Chest compression are the core of resuscitation efforts in any patient with confirmed or suspected cardiac arrest. Good CPR should not be thought as heart-only process, but a combination of heart and brain.
Standard cardiopulmonary resuscitation consists of manual chest compressions to maintain blood flow and
positive-pressure breathing to maintain oxygenation until spontaneous
circulation is restored. Chest compressions are interrupted frequently by ventilations
given as rescue breathing during the treatment of out-of-hospital cardiac
arrest. These interruptions reduce blood flow and potentially reduce the
effectiveness of CPR. Observational studies involving humans with
out-of-hospital cardiac arrest of presumed cardiac cause have suggested that
continuous compressions are associated with better survival than interrupted
compressions. Nichol et al. conducted a randomized trial to test whether
continuous chest compressions, as compared with chest compressions
interrupted for ventilation, during CPR performed by emergency medical
service (EMS) providers affected the rate of survival, neurologic function,
or the rate of adverse events.
In the
large randomized trial conducted by Nichol et al. involving adults with
out-of-hospital cardiac arrest, a strategy of continuous manual chest
compressions with positive-pressure ventilation was not associated with a
significantly higher rate of survival to discharge. During the
active-enrollment phase, 1129 of 12,613 patients (9.0%) in the intervention
group (which received continuous chest compression) and 1072 of 11,035 (9.7%)
in the control group (which received interrupted chest compressions) survived
to hospital discharge (difference with adjustment for cluster and sequential
monitoring, −0.7 percentage points; 95% confidence interval [CI], −1.5 to
0.1; P=0.07).
In the
study by Nichol et al., secondary outcomes included neurologic function at
discharge, which was measured with the use of the modified Rankin scale
(scores range from 0, indicating no symptoms, to 6, indicating death, with a
score of ≤3 indicating favorable neurologic function) on the basis of review
of the clinical record, and adverse events. Among patients with available
data on neurologic status, 883 of 12,560 patients (7.0%) in the intervention
group and 844 of 10,995 (7.7%) in the control group survived with a modified
Rankin scale score of 3 or less (difference with adjustment for cluster, −0.6
percentage points; 95% CI, −1.4 to 0.1; P=0.09).
Hospital-free
survival in the Nichol trial was defined as the number of days alive and
permanently out of the hospital during the first 30 days after the cardiac
arrest. Hospital-free survival was significantly shorter in the intervention
group than in the control group (mean difference, −0.2 days; 95% CI, −0.3 to −0.1;
P=0.004).
Previous
observational studies have shown large increases in survival rates among
patients with a shockable rhythm with the implementation of continuous
compressions by EMS providers versus compressions interrupted for
ventilations. Among patients with a noncardiac cause of cardiac arrest who
were treated by laypersons or those with a nonshockable rhythm who were
treated by EMS providers, continuous compressions were not associated with a
significant improvement in outcome. In these previous studies, participating
EMS agencies did not measure CPR process when implementing continuous
compressions, and implementation occurred simultaneously with other changes,
including directions to give intravenous epinephrine early, to use a
nonrebreather mask with passive ventilation, to defer airway insertion, and
to reduce the number of defibrillations given with each rhythm analysis. In
the initial reports of implementation of continuous compressions, most
patients received rescue breathing by means of positive-pressure ventilation
with a bag-valve mask. Other interventions that each patient received were
not reported. It seems plausible that some of the observed improvement in
these previous studies was due to improved CPR process (e.g., compression
rate and depth), concurrent improvements in the system of care, or Hawthorne
effects (changes in behavior resulting from awareness of being observed)
rather than to the implementation of continuous compressions alone.
In Summary...
- Rapid initiation of chest compression increases survival with better neurological outcome.
- Avoiding interruptions during chest compression is key for brain perfusion.
- Defibrillate for shockable rhythms.
- Teaching the general public on how to do high quality chest compressions can make a real difference.
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Thursday, December 3, 2015
Chest Compression During CPR ... Don't Forget The Brain !
