Interventions for the management of fluid around the lungs ( | Figure 1
%27%3e%3cg%20id=%27Group-14%27%20transform=%27translate(13.000000,%20103.176124)%27%3e%3cg%20id=%27Group-Copy-5%27%20transform=%27translate(0.000000,%20182.676124)%27%3e%3crect%20id=%27Rectangle-8%27%20fill=%27%23E2E0DE%27%20x=%270%27%20y=%270%27%20width=%2736%27%20height=%2736%27%20rx=%2718%27%3e%3c/rect%3e%3cpath%20d=%27M28,27.6503435%20C28,22.127496%2023.5228474,17.6503435%2018,17.6503435%20C12.4771525,17.6503435%208,22.127496%208,27.6503435%20M18,16.3472505%20C20.8165136,16.3472505%2023.099749,14.0640151%2023.099749,11.2475015%20C23.099749,8.43098783%2020.8165136,6.1477524%2018,6.1477524%20C15.1834863,6.1477524%2012.9002509,8.43098783%2012.9002509,11.2475015%20C12.9002509,14.0640151%2015.1834863,16.3472505%2018,16.3472505%20Z%27%20id=%27Combined-Shape%27%20fill=%27%23FFFFFF%27%20fill-rule=%27nonzero%27%3e%3c/path%3e%3c/g%3e%3c/g%3e%3c/g%3e%3c/g%3e%3c/svg%3e)
Deleted account
Some actions are only available when you log in.
Report case
Report this to our moderators
Interventions for the management of fluid around the lungs (pleural fluid) caused by cancer
You can view up to 4 cases without signing up Sign up for unlimited access
Review question
We reviewed the evidence on the effectiveness of different methods to manage a build‐up of fluid around the lungs in people where this is caused by cancer.
Background
Malignant pleural effusion (MPE) is a condition that affects people with cancer of the lining of the lung. This can cause fluid to build up in the space between the outside of the lungs and rib cage (pleural cavity), often resulting in breathlessness. Treatment options focus on controlling symptoms. These include removal of the fluid using a temporary chest drain, a camera examination of the pleural cavity (thoracoscopy) or a semi‐permanent chest drain tunnelled under the skin (an indwelling pleural catheter). Introducing a chemical into the pleural cavity can also be used to prevent the fluid coming back (pleurodesis). We wanted to find out which method was the most effective for preventing fluid re‐accumulation (pleurodesis failure) and which was best in terms of side effects (including pain and fever) and other important outcomes such as breathlessness and quality of life.
Study characteristics
We collected and analysed relevant studies to answer this question. We were interested in high quality research, so only searched for randomised controlled trials (in which participants are randomly allocated to the treatments being tested). We analysed most data using 'network meta‐analysis', which allows lots of different interventions to be compared in one analysis. This analysis ranks the interventions in order of their effectiveness.
Certainty of the evidence
We rated the certainty of the evidence from studies using four levels: very low, low, moderate or high. Very low‐certainty evidence means that we are very uncertain about the results. High‐certainty evidence means that we are very confident in the results. Many of the studies were of low quality and the individual studies were quite different to each other. This made it difficult to reach definite conclusions.
Key results
From our searches in June 2019, we found 80 studies (18 new) involving 5507 participants (2079 new).
In the network meta‐analysis, we found that giving talc through a chest tube after draining the fluid (talc slurry) resulted in fewer pleurodesis failures than other commonly used methods, such as the medicines doxycycline or bleomycin through a chest tube (low certainty). Using a thoracoscopy procedure to remove the fluid and blow talc into the chest (talc poudrage) is likely to be as effective as talc slurry (moderate certainty).
We had a low level of certainty that the risk of having a fever is similar between treatments. There may be little difference between treatments in the chance of having pain (low certainty for bleomycin, IPCs and doxycycline; very‐low certainty for talc poudrage).
Using an IPC, which allows intermittent drainage of fluid at home, may relieve breathlessness as much as a talc slurry procedure (low certainty).
