Search This Site
He stated he would bring small containers of olive oil. I am happy that I have lost the weight but thought that I would have lost a little more by now. All our own products are made with premium ingredients supported by science and formulated in the United States in GMP-certified facilities. Different mechanisms for the anti-diabetic effect of plants have been proposed: Talk about easy meals.
Follow by Email
This is what my tracking looks like. The next day I lost another pound overnight! I broke my weight loss stall! I still consumed my morning coffee with butter of course. Then I basically ate two meals a day that consisted of ground beef and butter.
Talk about easy meals. I might even do the egg fast again too. Both fasts are similar. As long as you eat protein with fats and very little to no carbs, you will lose weight. If you find yourself in a weight loss stall on the Ketogenic diet, you might try something similar. I personally believe the substitute sugars, even Keto approved ones, might cause you to stall at some point.
I also think dairy may have stalled me a bit too. Gosh, I love cheese. I suggest you do different tests of your own. This is the only way you will figure out what is making you stall in your weight loss efforts. I never once felt as though I was deprived when I ate ground beef with butter. I also only ate twice in a day.
I had coffee with butter in the morning 2 cups , and lunch and dinner were both ground beef with butter. Now when I look at my diet, I see more fat intake with moderate protein. When you think about your diet, what do you see? Head over here and sign up to get a free 7 day Keto Meal plan printable. We have a lot of fun and share tons of knowledge! This is what my breakfast looks like on a daily basis now! Bacon, Eggs, Avocado, and lots of butter! Join our Private Facebook Group for this challenge: Magnesium, Potassium and make sure to up your salt intake too!
I heard this advice over and over again from all the Keto experts at KetoCon too. I found your page through Pinterest, because the picture of the meat, cream cheese? Do you actually have that? I was glad I found this, because it is so nice to have an arsenal of techniques for keto! How has this affected your overall health blood work, etc? What supplements do you take besides magnesium, potassium, and salt? This is very interesting. I have been stalled for weeks and have been trying to figure out what is going on.
I usually fast until after I workout, but then eat 3 meals. I also usually eat pretty close to my 25 net carbs everyday, I find it helps with volume. Do others find they need to cut out the carbs completely? If you suffer from leg cramps the quickest way to get rid of them is to soak in a bathtub with a cup of epsom salts as your body absorbs magnesium quicker through your skin than in a supplement of buy a spray, this stops the leg cramps immediately. How do I find you on Facebook?
Hi Ronni, We have a facebook group and a page! I started to think that was it for my weight loss. I am so happy I found this pin. I was starting to gain weight again.
I started to eat the beef with butter for lunch every day for five days and lost 4 pounds. I look amazing I feel amazing and I just have to thank you for your amazing advice.
Anyone know if coconut like a fresh, real coconut, not dried or sweetened is ok on the keto diet? I love it, and it tastes like a treat! I did this fast for 4 days and lost 4. After the 4 days I made sure to track my food and fat intake so I could on the plan and figure out what caused me to stall in the first place. Most of my protein I ate after the stall had the same amount of fat in either butter or oils. Doubt, you just breakfast the coffe? Then lunch and dinner meat with butter?
Hello, i was interested in doing this. On the second day I added a small amount of grilled onion to the beef but very little because of the carb count. I also second the issues with keto approved sweeteners. I made some keto mini cheesecakes last weekend and my weight went up I only ate 2 in 2 days, everything else was normal keto for me Only time I have issues with major stalling or reversals is when I use sweeteners. Not going to make that mistake again! I did this and I lost weight.
Thank you for sharing this. I wanna do this again but I kinda wanna try something other than ground beef. Something simple and quick. Again thank you so much for sharing. Thank you for you post and all this information. I am still gathering as much info as I can. This was a great article. I had a question about the app you use. Does it have a bar code scanner or do you have to manual put in the nutrition values? When looking at your macros, how does your ground beef come out so low?
With a cup twice a day and 3 tbs butter each time my calories were at a little over with just those 2 meals, but yours also includes bpc and are still lower than mine. What app are you using to track it? Hi, I, too, had a stall on Keto. How did your body react when you went back to regular Keto? Did your weight fluctuate or did you keep losing? When I went back to my normal keto diet, I continued to lose but at a slower pace.
I was so excited it was still going down!!! If I stall again, I plan to do this same Beef and Butter fast again! Maybe a dumb question — but what percentage fat was the ground beef you used? Seems like the higher the better, right? Thank you so much for sharing your experience! My struggle with vegetables is making sure I get enough fiber — how would I do that without veggies in my diet?
