similar findings have been corroborated in other studies, where 12g/d BCAAs for 2y reduced risk of the following complications by 33% (HR 0.67, 95% CI 0.49-0.93): death by any cause, development of liver cancer, rupture of esophageal varices, or progress of hepatic failure (Muto 2005).

Conversely, Les et al found that administration of 30g BCAAs daily for approximately one year to 116 patients resulted in improvements in symptoms of minimal HE, but did not reduce rates of recurrence for having an episode of acute HE (2011). This may be in part due to the multifactorial nature of the influences on acute HE (see above sections). BCAAs as part of a more comprehensive nutritional and lifestyle approach might be of benefit in this respect.

Probiotics. Administration of probiotic bacteria has been shown to reduce ammonia levels by competing with urease- producing species such as Klebsiella and Proteus species (Pereg 2011). Malaguarnera found that compared to lactulose treated patients, those treated with Bifidobacterium had significantly improved mental functioning and lower ammonia levels (2010, 2007). Liu found that probiotics plus fiber lowered ammonia levels and improved Child-Turcotte-Pugh functional class in nearly 50% of cases with minimal HE (2004).

Acetyl L carnitine In advanced HE, use of intravenous acetyl L carnitine (ALC) in addition to BCAA has been shown to benefit neurological status (Glasgow coma scale); EEG parameters; serum ammonia; and improve HE grade from 4 to 3 in some patients (54% in one study) compared to BCAA alone (Malaguarnera 2006, 2009).

In earlier stages, oral ALC has shown benefit on neurophysiological function tests, prothrombin time (P < 0.001), bilirubin serum levels (P < 0.01), AST (P < 0.001), fasting serum ammonia levels (P < 0.001), and a significant increase in albumin serum levels (P < 0.005) (Malaguarnera 2008). Although the mechanism by which ALC exerts its effects in HE is unclear, carnitine is known to participate in ketone body production, facilitate mitochondrial function through transfer of acetylCoA, and aid production of acetylcholine (Shores 2008).

Zinc supplementation (225mg zinc acetate) for six months significantly decreased HE grade and blood ammonia levels (P = 0.03 and P = 0.01), and improved Child-Pugh score and neuropsychological tests compared with standard therapy (P = 0.04 and P = 0.02) in patients with grade 1 or 2 recurrent episodic HE unresponsive to standard therapies (lactulose and a proteinrestricted diet) (Takuma 2010). A smaller cross-over trial of 15 patients found lack of effect from 600mg zinc sulfate (Riggio 1991), while an earlier randomized double-blind trial of 22 HE patients did find benefit (Reding 1984). Authors postulated that zinc “probably improved hepatic encephalopathy by correcting the zinc deficiency that compromises conversion of ammonia to urea” (Reding 1984). Although these studies utilize very high dosages, it is possible that more modest dosages (~30mg) may also be of benefit.

Silymarin has not been studied specifically for HE, however it has been studied extensively as a hepatoprotective for liver cirrhosis. A randomized double blind placebo controlled trial of silymarin 140mg three times daily in patients with alcoholic liver cirrhosis found that silymarin significantly prolonged survival: 4-year survival rate 58% in silymarin-treated patients and 39% in the placebo group (P = 0.036) (Ferenci 1989). A more recent meta analysis by Saller including 19 trials found a lack of evidence of silymarin on progression of viral hepatitis, but a reduction in AST (p = 0.01) in alcoholic liver disease in silymarin-treated patients compared with placebo (2008). In liver cirrhosis, total mortality was 16.1% with silymarin and 20.5% with placebo (non-significant), and liver-related mortality was 10.0% with silymarin vs. 17.3% with placebo(p = 0.01) (Saller 2008).  

LOLA (L-ornithine, L-aspartate) is another intervention that has been demonstrated to lower ammonia and improve neurological function (Poo 2006). LOLA stimulates the urea cycle and glutamine synthesis which promote ammonia detoxification (Rees 2000).

