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1.
Dermatitis ; 27(3): 137-42, 2016.
Article En | MEDLINE | ID: mdl-27172309

BACKGROUND: Photoallergic contact dermatitis (PACD) is a hypersensitivity reaction that occurs when a previously photosensitized exogenous agent comes into contact with UV radiation. The best method for testing PACD is photopatch testing (PPT). OBJECTIVES: The primary objective of the study was to determine the frequency of PACD to 20 different photoallergens in common usage in China during a 10-year period. METHODS: All patients (n = 6153) who had PPTs done between 2005 and 2014 at the Department of Dermatology of Huashan Hospital, Fudan University, were included. RESULTS: A total of 3767 PACD reactions in 3668 subjects (59.61%) were recorded. Of these allergens, chlorpromazine (CPZ) (51.82%), para-aminobenzoic acid (11.94%), thimerosal (9.81%), potassium dichromate (6.37%), sulfanilamide (5.38%), and formaldehyde (4.7%) were the top 6 allergens that elicited PACD reactions. A comparison of PACD reactions between January 2005 to December 2009 and January 2010 to December 2014 revealed a statistically significant decrease in PACD reaction for chlorpromazine, potassium dichromate, p-aminobenzoic acid, and p-phenylenediamine. Formaldehyde showed a trend toward a statistically significant increase in sensitization over the 10-year period. CONCLUSIONS: In conclusion, positive PACD reactions were most frequent to chlorpromazine in our population. New allergens such as potassium dichromate and formaldehyde should be added to the test series.


Allergens/adverse effects , Dermatitis, Photoallergic/etiology , 4-Aminobenzoic Acid/adverse effects , Adolescent , Adult , Aged , Aged, 80 and over , Child , China/epidemiology , Chlorpromazine/adverse effects , Dermatitis, Photoallergic/diagnosis , Dermatitis, Photoallergic/epidemiology , Female , Formaldehyde/adverse effects , Humans , Male , Middle Aged , Patch Tests , Potassium Dichromate/adverse effects , Sulfanilamide , Sulfanilamides/adverse effects , Thimerosal/adverse effects , Young Adult
2.
Dermatitis ; 25(1): 22-6, 2014.
Article En | MEDLINE | ID: mdl-24407059

BACKGROUND: Photoallergic contact dermatitis (PACD) is of importance in a proportion of photodermatoses and can be evaluated through photopatch testing (PPT). OBJECTIVES: The objectives of this study were to evaluate the results of PPT and investigate the prevalence of PACD reactions to different photoallergens in Chinese patients at the Department of Dermatology of Huashan Hospital Fudan University during a 7-year period. METHODS: A retrospective PPT study was conducted. During the 7 years, 4957 patients attending for investigation of suspected photodermatoses were tested according to the European consensus methodology with up to 14 allergens prepared according to Chinese National Standards. The reactions were scored using the International Contact Dermatitis Research Group visual scoring system. RESULTS: A total of 3472 PACD reactions in 2454 subjects (49.5%) were recorded. The most common agents were chlorpromazine (44.3%), followed by para-aminobenzoic acid (14.7%), thimerosal (8.9%), and sulfanilamide (6.9%). Allergic contact dermatitis reactions comprised 409 reactions in 399 subjects (8%). Photoinhibition and photoaugmentation of allergic contact dermatitis compromised 3810 reactions in 2412 subjects and 11 reactions in 11 subjects, respectively. Irritant reactions (1928 reactions) were seen in 1140 subjects. CONCLUSIONS: The most predominant photoallergens in our region were chlorpromazine, para-aminobenzoic acid, thimerosal, and sulfanilamide, which likely reflected the particular exposures of this Chinese population.


Allergens/adverse effects , Dermatitis, Photoallergic/etiology , 4-Aminobenzoic Acid/adverse effects , Adolescent , Adult , Aged , Aged, 80 and over , Child , China , Chlorpromazine/adverse effects , Dermatitis, Allergic Contact/etiology , Female , Humans , Male , Middle Aged , Patch Tests , Retrospective Studies , Sulfanilamide , Sulfanilamides/adverse effects , Thimerosal/adverse effects , Ultraviolet Rays/adverse effects , Young Adult
5.
Inflamm Allergy Drug Targets ; 12(1): 61-7, 2013 Feb.
Article En | MEDLINE | ID: mdl-23004005

