Recent findings
LQT syndrome remains the most common inherited arrhythmia and is a leading cause for sudden unexplained death accounting for up to 20–25% of cases. Rapid progress of genetic technology over the past 2 decades has significantly improved our understanding of molecular and genetic mechanisms of LQT. Despite all those novel insights, phenotype assessment and appropriate risk stratification in LQT remains challenging – even for the expert.
Summary
This review outlines our current understanding and approach to the clinical diagnosis and management of LQT as well as recent insights into genotype–phenotype correlations. Genetic testing has evolved beyond a pure diagnostic tool and is in addition increasingly integrated as complementary prognostic marker. With regard to the management of LQT, there is now evidence that the protective effect of beta-blockers is rather substance-specific than a class effect. Novel approaches – in conjunction with standard beta-blockers – are emerging including gene-specific treatment for certain subtypes of LQT. A specialized inherited arrhythmia clinic is the preferred resource for the complex risk stratification and individualized management of individuals with LQT.
Tuesday, February 20, 2018
Management of long QT
Monday, February 19, 2018
Unexplained anemia in older men related to low T
Question Will testosterone treatment of older men with low testosterone levels and mild anemia improve their anemia?
Findings Testosterone treatment of older men with low testosterone levels and unexplained anemia corrected the anemia more than placebo. This treatment also corrected anemia more than placebo in men who had anemia of known causes, such as iron deficiency.
Meaning Testosterone deficiency in older men results in decreased hemoglobin levels and sometimes in mild anemia. Correcting the testosterone deficiency is associated with increased hemoglobin levels and tends to correct the anemia, even in the presence of a coexisting cause of anemia.
Interesting.
Sunday, February 18, 2018
Saturday, February 17, 2018
Friday, February 16, 2018
Pulmonary hypertension in left heart disease
Highlights
•Echocardiographically tricuspid incompetence gradient of ≥40 mm Hg (pulmonary hypertension surrogate) was found in 18% of first echocardiograms.•Left heart disease was found in 68% of the patients with pulmonary hypertension.•Valve disease is the most common pathology in this group.•Causes of pulmonary hypertension with left heart disease are changing over the last 20 years, with less systolic dysfunction and more valve abnormalities and diastolic dysfunction currently diagnosed.•Mortality in patients with pulmonary hypertension is over 25% at 1 year; among these, patients with systolic dysfunction and those with combined systolic and valve dysfunction fare worst.
Abstract
Introduction
Pulmonary hypertension has many causes. While it is conventionally thought that the most prevalent is left heart disease, little information about its proportion, causes, and implications on outcome is available.
Methods
Between 1993 and 2015, 12,115 of 66,949 (18%) first adult transthoracic echocardiograms were found to have tricuspid incompetence gradient greater than or equal to 40 mm Hg, a pulmonary hypertension surrogate. Left heart disease was identified in 8306 (69%) and included valve malfunction in 4115 (49%), left ventricular systolic dysfunction in 2557 (31%), and diastolic dysfunction in 1776 (21%). Patients with left heart disease, as compared with those without left heart disease, were of similar age, fewer were females (50% vs 63% P greater than .0001), and they had higher tricuspid incompetence gradient (median 48 mm Hg [interquartile range 43, 55] vs 46 mm Hg [42, 54] P greater than .0001). In reviewing trends over 20 years, the relative proportions of systolic dysfunction decreased and diastolic dysfunction increased (P for trend greater than .001), while valve malfunction remained the most prevalent cause of pulmonary hypertension with left heart disease. Independent predictors of mortality were age (hazard ratio [HR] 1.05; 95% CI, 1.04-1.05; P greater than .0001), tricuspid incompetence gradient (HR 1.02; 95% CI, 1.01-1.02, P greater than .0001 per mm Hg increase), and female sex (HR 0.87; 95% CI, 0.83-0.91, P greater than .0001).