Monday, September 7, 2015
DVT and Pregnancy
Although the absolute incidence of venous thromboembolism in pregnancy is low (1 or 2 cases per 1000 pregnancies), this risk is approximately five times as high as the risk among women who are not pregnant. These risks reflect the venous stasis and procoagulant changes in coagulation and fibrinolysis, which are considered to be part of physiologic preparation for the hemostatic challenge of delivery.
The clinical diagnosis of venous thrombosis is unreliable in pregnancy. Suggestive symptoms and signs, such as leg swelling and dyspnea, may be difficult to differentiate from the physiologic changes of pregnancy. As compared with deep-vein thrombosis in nonpregnant persons, deep-vein thrombosis in pregnant women occurs more frequently in the left leg (85%, vs. 55% in the left leg among nonpregnant persons) and is more often proximal (72% in the iliofemoral veins, vs. 9% in the iliofemoral veins among nonpregnant persons), with a greater risk of embolic complications and the post-thrombotic syndrome. Thrombotic events occur throughout pregnancy, with more than half occurring before 20 weeks of gestation. The risk increases further in the puerperium (the 6-week period after delivery), probably owing to endothelial damage to the pelvic vessels that occurs during delivery. Recent data indicate that an increased relative risk (but low absolute risk) persists until 12 weeks after delivery. However, approximately 80% of postpartum thromboembolic events occur in the first 3 weeks after delivery.
Suspected deep-vein thrombosis is best assessed by means of compression duplex ultrasonographic examination, including examination of the iliofemoral region. In women with a negative result on ultrasonography in whom clinical suspicion of deep-vein thrombosis is high, it may be prudent to repeat the test after 3 to 7 days. In cases in which iliocaval venous thrombosis is suspected but ultrasonography cannot detect a thrombus, magnetic resonance or conventional x-ray venography may be considered. Chest radiographic findings are normal in the majority of cases of pulmonary embolism, but they can show pulmonary features that point to an alternative diagnosis or nonspecific features of pulmonary embolism such as atelectasis or regional oligemia. Since deep-vein thrombosis is often present in patients with pulmonary embolism, ultrasonographic venography is useful in patients who have possible symptoms or signs of deep-vein thrombosis. If deep-vein thrombosis is detected, further radiologic studies do not have to be performed to confirm a pulmonary embolism. In women with normal findings on chest radiography, ventilation–perfusion lung scanning is often recommended, since it has a high negative predictive value, owing to the low prevalence of coexisting pulmonary problems that can result in indeterminate or false positive results. Moreover, the ventilation component can often be omitted, thereby minimizing the dose of radiation to the fetus. Whereas computed tomographic (CT) pulmonary angiography (CTPA), with its high sensitivity and specificity, is usually the first-line test to detect pulmonary embolism in nonpregnant patients, it is used less often in pregnant women.
One diagnostic study frequently used is the D-dimer. Pregnancy is a hyper coagulable state and therefore, D-dimer need to be adjusted. There is growing evidence that trimester adjusted D-dimer is safe, reduces testing without missing more clots. 1st trimester cut off can be 50% more than the normal laboratory value, during the 2nd trimester 100% and 3rd trimester 150% the normal value. Of note, D-dimers normalize to the pre-pregnancy value after 4-6 weeks.
