Objective: To evaluate the diagnostic utility of bone marrow (BM) samp
ling in HIV positive patients. Design: Retrospective cohort analysis.
Setting: Specialist HIV/AIDS service in London. Subjects: 215 consecut
ive HIV infected patients undergoing 246 BM samplings for investigatio
n of pyrexia without localising signs, haematological abnormalities, o
r staging/investigation of lymphoma. Main outcome measure: Diagnostic
yield from (and impact on management of) BM sampling. Results: Of 122
BM samples taken to investigate pyrexia, 33 (27%) revealed the cause o
n microscopy: unexpected lymphoma in seven (6%), mycobacteriosis in 25
(20%), and toxoplasmosis in one (1%). Marrow infiltration was confirm
ed in 11 of 38 BM samples taken for staging/investigation of lymphoma/
leukaemia. In afebrile patients, of 22 with pancytopenia, BM samples s
howed HN associated changes in 17 and specific diagnoses in five (myco
bacterial infection in three, haemophagocytic syndrome in one, and meg
aloblastic change due to vitamin B-12 deficiency in one); of 21 with i
solated thrombocytopenia, 20 (95%) BM samples showed immune thrombocyt
openic purpura to be the cause and the remaining patient had BM change
s of aplasia; of 29 with isolated anaemia, 28 had BM changes of HIV as
sociated dysplasia/erythroid dysplasia and one had unsuspected iron de
ficiency; all 10 with isolated leucopenia/neutropenia had BM changes a
scribed to HIV infection exacerbated by concurrent sepsis or medicatio
n; of four BM samples taken for other reasons, one showed mycobacteria
l infection. Conclusions: BM sampling has diagnostic utility in HIV in
fected patients with pyrexia without localising signs, pancytopenia, a
nd staging/investigation of lymphoma; this test has little value in th
e investigation of afebrile patients with isolated thrombocytopenia, a
naemia, or leucopenia as HIV is usually the underlying cause.