There may be little difference in the risk of death between treatments when compared to talc slurry (low certainty for bleomycin and IPC without daily drainage; very low certainty for talc poudrage and doxycycline).
The chance of needing another invasive procedure to remove fluid was lower after having an IPC than after talc slurry pleurodesis (moderate certainty).
Conclusions
The available evidence shows that talc poudrage and talc slurry are effective ways of managing MPEs, with lower pleurodesis failure rates than a number of other commonly used methods. However, it is also important to consider global experience of these agents and knowledge of their safety and side effects when selecting the most appropriate pleurodesis method.
IPCs are less likely to prevent pleural fluid from re‐accumulating than talc slurry, but may be as good at helping breathlessness. People who have an IPC are less likely to need another invasive procedure in the future to manage the pleural effusion.
Further research is required to look at particular patient groups and explore outcomes such as breathlessness and quality of life in more detail. Ideally a fuller understanding of the potential harms of the treatments from the patients' perspective would also be beneficial.
Read the full Cochrane Review here
More about this case
ResolvedVerified literature
Why you should join Figure 1
Share your knowledge with our global community of healthcare professionals
Get help from experts in your field
Learn from our library of real-world cases and quizzes
Similar cases
\ \ We reviewed the evidence for the effect of Roux‐en‐Y compared to Billroth‐I reconstruction after surgery for gastric cancer. We found eight studies.\ Background\ Gastric (stomach) cancer is one of the most common cancers worldwide. Recently, early detection rates of gastric cancer and treatment technology have improved. As a result, people can survive longer after surgery, and the importance of quality of life after surgery has been discussed. Billroth‐I and Roux‐en‐Y are both options for reconstruction of continuity of the gastrointestinal system after distal gastrectomy (removal of the lower part of the stomach).\ However, there are no standards on which reconstructive procedure to select; guidelines do not describe which procedure should be a priority. It was therefore important to perform a review of the available evidence to aid decision making for people undergoing surgery, surgeons, physicians, medical staff, and policymakers.\ Study characteristics\ The evidence is current to 4 May 2021.\ We identified eight trials including 942 participants with gastric cancer who underwent distal gastrectomy.\ The evidence suggests that Roux‐en‐Y reconstruction may result in little to no difference in quality of life 12 months after surgery. However, these findings must be interpreted with caution because the study investigators measured quality of life in different ways. The evidence is very uncertain for the effect of the interventions on leakage through the reconstructed connection (anastomotic leakage).\ Billroth‐I reconstruction may result in little to no difference in loss of body weight; probably increases bile reflux into the remnant stomach; and may reduce overall complications after surgery compared to Roux‐en‐Y reconstruction. The evidence is very uncertain for the effect of the procedures on length of hospital stay.\ The certainty of the evidence for quality of life was low due to limitations in how the studies were designed and conducted, and because there are not enough studies to be certain about the results for this outcome. The certainty of the evidence for the other outcomes ranged from very low to moderate. Further research is needed to look at the effects over a longer time period.](https://app.figure1.com/case-detail/14754f12-b3e0-4a94-a4a7-8c862b337979)
](https://app.figure1.com/case-detail/158ab635-91d1-43ab-8746-5ea3d60105ae)
The Cochrane Review "Paracetamol (acetaminophen) for patent ductus arteriosus in preterm or low birth weight infants" has been updated and the conclusions changed. "Moderate‐certainty evidence suggests that there is probably little or no difference in effectiveness between paracetamol and ibuprofen; low‐certainty evidence suggests that there is probably little or no difference in effectiveness between paracetamol and indomethacin; low‐certainty evidence suggests that prophylactic paracetamol may be more effective than placebo/no intervention; low‐certainty evidence suggests that early paracetamol treatment may be more effective than placebo/no intervention; low‐certainty evidence suggests that there is probably little or no difference between late paracetamol treatment and placebo, and probably little or no difference in effectiveness between the combination of paracetamol plus ibuprofen versus ibuprofen alone for the closure of PDA after the first course of treatment. The majority of neonates included in these studies were of moderate preterm gestation. Thus, establishing the efficacy and safety of paracetamol for PDA treatment in extremely low birth weight (ELBW: birth weight < 1000 grams) and extremely low gestational age neonates (ELGANs < 28 weeks' gestation) requires further studies." www.cochranelibrary.com