Anticoagulation in pregnancy typically involves unfractionated heparin or low-molecular-weight heparin, which do not cross the placenta or enter breast milk. In contrast, vitamin K antagonists such as warfarin are contraindicated in pregnancy, since they cross the placenta and their use is associated with embryopathy, central nervous system abnormalities, pregnancy loss, and fetal anticoagulation with possible bleeding. Low-molecular-weight heparins have largely replaced unfractionated heparin for the management of venous thromboembolism in pregnancy. Typical agents include dalteparin (at a dose of 200 IU per kilogram of body weight daily or 100 IU per kilogram twice daily), enoxaparin (1.5 mg per kilogram daily or 1 mg per kilogram twice daily), and tinzaparin (175 units per kilogram daily). Data are limited regarding the use of fondaparinux in pregnancy. Oral direct thrombin inhibitors such as dabigatran and anti–factor Xa inhibitors such as rivaroxaban should generally be avoided during pregnancy. These agents may cross the placenta with possible adverse fetal effects. Thrombolysis in pregnancy is reserved for massive life-threatening pulmonary embolism with hemodynamic compromise or for proximal deep-vein thrombosis that is threatening leg viability. Caval filters are sometimes used in women who have recurrent pulmonary embolisms despite adequate anticoagulation or in whom anticoagulation is contraindicated, or in women in whom acute deep-vein thrombosis has developed close to the time of delivery.
Women should be advised to discontinue injections of heparin if labor starts or is suspected. Neuraxial anesthesia is usually deferred until at least 24 hours after the last dose, given a small risk of epidural hematoma associated with administration of neuraxial anesthesia before that time. After delivery, low-molecular-weight heparin should not be administered for at least 4 hours after spinal anesthesia or removal of an epidural catheter. After delivery, anticoagulant treatment is continued for at least 6 weeks, with a minimum total duration of 3 months.
Women should be advised to discontinue injections of heparin if labor starts or is suspected. Neuraxial anesthesia is usually deferred until at least 24 hours after the last dose, given a small risk of epidural hematoma associated with administration of neuraxial anesthesia before that time. After delivery, low-molecular-weight heparin should not be administered for at least 4 hours after spinal anesthesia or removal of an epidural catheter. After delivery, anticoagulant treatment is continued for at least 6 weeks, with a minimum total duration of 3 months.
Thursday, August 6, 2015
Heparin Induced Thrombocytopenia
Although the use of heparin is relatively common in the ED, rarely we encounter this complication. In contrast to other conditions caused by enhanced consumption, impaired production, or destruction of platelets, which lead to bleeding complications, immune-mediated heparin-induced thrombocytopenia (HIT) does not induce bleeding but rather results in a paradoxical prothrombotic state. Thromboembolic complications develop in approximately 50% of patients with confirmed HIT. Venous thrombosis of the large vessels of the lower limbs and pulmonary embolism are the most frequent complications, followed by peripheral arterial thrombosis and then stroke; myocardial infarction is uncommon.
HIT occurs in approximately 1 in 5000 hospitalized patients. The risk of HIT depends on the type of heparin and the patient population. The incidence is up to 10 times as high among patients receiving unfractionated heparin as it is among those receiving low-molecular-weight heparin, and HIT occurs more frequently among patients who have had major surgery than among those who have had minor surgery or are receiving medical therapy. HIT is rare in obstetrical patients, although in contexts other than pregnancy, women are at slightly higher risk than men.
The onset of HIT characteristically occurs between 5 and 10 days after heparin is started, both in patients who receive heparin for the first time and in patients with reexposure. However, there are exceptions. In persons who have received heparin within the previous 90 days (especially, ≤30 days), there may be persistent circulating anti–platelet factor 4 (PF4)–heparin antibodies, and HIT can start abruptly on reexposure to heparin (rapid-onset HIT); in this case, HIT is sometimes complicated by an anaphylactoid reaction within 30 minutes after a heparin bolus. The fall in platelet count in HIT occurs rapidly (over a period of 1 to 3 days) and is assessed relative to the highest platelet count after the start of heparin. The typical nadir is 40,000 to 80,000 platelets per cubic millimeter, but the count may remain in the normal range (e.g., a decline from 500,000 to 200,000 per cubic millimeter). In less than 10% of patients, the decrease in platelet count is less pronounced (30 to 50% of the highest preceding value). Rarely, the platelet count may fall below 20,000 per cubic millimeter, especially when HIT is associated with other causes of thrombocytopenia, such as consumptive coagulopathy.