I avoid all grains and legumes. There is a podcast called 2ketodudes. They go into the nitty gritty science of how and why keto works. But for a nutshell answer to this question: This is why when starting on keto you urinate a tremendous amount. However, as your body flushes out water it also flushes out electrolytes sodium, potassium and chloride.
Magnesium is also important. Low electrolytes can cause leg cramps, headaches, heart palpitations and some other nasty symptoms. Colored salts pink, gray contain minerals such as potassium and magnesium so those can be helpful on a keto diet. Under these plans, claims for weight reduction medications and for physician supervision of weight reduction programs will be denied based on that exclusion.
Please check benefit plan descriptions for details. The medical necessity criteria set forth below do not apply to health plans that specifically exclude services and supplies for or related to treatment of obesity or for diet or weight control. Under these plans, claims for weight loss drugs will be denied based on this exclusion.
For members whose medical policies do not exclude weight reduction medications or services and supplies for or related to weight reduction programs, Aetna covers these drugs under the medical benefit, not the pharmacy benefit. Weight reduction medications are considered medically necessary for members who have failed to lose at least one pound per week after at least 6 months on a weight loss regimen that includes a low calorie diet, increased physical activity, and behavioral therapy, and who meet either of the following selection criteria below:.
Weight reduction medications are considered experimental and investigational when these criteria are not met. VLCDs extending beyond 16 weeks are subject to medical review to determine if additional services are medically necessary.
Prepackaged food supplements or substitutes and grocery items are generally excluded from coverage under most benefit plans. Diagnostic tests required by, for or as a result of non-covered weight loss programs e. Under most benefit plans, the following services and supplies for weight reduction are specifically excluded from coverage please check benefit plan descriptions for details. Weight reduction medications should be used as an adjunct to caloric restriction, exercise, and behavioral modification, when these measures alone have not resulted in adequate weight loss.
Factors influencing successful weight loss are: Weight loss due to weight reduction medication use is generally temporary. In addition, the potential for development of physical dependence and addiction is high. Individuals who cannot maintain weight loss through behavioral weight loss therapy and are at risk of medical complications of obesity are an exception to this; for these persons, the risk of physical dependence or other adverse effects may present less of a risk than continued obesity.
For such individuals, use of weight reduction medication may need to be chronic. Tests with weight loss drugs have shown that initial responders tend to continue to respond, while initial non-responders are less likely to respond even with an increase in dosage. If a person does not lose 2 kg 4.
If weight is lost in the initial 6 months of therapy or is maintained after the initial weight loss phase, this should be considered a success and the drug may be continued. Orlistat is a reversible inhibitor of gastric and pancreatic lipases. Binding of orlistat to these enzymes forms inactive intermediates in the gut.
Rather, an oil phase that includes triglycerides and cholesterol is excreted in feces. This effect may lead to weight loss. It is also indicated to reduce the risk for weight regain after prior weight loss. Orlistat is available as Xenical in mg capsules and as Alli in 60mg capsules.
Recommended dosage of Xenical is one mg capsule three times a day with each main meal containing fat during or up to 1 hour after the meal. Comorbidities associated with obesity appear to be improved through weight loss in orlistat treated patients. However, studies are limited in time span and comparison with other pharmacologic agents is needed to determine place in therapy. Dosage reductions of hypoglycemic agents may be necessary when glycemic control is improved with weight loss.
Pharmacologic treatment of exogenous obesity should be adjunctive to caloric restriction, increased physical activity, and behavioral modification. Other than orlistat Xenical , which is approved for use in adolescents aged 12 years or older, weight reduction medications have not been proven to be safe and effective for treatment of obesity in children and adolescents.
Orlistat Xenical is contraindicated in persons with chronic malabsorption syndromes and cholestasis. Belviq is contraindicated in pregnancy. Ioannides-Demos et al stated that there is limited safety and effectiveness data for amfepramone diethylpropion and phentermine and their approvals for the management of obesity are limited to short-term use. The authors stated that, although the benefit-risk profiles of sibutramine and orlistat appear positive, sibutramine continues to be monitored because of long-term safety concerns.
The safety and effectiveness of currently approved drug therapies have not been evaluated in children and elderly patient populations. Available evidence does not support the use of whole body DEXA for managing obesity. There is currently no established role for whole body bioimpedance for weight reduction or other indications. Nowadays, medicinal plants and natural treatments are becoming more and more popular.