\ \ Introduction and aims\ Sprains, strains, and bruises are common injuries, and people with these injuries often require pain relief, given as a tablet or capsule that is swallowed (oral). Many types of oral painkillers are available to treat such injuries. We wanted to know whether there were any differences in people's pain, swelling, function, or unwanted side effects when sprains, strains, and bruises were treated with oral non‐steroidal anti‐inflammatory drugs (NSAIDs, e.g. ibuprofen) compared with paracetamol, opioids (e.g. codeine), complementary or alternative medicines, or combinations of these.\ This is an update of a Cochrane review published in 2015.\ What did we do?\ We searched medical databases up to January 2020 for studies that compared NSAIDs with other painkillers in people with sprains, strains, and bruises. Study participants could be any age. We assessed the included studies to judge the reliability (certainty) of the evidence. We categorised the evidence as being of high, moderate, low, or very low certainty. High certainty means we are confident in the evidence, moderate certainty means we are fairly confident, low or very low certainty means that we are unsure or very unsure of the reliability of the evidence.\ Results of our search and description of studies\ We included 20 studies, with 3305 participants. Seven studies included people with ankle sprain only. Three studies included children only. Most of the participants of the other studies were young adults, and there were slightly more men than women. Few participants were aged over 65 years. Eleven studies compared NSAIDs with paracetamol, six studies compared NSAIDs with opioids, and four studies compared NSAIDs with paracetamol combined with an opioid. Studies reported outcomes at times varying from one hour after taking the medication, up to 10 to 14 days.\ Main results\ There is no difference between NSAIDs and paracetamol in pain after one to two hours, or after two to three days (high‐certainty evidence), and there may be no difference after a week or more (low‐certainty evidence). There is low‐certainty evidence that NSAIDs may make little difference to swelling after a week or more. We are uncertain whether NSAIDs make a difference to return to function after a week or more (very low‐certainty evidence). There is low‐certainly evidence that NSAIDs may slightly increase unwanted side effects related to the gut.\ There is probably no difference between NSAIDs and opioids in pain at one hour (moderate‐certainly evidence), and there may be no difference four or seven days after taking medication (low‐certainty evidence). We are uncertain whether NSAIDs make a difference to swelling after 10 days (very low‐certainty evidence). There is low‐certainty evidence that NSAIDs may increase return to function in 7 to 10 days. There is moderate‐certainty evidence that NSAIDs probably result in fewer unwanted side effects, such as nausea and dizziness, compared with opioids.\ The evidence suggests that there is little or no difference between NSAIDs and paracetamol combined with opioids in pain, swelling, return to function, or unwanted side effects. However, the evidence was very low certainty, so we are uncertain of these results.\ No studies reported the risk of re‐injury after treatment.\ We found no studies comparing NSAIDs with complementary or alternative medicines.\ Conclusions\ The body of evidence to date has found no difference between NSAIDs and other pain killers for pain relief for strains, sprains, and bruises in younger people. However, we need more, and better evidence on return to function and unwanted side effects in all age groups, particularly in older people.](https://app.figure1.com/case-detail/1b22ae79-f8d2-4864-a092-abfc66c02fca)
