Using antibiotics as well as cleaning by a dental care profe | Figure 1
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Using antibiotics as well as cleaning by a dental care professional to treat gum disease
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What are the benefits and risks of using antibiotics as well as cleaning by a dental care professional to treat gum disease?
Why is this question important?
Gum disease is a common condition in which the gums become swollen, sore or infected. It is caused by bacteria that accumulate on gums and teeth. Diseased gums may bleed when people brush their teeth, and may cause bad breath. If gum disease is not treated, teeth can become loose and eventually fall out. This can affect a person’s ability to chew and speak. It can also make people feel self‐conscious about their appearance.
Dental‐care professionals can clean teeth and gums to remove excess bacteria from the mouth. They use special instruments – typically, an ultrasound scraper followed by specialised hand‐held instruments – to scrape bacteria from the teeth, and stop these from affecting the gums.
Antibiotics (medicines that kill bacteria) taken by mouth (orally) can be used alongside professional cleaning, to remove bacteria from the area between the teeth and gums. However, there are potential risks associated with antibiotics, such as allergic reactions and antibiotic resistance (changes in bacteria after exposure to antibiotics, that allow the bacteria to survive future antibiotic treatment).
We conducted a review of the evidence from research studies to find out about the benefits and risks of using antibiotics alongside professional dental cleaning to treat gum disease. We also wanted to know if some antibiotics work better than others in this situation.
How did we identify and evaluate the evidence?
First, we searched for randomized controlled studies (clinical studies where people are randomly put into one of two or more treatment groups), because these studies provide the most robust evidence about the effects of a treatment. We then compared the results, and summarized the evidence from all the studies. Finally, we rated our confidence in the evidence, based on factors such as study methods and sizes, and the consistency of findings across studies.
What did we find?
We found 45 studies that involved a total of 2664 people over the age of 18 who had gum disease. The studies compared professional cleaning plus antibiotics against professional cleaning alone, or compared different antibiotics used alongside professional cleaning against one another.
We cannot tell whether antibiotics reduce gum disease in the long term (one year or more after treatment), or whether some antibiotics are better than others. This is because we have very little confidence in the evidence we found.
We cannot tell whether antibiotics are associated with unwanted effects, because we have too little confidence in the evidence. The most commonly reported unwanted effects were temporary, mild gastrointestinal disturbances, such as nausea, vomiting, diarrhoea, or a metallic taste in the mouth. No serious unwanted effects were reported.
No studies reported on antimicrobial resistance or changes in people’s quality of life.
What does this mean?
We do not know whether:
‐ using antibiotics alongside professional cleaning is beneficial for treating gum disease in the long term (more than one year after treatment);
‐ using antibiotics alongside professional cleaning is associated with unwanted effects; or
‐ some antibiotics are better than others for treating gum disease alongside professional cleaning.
Our confidence in the available evidence is very low. The results of our review are likely to change if more evidence becomes available. Future studies should clearly define what qualifies as a minimally important improvement in gum disease.
How‐up‐to date is this review?
The evidence in this Cochrane Review is current to March 2020.
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\ \ Benefits and risks of antibiotics taken orally or given as an injection to treat chronic suppurative otitis media (persistent or recurring ear infection with discharge)\ Why is this question important?\ Chronic suppurative otitis media (CSOM), also known as chronic otitis media (COM), is an inflammation and infection of the middle ear that lasts for two weeks or more. People with CSOM usually experience recurrent or persistent discharge – fluid that leaks out from a hole or tear in the eardrum – and hearing loss.\ CSOM can be treated with antibiotics (medicines that fight bacterial infections) taken orally or given as an injection (i.e. systemic treatment in which the whole body is treated). Systemic antibiotics can be used:\ ‐ alone;\ ‐ in combination with antibiotics in the form of drops, sprays, ointments or creams (topical, i.e. localised surface treatment); or\ ‐ in combination with other treatments such as steroids (anti‐inflammation medicines) or antiseptics (substances that stop or slow down the growth of micro‐organisms).\ To find out how effective systemic antibiotics are for treating CSOM, and whether they lead to side effects, we reviewed the evidence from research studies.\ How did we identify and evaluate the evidence?\ First, we searched the medical literature for studies that followed people with CSOM for at least one week and compared:\ ‐ a systemic antibiotic used alone against a placebo (dummy) treatment, no treatment or another systemic antibiotic;\ ‐ a systemic antibiotic combined with another treatment, against that treatment alone.\ We then compared the results, and summarised the evidence from all the studies. Finally, we rated our confidence in the evidence, based on factors such as study methods and sizes, and the consistency of findings across studies.\ What did we find?