Phosphatidylcholine Although better studied for NAFLD, a single study reports benefits with use of 2.0g daily of an intravenous formula of “essential phospholipids” including phosphatidylcholine (PC) in patients with stage 3-4 HE (Bruha 2000). Ammonia reductions of ~50% were reported in the treatment group but none in the control group, and survival time was longer in the treatment group: 50.3 versus 34.7 days. A second study reports improvements in liver function (AST, bilirubin) with 1.5g polyenylphosphatidylcholine in subgroups of patients out of a cohort of veterans with chronic alcohol abuse; the groups that benefited most were those with hepatitis C and heavy drinkers (Lieber 2003). It is possible that oral PC may also be of benefit in earlier stages of HE/ cirrhosis.

Other agents for which evidence specific to cirrhosis/ HE is lacking at present, but which may be of benefit based on their mechanism of action include alpha lipoic acid, N-acetyl-cysteine, eicosapentanoic acid, and betaine.

Conclusion

Liver cirrhosis severity ranges from having little or no symptoms (compensated disease), to having minimal-tosevere HE, ascites, and other complications as the pathology progresses. Conventional treatment for cirrhosis and HE remain limited. A selection of natural interventions has shown promise in ameliorating symptoms associated with HE when present, and potentially delaying the onset and progression of HE and cirrhosis, respectively in earlier stages. In addition to specific dietary guidelines, these agents include BCAAs, probiotics, acetyl L carnitine, silymarin, zinc, LOLA, and phosphatidylcholine.

Table 3. Natural Interventions for Liver Cirrhosis
Table 3. Natural Interventions for Liver Cirrhosis

References

Bémeur C, Desjardins P, Butterworth RF. Role of nutrition in the management of hepatic encephalopathy in end-stage liver failure. J Nutr Metab. 2010;2010:489823.

Brůha R, Marecek Z. [Essential phospholipids in the treatment of hepatic encephalopathy]. Vnitr Lek. 2000 Apr;46(4):199-204.

Cabral CM, Burns DL. Low-protein diets for hepatic encephalopathy debunked: let them eat steak. Nutr Clin Pract. 2011 Apr;26(2):155-9.

Chadalavada R, Sappati Biyyani RS, Maxwell J, Mullen K. Nutrition in hepatic encephalopathy. Nutr Clin Pract. 2010 Jun;25(3):257-64.

Córdoba J, López-Hellín J, Planas M, Sabín P, Sanpedro F, Castro F, Esteban R, Guardia J. Normal protein diet for episodic hepatic encephalopathy: results of a randomized study. J Hepatol. 2004 Jul;41(1):38-43.

Egberts EH, Schomerus H, Hamster W, Jürgens P. [Branched-chain amino acids in the treatment of latent porto-systemic encephalopathy. A placebo-controlled doubleblind cross-over study]. Z Ernahrungswiss. 1986 Mar;25(1):9-28.

Ferenci P, Dragosics B, Dittrich H, Frank H, Benda L, Lochs H, Meryn S, Base W, Schneider B. Randomized controlled trial of silymarin treatment in patients with cirrhosis of the liver. J Hepatol. 1989 Jul;9(1):105-13.

Foster KJ, Lin S, Turck CJ. Current and emerging strategies for treating hepatic encephalopathy. Crit Care Nurs Clin North Am. 2010 Sep;22(3):341-50.

Gheorghe L, Iacob R, Vădan R, Iacob S, Gheorghe C. Improvement of hepatic encephalopathy using a modified high-calorie high-protein diet. Rom J Gastroenterol. 2005 Sep;14(3):231-8.

Higuchi K, Shimizu Y, Nambu S, Miyabayashi C, Takahara T, Saito S, Hioki O, Kuwabara Y, Watanabe A. Effects of an infusion of branched-chain amino acids on neurophysiological and psychometric testings in cirrhotic patients with mild hepatic encephalopathy. J Gastroenterol Hepatol. 1994 Jul-Aug;9 (4):366-72.