Although monitoring of platelet counts facilitates the recognition of HIT, it is difficult to justify in many patients, especially outpatients. Monitoring should be considered when the risk of HIT is relatively high (>1%), such as among patients who have undergone cardiac surgery and those receiving unfractionated heparin after major surgery (other than heparin received for intraoperative flushes or catheter-related flushes). Scoring systems can be helpful in estimating the probability of HIT. A widely used scoring system is the 4T score, which evaluates four indicators: the relative platelet-count fall, the timing of the onset of the platelet-count fall, the presence or absence of thrombosis, and the likelihood of another cause, with scores on the individual components ranging from 0 to 2 and higher scores indicating a higher likelihood of HIT. For those whose score is intermediate or high, laboratory tests are needed to rule out HIT. Anti–PF4–heparin enzyme immunoassays have an excellent negative predictive value (98 to 99%) but a low positive predictive value, owing to the detection of clinically insignificant anti–PF4–heparin antibodies. Diagnostic accuracy for HIT is improved with the use of both an anti–PF4–heparin enzyme immunoassay and a functional test (e.g., a platelet-activation assay).
Key interventions in patients with highly suspected or confirmed acute HIT are the prompt cessation of heparin (if still being administered) and the initiation of an alternative anticoagulant at a therapeutic dose. Prophylactic-dose anticoagulation is insufficient to compensate for massive thrombin generation, even if the patient has no apparent thrombosis. Vitamin K antagonists (e.g., warfarin and phenprocoumon) must not be given until HIT has abated (e.g., the platelet count has increased to >150,000 per cubic millimeter at a stable plateau for 2 consecutive days), because they increase the risk of venous limb gangrene and limb loss by decreasing the level of protein C. Two drugs are approved for the treatment of HIT — the direct thrombin inhibitor argatroban (in the United States, Canada, the European Union, and Australia) and the antithrombin-dependent factor Xa inhibitor danaparoid (in Canada, the European Union, and Australia). Argatroban is frequently used in critically ill patients. It has a relatively short half-life, which is independent of renal function, but it requires intravenous administration. Fondaparinux and bivalirudin are also used in this context, although they have not been approved by the Food and Drug Administration for this indication. Prophylactic platelet transfusions should be avoided in patients with HIT. The risk of bleeding is very low, and such transfusions can increase the risk of thrombosis.
Thursday, July 23, 2015
Potassium metabolism... enough to make you go Bananas!
Potassium metabolism is one of those things we
just have to know. We can really hurt people if get this one wrong. Here is a
review on the topic. Now, go a eat some bananas !
The plasma potassium level is normally maintained
within narrow limits (typically, 3.5 to 5.0 mmol per liter) by multiple
mechanisms that collectively make up potassium homeostasis. Such strict
regulation is essential for a broad array of vital physiologic processes. The
importance of potassium homeostasis is underscored by the well-recognized
finding that patients with hypokalemia or hyperkalemia have an increased rate
of death from any cause. In addition, derangements of potassium homeostasis
have been associated with pathophysiologic processes, such as progression of
cardiac and kidney disease and interstitial fibrosis.
External
potassium homeostasis regulates renal potassium excretion to balance
potassium intake, minus extrarenal potassium loss and correction for any
potassium deficits. External potassium balance involves three control
systems. Two systems can be categorized as “reactive,” whereas a third system
is considered to be “predictive.” A negative-feedback system reacts to
changes in the plasma potassium level and regulates the potassium balance.
Potassium excretion increases in response to increases in the plasma
potassium level, leading to a decrease in the plasma level. A reactive
feed-forward system that responds to potassium intake in a manner that is
independent of changes in the systemic plasma potassium level has also been
recognized. A predictive system appears to modulate the effect of reactive
systems, enhancing physiologic mechanisms at the time of day when food intake
characteristically occurs — typically, during the day in humans and at night
in nocturnal rodents. This predictive system is driven by a circadian
oscillator in the suprachiasmatic nucleus of the brain and is entrained to
the ambient light–dark cycle. The central oscillator (clock) entrains
intracellular clocks in the kidney that generate the cyclic changes in
excretion. When food intake is evenly distributed over 24 hours, and physical
activity and ambient light are held constant, this system produces a cyclic
variation in potassium excretion.