Peyronie's Disease (PD) is a connective tissue disorder involving the growth of fibrous plaques in penile corpora cavernosa (tunica albuginea). The conservative treatment is indicated in the development stage of PD for at least one year after diagnosis and in case of penile pain. This study was conducted to demonstrate the possible effectiveness of the new substances of Peironimev-plus®. Sixty four patients (age: 29-65 years, mean: 52.57 ± 9.06) diagnosed with PD were enrolled in a medical treatment. All patients underwent the following diagnostic tests: penile ultrasound, photographic documentation of penile curvature, IIEF questionnaire (erectile function score), pain evaluation with Visual Analogue pain Scale (VAS). The patients were divided into two treatment groups with different combinations of drugs: A = Peironimev-plus/oral/one tablet-daily + Verapamil injection (peri-lesional) 10 mg/every two weeks + Verapamil iontophoresis/5 mg/three times a week - for 6 months; B = Verapamil injection (peri-lesional) 10 mg/every two weeks + Verapamil iontophoresis/5 mg/three times a week - for 6 months. Intergroup analysis revealed statistically significant differences: in group A the effective plaque size reduction was -30.8% while in the group B the reduction was -18.0% (p=0.000). In group A the improvement of curvature occurred in 85.1% of the cases while in group B this occurred only in 53.5% (p=0.024), moreover the mean curvature decrease was respectively - 8.7° and - 4.6° (p=0.002). IIEF score was significantly improved in group A patients with erectile dysfunction (p=0.02). Our results suggest that Peironimev-plus is an effective drug in treating PD and it may help to prevent the progression of PD.


4-Aminobenzoic Acid/therapeutic use , Anthocyanins/therapeutic use , Antioxidants/administration & dosage , Biological Therapy/methods , Erectile Dysfunction/prevention & control , Inflammation/drug therapy , Isoflavones/therapeutic use , Penile Induration/drug therapy , Penis/drug effects , Plant Extracts/therapeutic use , Propolis/therapeutic use , Verapamil/therapeutic use , Vitamin E/therapeutic use , 4-Aminobenzoic Acid/adverse effects , Adult , Aged , Anthocyanins/adverse effects , Antioxidants/adverse effects , Antioxidants/therapeutic use , Chronic Disease , Dietary Supplements , Drug Combinations , Erectile Dysfunction/etiology , Humans , Inflammation/complications , Isoflavones/adverse effects , Male , Middle Aged , Penile Induration/complications , Penile Induration/immunology , Penis/pathology , Plant Extracts/adverse effects , Propolis/adverse effects , Vitamin E/adverse effects , Vitamin E/analogs & derivatives
6.
Int J Androl ; 35(3): 424-36, 2012 Jun.
Article En | MEDLINE | ID: mdl-22612478

Today, topical application of sunscreens, containing ultraviolet-filters (UV-filters), is preferred protection against adverse effects of ultraviolet radiation. Evidently, use of sunscreens is effective in prevention of sunburns in various models. However, evidence for their protective effects against melanoma skin cancer is less conclusive. Three important observations prompted us to review the animal data and human studies on possible side effects of selected chemical UV-filters in cosmetics. (1) the utilization of sunscreens with UV-filters is increasing worldwide; (2) the incidence of the malignant disorder for which sunscreens should protect, malignant melanoma, is rapidly increasing and (3) an increasing number of experimental studies indicating that several UV-filters might have endocrine disruptive effects. The selected UV-filters we review in this article are benzophenone-3 (BP-3), 3-benzylidene camphor (3-BC), 3-(4-methyl-benzylidene) camphor (4-MBC), 2-ethylhexyl 4-methoxy cinnamate (OMC), Homosalate (HMS), 2-ethylhexyl 4-dimethylaminobenzoate (OD-PABA) and 4-aminobenzoic acid (PABA). The potential adverse effects induced by UV-filters in experimental animals include reproductive/developmental toxicity and disturbance of hypothalamic-pituitary-thyroid axis (HPT). Few human studies have investigated potential side effects of UV-filters, although human exposure is high as UV-filters in sunscreens are rapidly absorbed from the skin. One of the UV-filters, BP-3, has been found in 96% of urine samples in the US and several UV-filters in 85% of Swiss breast milk samples. It seems pertinent to evaluate whether exposure to UV-filters contribute to possible adverse effects on the developing organs of foetuses and children.