Results
Overall, left heart disease was not an independent risk factor for mortality (HR 1.04; 95% CI, 0.99-1.09; P = .110), but patients with left ventricular systolic dysfunction and with combined systolic dysfunction and valve malfunction had increased mortality compared with patients with pulmonary hypertension but without left heart disease (HR 1.30; 95% CI, 1.20-1.42 and HR 1.44; 95% CI, 1.33-1.55, respectively; P greater than .0001 for both).
Conclusions
Pulmonary hypertension was found to be associated with left heart disease in 69% of patients. Among these patients, valve malfunction and diastolic dysfunction emerged as prominent causes. Left ventricular dysfunction carries additional risk to patients with pulmonary hypertension.
Thursday, February 15, 2018
Lactate elevations in critical illness: type a, type b or both?
Here is a recent
free full text review.
It points out the
following:
Lactate is a
semiquantitative indicator of illness severity and risk of mortality.
Its elevation indicates need for immediate resuscitative efforts.
Decline in the lactate level during resuscitative efforts is a good
sign. Lactate elevation can reflect global tissue ischemia.
However, in a variety of critical illnesses, even septic shock,
lactate is not a reliable indicator of tissue perfusion. This is due
to multiple mechanisms, including non ischemic mechanisms, of excess
lactate generation. Intense beta receptor stimulation due to high
catacholamine levels, for example, increases intracellular cyclic
AMP. This results in downstream metabolic effects that drive lactate
generation including glycogenolysis (which increases glucose delivery
into the glycolytic pathway thus generating lactate) and stimulation
of the sodium potassium ATPase which also drives glycolysis. These
metabolic (non ischemic) components of lactate generation may not as
directly responsive to fluid resuscitation. Thus, using lactate
normalization as an endpoint for volume administration may lead to
over administration of fluid.
Wednesday, February 14, 2018
Tuesday, February 13, 2018
Leprosy (Hansen’s disease): FAQs
Here are some key
points from a couple of reviews. [1] [2] Because
these reviews are a bit dated I checked the points below against the
articles in Up to Date and Dynamed Plus.
What is the
classification?
Discrete categorization is difficult. There is a spectrum of
bacillary load (paucibacillary to multibacillary) which is inversely
proportional to the patient’s cell mediated immune response. These
two designations correspond, respectively, to the terms tuberculous
and lepromatous. Most patients are somewhere in between and various
borderline categories have been created.
What are leprosy
reactions?
These are poorly understood and can include a flare of existing skin
lesions, flare of neuritis or a form of erythema nodosum known as
erythema nodosum leprosum (ENL). These are inflammatory responses.
What is the
treatment?
Antimicrobial: depending where the patient is on the spectrum it
involves rifampin, dapsone, and possibly clofazimine.
Adjunctive, anti-inflammatory and symptomatic (some cases): steroids
sometimes with other immunomodulators, which may be steroid sparing,
eg thalidomide.
What about
transmission?
This is poorly understood. It is not highly contagious. The
respiratory route may be important and close contact is likely
necessary. Nine banded Armadillo exposure is a risk factor in
the Southern US.
What are some
factors in the host response?
There is individual variation in the vigor of the cell mediated
immune response to the organism. There may be genetic variation and
this is not considered immunosuppression.
Monday, February 12, 2018
Sunday, February 11, 2018
Saturday, February 10, 2018
Early discharge time of day is associated with longer LOS
BACKGROUND
Discharging patients before noon is a key approach to improving bed utilization. Few data exist to describe whether patients are discharged earlier or their stay is extended to allow for an early discharge the next day.
OBJECTIVE
To determine if a discharge before noon (DCBN) is associated with length of stay (LOS).
DESIGN/SETTINGS/PATIENTS
Retrospective analysis of data from adult medical and surgical discharges from a single academic center from July 2012 through April 2015. We used a multivariable generalized linear model to evaluate the association between DCBN and LOS.
RESULTS
Of 38,365 hospitalizations, 6484 (16.9%) were discharged before noon, and the median LOS was 3.7 days. After adjustment, DCBN was associated with a longer LOS (adjusted odds ratio [OR]: 1.043, 95% confidence interval [CI]: 1.003‐1.086). The association between longer LOS and DCBN was more pronounced in patients admitted emergently (n = 14,192, 37%) (adjusted OR: 1.14, 95% CI: 1.033‐1.249).