Internal
potassium homeostasis is the maintenance of an asymmetric distribution of
total body potassium between the intracellular and extracellular fluid
(approximately 98% intracellular and only a small fraction, approximately 2%,
extracellular), which occurs by the balance of active cellular uptake by sodium–potassium
adenosine triphosphatase, an enzyme that pumps sodium out of cells while
pumping potassium into cells (called the sodium–potassium pump rate), and
passive potassium efflux (called the leak rate). Little increase in the
plasma potassium level occurs during potassium absorption from the gut in
normal persons owing to potassium excretion by the kidney and potassium
sequestration by the liver and muscle. Insulin, catecholamines, and
mineralocorticoids stimulate potassium uptake into muscle and other tissues.
Between meals, the plasma potassium level is nearly constant, as potassium
excretion is balanced by the release of sequestered intracellular potassium.
The
healthy kidney has a robust capacity to excrete potassium, and under normal
conditions, most persons can ingest very large quantities of potassium (400
mmol per day or more) without clinically significant hyperkalemia. Potassium
that is filtered at the glomerulus is largely reabsorbed in the proximal
tubule and the loop of Henle. Consequently, the rate of renal potassium
excretion is determined mainly by the difference between potassium secretion
and potassium reabsorption in the cortical distal nephron and collecting
duct. Both of these processes are regulated — potassium ingestion stimulates
potassium secretion and inhibits potassium reabsorption. Factors that
regulate potassium secretion and reabsorption can be divided into those that
serve to preserve potassium balance (homeostatic) and those that affect
potassium excretion without intrinsically acting to preserve potassium
balance (contra-homeostatic). Examples of the latter include flow rate in the
renal tubular lumen and the luminal sodium level. The acid–base balance also
affects potassium excretion. The predominant effect of acidosis is to inhibit
potassium clearance, whereas the predominant effect of alkalosis is to
stimulate potassium clearance.
In
vertebrates, a central clock in the suprachiasmatic nucleus of the brain and
peripheral clocks that are present in virtually all cells regulate circadian
rhythms. Among the many physiologic functions in humans that show circadian
rhythms, few are more consistent and stable than the circadian rhythm of
urinary potassium excretion. The timing signals from the central clock to the
peripheral clocks remain uncertain, but adrenal corticosteroids and agents
from other loci have been proposed or identified. Although the action of
cortisol in promoting potassium excretion would suggest a direct (nonclock)
hormonal effect, studies by Moore-Ede and colleagues indicate that cortisol
serves as a clock synchronizer. Aldosterone also affects certain circadian
clocks and, in particular, acutely induces the expression of period circadian
clock 1 (PER1) in the kidney.
Having a basic understanding of the metabolism of this mineral is important when deciding therapies to treat or prevent potassium plasma level variations. Now you know... be careful when writing for potassium or telling patients to take supplements.
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Sunday, June 14, 2015
PID is not just an STD, get help from your GYN.
Yes, we do see pelvic pain in the ED (a lot of them), and pelvic inflammatory disease is not an uncommon cause of many of those cases. PID is an infection-induced inflammation of the female upper reproductive tract (the endometrium, fallopian tubes, ovaries, or pelvic peritoneum). Many women have clinically silent spread of infection to the upper genital tract, which results in subclinical pelvic inflammatory disease. Pelvic inflammatory disease is a major concern because it can result in long-term reproductive disability, including infertility, ectopic pregnancy, and chronic pelvic pain.
