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Hypercalcaemia preceding diagnosis of Pneumocystis jirovecii pneumonia in renal transplant recipients.
Ling, Jonathan; Anderson, Tara; Warren, Sanchia; Kirkland, Geoffrey; Jose, Matthew; Yu, Richard; Yew, Steven; Mcfadyen, Samantha; Graver, Alison; Johnson, William; Jeffs, Lisa.
Afiliação
  • Ling J; Department of Nephrology, Royal Hobart Hospital, Hobart, Tasmania, Australia.
  • Anderson T; Department of Infectious Diseases, Royal Hobart Hospital, Hobart, Tasmania, Australia.
  • Warren S; Department of Infectious Diseases, Royal Hobart Hospital, Hobart, Tasmania, Australia.
  • Kirkland G; Department of Nephrology, Royal Hobart Hospital, Hobart, Tasmania, Australia.
  • Jose M; Department of Nephrology, Royal Hobart Hospital, Hobart, Tasmania, Australia.
  • Yu R; School of Medicine, University of Tasmania, Hobart, Tasmania, Australia.
  • Yew S; Department of Nephrology, Royal Hobart Hospital, Hobart, Tasmania, Australia.
  • Mcfadyen S; Department of Nephrology, Royal Hobart Hospital, Hobart, Tasmania, Australia.
  • Graver A; Department of Nephrology, Royal Hobart Hospital, Hobart, Tasmania, Australia.
  • Johnson W; Department of Nephrology, Royal Hobart Hospital, Hobart, Tasmania, Australia.
  • Jeffs L; Department of Nephrology, Royal Hobart Hospital, Hobart, Tasmania, Australia.
Clin Kidney J ; 10(6): 845-851, 2017 Dec.
Article em En | MEDLINE | ID: mdl-29225815
ABSTRACT

BACKGROUND:

The overall incidence of Pneumocystis jirovecii pneumonia (PJP) in solid organ transplant recipients is 5-15%. A timely diagnosis of PJP is difficult and relies on imaging and detection of the organism.

METHODS:

We present a case series of four patients displaying hypercalcaemia with an eventual diagnosis of PJP and document the management of the outbreak with a multidisciplinary team approach. We discuss the underlying pathophysiology and previous reports of hypercalcaemia preceding a diagnosis of PJP. We also reviewed the evidence concerning PJP diagnosis and treatment.

RESULTS:

Within our renal transplant cohort, four patients presented within 7 months with hypercalcaemia followed by an eventual diagnosis of PJP. We measured their corrected calcium, parathyroid hormone (PTH), 1,25-dihydroxycholecalciferol [1,25-(OH)2D3] and 25-hydroxycholecalciferol [25(OH)D] levels at admission and following treatment of PJP. All four patients diagnosed with PJP were 4-20 years post-transplantation. Three of the four patients demonstrated PTH-independent hypercalcaemia (corrected calcium >3.0 mmol/L). The presence of high 1,25(OH)2D3 and low 25(OH)D levels suggest negation of the negative feedback mechanism possibly due to an extrarenal source; in this case, the alveolar macrophages. All four patients had resolution of their hypercalcaemia after treatment of PJP.

CONCLUSIONS:

Given the outbreak of PJP in our renal transplant cohort, and based on previous experience from other units nationally, we implemented cohort-wide prophylaxis with trimethoprim-sulphamethoxazole for 12 months in consultation with our local infectious diseases unit. Within this period there have been no further local cases of PJP.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Revista: Clin Kidney J Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Austrália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Revista: Clin Kidney J Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Austrália