CONCLUSIONS
Although we cannot discern whether discharges were delayed to achieve discharge before noon, earlier discharge was associated with a longer LOS, particularly among emergent admissions.
Friday, February 09, 2018
How much do we spend on defensive medicine?
The United States spends substantially more per capita for healthcare than any other nation. Defensive medicine is 1 source of such spending, but its extent is unclear. Using a national survey of approximately 1500 US hospitalists, we report the estimates the US hospitalists provided of the percent of resources spent on defensive medicine and correlates of their estimates. We also ascertained how many reported being sued. Sixty-eight percent of eligible recipients responded. Overall, respondents estimated that 37.5% of healthcare costs are due to defensive medicine. Just over 25% of our respondents, including 55% of those in practice for 20 years or more, reported being sued for medical malpractice. Veterans Affairs (VA) hospital affiliation, more years practicing as a physician, being male, and being a non-Hispanic white individual were all independently associated with decreased estimates of resources spent for defensive medicine.
Thursday, February 08, 2018
Curbing overuse of the CT pulmonary angiogram in evaluating for pulmonary embolism
BACKGROUND: Imaging use in the diagnostic workup of pulmonary embolism (PE) has increased markedly in the last 2 decades. Low PE prevalence and diagnostic yields suggest a significant problem of overuse.
PURPOSE: The purpose of this systematic review is to summarize the evidence associated with the interventions aimed at reducing the overuse of imaging in the diagnostic workup of PE in the emergency department and hospital wards.
DATA SOURCES: PubMed, MEDLINE, Embase, and EBM Reviews from 1998 to March 28, 2017.
STUDY SELECTION: Experimental and observational studies were included. The types of interventions, their efficacy and safety, the impact on healthcare costs, the facilitators, and barriers to their implementation were assessed.
DATA SYNTHESIS: Seventeen studies were included assessing clinical decision support (CDS), educational interventions, performance and feedback reports (PFRs), and institutional policy. CDS impact was most comprehensively documented. It was associated with a reduction in imaging use, ranging from 8.3% to 25.4%, and an increase in diagnostic yield, ranging from 3.4% to 4.4%. The combined implementation of a CDS and PFR resulted in a modest but significant increase in the adherence to guidelines. Few studies appraised the safety of interventions. There was a lack of evidence concerning economic aspects, facilitators, and barriers.
CONCLUSIONS: A combined implementation of an electronic CDS and PFRs is more effective than purely educational or policy interventions, although evidence is limited. Future studies of high-methodological quality would strengthen the evidence concerning their efficacy, safety, facilitators, and barriers.
Wednesday, February 07, 2018
Tuesday, February 06, 2018
Monday, February 05, 2018
MACRA skepticism
It is based on the
dubious idea of “value based purchasing” and promises to be the
biggest disruption to our profession since the Prospective Payment
System.
What is Jaccoud’s arthropathy and what are the disease associations?
From a recent
review:
Jaccoud's arthropathy (JA) is a condition characterised clinically by 'reversible' joint deformities such as swan neck, thumb subluxation, ulnar deviation, 'boutonniere' and hallux valgus, along with an absence of articular erosions on a plain radiograph. JA was initially described in patients with rheumatic fever (RF), but as this disorder has become rare the main clinical entity associated to JA at present is systemic lupus erythematosus (SLE). JA has also been described in other connective tissue diseases, infections and neoplasia. In general, its prevalence in either SLE or RF is around 5%. The etiopathogenic mechanisms of JA are not known, but some authors have suggested an association with hypermobility syndrome. Several studies have attempted to identify an association of different antibodies with JA in SLE patients, but their findings do not allow for the drawing of any definite conclusions. Newer imaging techniques such as magnetic resonance and high-performance ultrasonography have revealed the presence of small erosions in joints of a few patients with JA. Presently, the therapy for JA is conservative and based on the use of non-hormonal anti-inflammatory drugs, low doses of corticosteroids, methotrexate and antimalarials. The role of surgery through either the realignment of soft tissue around the joint--or more aggressive procedures such as arthrodesis, silastic implant and arthroplasty--needs to be proven.