\ \ Intranasal corticosteroids for non‐allergic rhinitis\ Review question\ We wanted to find out whether intranasal corticosteroids (steroids applied into the nose) are effective for the treatment of rhinitis that is not caused by allergy.\ Background\ Non‐allergic rhinitis is a chronic disease of the nose, which is not caused by infection or allergies. People with non‐allergic rhinitis experience symptoms that affect their quality of life, such as nasal obstruction, runny nose and sneezing. Non‐allergic rhinitis patients can be divided into different subgroups who have different underlying causes for their disease. The underlying causes of non‐allergic rhinitis are not fully understood, therefore treatment is often unsuccessful in these patients.\ Topical (intranasal) corticosteroids are used with the aim of reducing inflammation. They are the most commonly prescribed drug in other chronic diseases of the nose and sinuses, such as allergic rhinitis and chronic rhinosinusitis. Intranasal corticosteroid treatment can be delivered with sprays or drops and for different time periods.\ Study characteristics\ We included 34 randomised controlled trials (RCTs) with a total of 4452 participants in this review. Most of the studies were relatively small, although the largest study had 983 patients in total. All of the patients were either adults or adolescents (aged between 12 and 18 years old) with non‐allergic rhinitis. The studies looked at a range of types, doses and methods of administration (e.g. spray, drops) of intranasal corticosteroids. Nine studies were sponsored by the pharmaceutical industry or had commercial sponsors. One study was funded by the government. In several studies, the pharmaceutical industry or commercial sponsor may have provided medications, but the funding role was unclear. Funding was not reported in eight studies.\ Key results\ Intranasal corticosteroids compared with placebo\ It is uncertain whether intranasal corticosteroids reduce patient‐reported disease severity in non‐allergic rhinitis patients compared with placebo when measured at up to three months. They may improve patient‐reported disease severity compared with placebo at up to four weeks, however this evidence is of low certainty. Treatment with intranasal corticosteroids probably increases the risk of epistaxis (nosebleed) but there is no difference in the risk of other adverse effects. It is not possible to tell from this review whether there is a difference between the different concentrations, delivery methods or treatment plans of intranasal corticosteroids. There are no good‐quality studies assessing changes in quality of life with intranasal corticosteroids.\ Intranasal corticosteroids compared with other treatments\ There is not enough evidence to know whether intranasal corticosteroid treatment is better, worse or the same as using other treatment strategies such as saline irrigation, intranasal antihistamines, capsaicin or ipratropium bromide for non‐allergic rhinitis.\ Certainty of the evidence\ Overall, the evidence for intranasal corticosteroids compared with placebo for most outcomes was either low‐certainty (our confidence in the effect estimate is low) or very low‐certainty (our confidence in the effect estimate is very low). This was because most studies were very small and used different methods to measure the same outcome. This evidence is up to date to July 2019.](https://app.figure1.com/case-detail/2865d0f1-cb87-462c-9572-147257a9c499)
Trending now
\ \ A 52-year-old man presented with a 20-minute history of chest pain radiating to the left shoulder and neck, associated with dyspnea and diaphoresis.\ He had a history of hypertension, long-term smoking, and a sedentary lifestyle.\ On physical examination, bibasilar crackles were noted on lung auscultation. An electrocardiogram (ECG) was performed in the primary care setting, and the patient was promptly referred to the emergency department.](https://app.figure1.com/case-detail/ae0fe999-6875-4474-94f0-ad823dbb9b3a)
\ \ A 28-year-old woman presented with a 3-day history of intense pruritus over the lower back. She reported no recent travel or exposure to new environments. She cares for a small kennel with approximately eight dogs rescued from the streets.\ Physical examination revealed multiple small vesicles, some clustered and others scattered, predominantly involving the lumbar region and the left gluteal area.](https://app.figure1.com/case-detail/c271070f-2bc7-4052-9895-635277e1a7d5)
\ \ A 4-month-old male infant presented with skin lesions localized to the chin for the past 3 days. Physical examination revealed multiple small pustules with surrounding inflammatory signs on the chin, along with a few scattered papules on the chest.](https://app.figure1.com/case-detail/48f41642-b9db-4089-b120-a94ee52328de)
\ \ patient in late teens presenting after a collapse, no chest pain, no previous cardiac history, no history of sudden death in family, are there any features in this ekg that would warrant further work-up or is this just a pediatric ekg?](https://app.figure1.com/case-detail/2af390e1-ace8-40ed-ba1c-98fb2d72f4c5)