Endocrine Disruptors/pharmacology , Sunburn/prevention & control , Sunscreening Agents/adverse effects , 4-Aminobenzoic Acid/adverse effects , Animals , Benzyl Compounds/adverse effects , Camphor/adverse effects , Camphor/analogs & derivatives , Cinnamates/adverse effects , Humans , Hypothalamo-Hypophyseal System/drug effects , Melanoma/chemically induced , Receptors, Estrogen/drug effects , Salicylates/adverse effects , Skin Neoplasms/chemically induced , Skin Neoplasms/prevention & control , Thyroid Gland/drug effects , Ultraviolet Rays/adverse effects , para-Aminobenzoates
7.
Dermatitis ; 22(6): 332-4, 2011.
Article En | MEDLINE | ID: mdl-22653006

BACKGROUND: p-Phenylenediamine (PPD) is an important allergen; 5.0% of patients tested positive to PPD when patch-tested, according to the North American Contact Dermatitis Group. Hair dyes are the main source of exposure. OBJECTIVE: To assess the significance of PPD allergy at the Ottawa Patch Test Clinic. METHODS: We assessed the epidemiology of PPD allergies and determined the cross-reactivity with other para-amino compounds. Charts of patients visiting the Ottawa Patch Test Clinic between May 1997 and July 2009 were reviewed. RESULTS: One hundred thirty-four patients were found to have a contact allergy to PPD; 75.4% were female, 24.6% were male, 13.4% were hairdressers, 18.7% had a history of atopy, 90.3% were sensitized by hair dye, 2.2% were sensitized by henna tattoos, and 7.5% were sensitized by other sources. Positive patch-test reactions to textile dyes were seen in 24.6%, 7.5% reacted to benzocaine, 6.0% reacted to sulfa drugs, 1.5% reacted to isopropyl-para-phenylenediamine, and 1.5% reacted to para-aminobenzoic acid. CONCLUSIONS: PPD is an important source of allergic contact allergy. Our results show a significant relationship of PPD with other related para-amino compounds.


4-Aminobenzoic Acid/adverse effects , Allergens/adverse effects , Coloring Agents/adverse effects , Dermatitis, Allergic Contact/epidemiology , Phenylenediamines/adverse effects , Amines/adverse effects , Azo Compounds/adverse effects , Canada/epidemiology , Cross Reactions , Dermatitis, Allergic Contact/etiology , Female , Hair Dyes/adverse effects , Humans , Male , Occupational Exposure/adverse effects , Ontario/epidemiology , Patch Tests , Sulfonamides/adverse effects , Textiles , Time Factors
8.
Dermatitis ; 21(4): 185-98, 2010.
Article En | MEDLINE | ID: mdl-20646669

BACKGROUND: Rising use of sunscreen products has led to increased reporting of adverse reactions to sunscreens. OBJECTIVE: To investigate possible photoallergic reactions in patients who identified themselves as "being allergic" to sunscreens. METHODS: Patients filled out questionnaires about types of sunscreens they used and timing of their "allergic" reactions. Next, they consented to be photopatch-tested with active sunscreen ingredients, including the new sunscreen Anthelios SX (containing Mexoryl SX) and the new ultraviolet filters Tinosorb M and Tinosorb S. Standard allergen patch testing was also done. RESULTS: Twenty-seven patients self-reported "sunscreen allergy." Photopatch testing is difficult for patients; hence, only 11 agreed to proceed with the testing. Eight patients had negative patch testing results. One patient reacted to benzophenone-2. Another had a prior reaction to titanium dioxide and titanium oxalate but did not react to the silicone-coated titanium in our study. Yet another patient had relevant photopatch reactions to benzophenone-3 and ethylhexyl dimethyl para-aminobenzoic acid (PABA). None reacted to the Tinosorbs or Anthelios SX. Few positive reactions to the standard allergens were not relevant. CONCLUSION: Although small, this study parallels prior studies in concluding that true delayed type IV hypersensitivity (allergic contact dermatitis and photoallergy) to sunscreens is more infrequent than patients tend to believe.