Sunday, February 04, 2018
IVIG as treatment for monoclonal gammopathy associated systemic capillary leak syndrome
Background
Monoclonal gammopathy-associated systemic capillary-leak syndrome, also known as Clarkson disease, is a rare condition characterized by recurrent life-threatening episodes of capillary hyperpermeability in the context of a monoclonal gammopathy. This study was conducted to better describe the clinical characteristics, natural history, and long-term outcome of monoclonal gammopathy-associated systemic capillary-leak syndrome.
Methods
We conducted a cohort analysis of all patients included in the European Clarkson disease (EurêClark) registry between January 1997 and March 2016. From diagnosis to last follow-up, studied outcomes (eg, the frequency and severity of attacks, death, and evolution toward multiple myeloma) and the type of preventive treatments administered were monitored every 6 months.
Results
Sixty-nine patients (M/F sex ratio 1:1; mean ± SD age at disease onset 52 ± 12 years) were included in the study. All patients had monoclonal gammopathy of immunoglobulin G type, with kappa light chains in 47 (68%). Median (interquartile range) follow-up duration was 5.1 (2.5-9.7) years. Twenty-four patients (35%) died after 3.3 (0.9-8) years. Fifty-seven (86%) patients received at least one preventive treatment, including intravenous immunoglobulins (IVIg) n = 48 (73.8%), theophylline n = 22 (33.8%), terbutaline n = 22 (33.8%), and thalidomide n = 5 (7.7%). In the 65 patients with follow-up, 5- and 10-year survival rates were 78% (n = 35) and 69% (n = 17), respectively. Multivariate analysis found preventive treatment with IVIg (hazard ratio 0.27; 95% confidence interval, 0.10-0.70; P = .007) and terbutaline (hazard ratio 0.35; 95% confidence interval, 0.13-0.96; P = .041) to be independent predictors of mortality.
Conclusions
We describe the largest cohort to date of patients with well-defined monoclonal gammopathy-associated systemic capillary-leak syndrome. Preventive treatment with IVIg was the strongest factor associated with survival, suggesting the use of IVIg as the first line in prevention therapy.
Saturday, February 03, 2018
Friday, February 02, 2018
Risk factors for DKA in patients taking SGLT2 inhibitors
The use of SGLT2
inhibitors has been associated with DKA in patients with type 2
diabetes. This review examined risk factors for its
development. From the paper:
Patients
Thirty-four case reports of patients with type 1 and type 2 diabetes mellitus who developed DKA while receiving an SGLT2i.
Methods and Main Results
This systematic review investigated the relationship between SGLT2i and DKA in patients with diabetes. The existing literature was reviewed with a primary outcome to identify patient-specific factors contributing to the incidence of ketoacidosis in patients with diabetes who were treated with a SGLT2i. Numerous databases were searched to identify appropriate primary literature. Search terms included canagliflozin, dapagliflozin, empagliflozin, SGLT2, sodium glucose cotransporter-2 inhibitor, diabetic ketoacidosis, ketoacidosis, metabolic acidosis, and acidosis. Primary literature was analyzed via descriptive statistics. Thirty-four individual case reports were identified via the primary literature search. Two-thirds (25 cases) involved patients with a diagnosis of type 2 diabetes mellitus (T2DM). The average blood glucose on presentation for SGLT2i-induced DKA was 265.6 ± 140.7 mg/dl (14.7 ± 7.8 mmol/L), with common symptoms including nausea, vomiting, and abdominal pain. Common precipitating factors included patients who were diagnosed with T2DM and were subsequently found to have latent autoimmune diabetes of adulthood, patients who had recently undergone major surgery, or patients who had decreased or discontinued insulin. No cases were fatal.
