Online Clinical Case Study (March 2004)

Clinical Cardiology Series
臨床心臟科個案研究

The content of the Office Cardiology Series is provided by:
Dr. Cheng Cheung Wah, Boron
M.B.,B.S.(H.K.), M.R.C.P.(U.K.), F.H.K.A.M., F.H.K.C.P., Specialist in Cardiology
Dr. Wong Shou Pang, Alexander
F.R.C.P., F.H.K.A.M.(Med.), F.H.K.C.P., Specialist in Cardiology
Dr. Li Siu Lung, Steven
M.B.,B.S.(H.K.), M.R.C.P.(U.K.), F.H.K.A.M., F.H.K.C.P., F.R.C.P.(Glasg.), F.R.C.P.
(Edin.), Specialist in Cardiology

臨床心臟科個案研究之內容誠蒙鄭長華醫生、王壽鵬醫生及李少隆醫生提供。

Questions on the use of angiotensin converting enzyme inhibitors (ACEI).

Answers

1.

A 43 year old gentleman with good past health presents to you with a left sided weakness. Physical examination is unremarkable. A CAT scan of brain confirms two small right parietal infarcts. Routine blood tests are normal, including a 75gm OGTT and a fasting lipid profile. The EKG is in sinus rhythm. The autoimmune markers and clotting factors screening are normal. What will be the next most appropriate investigation?
(A) Holter study
(B) Echocardiography
(C) MRA
(D) Transcranial Doppler

(B) This is a young patient with cryptogenic stroke. The presence of two small right parietal infarcts points to an embolic phenomenon. An echocardiogram (transthroacic and transesophageal) will help to rule out any cardiac source of emboli.

 

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2.

Patent foramen ovale is associated with cryptogenic stroke. True or false?

Several case control studies using contrast echocardiography have established a strong association between the diagnosis of cryptogenic stroke and the presence of patent foramen ovale (PFO) in young adults less than 55 years of age (1,2,3,4,5) . Therefore, contrast echocardiography with agitated saline and Valsalva maneuver is required to rule out the presence of PFO. At the same time, one needs to look for any high risk characteristics of PFO which predispose patients for paradoxical embolism and stroke. Such features include a large PFO size, a greater degree of right to left shunt as assessed by the amount of crossing microbubbles and atrial septal aneurysm.

 

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3.

What are the treatment options of cryptogenic stroke and the recurrent risk of ischemic events?

 

In this case, contrast echocardiography confirms the presence of a PFO with instantaneous right to left shunt. There are no other high risk characteristics. One may conclude that this gentleman has cryptogenic stroke with presumed paradoxical embolism. Three treatment modalities are currently available: Antiplatelet (aspirin, clopidogrel), antithrombotic agent (warfarin) and PFO closure (surgical or percutaneous). The risk of recurrent neurological events during medical treatment with either aspirin or oral anticoagulant has been retrospectively examined in patients with PFO and cryptogenic stroke less than 60 years of age. The average annual rate of recurrence was 3.4% for the combined endpoint of TIA and CVA (6) . In another study, the average annual recurrence rate was 3.8% with no significant difference between aspirin and anticoagulant (7) . With the availability of percutaneous PFO closure technique, surgical PFO closure is not the procedure of choice in most patients. Concerning the risk of recurrent neurological events after percutaneous PFO closure, Windecker S et al showed that the annual risk of recurrent ischemic events was 3.4% (8) . After all, the best therapeutic modality remains unknown at this time because no head to head comparison between these therapeutic options is available.

 

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4.

This gentleman has recurrent transient ischemic events seven months after the initial event despite sequential treatment with aspirin and warfarin. Once again, all the investigations are normal. What is your management strategy?

 

PFO-occluder is indicated in this gentleman. In April 2002, U.S. Food and Drug Administration (FDA) approved the Amplatzer-PFO-occluder for the non-surgical closure of a patent foramen ovale (PFO) in patients with recurrent cryptogenic stroke due to presumed paradoxical embolism through a PFO and who have failed conventional drug therapy. It is also the authors' practice to reserve percutaneous PFO closure for those patients with failed conventional drug treatment only.