More than 85% of infections are due to sexually transmitted cervical pathogens or bacterial vaginosis–associated microbes, and approximately 15% are due to respiratory or enteric organisms that have colonized the lower genital tract. Ascending infection from the cervix is often due to sexually acquired infections with Neisseria gonorrhoeae or Chlamydia trachomatis. Acute pelvic inflammatory disease has classically been defined by the abrupt onset of severe lower abdominal pain during or shortly after menses, although it is now well recognized that both the onset and severity of symptoms can be more ill-defined and subtle. Atypical, milder clinical manifestations have become more common as rates of N. gonorrhoeae infection have fallen. The symptoms associated with acute pelvic inflammatory disease include pelvic or lower abdominal pain of varying severity, abnormal vaginal discharge, intermenstrual or postcoital bleeding, dyspareunia, and dysuria. Fever can occur, but systemic manifestations are not a prominent feature of pelvic inflammatory disease.
The clinical diagnosis of pelvic inflammatory disease is based on the finding of pelvic organ tenderness, as indicated by cervical motion tenderness, adnexal tenderness, or uterine compression tenderness on bimanual examination, in conjunction with signs of lower genital tract inflammation. Signs of lower genital tract inflammation include cervical mucopus, which is visible as an exudate from the endocervix or as yellow or green mucous on a cotton-tipped swab placed gently into the cervical os (positive “swab test”); cervical friability (easily induced columnar epithelial bleeding); or increased numbers of white cells observed on saline microscopic examination of vaginal secretions (wet mount). All patients with suspected pelvic inflammatory disease should undergo cervical or vaginal nucleic acid amplification tests for N. gonorrhoeae and C. trachomatis infection; if the results are positive, the probability that pelvic inflammatory disease is present increases substantially. Transvaginal ultrasonography and magnetic resonance imaging (MRI) revealing thickened, fluid-filled tubes are timely and highly specific for salpingitis. However, the sensitivity of ultrasonography is only fair, and although MRI has high sensitivity, it is expensive and not typically available in resource-poor settings. Power Doppler studies showing increased fallopian-tube blood flow are highly suggestive of infection.
Most patients are successfully treated as outpatients with single-dose intramuscular ceftriaxone, cefoxitin plus probenicid, or another third-generation cephalosporin (cefotaxime or ceftizoxime), followed by oral doxycycline with or without metronidazole for 2 weeks. For hospitalized patients, therapy with cefotetan or cefoxitin (administered parenterally until 24 to 48 hours after clinical improvement) together with doxycycline and followed by doxycycline with or without metronidazole to complete 2 weeks of treatment is recommended. An alternative regimen of clindamycin and an aminoglycoside may be particularly appropriate for patients with a tubo-ovarian abscess. Adjunctive nonsteroidal anti-inflammatory drugs do not improve the clinical outcome. Removal of an intrauterine device (IUD) does not hasten clinical resolution (and may delay it), and in most cases the IUD is left in place.
Although more than 90% of patients with pelvic inflammatory disease will have a clinical response to CDC-recommended treatment, the long-term outcome of treatment is still suboptimal. It remains unclear why the long-term outcome of treated pelvic inflammatory disease remains so dismal, given the high rates of clinical response. Perhaps infection-induced damage to the fallopian tubes has occurred by the time treatment is first given. This observation, together with the frequent occurrence of subclinical pelvic inflammatory disease, have highlighted the importance of recognizing prevention of pelvic inflammatory disease as a major public heath priority. The U.S. Preventive Services Task Force, CDC, and other professional organizations recommend annual C. trachomatis screening for all sexually active women younger than 25 years of age and older women at increased risk for infection (e.g., women with multiple or new sex partners). These groups also recommend testing for N. gonorrhoeae among women at increased risk for infection (e.g., women with multiple sex partners or previous gonorrhea infection and women living in communities with a high prevalence of disease).
Wednesday, May 20, 2015
Oxygen IS a drug, use it with caution, only when is needed.
This is a quick review on the potentially harmful effects of too much oxygen, published in this month's EPM magazine.
