Uvavanyo lwee-electrolyte zokubila

I-sweat electrolyte luvavanyo olulinganisa inqanaba le-chloride ekubileni. Uvavanyo lwe-sweat chloride luvavanyo oluqhelekileyo olusetyenziselwa ukufumanisa i-cystic fibrosis.

Imichiza engenambala, engenavumba ebangela ukubila ifakwa kwindawo encinci engalweni okanye emlenzeni. Umbane ubotshelelwe kuloo ndawo. Umbane wombane obuthathaka uthunyelwa kuloo ndawo ukukhuthaza ukubila.

Abantu banokuziva ngathi bayarhawuzela kuloo ndawo, okanye imvakalelo yobushushu. Eli candelo lenkqubo lihlala malunga nemizuzu emi-5.

Okulandelayo, indawo evuselelweyo iyacocwa kwaye ukubila kuqokelelwa kwisiqwenga sephepha lokucoca okanye i-gauze, okanye kwikhoyili yeplastiki.

Emva kwemizuzu engama-30, ukubila okuqokelelweyo kuthunyelwa kwilebhu yasesibhedlele ukuze kuvavanywe. Ingqokelela ithatha malunga neyure.

Akukho manyathelo akhethekileyo ayimfuneko ngaphambi kovavanyo.

Uvavanyo alubuhlungu. Abanye abantu banemvakalelo yokutswina kwindawo ye-electrode. Olu luvo lunokubangela ukungonwabi kubantwana abancinci.

Uvavanyo lwe-sweat yindlela esemgangathweni yokufumanisa isifo se-cystic fibrosis. Abantu abane-cystic fibrosis banexabiso eliphezulu le-sodium kunye ne-chloride ekubilo kwabo okufunyanwa kuvavanyo.

Abanye abantu bavavanywa ngenxa yeempawu abanazo. E-United States, iinkqubo zovavanyo lweentsana ezisandul 'ukuzalwa kuvavanyo lwe-cystic fibrosis. Uvavanyo lokubila lusetyenziselwa ukuqinisekisa ezi ziphumo.

Iziphumo eziqhelekileyo zibandakanya:

• Iziphumo zovavanyo lwe-sweat chloride ezingaphantsi kwama-30 mmol / L kubo bonke abantu zithetha ukuba i-cystic fibrosis ayinakufane yenzeke.
• Isiphumo esiphakathi kwama-30 ukuya kuma-59 mmol / L asibonisi ngokucacileyo. Olunye uvavanyo luyafuneka.
• Ukuba iziphumo zingama-60 mmol / L okanye ngaphezulu, kukho icystic fibrosis.

Qaphela: mmol / L = millimole ilitha nganye

Amaxabiso esiqhelo ahluka kancinci phakathi kweelebhu ezahlukeneyo. Thetha nomboneleli wakho wezempilo malunga nentsingiselo yeziphumo zakho zovavanyo.

Ezinye iimeko, ezinjengokuphelelwa ngamanzi emzimbeni okanye ukudumba (i-edema) kunokuchaphazela iziphumo zovavanyo.

Uvavanyo olungaqhelekanga lunokuthetha ukuba umntwana une-cystic fibrosis. Iziphumo zinokuqinisekiswa kwakhona luvavanyo lwecandelo lokutshintsha kweCF.

Uvavanyo lokubila; Ukubila i-chloride; Uvavanyo lwe-Iontophoretic sweat; Uvavanyo lweCF - ukubila; Uvavanyo lweCystic fibrosis - ukubila

• Uvavanyo lokubila
• Uvavanyo lokubila

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I-Farrell PM, i-White TB, i-Ren CL, okqhubekayo. Ukuchongwa kwecystic fibrosis: izikhokelo zemvumelwano ezivela kwiCystic Fibrosis Foundation. J Isilwanyana. Ngo-2017; 181S: S4-S15.e1. IINKCUKACHA: 28129811 www.ncbi.nlm.nih.gov/pubmed/28129811.

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