 

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  1. Webster MW, Chancellor AM, Smith HJ, Swift DL, Sharpe DN, Bass NM, Glasgow GL. Patent foramen ovale in young stroke patients Lancet. 1988 Jul 2;2(8601):11-2

  2. Lechat P, Mas JL, Lascault G, Loron P, Theard M, Klimczac M, Drobinski G, Thomas D, Grosgogeat Y. Prevalence of patent foramen ovale in patients with stroke. N Engl J Med. 1988 May 5;318(18):1148-52.

  3. Hausmann D, Mugge A, Becht I, Daniel WG. Diagnosis of patent foramen ovale by transesophageal echocardiography and association with cerebral and peripheral embolic events. Am J Cardiol. 1992 Sep 1;70(6):668-72.

  4. Cabanes L, Mas JL, Cohen A, Amarenco P, Cabanes PA, Oubary P, Chedru F, Guerin F, Bousser MG, de Recondo J. Atrial septal aneurysm and patent foramen ovale as risk factors for cryptogenic stroke in patients less than 55 years of age. A study using transesophageal echocardiography. Stroke. 1993 Dec;24(12):1865-73.

  5. de Belder MA, Tourikis L, Leech G, Camm AJ. Risk of patent foramen ovale for thromboembolic events in all age groups. Am J Cardiol. 1992 May 15;69(16):1316-20.

  6. Mas JL, Zuber M. Recurrent cerebrovascular events in patients with patent foramen ovale, atrial septal aneurysm, or both and cryptogenic stroke or transient ischemic attack. French Study Group on Patent Foramen Ovale and Atrial Septal Aneurysm. Am Heart J. 1995 Nov;130(5):1083-8.

  7. Bogousslavsky J, Garazi S, Jeanrenaud X, Aebischer N, Van Melle G. Stroke recurrence in patients with patent foramen ovale: the Lausanne Study. Lausanne Stroke with Paradoxical Embolism Study Group. Neurology. 1996 May;46(5):1301-5.

  8. Windecker S, Wahl A, Chatterjee T, Garachemani A, Eberli FR, Seiler C, Meier B. Percutaneous closure of patent foramen ovale in patients with paradoxical embolism: long-term risk of recurrent thromboembolic events. Circulation. 2000 Feb 29;101(8):893-8.


Dermatology Series 皮膚科病例研究

An 8 year old boy presented with sudden onset of painful skin rash over both hands for few days. The lesions started as small erythematous macules which enlarged and ruptured easily. There had been two similar attacks within recent 12 months. His past health and family history was unremarkable and there was no history of recent travel. Physical examination revealed superficial erosions and pustules over palms and dorsum of both hands

The content of the Dermatology Series is provided by:
Dr. Chan Loi Yuen and Dr. Tang Yuk Ming, William
Specialist in Dermatology & Venereology

皮膚科病例研究之內容誠蒙陳來源醫生鄧旭明醫生提供。

Answers

1. What is the clinical diagnosis?

The diagnosis is impetigo contagiosa. This is the most common bacterial skin infection in children. Staphylococcus aureus is the most common pathogen. Group A beta-haemolytic streptococcus may also be isolated. In some cases, both organisms can be cultured. The bacteria enter through damaged skin. Impetigo is very contagious and can be spread by direct contact or scratching.

 

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2.

What are the clinical differential diagnoses?

The differential diagnoses include infected eczema, herpes simplex, pustular drug eruption, erythema multiforme, and subcorneal pustular dermatosis.

 

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3. What are the investigations?

A Gram stain of the blister fluid will reveal gram-positive cocci. A skin swab from pustules should be taken for culture and sensitivity test. In patients with recurrent staphylococcal impetigo, nasal swab should be taken as they may be nasal carrier of Staphylococcus aureus.

 

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4. What are the possible complications?

Infection due to nephritogenic Group A beta-haemolytic s t reptococci could be complicated by acute glomerulonephritis occurring in 10-15%. Sepsis may also develop in neonates.

 

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5.

What is the treatment?

The wound should be dressed with antiseptic followed by application of topical antibiotics such as fucidin, mupirocin or bacitracin. Systemic antibiotic is indicated except in mildest cases and may include semisynthetic penicillin (e.g., cloxacillin or erythromycin), first-generation cephalosporins (e.g., cephalexin) or fusidic acid. As the condition is contagious, the patient should not return to school until all lesions clear. Topical mupirocin or systemic rifampicin should be given to eradicate nasal carriage of Staphylococcus aureus if present.

 

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