THE POTENTIAL HARM OF OXYGEN THERAPY IN MEDICAL EMERGENCIES
Cornet, A.D., et al, Crit Care 17(2):313, April 18, 2013
These Dutch authors comment on possible harm from routine use of supplemental oxygen in patients with a medical emergency. Several early studies reported high-flow oxygen in myocardial infarction patients was associated with reduced cardiac output and stroke volume with an increase in systemic vascular resistance and arterial blood pressure, largely due to vasoconstriction, with no evidence of a benefit of hyperoxia on myocardial ischemia. Clinical trials of supplemental oxygen in patients with cardiac emergencies are limited, but a 2010 Cochrane review reported increased mortality in MI patients receiving supplemental oxygen (RR 3.0). Experimental evidence also suggests an adverse hemodynamic effect of oxygen in patients with congestive heart failure. The adverse effects of supplemental oxygen are more widely appreciated in patients with chronic obstructive pulmonary disease (COPD), and a recent randomized trial noted decreased mortality in COPD patients receiving titrated rather than high-concentration oxygen.
Cornet, A.D., et al, Crit Care 17(2):313, April 18, 2013
These Dutch authors comment on possible harm from routine use of supplemental oxygen in patients with a medical emergency. Several early studies reported high-flow oxygen in myocardial infarction patients was associated with reduced cardiac output and stroke volume with an increase in systemic vascular resistance and arterial blood pressure, largely due to vasoconstriction, with no evidence of a benefit of hyperoxia on myocardial ischemia. Clinical trials of supplemental oxygen in patients with cardiac emergencies are limited, but a 2010 Cochrane review reported increased mortality in MI patients receiving supplemental oxygen (RR 3.0). Experimental evidence also suggests an adverse hemodynamic effect of oxygen in patients with congestive heart failure. The adverse effects of supplemental oxygen are more widely appreciated in patients with chronic obstructive pulmonary disease (COPD), and a recent randomized trial noted decreased mortality in COPD patients receiving titrated rather than high-concentration oxygen.
Hyperoxia in stroke has been noted to be associated with a decrease in cerebral blood flow and increased mortality, and use of supplemental oxygen for most ischemic stroke patients is not supported in American Stroke Association guidelines. Several large studies reported increased mortality and poor neurologic outcomes in hyperoxic patients after resuscitation from cardiac arrest. Although it is possible that vasoconstriction due to hyperoxia might be beneficial in patients with shock, no studies have demonstrated a benefit of supranormal oxygen levels in this setting. The authors advise caution with the routine use of supplemental oxygen for medical emergencies. While hypoxemia should be treated promptly, they recommend slow stepwise titration and feel that an oxygen saturation of 90-94% may be reasonable. 61 references (cornet@vumc.nl – no reprints)
Conclusions:
- Oxygen IS toxic when used in high concentrations and for prolonged periods of time.
- Hyperoxia causes cellular dysfunction
- Use it only when patient is hypoxic and when hypoxia has been corrected, titrate down to maintain normoxia.
- Share the knowledge and stop the ritual of putting every patient on oxygen !
- Oxygen IS toxic when used in high concentrations and for prolonged periods of time.
- Hyperoxia causes cellular dysfunction
- Use it only when patient is hypoxic and when hypoxia has been corrected, titrate down to maintain normoxia.
- Share the knowledge and stop the ritual of putting every patient on oxygen !
Sunday, May 10, 2015
Emergency Contraception.. the only "REAL" emergency!
You: Hi.. I am Dr
X, what can I do for you today?
Patient: Uhhh...
my boyfriend and I were... uhhh, you know... (silence)
You: Yes...
Patient: My
boyfriend and I were having sex and... (silence)
You: Uh-hu....
Patient: You
know, he didn't pull out on time. (in soft voice)
Boyfriend: I told
you do move, but you didn't move! (Obviously angry)
Patient: Shut up!
Do you think I want to be here?
You: It's OK, no need to argue. You want to make sure you don't get pregnant, correct?
Patient: YES !!
That's right doc. You gotta help me. I am going to school, work 2 jobs, my mom
is going to kill me and .... and....