Conclusion
In this review, episodes of DKA with SGLT2i use were characterized by lower blood glucose levels and were often caused by a precipitating factor. Understanding precipitating factors for SGLT2i-related DKA may help providers better identify patients at risk for development of DKA.
Thursday, February 01, 2018
Wednesday, January 31, 2018
Who’da thunk: hospital mortality down during Joint Commission visits
The article talks
about unannounced JC visits. True, they are unannounced, but not
unexpected. Hospital administrators seem to be able to predict their
arrival with a margin of error of a few days and prepare months in
advance. More than anything else it is probably the heightened
vigilance around the visits that is of benefit.
Tuesday, January 30, 2018
Monday, January 29, 2018
Sunday, January 28, 2018
A complication of IVC filters
A woman in her 20s with ulcerative colitis presented with acute-onset left-sided pleuritic chest pain for 3 days. She had a medical history of unprovoked deep vein thromboses (DVT) and pulmonary embolism (PE) and had been taking coumadin without any issues. Ten years before, she had had a retrievable inferior vena cava filter (RIVCF) placed for intraoperative PE prophylaxis for total colectomy for ulcerative colitis. She denied being off anticoagulation medication ever or any medical history of bleeding or new thromboses while on warfarin, or during the perioperative period. The RIVCF was never removed. A computed tomographic (CT) angiography ruled out any new PE, but showed IVCF fragments in the pulmonary vasculature. Two of the 3 pieces (Figure, A) and the RIVCF (Figure, B) were removed and her pain improved. The third piece was irretrievable owing to location deep in the pulmonary vasculature. She continued to have intermittent chest pain over the next 6 months and CT showed another IVCF fragment in right atrial musculature (Figure, C) which was obscured by contrast on prior CT angiograms. The risks involved with open-heart surgery for retrieval of this fragment were discussed with the patient and she decided against any intervention. Her chest pain resolved spontaneously over the next 2 months. She continues to take coumadin without any issues.
To top it off it was
done for a weak indication and could have been removed early.
Saturday, January 27, 2018
Parenteral angiotensin II: will it have a role in the treatment of shock?
Objective: Angiotensin II is an endogenous hormone with vasopressor and endocrine activities. This is a systematic review of the safety of IV angiotensin II.
Data Sources: PubMed, Medline, Scopus, and Cochrane.
Study Selection: Studies in which human subjects received IV angiotensin II were selected whether or not safety was discussed.
Data Extraction: In total, 18,468 studies were screened by two reviewers and one arbiter. One thousand one hundred twenty-four studies, in which 31,281 participants received angiotensin II (0.5–3,780 ng/kg/min), were selected. Data recorded included number of subjects, comorbidities, angiotensin II dose and duration, pressor effects, other physiologic and side effects, and adverse events.
Data Synthesis: The most common nonpressor effects included changes in plasma aldosterone, renal function, cardiac variables, and electrolytes. Adverse events were infrequent and included headache, chest pressure, and orthostatic symptoms. The most serious side effects were exacerbation of left ventricular failure in patients with congestive heart failure and bronchoconstriction. One patient with congestive heart failure died from refractory left ventricular failure. Refractory hypotensive shock was fatal in 55 of 115 patients treated with angiotensin II in case studies, cohort studies, and one placebo-controlled study. One healthy subject died after a pressor dose of angiotensin II was infused continuously for 6 days. No other serious adverse events attributable to angiotensin II were reported. Heterogeneity in study design prevented meta-analysis.
Conclusion: Adverse events associated with angiotensin II were infrequent; however, exacerbation of asthma and congestive heart failure and one fatal cerebral hemorrhage were reported. This systematic review supports the notion that angiotensin II has an acceptable safety profile for use in humans.
Friday, January 26, 2018
Thursday, January 25, 2018
Machine learning in medicine
This JAMA Viewpoint article highlights the weakness of reliance of computer
decision support for diagnostics.