Dermatitis, Photoallergic/epidemiology , Dermatitis, Photoallergic/etiology , Sunscreening Agents/adverse effects , 4-Aminobenzoic Acid/adverse effects , Benzophenones/adverse effects , Camphanes/adverse effects , Chalcones/adverse effects , Cyanoacrylates/adverse effects , Dermatitis, Photoallergic/diagnosis , Drug Combinations , Female , Humans , Male , Middle Aged , Oxalates/adverse effects , Patch Tests , Phenols/adverse effects , Sulfonic Acids/adverse effects , Surveys and Questionnaires , Titanium/adverse effects , Triazines/adverse effects
9.
Eur J Dermatol ; 20(2): 217-9, 2010.
Article En | MEDLINE | ID: mdl-20153994

A 51-year-old man suffered from an acute eczematous rash confined to the air- and light-exposed areas of the skin. As a construction worker he was exposed to common occupational allergens such as epoxy resins, but there was also remarkable holiday-associated sun exposure. He did not use any sunscreen agents. Several weeks before the onset of skin eruptions, conservative treatment of Peyronie's disease with oral PotabaTM (potassium paraaminobenzoate) had been started. Airborne contact dermatitis to volatile allergens was ruled out, while photopatchtesting revealed photoallergy to paraaminobenzoic acid (PABA). In sunscreens, PABA has mostly been abandoned due to its known topical photosensitization properties, but it has not yet been recognized as a systemic photosensitizer.


4-Aminobenzoic Acid/adverse effects , Dermatitis, Photoallergic/etiology , Penile Induration/drug therapy , Vitamin B Complex/adverse effects , 4-Aminobenzoic Acid/administration & dosage , Humans , Male , Middle Aged , Occupations , Vitamin B Complex/administration & dosage
11.
Drugs Today (Barc) ; 45(1): 21-31, 2009 Jan.
Article En | MEDLINE | ID: mdl-19271029

Osteoarthritis (OA) is the most common arthritis affecting the aging population. This degenerative disease can cause significant pain and functional disability in affected individuals. Despite advances in the retardation of rheumatoid arthritis with disease-modifying agents, comparable oral agents have been relatively unavailable for OA. The mainstays of therapy continue to be acetaminophen and nonsteroidal antiinflammatory medications to manage symptoms. Unfortunately, these medications can precipitate severe adverse events in some patients or may be contraindicated, leaving few choices remaining to control pain and suffering. Glucosamine sulfate and chondroitin sulfate have been evaluated in many studies as agents to relieve pain, improve functional activity, and slow disease progression in OA especially of the hip and knee. Studies have reported conflicting results regarding improvement in the pain and disability associated with OA with the use of glucosamine and chondroitin as single agents; however, when improvement has been demonstrated, the formulation has primarily been glucosamine sulfate combined with chondroitin sulfate. Recently, as a result of information implicating the role of reactive oxygen species and oxidative cellular stress reactions on the onset of neurodegenerative and inflammatory disorders, it has been theorized that medications that could control or alter these reactions might improve or prevent the onset of these conditions. Primorine is a combination of products thought to alter these biochemical oxidative byproducts. Based on current evidence, the use of a combination product of glucosamine sulfate and chondroitin sulfate seems to have the greatest potential as a therapeutic intervention for patients at increased risk from the adverse events of accepted current oral therapies. The use of primorine and its combination of products as an intervention in OA has theoretical advantages but its benefits are unproven. A new product, relamine, is a combination of these three formulations. While no studies have evaluated glucosamine sulfate, chondroitin sulfate and primorine in a single product, it may be an option for those who wish to try an alternate therapy for OA, as there appears to be a low risk for serious adverse events.


Osteoarthritis/drug therapy , 4-Aminobenzoic Acid/administration & dosage , 4-Aminobenzoic Acid/adverse effects , 4-Aminobenzoic Acid/therapeutic use , Aged , Chondroitin Sulfates/administration & dosage , Chondroitin Sulfates/adverse effects , Chondroitin Sulfates/therapeutic use , Clinical Trials as Topic , Drug Combinations , Glucosamine/administration & dosage , Glucosamine/adverse effects , Glucosamine/therapeutic use , Humans , Osteoarthritis/physiopathology , Thioctic Acid/administration & dosage , Thioctic Acid/adverse effects , Thioctic Acid/therapeutic use , Vitamin E/administration & dosage , Vitamin E/adverse effects , Vitamin E/therapeutic use
12.
J Sex Med ; 5(12): 2967-9, 2008 Dec.
Article En | MEDLINE | ID: mdl-18624965

INTRODUCTION: Potassium para-aminobenzoate is an agent used in the treatment of sclerotic diseases including Peyronie's disease of the penis. It has been reported that this medication may have been responsible for cases of acute liver injury. AIM: To inform clinicians of the possibility of an adverse drug event associated with the oral intake of potassium para-aminobenzoate by reporting an additional case and compiling information from previous reports. METHODS: The affected patient's medical records were diligently reviewed; all available and relevant information pertaining to this adverse event is reported. Similar case reports were analyzed and compared, and relevant information was compiled in this report. RESULTS: The patient enjoyed a full biochemical recovery from his hepatitis 4 months after discontinuation of potassium para-aminobenzoate. CONCLUSION: To date, the oral use of potassium para-aminobenzoate has been reported to be linked to acute liver injury in six individuals. Appropriate management of this adverse drug event is the immediate discontinuation of the offending drug and general patient support measures.