You get the idea!
Emergency
contraception is one of those issues that sound simple, but it is not. Matching
the right method to the right patient requires some understanding of the
pharmacology of these agents and also knowing more about your patient's
history. Here is a review from this months, NEJM. Enjoy!
Oral
emergency contraceptive pills are the most commonly used form of emergency
contraception. Two regimens are currently marketed in the United States:
ulipristal acetate (30 mg) and levonorgestrel (1.5 mg). In 39 clinical trials
that included a combined total of more than 18,000 women, rates of pregnancy
after use of one of these two regimens ranged from 0 to 6.5%. Interpretation of
these numbers is problematic because the likelihood of pregnancy in the absence
of emergency contraception was not directly assessed; estimates that were based
on the days of the menstrual cycle on which the participants had sex suggest
that use of each of these regimens reduces the risk of pregnancy after a single
sex act by 40 to 90%. In the United States, products containing 1.5 mg of
levonorgestrel in one tablet may legally be sold over the counter to women and
men of all ages. Although the ulipristal regimen was recently approved for
nonprescription sale in Europe, it still requires a prescription in the United
States; consequently, use of this regimen in the United States is limited. Some
but not all data suggest reduced efficacy of the levonorgestrel regimen in
obese women with BMI’s as low as 25. If you think about it, it is not that
much!
The
levonorgestrel regimen is effective for at least 4 or 5 days after sex but may
be more effective the sooner it is taken; data on the ulipristal regimen have
not indicated a decrease in efficacy through 120 hours after sex. However,
since both regimens work largely by delaying or inhibiting ovulation, and since
women are usually unaware of whether ovulation is imminent, prompt use is
prudent. Neither of these two oral emergency contraceptive regimens has any
recognized contraindications.
The
most effective form of emergency contraception is the copper IUD. A review of
42 studies showed that, of 7034 women who received IUDs up to 10 days after
unprotected sex, only 0.09% subsequently became pregnant. Recent analyses
suggest that the IUD is effective for emergency contraception throughout the
menstrual cycle and can be inserted at any point if pregnancy is ruled out. A
key advantage of the IUD over oral emergency contraceptive pills is that the
IUD can provide ongoing contraception for at least 10 years. Almost all women
can safely use an IUD for emergency contraception; the only recognized
contraindications are pregnancy, cancer of the genital tract, uterine
malformation preventing device placement, copper allergy, mucopurulent
cervicitis, current pelvic inflammatory disease, and known current cervical
infection with chlamydia or gonorrhea. These conditions can be reasonably ruled
out on the basis of interview, examination, and, if indicated, pregnancy test;
routine testing for cervical infection is not necessary.
No
deaths or serious complications have been causally linked to either oral
emergency contraception regimen. Previous studies over the past decades have
not revealed adverse effects of levonorgestrel exposure during pregnancy on
either the woman or the conceptus. Data on ulipristal exposure during pregnancy
are limited, but combined data from postmarketing surveillance and clinical
trials showed that among 232 pregnancies with a known outcome in which the
woman and conceptus were exposed to ulipristal, no teratogenic effects were
seen. The incidence of pelvic inflammatory disease after IUD insertion is less
than 5% even when the device is inserted through an infected cervix; whether
IUD insertion itself increases this incidence has not been definitively
established. IUD insertion can be uncomfortable, and some women have vaginal
bleeding and cramping after insertion. In the one published study of IUD
insertion for emergency contraception, which was conducted in community
clinics, the IUD insertion attempt was unsuccessful in 18% of women; this
proportion is higher than that reported in clinical trials of IUD insertion for
routine contraception.
Key points:
- IDU is the king of emergency contraception. However, not for all women.
- Oral hormonal options, mainly levonogestrel and ulipristal, have failure rates that vary from 0-6%.
- Women with higher BMI's are at risk for failure of the oral forms.
- The sooner you take them, the better.
- It is good to have a plan C and D, when B doesn't work.
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