\ We found 18 studies that involved a total of 2135 people with CSOM. People were treated for between five days and 12 weeks, and were followed for up to one year. Four studies provided information about how they were funded or who supplied the medicines: two were publicly funded, and medicines were provided by pharmaceutical companies in the other two studies.\ Studies compared:\ ‐ systemic antibiotics against no treatment (one study);\ ‐ systemic antibiotics plus topical antibiotics against topical antibiotics alone (six studies);\ ‐ systemic antibiotics plus other treatments (other than topical antibiotics alone), against these same treatments without systemic antibiotics (four studies);\ ‐ different systemic antibiotics against one another (eight studies).\ Systemic antibiotics alone against no treatment\ We cannot determine from the only study we found whether systemic antibiotics alone are better or worse than no treatment. This is mainly because the study:\ ‐ was small;\ ‐ was conducted in ways that could have introduced error in the results; and\ ‐ reported limited information.\ Systemic antibiotics plus topical antibiotics against topical antibiotics alone\ Systemic antibiotics plus topical antibiotics may have little to no effect on whether discharge stops after one to two weeks, compared against topical antibiotics alone (five studies). We do not know if systemic antibiotics added to topical antibiotics have any other positive or negative effects, because:\ ‐ there are too few studies;\ ‐ available studies were small and may have been conducted in ways that introduce error in their results.\ Systemic antibiotics plus other treatments (other than topical antibiotics alone), against these same treatments without systemic antibiotics\ We cannot determine from the evidence available whether systemic antibiotics are effective or lead to adverse events when added to treatments other than topical antibiotics only. This is mainly because the few studies available reported limited information.\ Comparisons between different systemic antibiotics\ We do not know whether some systemic antibiotics are better than others. This is mainly because the way studies were conducted is likely to have introduced error in their results.\ What does this mean?\ There is insufficient robust evidence to determine whether systemic antibiotics are effective treatments for CSOM, and whether they lead to side effects. Evidence about side effects is particularly limited. When added to topical antibiotics, systemic antibiotics may make little to no difference to whether discharge resolves after one to two weeks. We do not know if some systemic antibiotics are better than others.\ How‐up‐to date is this review?\ The evidence in this Cochrane Review is current to March 2020.](https://app.figure1.com/case-detail/2a9fc52f-5f63-4054-bbac-2f00bea18998)
\ \ Cochrane Review; no studies were identified for inclusion in the review.\ Question\ Are oral antibiotics (taken by mouth) or inhaled antibiotics more effective for reducing the duration and frequency of infective episodes of bronchiectasis, admissions to hospital and side effects, as well as reducing the risk of chest infections not responding to treatment with antibiotics?\ Background\ Bronchiectasis is a long-term incurable condition where people get repeated bacterial chest infections that lead to frequent cough, breathlessness and mucus production.\ Antibiotics are commonly used to treat chest infections in people with bronchiectasis, to eliminate the specific types of bacteria that cause the infection. However it is currently unknown which method of administering antibiotics, orally or by inhalation, is most effective.\ Study characteristics\ While there have been a few studies investigating the benefits of antibiotics for people with bronchiectasis, none have compared orally administered antibiotics with inhaled antibiotics.\ Quality of the evidence\ There is no high-quality evidence available to determine whether oral or inhaled antibiotics are more helpful for people with bronchiectasis. More studies are needed.](https://app.figure1.com/case-detail/3ca8cb7f-077f-486b-8ff2-7a03c9925103)
\ \ Is chloroquine or hydroxychloroquine useful in treating people with COVID‐19, or in preventing infection in people who have been exposed to the virus?\ What is the aim of this review?\ COVID‐19 is an infectious respiratory disease caused by a coronavirus called SARS‐CoV‐2. If the infection becomes severe, people may need intensive care and support in hospital, including mechanical ventilation.\ Drugs used for other diseases were tried out in COVID‐19, and this included chloroquine, used for malaria; and hydroxychloroquine used for rheumatic diseases, such as rheumatoid arthritis or systemic lupus erythematosus. We sought evidence of the effects of these drugs in treating people ill with the disease; in preventing the disease in people at risk of getting the disease, such as health workers; and people exposed to the virus developing the disease.\ Key messages\ Hydroxychloroquine does not reduce deaths from COVID‐19, and probably does not reduce the number of people needing mechanical ventilation.\ Hydroxychloroquine caused more unwanted effects than a placebo treatment, though it did not appear to increase the number of serious unwanted effects.\ We do not think new studies of hydroxychloroquine should be started for treatment of COVID‐19.\ What was studied in the review?\ We searched for studies that looked at giving chloroquine and hydroxychloroquine to people with COVID‐19; people at risk of being exposed to the virus; and people who have been exposed to the virus.\ We found 14 relevant studies: 12 studies of chloroquine or hydroxychloroquine used to treat COVID‐19 in 8569 adults; two studies of hydroxychloroquine to stop COVID‐19 in 3346 adults who had been exposed to the virus but had no symptoms of infection. We did not find any completed studies of these medicines to stop COVID‐19 in people who were at risk of exposure to the virus; studies are still under way.