4-Aminobenzoic Acid/adverse effects , Chemical and Drug Induced Liver Injury/etiology , Penile Induration/drug therapy , 4-Aminobenzoic Acid/therapeutic use , Administration, Oral , Aged , Chemical and Drug Induced Liver Injury/diagnosis , Chemical and Drug Induced Liver Injury/therapy , Follow-Up Studies , Humans , Liver Function Tests , Male , Treatment Outcome
14.
J Pharmacol Sci ; 102(2): 205-12, 2006 Oct.
Article En | MEDLINE | ID: mdl-17031069

We investigated the effects of 4-(N-{1-[2-(4-cyanophenyl)ethyl]-4-hydroxypiperidin-4-ylmethyl}-N-methylamino)benzoic acid monohydrochloride (M58996), a novel analgesic, on persistent and neuropathic pain in rats. In the formalin test, oral M58996 (0.3 - 10 mg/kg) reduced nociceptive behaviors only in the late phase. In the neuropathic pain model, oral M58996 (1 - 10 mg/kg) attenuated mechanical allodynia and heat hyperalgesia in the nerve-injured paw without affecting normal responses of the uninjured paw. High doses (10 - 100 mg/kg) of oral M58996 did not influence normal motor function. Thus, M58996 had a wide dose range showing antinociceptive, antiallodynic, and antihyperalgesic effects without motor dysfunction. In addition, we studied the possible mechanisms involved in the M58996-induced antinociception. The antinociceptive effect of M58996 was reversed by intrathecal pertussis toxin, an inhibitor of the inhibitory- and other-GTP-binding protein (G(i/o) protein), but not by subcutaneous naloxone, an opioid-receptor antagonist. This effect was also reversed by intracerebroventricular or intrathecal tropisetron, a 5-hydroxytryptamine(3) (5-HT(3))-receptor antagonist, and intraperitoneal bicuculline, a gamma-aminobutyric acid(A) (GABA(A))-receptor antagonist. These results suggest that M58996 produces its antinociceptive effect by a pertussis toxin-sensitive G protein mechanism. In addition, the GABA released by the activation of supraspinal and/or spinal 5-HT(3) receptors is likely to contribute to the M58996-induced antinociception.


Analgesics , Behavior, Animal/drug effects , Pain/drug therapy , Piperidines , Sciatic Neuropathy/drug therapy , para-Aminobenzoates , 4-Aminobenzoic Acid/adverse effects , 4-Aminobenzoic Acid/pharmacology , 4-Aminobenzoic Acid/therapeutic use , Administration, Oral , Analgesics/adverse effects , Analgesics/pharmacology , Analgesics/therapeutic use , Animals , Biogenic Monoamines/metabolism , Disease Models, Animal , Dose-Response Relationship, Drug , Male , Motor Activity/drug effects , Pain/metabolism , Pain/physiopathology , Pain Measurement , Piperidines/adverse effects , Piperidines/pharmacology , Piperidines/therapeutic use , Rats , Rats, Wistar , Receptors, GABA/metabolism , Sciatic Neuropathy/metabolism , Sciatic Neuropathy/physiopathology
15.
J Spinal Disord Tech ; 19(4): 302-4, 2006 Jun.
Article En | MEDLINE | ID: mdl-16778669

Methemoglobinemia, a condition associated with cyanosis and diminished pulse oximetry values, has been reported after use of local anesthetics to facilitate fiberoptic intubation. The majority of reports in the literature detail this development during diagnostic procedures such as endoscopy and bronchoscopy. A case of methemoglobinemia in a multiple-injury patient with an unstable compressive-flexion injury of the cervical spine undergoing fiberoptic intubation is presented. A literature review of this entity is also presented. The patient underwent fiberoptic intubation using topical pharyngeal anesthetics before planned cervical corpectomy, strut grafting and instrumentation. He became acutely cyanotic with abruptly diminished pulse oximetry readings. Subsequent blood gas analysis demonstrated methemoglobinemia. Intravenous methylene blue administration led to an uncomplicated resolution of the condition. Surgeons and anesthesiologists who manage such patients should be aware of methemoglobinemia, a rare but potentially fatal complication related to topical airway anesthetics.


