Hereditary spherocytosis secondary prevention: Difference between revisions
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{{Hereditary spherocytosis}} | {{Hereditary spherocytosis}} | ||
{{CMG}} {{ | {{CMG}} {{shyam}} {{AE}} | ||
{{ | |||
==Overview== | ==Overview== | ||
The administration of [[Vaccine|vaccines]] including [[Pneumococcal vaccine|pneumococcal]], [[Haemophilus influenzae|hemophilus influenzae]], [[Neisseria meningitidis|meningococcal]] and [[Influenza vaccine|influenza]] should be given two to three weeks before [[splenectomy]]. [[Folic Acid|Folic acid]] supplementation as well as oral [[penicillin]] is also suggested for postsplenectomy [[Patient|patients]] untill reaching [[Adult|adulthood]]. | |||
==Secondary Prevention== | ==Secondary Prevention== | ||
* In general, once the diagnosis and baseline severity of | * The administration of [[Vaccine|vaccines]] ([[Pneumococcal vaccine|pneumococcal]], [[haemophilus influenzae type b]], [[Neisseria meningitidis|meningococcal group C]] and [[Influenza vaccine|influenza]]) is indicated 2 to 3 weeks before [[splenectomy]].<ref>{{Cite journal | ||
| author = [[Sayeeda Huq]], [[Mark A. C. Pietroni]], [[Hafizur Rahman]] & [[Mohammad Tariqul Alam]] | |||
| title = Hereditary spherocytosis | |||
| journal = [[Journal of health, population, and nutrition]] | |||
| volume = 28 | |||
| issue = 1 | |||
| pages = 107–109 | |||
| year = 2010 | |||
| month = February | |||
| pmid = 20214092 | |||
}}</ref> | |||
* Postsplenectomy [[Patient|patients]] should also be given 1mg of [[Folic Acid|folic acid]] daily for preventing secondary [[folic acid deficiency]] and oral [[penicillin]] ([[penicillin V]]) for preventing [[secondary infection]] until reaching [[Adult|adulthood]]. | |||
* In general, once the [[diagnosis]] and baseline severity of [[hereditary spherocytosis]] in a [[child]] are established, it is not necessary to perform repeated [[Blood test|blood tests]] unless there is an additional [[clinical]] [[Indication (medicine)|indication]] (such as intercurrent [[infection]] and [[pallor]], or an increase in [[jaundice]]).<ref>{{cite web |url=http://dx.doi.org/10.1136/adc.2003.034587 |title=Hereditary spherocytosis; new guidelines | Archives of Disease in Childhood |format= |work= |accessdate=}}</ref> | |||
* Avoidance of precipitants of hemolysis (such as sulfa drugs or quinines) and certain foods (such as fava beans) may help prevent hemolysis. | |||
==References== | ==References== | ||
Latest revision as of 04:03, 19 December 2018
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Shyam Patel [2] Associate Editor(s)-in-Chief:
Overview
The administration of vaccines including pneumococcal, hemophilus influenzae, meningococcal and influenza should be given two to three weeks before splenectomy. Folic acid supplementation as well as oral penicillin is also suggested for postsplenectomy patients untill reaching adulthood.
Secondary Prevention
- The administration of vaccines (pneumococcal, haemophilus influenzae type b, meningococcal group C and influenza) is indicated 2 to 3 weeks before splenectomy.[1]
- Postsplenectomy patients should also be given 1mg of folic acid daily for preventing secondary folic acid deficiency and oral penicillin (penicillin V) for preventing secondary infection until reaching adulthood.
- In general, once the diagnosis and baseline severity of hereditary spherocytosis in a child are established, it is not necessary to perform repeated blood tests unless there is an additional clinical indication (such as intercurrent infection and pallor, or an increase in jaundice).[2]
- Avoidance of precipitants of hemolysis (such as sulfa drugs or quinines) and certain foods (such as fava beans) may help prevent hemolysis.
References
- ↑ Sayeeda Huq, Mark A. C. Pietroni, Hafizur Rahman & Mohammad Tariqul Alam (2010). "Hereditary spherocytosis". Journal of health, population, and nutrition. 28 (1): 107–109. PMID 20214092. Unknown parameter
|month=ignored (help) - ↑ "Hereditary spherocytosis; new guidelines | Archives of Disease in Childhood".