Diabetes has historically been treated with plants or plant-derived formulations in different cultures, mainly in China, Asia and India. Different mechanisms for the anti-diabetic effect of plants have been proposed: The scientific evidences for most of these plants are still incomplete. The large market for plant remedies has resulted in an array of unauthorized products or marketed as dietary supplements and, at the same time, no reliable pharmaceutical-grade products are registered for this purpose.
Borel et al conducted a prospective intervention study in viscerally obese men classified according to their glucose tolerance status. The results showed insulin sensitivity improved in assocication with decreases inboth visceral VAT and subcutaneous adiposity SAT as well as improvement in CRF, regardless of baseline glucose tolerance.
The results of this study also shoed that reduction in VAT was associated with an improvement in homeostasis model assessment of insulin resistance, whereas reduction in SAT was rather associated with improvement of the insulin sensitivity index of Matsuda. Subjects were randomly assigned to placebo, 7. Mulholland et al stated that evidence from the literature supports the safe use of very-low-energy diets VLED for up to 3 months in supervised conditions for patients who fail to meet a target weight loss using a standard low-fat, reduced-energy approach.
There is, however, a need for longer-term outcomes on obesity and associated morbidities following a VLED. These researchers investigated longer-term outcomes from studies using VLED, with a minimum duration of 12 months, published between January and December Reference lists of studies and reviews were manually searched. Weight loss or prevention of weight gain and morbidities were the main outcomes assessed.
A total of 32 out of articles met the inclusion criteria. The duration of the studies ranged from 12 months to 5 years. Periods of VLED ranged from 25 d to 9 months. Several studies incorporated aspects of behavior therapy, exercise, low-fat diets, low-carbohydrate diets or medication. Current evidence demonstrated significant weight loss and improvements in blood pressure, waist circumference and lipid profile in the longer term following a VLED. Interpretation of the results, however, was restricted and conclusions with which to guide best practice were limited due to heterogeneity between the studies.
The authors concluded that the present review clearly identified the need for more evidence and standardized studies to assess the longer-term benefits from weight loss achieved using VLED.
Clinicians supposedly can screen for abnormally low metabolic rates, teach energy balance, and identify the precise caloric intake needed for weight loss. Clinical applications of indirect calorimetry include obesity treatment, as well as treating obesity related diseases such as diabetes, dysmetabolic syndrome X, hypothyroidism, hyperthyroidism, hypertension, cardiovascular disease, as well as sleep apnea.
Under strict laboratory protocol, indirect calorimetry can also be used to measure basal metabolic rate. Published studies of indirect calorimetry in weight management have focused on its accuracy Frankenfeld, et al. Difference in weight loss between the treatment and usual care group were —4. The investigators noted that study limitations include small sample size, short duration, and small treatment effect.
An additional issue is the generalizability of the findings, given that, at the time of the study, the Air Force had regulations that all personnel maintain a desired body weight and body fat percentage, or these individuals could be discharged from service.
The investigators stated that future research is needed to determine the long-term efficacy of using indirect calorimetry as part of a comprehensive weight control program.
Close to one-half of cancer patients being evaluated in an outpatient cachexia clinic are noted to be hypermetabolic by indirect calorimetry. Whiting et al stated that capsaicinoids are a group of chemicals naturally occurring in chilli peppers with bioactive properties that may help to support weight management. These investigators conducted a meta-analysis investigating the potential effects of capsaicinoids on energy intake, clarified previous observations and formed evidence-based conclusions about possible weight management roles.
Medical databases Medline, Web of Knowledge and Scopus were systematically searched for papers. Of the 74 clinical trials identified, 10 were included, 8 of which provided results suitable to be combined in analysis participants. From the studies, 19 effect sizes were extracted and analyzed using MIX meta-analysis software. Data analysis showed that capsaicinoid ingestion prior to a meal reduced ad libitum energy intake by Study findings suggested a minimum dose of 2 mg of capsaicinoids is needed to contribute to reductions in ad libitum energy intake, which appears to be attributed to an altered preference for carbohydrate-rich foods over foods with a higher fat content.
The authors concluded that meta-analysis findings suggested that daily consumption of capsaicinoids may contribute to weight management through reductions in energy intake. Subsequently, there may be potential for capsaicinoids to be used as long-term, natural weight-loss aids.
They stated that further long-term randomized trials are now needed to investigate these effects. In a systematic review, Onakpoya et al a evaluated the evidence for or against the effectiveness of glucomannan, a soluble fiber, in body weight reduction. Hand searches of bibliography were also conducted.