Benzalkonium Compounds/adverse effects , Benzocaine/adverse effects , Cetrimonium Compounds/adverse effects , Intubation/adverse effects , Methemoglobinemia/chemically induced , Methemoglobinemia/diagnosis , Spinal Fractures/pathology , Spinal Fractures/surgery , Tetracaine/adverse effects , para-Aminobenzoates , 4-Aminobenzoic Acid/adverse effects , 4-Aminobenzoic Acid/therapeutic use , Adult , Anesthetics, Local/adverse effects , Anesthetics, Local/therapeutic use , Benzalkonium Compounds/therapeutic use , Benzocaine/therapeutic use , Cetrimonium Compounds/therapeutic use , Drug Combinations , Fiber Optic Technology/instrumentation , Humans , Male , Methemoglobinemia/prevention & control , Tetracaine/therapeutic use
16.
J Voice ; 20(2): 282-90, 2006 Jun.
Article En | MEDLINE | ID: mdl-16314075

The application of topical anesthesia to the oropharynx is a common clinical practice during oral and nasal laryngoscopy. Clinically, questions have been raised about whether topical anesthesia alters laryngeal secretions, which distorts clinical impressions. A double-blind, placebo controlled design was employed to address this issue. Ten premenopausal women with healthy vocal folds and 10 premenopausal women with phonotraumatic lesions underwent oral videolaryngoscopic examinations on subsequent days under both anesthesia and placebo conditions, in counterbalanced order. Video segments were rated by three judges. Dependent variables were balling and pooling of secretions, as previously described in the literature. Statistical analyses failed to reveal any clear effect of topical anesthesia on either secretion balling or pooling for the collapsed data set, but one cannot exclude changes in individual cases. Moreover, there was no evidence that secretions were differentially affected by anesthesia across subject groups. Null results in this data set replicate and extend previously reported findings by other authors. An incidental but potentially interesting finding was that the order of treatment condition (anesthesia versus placebo first) seemed relevant for secretions: Subjects who received the anesthesia condition first tended to show more secretion balling in general, as compared with subjects who received the placebo condition first. Speculation is entertained regarding possible physiological pathways for these incidental findings, which could be relevant for some clinical practice.


Anesthesia, Local/adverse effects , Laryngoscopy , Larynx/metabolism , 4-Aminobenzoic Acid/administration & dosage , 4-Aminobenzoic Acid/adverse effects , Administration, Topical , Adult , Anesthetics, Local/administration & dosage , Anesthetics, Local/adverse effects , Benzalkonium Compounds/administration & dosage , Benzalkonium Compounds/adverse effects , Benzocaine/administration & dosage , Benzocaine/adverse effects , Cetrimonium Compounds/administration & dosage , Cetrimonium Compounds/adverse effects , Cross-Over Studies , Double-Blind Method , Drug Combinations , Female , Humans , Larynx/drug effects , Oropharynx , Regression Analysis , Tetracaine/administration & dosage , Tetracaine/adverse effects , para-Aminobenzoates
19.
J Clin Gastroenterol ; 38(3): 225-9, 2004 Mar.
Article En | MEDLINE | ID: mdl-15128067

During upper gastrointestinal endoscopy, topical oropharyngeal anesthesia with lidocaine and/or benzocaine is used routinely by many endodscopists. Although such a practice is usually safe, there have been a number of reports of methemoglobinemia induced by topical anesthesia. Early treatment is extremely important as the development of methemoglobinemia is potentially fatal. Methemoglobinemia should be considered when oxygen desaturation occurs without another explanation. In this case series, we report 4 cases of methemoglobinemia that followed the liberal application of Cetacaine for ERCP. All patients recovered after appropriate treatment but these cases serve to highlight the potential problem, the importance of early recognition and treatment, and the most appropriate treatment options.


4-Aminobenzoic Acid/adverse effects , Anesthetics, Local/adverse effects , Benzalkonium Compounds/adverse effects , Benzocaine/adverse effects , Cetrimonium Compounds/adverse effects , Cholangiopancreatography, Endoscopic Retrograde/methods , Methemoglobinemia/chemically induced , Tetracaine/adverse effects , para-Aminobenzoates , Administration, Topical , Aged , Drug Combinations , Female , Humans , Male , Methemoglobinemia/diagnosis , Methemoglobinemia/therapy , Middle Aged
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