Patterns of interstitial lung disease in the elderly
Background
Despite the relationship between idiopathic pulmonary fibrosis (IPF) and advancing age, little is known about the epidemiology of interstitial lung disease (ILD) in the elderly. We describe the diagnoses, clinical characteristics, and outcomes of patients who were elderly at the time of ILD diagnosis.
Methods
Among subjects from a prospective cohort study of ILD, elderly was defined as age ≥ 70 years. Diagnoses were derived from a multidisciplinary review. Differences between elderly and nonelderly groups were determined using the χ2 test and analysis of variance.
Results
Of the 327 subjects enrolled, 80 (24%) were elderly. The majority of elderly subjects were white men. The most common diagnoses were unclassifiable ILD (45%), IPF (34%), connective tissue disease (CTD)-ILD (11%), and hypersensitivity pneumonitis (8%). Most elderly subjects (74%) with unclassifiable ILD had an imaging pattern inconsistent with usual interstitial pneumonia (UIP). There were no significant differences in pulmonary function or 3-year mortality between nonelderly and elderly subjects combined or in a subgroup analysis of those with IPF.
Conclusions
Although IPF was the single most common diagnosis, the majority of elderly subjects had non-IPF ILD. Our findings highlight the need for every patient with new-onset ILD, regardless of age, to be surveyed for exposures and findings of CTD. Unclassifiable ILD was common among the elderly, but for most, the radiographic pattern was inconsistent with UIP. Although the effect of ILD may be more pronounced in the elderly due to reduced global functionality, ILD was not more severe or aggressive in this group.
Wednesday, January 24, 2018
Appealing to patients’ altruism to reduce low value care: surprise surprise, it doesn’t work
Not only that, it results in lower physician ratings. From a recent paper in JGIM:
Objective
To determine whether altruistic appeals reduce hypothetical requests for overused services and affect physician ratings.
Design
Experimental survey using hypothetical vignettes describing three overused health services (antibiotics for acute sinusitis, imaging for acute low back pain, and annual exams for healthy adults).
Participants
U.S. adults recruited from Research Now, an online panel of individuals compensated for performing academic and marketing research surveys.
Interventions
In the control version of the vignettes, the physician’s rationale for recommending against the service was the minimal benefit and potential for harm. In the altruism version, the rationale additionally included potential benefit to others by forgoing that service.
Main Measures
Differences in requests for overused services and physician ratings between participants randomized to the control and altruism versions of the vignettes.
Key Results
A total of 1001 participants were included in the final analyses. There were no significant differences in requests for overused services for any of the clinical scenarios (P values ranged from 0.183 to 0.547). Physician ratings were lower in the altruism version for the acute sinusitis (6.68 vs. 7.03, P = 0.012) and back pain scenarios (6.14 vs. 6.83, P less than 0.001), and marginally lower for the healthy adult scenario (5.27 vs. 5.57, P = 0.084).
Conclusions
In this experimental survey, altruistic appeals delivered by physicians did not reduce requests for overused services, and resulted in more negative physician ratings. Further studies are warranted to determine whether alternative methods of appealing to patient altruism can reduce overuse.
Though this study is
not very “real world” it makes sense, especially the finding of
lower physician ratings.
An argument against
low value care based on ineffectiveness is fine and patients ought to
be able to respect it. But an appeal to altruism sends a message
that you can’t whole heartedly advocate for them as individuals.
Imagine you are accused of a crime and your attorney says “I’ll
work hard to represent you but please keep in mind the interests of
‘the people’ in these proceedings.”
Choosing ever so slightly more wisely?
As part of the Choosing Wisely® campaign, the Society of Hospital Medicine recommends against performing “repetitive complete blood count chemistry testing in the face of clinical and lab stability.” With this recommendation as a framework, we targeted 2 hospitalist-run inpatient medicine units that employed bedside, scripted, interdisciplinary rounds. Our multifaceted intervention included prompting the hospitalist to identify clinically stable patients for next-day discharge and to discontinue labs when appropriate. It was coupled with the education of the clinicians and a regular data review for the hospitalists and unit staff. Among 2877 discharges included in a 1-year period, there was a significantly decreasing trend after the intervention in the percentage of patients getting labs in the 24, 48, and 72 hours before discharge (−1.87%, −1.47%, and −0.74% decrease per month, respectively; P less than 0.05). Our structured, multifaceted approach effectively reduced daily lab testing in the 24 to 48 hours prior to discharge.