Iwasa M, Matsumura K, Watanabe Y, Yamamoto M, Kaito M, Ikoma J, Gabazza EC, Takeda K, Adachi Y. Improvement of regional cerebral blood flow after treatment with branched-chain amino acid solutions in patients with cirrhosis. Eur J Gastroenterol Hepatol. 2003 Jul;15(7):733-7.

Kawamura E, Habu D, Morikawa H, Enomoto M, Kawabe J, Tamori A, Sakaguchi H, Saeki S, Kawada N, Shiomi S. A randomized pilot trial of oral branched-chain amino acids in early cirrhosis: validation using prognostic markers for pre-liver transplant status. Liver Transpl. 2009 Jul;15(7):790-7.

Kobayashi M, Ikeda K, Arase Y, Suzuki Y, Suzuki F, Akuta N, Hosaka T, Murashima N, Saitoh S, Someya T, Tsubota A, Kumada H. Inhibitory effect of branched-chain amino acid granules on progression of compensated liver cirrhosis due to hepatitis C virus. J Gastroenterol. 2008;43(1):63-70.

Les I, Doval E, García-Martínez R, Planas M, Cárdenas G, Gómez P, Flavià M, Jacas C, Mínguez B, Vergara M, Soriano G, Vila C, Esteban R, Córdoba J. Effects of branched-chain amino acids supplementation in patients with cirrhosis and a previous episode of hepatic encephalopathy: a randomized study. Am J Gastroenterol. 2011 Jun;106(6):1081-8.

Lieber CS, Weiss DG, Groszmann R, Paronetto F, Schenker S; Veterans Affairs Cooperative Study 391 Group. II. Veterans Affairs Cooperative Study of polyenylphosphatidylcholine in alcoholic liver disease. Alcohol Clin Exp Res. 2003 Nov;27(11):1765-72.

Liu Q, Duan ZP, Ha DK, Bengmark S, Kurtovic J, Riordan SM. Synbiotic modulation of gut flora: effect on minimal hepatic encephalopathy in patients with cirrhosis. Hepatology. 2004 May;39(5):1441-9.

Loguercio C, Del Vecchio Blanco C, Coltorti M. Enterococcus lactic acid bacteria strain SF68 and lactulose in hepatic encephalopathy: a controlled study. J Int Med Res. 1987 Nov-Dec;15(6):335-43.

Malaguarnera M, Gargante MP, Malaguarnera G, Salmeri M, Mastrojeni S, Rampello L, Pennisi G, Li Volti G, Galvano F. Bifidobacterium combined with fructo-oligosaccharide versus lactulose in the treatment of patients with hepatic encephalopathy. Eur J Gastroenterol Hepatol. 2010 Feb;22(2):199-206.

Malaguarnera M, Risino C, Cammalleri L, Malaguarnera L, Astuto M, Vecchio I, Rampello L. Branched chain amino acids supplemented with L-acetylcarnitine versus BCAA treatment in hepatic coma: a randomized and controlled double blind study. Eur J Gastroenterol Hepatol. 2009 Jul;21(7):762-70.

Malaguarnera M, Gargante MP, Cristaldi E, Vacante M, Risino C, Cammalleri L, Pennisi G, Rampello L. Acetyl-L-carnitine treatment in minimal hepatic encephalopathy. Dig Dis Sci. 2008 Nov;53(11):3018-25.

Malaguarnera M, Greco F, Barone G, Gargante MP, Malaguarnera M, Toscano MA. Bifidobacterium longum with fructo-oligosaccharide (FOS) treatment in minimal hepatic encephalopathy: a randomized, double-blind, placebo-controlled study. Dig Dis Sci. 2007 Nov;52(11):3259-65.

Malaguarnera M, Pistone G, Astuto M, Vecchio I, Raffaele R, Lo Giudice E, Rampello L. Effects of L-acetylcarnitine on cirrhotic patients with hepatic coma: randomized double-blind, placebo-controlled trial. Dig Dis Sci. 2006 Dec;51(12):2242-7.