Outcomes of interest were body weight and BMI. A total of 18 trials were identified, and 9 were included. There was a variation in the reporting quality of the included RCTs. A meta-analysis random effect model of 8 RCTs revealed a non-statistically significant difference in weight loss between glucomannan and placebo mean difference [MD]: Adverse events included abdominal discomfort, diarrhea, and constipation.
The authors concluded that the evidence from available RCTs does not show that glucomannan intake generates statistically significant weight loss. They stated that future trials should be more rigorous and better reported. Onakpoya et al b noted that several slimming aids being sold as food supplements are widely available.
One of them is pyruvate. Its effectiveness in causing weight reduction in humans has not been fully established. The objective of this systematic review was to examine the effectiveness of pyruvate in reducing body weight. Electronic and non-electronic searches were conducted to identify all relevant human RCTs. The bibliographies of all located articles were also searched.
No restrictions in language or time were applied. Two independent reviewers extracted the data according to predefined criteria. A total of 9 trials were identified and 6 were included. All had methodological weaknesses. The meta-analysis revealed a statistically significant difference in body weight with pyruvate compared to placebo MD: The magnitude of the effect is small, and its clinical relevance is uncertain.
Adverse events included gas, bloating, diarrhea, and increase in low-density lipoprotein LDL cholesterol. The authors concluded that the evidence from RCTs does not convincingly show that pyruvate is effective in reducing body weight; limited evidence exists about the safety of pyruvate.
They stated that future trials involving the use of this supplement should be more rigorous and better reported. The labeling of Saxenda states that liraglutide should not be used with insulin FDA, It also states that the the effects of liraglutide on cardiovascular morbidity and mortality have not been established.
The labeling states that the safety and efficacy of coadministration with other products for weight loss have not been established. In addition, liraglutide has not been studied in patients with a history of pancreatitis. Liraglutide for chronic weight management is contraindicated in the following conditions: Trial data showed that liraglutide, in combination with a reduced-calorie diet and increased physical activity, resulted in significantly greater weight loss than diet and physical activity alone.
The SCALE phase 3 clinical trial program of the safety and effectiveness of liraglutide for chronic weight management included three clinical trials that included approximately 4, obese and overweight patients with and without significant weight-related conditions FDA, All patients received counseling regarding lifestyle modifications that consisted of a reduced-calorie diet and regular physical activity.
Results from a clinical trial that enrolled patients without diabetes showed that patients had an average weight loss of 4. In this trial, 62 percent of patients treated with liraglutide lost at least 5 percent of their body weight compared with 34 percent of patients treated with placebo. Results from another clinical trial that enrolled patients with type 2 diabetes showed that patients had an average weight loss of 3. In this trial, 49 percent of patients treated with liraglutide lost at least 5 percent of their body weight compared with 16 percent of patients treated with placebo.
The FDA approved labeling states that patients using liraglutide should be evaluated after 16 weeks to determine if the treatment is working FDA, If a patient has not lost at least 4 percent of baseline body weight, liraglutide should be discontinued, as it is unlikely that the patient will achieve and sustain clinically meaningful weight loss with continued treatment.
Saxenda is a glucagon-like peptide-1 GLP-1 receptor agonist and should not be used in combination with any other drug belonging to this class, including Victoza, a treatment for type 2 diabetes FDA, Saxenda and Victoza contain the same active ingredient liraglutide at different doses 3 mg and 1. However, Saxenda is not indicated for the treatment of type 2 diabetes, as the safety and efficacy of Saxenda for the treatment of diabetes has not been established.
Saxenda has a boxed warning stating that thyroid C-cell tumors have been observed in rodent studies with liraglutide but that it is unknown whether liraglutide causes thyroid C-cell tumors, including medullary thyroid carcinoma MTC , in humans FDA, Liraglutide causes dose-dependent and treatment-duration-dependent thyroid C-cell tumors at clinically relevant exposures in both genders of rats and mice.
It is unknown whether liraglutide causes thyroid C-cell tumors, including MTC, in humans, as the human relevance of liraglutide-induced rodent thyroid C-cell tumors has not been determined. The labeling states that liraglutide is contraindicated in patients with a personal or family history of MTC or in patients with multiple endocrine neoplasia syndrome type 2 MEN 2 FDA, The labeling states that patients should be counseled regarding the risk of MTC with use of liraglutide and informed of symptoms of thyroid tumors e.
The labeling states that routine monitoring of serum calcitonin or using thyroid ultrasound is of uncertain value for early detection of MTC in patients treated with liraglutide. Serious side effects reported in patients treated with liraglutide for chronic weight management include pancreatitis, gallbladder disease, renal impairment, and suicidal thoughts FDA, Liraglutide can also increase heart rate and should be discontinued in patients who experience a sustained increase in resting heart rate.