\ The studies took place in China, Brazil, Egypt, Iran, Taiwan, North America, and Europe; one study was worldwide. Some studies were partly funded by pharmaceutical companies that manufacture hydroxychloroquine.\ What are the main results of our review?\ Treating COVID‐19\ Compared with usual care or placebo, hydroxychloroquine:\ · clearly did not affect how many people died (of any cause; 9 studies in 8208 people);\ · probably did not affect how many people needed mechanical ventilation (3 studies; 4521 people);\ · may not affect how many people still tested positive for the virus after 14 days (3 studies; 213 people).\ We are uncertain whether hydroxychloroquine affected the number of people whose symptoms improved after 28 days.\ Compared with other antiviral treatment (lopinavir plus ritonavir), chloroquine made little or no difference to the time taken for symptoms to improve (1 study; 22 people).\ Compared with usual care in one study in 444 people, hydroxychloroquine given with azithromycin (an antibiotic) made no difference to:\ · how many people died;\ · how many needed mechanical ventilation; or\ · time spent in hospital.\ Compared with febuxostat (a medicine to treat gout), hydroxychloroquine made no difference to how many people were admitted to hospital or to changes seen on scans of people's lungs; no deaths were reported (1 study; 60 people).\ Preventing COVID‐19 in people exposed to it\ We are uncertain whether hydroxychloroquine affected how many people developed COVID‐19, or how many people were admitted to hospital with COVID‐19, compared with those receiving a placebo treatment (1 study; 821 people).\ Compared with usual care, hydroxychloroquine made no difference to the risk of developing COVID‐19, or antibodies to the virus, in people exposed to it (1 study; 2525 people).\ Unwanted effects\ When used for treating COVID‐19, compared with usual care or placebo, hydroxychloroquine:\ · probably increases the risk of mild unwanted effects (6 studies; 1394 people);\ · may not increase the risk of serious harmful effects (6 studies; 1004 people).\ When given along with azithromycin, hydroxychloroquine increased the risk of any unwanted effects, but made no difference to the risk of serious unwanted effects (1 study; 444 people).\ Compared with lopinavir plus ritonavir, chloroquine made little or no difference to the risk of unwanted effects (1 study; 22 people).\ When used for preventing COVID‐19, hydroxychloroquine probably causes more unwanted effects than placebo, but may not increase the risk of serious, harmful unwanted effects (1 study; 700 people).\ How confident are we in our results?\ We are confident about our results for how many people died and moderately confident about how many needed mechanical ventilation. We are moderately confident about the unwanted effects of hydroxychloroquine treatment, but less confident about our results for serious unwanted effects; these results might change with further evidence.\ How up‐to‐date is this review?\ We included evidence published up to 15 September 2020.](https://app.figure1.com/case-detail/47eaf351-8332-42a9-9ffc-cd099dc20b03)
\ \ Background\ Epilepsy is a neurological disorder which causes people to have seizures. Most people can control their epilepsy with a single antiepileptic drug. Some people, however, require multiple antiepileptic drugs to control their epilepsy, and are said to have drug‐resistant epilepsy. Oxcarbazepine is an antiepileptic drug and is similar to an older antiepileptic drug, carbamazepine. Oxcarbazepine can be taken as an add‐on treatment, alongside other antiepileptic medication, to treat drug‐resistant epilepsy.\ Aim of the review\ This review examined whether oxcarbazepine is tolerable and effective when used alongside other antiepileptic medication by people with drug‐resistant focal epilepsy (epilepsy that originates from one area of the brain).\ Results\ We included six clinical trials that investigated oxcarbazepine as an add‐on treatment for people with drug‐resistant focal epilepsy. There were 1593 people across the studies and they were aged from 1 month to 65 years.\ People who received oxcarbazepine in addition to their normal antiepileptic medication were more likely to have a 50% or greater reduction in the frequency of their seizures compared to people who were on a control treatment, which is believed to have little or no effect. They were also nearly three times more likely to be free from all seizures than those receiving control treatment. Both of these findings suggest that oxcarbazepine is effective at treating drug‐resistant focal epilepsy. These findings are, however, based on evidence that was of low certainty. This means that we are not confident that the findings that we have reported are accurate.\ People who received oxcarbazepine add‐on treatment were also more likely to withdraw from the studies and were more likely to experience side effects, including dizziness and drowsiness, than people receiving control add‐on treatment. The evidence for treatment withdrawal was of moderate certainty, and this means that we can be fairly confident that this is a true effect.\ Authors' conclusions\ As a result of the low‐certainty evidence, we cannot be sure that oxcarbazepine is an effective add‐on treatment for people with drug‐resistant focal epilepsy. Instead, we have concerns about the tolerability of oxcarbazepine because of the increased number of people who withdrew from treatment and who experienced side effects.\ The evidence is current to September 2018.](https://app.figure1.com/case-detail/658ac7c2-7da7-446f-9835-d52d25ea0a1b)
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