Malaguarnera M, Pistone G, Elvira R, Leotta C, Scarpello L, Liborio R. Effects of L-carnitine in patients with hepatic encephalopathy. World J Gastroenterol. 2005 Dec 7;11(45):7197-202.

Malaguarnera M, Pistone G, Astuto M, Dell’Arte S, Finocchiaro G, Lo Giudice E, Pennisi G. L-Carnitine in the treatment of mild or moderate hepatic encephalopathy. Dig Dis. 2003;21(3):271-5.

Marchesini G, Dioguardi FS, Bianchi GP, Zoli M, Bellati G, Roffi L, Martines D, Abbiati R. Long-term oral branched-chain amino acid treatment in chronic hepatic encephalopathy. A randomized double-blind casein-controlled trial. The Italian Multicenter Study Group. J Hepatol. 1990 Jul;11(1):92-101.

The Merck Manual of Diagnosis and Therapy, Nineteenth Edition. Cirrhosis. Ed. Eldon A. Shaffer. Updated 2011. http://www.merckmanuals.com/professional/hepatic_

and_biliary_disorders/fibrosis_and_cirrhosis/cirrhosis.html Accessed 14 April 2012.

Muto Y, Sato S, Watanabe A, Moriwaki H, Suzuki K, Kato A, Kato M, Nakamura T, Higuchi K, Nishiguchi S, Kumada H; Long-Term Survival Study Group. Effects of oral branched-chain amino acid granules on event-free survival in patients with liver cirrhosis. Clin Gastroenterol Hepatol. 2005 Jul;3(7):705-13.

O’Keefe SJ, Ogden J, Dicker J. Enteral and parenteral branched chain amino acidsupplemented nutritional support in patients with encephalopathy due to alcoholic liver disease. JPEN J Parenter Enteral Nutr. 1987 Sep-Oct;11(5):447-53.

Olson JC, Wendon JA, Kramer DJ, Arroyo V, Jalan R, Garcia-Tsao G, Kamath PS. Intensive care of the patient with cirrhosis. Hepatology. 2011 Nov;54(5):1864-72. doi: 10.1002/hep.24622.

Pereg D, Kotliroff A, Gadoth N, Hadary R, Lishner M, Kitay-Cohen Y. Probiotics for patients with compensated liver cirrhosis: a double-blind placebo-controlled study. Nutrition. 2011 Feb;27(2):177-81.

Plauth M, Cabré E, Riggio O, Assis-Camilo M, Pirlich M, Kondrup J; DGEM (German Society for Nutritional Medicine), Ferenci P, Holm E, Vom Dahl S, Müller MJ, Nolte W; ESPEN (European Society for Parenteral and Enteral Nutrition). ESPEN Guidelines on Enteral Nutrition: Liver disease. Clin Nutr. 2006 Apr;25(2):285-94.

Plauth M, Egberts EH, Hamster W, Török M, Müller PH, Brand O, Fürst P, Dölle W. Long-term treatment of latent portosystemic encephalopathy with branched-chain amino acids. A double-blind placebo-controlled crossover study. J Hepatol. 1993 Mar;17(3):308-14.

Poo JL, Góngora J, Sánchez-Avila F, Aguilar-Castillo S, García-Ramos G, Fernández- Zertuche M, Rodríguez-Fragoso L, Uribe M. Efficacy of oral L-ornithine-L-aspartate in cirrhotic patients with hyperammonemic hepatic encephalopathy. Results of a randomized, lactulose-controlled study. Ann Hepatol. 2006 Oct-Dec;5(4):281-8.

Reding P, Duchateau J, Bataille C. Oral zinc supplementation improves hepatic encephalopathy. Results of a randomised controlled trial. Lancet. 1984 Sep 1;2(8401):493-5.

Rees CJ, Oppong K, Al Mardini H, Hudson M, Record CO. Effect of L-ornithine- L-aspartate on patients with and without TIPS undergoing glutamine challenge: a double blind, placebo controlled trial. Gut. 2000 Oct;47(4):571-4.