Based on spontaneous postmarketing reports, acute pancreatitis, including fatal and non-fatal hemorrhagic or necrotizing pancreatitis, has been observed in patients treated with liraglutide Novo Nordisk, After initiation of liraglutide, patients should be observed for signs and symptoms of pancreatitis including persistent severe abdominal pain, sometimes radiating to the back and which may or may not be accompanied by vomiting. If pancreatitis is suspected, liraglutide should promptly be discontinued and appropriate management should be initiated.
If pancreatitis is confirmed, liraglutide should not be restarted. Substantial or rapid weight loss can increase the risk of cholelithiasis; however, the incidence of acute gallbladder disease was greater in liraglutide-treated patients than in placebo-treated patients even after accounting for the degree of weight loss Novo Nordisk, If cholelithiasis is suspected, gallbladder studies and appropriate clinical follow-up are indicated.
When liraglutide is used with an insulin secretagogue e. The labeling recommends lowering the dose of the insulin secretagogue to reduce the risk of hypoglycemia. Renal impairment has been reported postmarketing, usually in association with nausea, vomiting, diarrhea, or dehydration, which may sometimes require hemodialysis Novo Nordisk, The labeling recommends using caution when initiating or escalating doses of liraglutide in patients with renal impairment.
Serious hypersensitivity reactions e. The labeling recommends that patients stop taking liraglutide and seek medical advice if symptoms of hypersensitivity reactions occur. Liraglutide should be discontinued in patients who experience suicidal thoughts or behaviors. Liraglutide should be avoided in patients with a history of suicidal attempts or active suicidal ideation.
The labeling states that nursing mothers should either discontinue liraglutide for chronic weight management or discontinue nursing Novo Nordisk, The labeling states that the safety and effectiveness of liraglutide have not been established in pediatric patients and is not recommended for use in pediatric patients.
In addition, the cardiovascular safety of liraglutide is being investigated in an ongoing cardiovascular outcomes trial. Lingwood stated that there is a critical need for improved technologies to monitor fluid balance and body composition in neonates, particularly those receiving intensive care.
Bioelectrical impedance analysis BIA meets many of the criteria required in this environment and appears to be effective for monitoring physiological trends. These researchers reviewed the literature regarding the use of bioelectrical impedance in neonates. It was found that prediction equations for total body water, extracellular water and fat-free mass have been developed, but many require further testing and validation in larger cohorts.
Alternative approaches based on Hanai mixture theory or vector analysis are in the early stages of investigation in neonates. The authors concluded that further research is needed into electrode positioning, bioimpedance spectroscopy and Cole analysis in order to realize the full potential of this technology. These investigators reviewed available information on the short- and long-term effects of intervention treatment on body fat composition of overweight and obese children and adolescents and, to obtain a further understanding on how different body composition techniques detect longitudinal changes.
A total of 13 papers were included; 7 included a multi-disciplinary intervention component, 5 applied a combined dietary and physical activity intervention and 1 a physical activity intervention.
Body composition techniques used included anthropometric indices, BIA, and dual energy X-ray absorptiometry. Percentage of fat mass change was calculated in when possible. Findings suggested, no changes were observed in fat free mass after 16 weeks of nutritional intervention and the lowest decrease on fat mass percentage was obtained.
However, the highest fat mass percentage with parallel increase in fat free mass, both assessed by DXA was observed in a multi-component intervention applied for 20 weeks. The authors concluded that more studies are needed to determine the best field body composition method to monitor changes during overweight treatment in children and adolescents. Two reviewers independently screened titles and abstracts for inclusion, extracted data and rated methodological quality of the included studies.
These investigators performed a best evidence synthesis to synthesize the results, thereby excluding studies of poor quality. They included 50 published studies. Mean differences between BIA and reference methods gold standard [criterion validity] and convergent measures of body composition [convergent validity] were considerable and ranged from negative to positive values, resulting in conflicting evidence for criterion validity.
These investigators found strong evidence for a good reliability, i. However, test-retest mean differences ranged from 7. However, they stated that validity and measurement error were not satisfactory. Goldberg et al stated that the sensory and gastro-intestinal changes that occur with aging affect older adults' food and liquid intake. Any decreased liquid intake increases the risk for dehydration. This increased dehydration risk is compounded in older adults with dysphagia. The availability of a non-invasive and easily administered way to document hydration levels in older adults is critical, particularly for adults in residential care.