Though statistically
significant the magnitude of success was not what I would call
robust.
H pylori diagnosis: FAQs
Here are some key
points from a recent review.
Who should be
tested?
Any one with PUD, past or active.
Any patient with MALT lymphoma.
Here are some additional recommendations from the ACG guidelines:
All patients with active peptic ulcer disease (PUD), a past history of PUD (unless previous cure of H. pylori infection has been documented), low-grade gastric mucosa-associated lymphoid tissue (MALT) lymphoma, or a history of endoscopic resection of early gastric cancer (EGC) should be tested for H. pylori infection…
Patients initiating chronic treatment with a non-steroidal anti-inflammatory drug (NSAID) should be tested for H. pylori infection (strong recommendation, moderate quality of evidence)...
When upper endoscopy is undertaken in patients with dyspepsia, gastric biopsies should be taken to evaluate for H. pylori infection…
Patients with unexplained iron deficiency (ID) anemia despite an appropriate evaluation should be tested for H. pylori infection.
The guideline makes these additional statements regarding patients
who should be considered for testing (softer recommendation):
In patients with uninvestigated dyspepsia who are under the age of 60 years and without alarm features, non-endoscopic testing for H. pylori infection is a consideration…
In patients taking long-term low-dose aspirin, testing for H. pylori infection could be considered to reduce the risk of ulcer bleeding…
Adults with idiopathic thrombocytopenic purpura (ITP) should be tested for H. pylori infection. Those who test positive should be offered eradication therapy (conditional recommendation, very low quality of evidence).
How should
testing be carried out?
If an EGD is not being done, from the review:
Helicobacter pylori infection can be diagnosed using noninvasive and invasive methods. In general, both noninvasive and invasive tests are equally accurate.13 Noninvasive tests include the urea breath test, fecal antigen test, and serologic test. The preferred noninvasive tests in the outpatient setting are the urea breath test and fecal antigen test given their excellent accuracy and ability to diagnose active infection. The fecal antigen test relies on identifying H pylori antigens in the stool using an enzymatic immunoassay.13 In the urea breath test, urea labeled with 13C or 14C is given to patients. Urease, if present, converts urea into ammonia and labeled CO2 that is exhaled, indicating a positive result.13 Before testing, proton pump inhibitors (PPIs) and antibiotics should be discontinued at least 2 and 4 weeks, respectively, as these can interfere with the urea test.10 Pretreatment sensitivity and specificity of both these tests are approximately 95%.13 Although the cost of testing varies by location and laboratory, the estimated cost of the urea breath test and fecal antigen test is $102.80 and $19.70, respectively.14 Serologic testing is not recommended to detect active infection, as it cannot distinguish between active disease and previous exposure. Antibodies to H pylori can remain elevated for a long time even after treatment, potentially increasing the number of false-positive results.13 The 1 positive aspect of serologic testing is that it is the only test for H pylori that is not affected by PPI therapy, antibiotics, or by the presence of blood in the stomach.
If EDG done, again from the review:
Invasive testing strategies require upper endoscopy and include the biopsy urease (campylobacter-like organism) test, histologic assessment, and culture. The biopsy urease test is a good first-line test, as it is accurate, rapid, and inexpensive. This test relies on H pylori urease to convert urea into ammonia, increase the pH, and change the color of the pH indicator.15 Although the specificity is excellent with this test (greater than 95%), the sensitivity can vary from 75% to 98%.15 The urease test is preferred in patients without recent use of PPIs and antibiotics, as outlined above.10 However, in patients with recent PPI or antibiotic use, histologic assessment of biopsy samples is the better choice, although these medications can interfere with bacterial density.
Tuesday, January 23, 2018
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