Riggio O, Ariosto F, Merli M, Caschera M, Zullo A, Balducci G, Ziparo V, Pedretti G, Fiaccadori F, Bottari E, et al. Short-term oral zinc supplementation does not improve chronic hepatic encephalopathy. Results of a double-blind crossover trial. Dig Dis Sci. 1991 Sep;36(9):1204-8.

Saller R, Brignoli R, Melzer J, Meier R. An updated systematic review with metaanalysis for the clinical evidence of silymarin. Forsch Komplementmed. 2008 Feb;15(1):9-20. Sherman KE. Advanced liver disease: what every hepatitis C virus treater should know. Top Antivir Med. 2011 Aug-Sep;19(3):121-5.

Shores NJ, Keeffe EB. Is oral L-acyl-carnitine an effective therapy for hepatic encephalopathy? Review of the literature. Dig Dis Sci. 2008 Sep;53(9):2330-3. Starr SP, Raines D. Cirrhosis: diagnosis, management, and prevention. Am Fam Physician. 2011 Dec 15;84(12):1353-9.

Stauch S, Kircheis G, Adler G, Beckh K, Ditschuneit H, Görtelmeyer R, Hendricks R, Heuser A, Karoff C, Malfertheiner P, Mayer D, Rösch W, Steffens J. Oral L-ornithine- L-aspartate therapy of chronic hepatic encephalopathy: results of a placebo-controlled double-blind study. J Hepatol. 1998 May;28(5):856-64.

Takeshita S, Ichikawa T, Nakao K, Miyaaki H, Shibata H, Matsuzaki T, Muraoka T, Honda T, Otani M, Akiyama M, Miuma S, Ozawa E, Fujimito M, Eguchi K. A snack enriched with oral branched-chain amino acids prevents a fall in albumin in patients with liver cirrhosis undergoing chemoembolization for hepatocellular carcinoma. Nutr Res. 2009 Feb;29(2):89-93.

Takuma Y, Nouso K, Makino Y, Hayashi M, Takahashi H. Clinical trial: oral zinc in hepatic encephalopathy. Aliment Pharmacol Ther. 2010 Nov;32(9):1080-90.

Tamayo C, Diamond S. Review of clinical trials evaluating safety and efficacy of milk thistle (Silybum marianum [L.] Gaertn.). Integr Cancer Ther. 2007 Jun;6(2):146-57.

Wolf, D. Cirrhosis. Medscape Reference. Updated Sept 22 2011. http://emedicine. medscape.com/article/185856-overview Accessed 14 April 2012

Risks and benefits of planned vaginal birth versus elective repeat caesarean

0

This prospective restricted cohort study was conducted to compare risks and benefits of a planned elective repeat caesarean (ERC) with planned vaginal birth after caesarean (VBAC). Subjects included 2,345 women with one prior caesarean, eligible for VBAC at term. Women were assigned by patient preference (N = 2,323) or randomization (N = 22) to planned VBAC (1,225 patient preference, 12 randomized) or planned ERC (1,098 patient preference, ten randomized). The risk of fetal death or liveborn infant death prior to discharge or serious infant outcome was significantly lower for infants born in the planned ERC group compared with infants in the planned VBAC group (0.9% vs 2.4%; RR 0.39; 95% CI 0.19-0.80). Fewer women in the planned ERC group compared with women in the planned VBAC had a major haemorrhage, defined as blood loss ≥1,500 ml and/or blood transfusion (0.8% vs 2.3%; RR 0.37; 95% CI 0.17-0.80). The authors concluded that among women with one prior caesarean, planned ERC compared with planned VBAC was associated with a lower risk of fetal and infant death, serious infant outcome, and major maternal haemorrhage, with no increase in maternal or perinatal complications to time of hospital discharge. PLoS Med. 2012 Mar;9(3):e1001192. PMID: 22427749